Long COVID: major findings, mechanisms and recommendations.

Davis HE; McCorkell L; Vogel JM; Topol EJ

doi:10.1038/s41579-022-00846-2

Long COVID: major findings, mechanisms and recommendations.

Affiliations

1. Patient-Led Research Collaborative, New York, NY, USA.
Authors
Davis HE¹
(1 author)
2. Patient-Led Research Collaborative, Oakland, CA, USA.
Authors
McCorkell L²
(1 author)
3. Scripps Research Translational Institute, Scripps Research, La Jolla, CA, USA.
Authors
Vogel JM³
Topol EJ³
(2 authors)

ORCIDs linked to this article

Nature reviews. Microbiology, 13 Jan 2023, 21(3):133-146
https://doi.org/10.1038/s41579-022-00846-2 PMID: 36639608 PMCID: PMC9839201

Review

This article is in the Europe PMC Open access subset. Refer to the copyright information in the article for licensing details.

Free full text in Europe PMC

This article has been corrected. See Nat Rev Microbiol. 2023 Jun;21(6):408. doi: 10.1038/s41579-023-00896-0.

Abstract

Long COVID is an often debilitating illness that occurs in at least 10% of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections. More than 200 symptoms have been identified with impacts on multiple organ systems. At least 65 million individuals worldwide are estimated to have long COVID, with cases increasing daily. Biomedical research has made substantial progress in identifying various pathophysiological changes and risk factors and in characterizing the illness; further, similarities with other viral-onset illnesses such as myalgic encephalomyelitis/chronic fatigue syndrome and postural orthostatic tachycardia syndrome have laid the groundwork for research in the field. In this Review, we explore the current literature and highlight key findings, the overlap with other conditions, the variable onset of symptoms, long COVID in children and the impact of vaccinations. Although these key findings are critical to understanding long COVID, current diagnostic and treatment options are insufficient, and clinical trials must be prioritized that address leading hypotheses. Additionally, to strengthen long COVID research, future studies must account for biases and SARS-CoV-2 testing issues, build on viral-onset research, be inclusive of marginalized populations and meaningfully engage patients throughout the research process.

Free full text

Nat Rev Microbiol. 2023; 21(3): 133–146.

Published online 2023 Jan 13. https://doi.org/10.1038/s41579-022-00846-2

PMCID: PMC9839201

PMID: 36639608

Long COVID: major findings, mechanisms and recommendations

Hannah E. Davis,¹ Lisa McCorkell,² Julia Moore Vogel,³ and Eric J. Topol³

Author information Article notes Copyright and License information Disclaimer

This article has been corrected. See Nat Rev Microbiol. 2023 April 17; 21(6): 408.

This article has been cited by other articles in PMC.

Go to:

Abstract

Subject terms: SARS-CoV-2, Viral infection, Research data

Go to:

Introduction

Long COVID (sometimes referred to as ‘post-acute sequelae of COVID-19’) is a multisystemic condition comprising often severe symptoms that follow a severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. At least 65 million individuals around the world have long COVID, based on a conservative estimated incidence of 10% of infected people and more than 651 million documented COVID-19 cases worldwide¹; the number is likely much higher due to many undocumented cases. The incidence is estimated at 10–30% of non-hospitalized cases, 50–70% of hospitalized cases^2,3 and 10–12% of vaccinated cases^4,5. Long COVID is associated with all ages and acute phase disease severities, with the highest percentage of diagnoses between the ages of 36 and 50 years, and most long COVID cases are in non-hospitalized patients with a mild acute illness⁶, as this population represents the majority of overall COVID-19 cases. There are many research challenges, as outlined in this Review, and many open questions, particularly relating to pathophysiology, effective treatments and risk factors.

Hundreds of biomedical findings have been documented, with many patients experiencing dozens of symptoms across multiple organ systems⁷ (Fig. 1). Long COVID encompasses multiple adverse outcomes, with common new-onset conditions including cardiovascular, thrombotic and cerebrovascular disease⁸, type 2 diabetes⁹, myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS)^10,11 and dysautonomia, especially postural orthostatic tachycardia syndrome (POTS)¹² (Fig. 2). Symptoms can last for years¹³, and particularly in cases of new-onset ME/CFS and dysautonomia are expected to be lifelong¹⁴. With significant proportions of individuals with long COVID unable to return to work⁷, the scale of newly disabled individuals is contributing to labour shortages¹⁵. There are currently no validated effective treatments.

Fig. 1

Long COVID symptoms and the impacts on numerous organs with differing pathology.

The impacts of long COVID on numerous organs with a wide variety of pathology are shown. The presentation of pathologies is often overlapping, which can exacerbate management challenges. MCAS, mast cell activation syndrome; ME/CFS, myalgic encephalomyelitis/chronic fatigue syndrome; POTS, postural orthostatic tachycardia syndrome.

Fig. 2

SARS-CoV-2 infection, COVID-19 and long COVID increases the risk of several medical conditions.

Because diagnosis-specific data on large populations with long COVID are sparse, outcomes from general infections are included and a large proportion of medical conditions are expected to result from long COVID, although the precise proportion cannot be determined. One year after the initial infection, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections increased the risk of cardiac arrest, death, diabetes, heart failure, pulmonary embolism and stroke, as studied with use of US Department of Veterans Affairs databases. Additionally, there is clear increased risk of developing myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) and dysautonomia. Six months after breakthrough infection, increased risks were observed for cardiovascular conditions, coagulation and haematological conditions, death, fatigue, neurological conditions and pulmonary conditions in the same cohort. The hazard ratio is the ratio of how often an event occurs in one group relative to another; in this case people who have had COVID-19 compared with those who have not. Data sources are as follows: diabetes⁹, cardiovascular outcomes⁸, dysautonomia^12,201, ME/CFS^10,202 and breakthrough infections⁴.

There are likely multiple, potentially overlapping, causes of long COVID. Several hypotheses for its pathogenesis have been suggested, including persisting reservoirs of SARS-CoV-2 in tissues^16,17; immune dysregulation^17–20 with or without reactivation of underlying pathogens, including herpesviruses such as Epstein–Barr virus (EBV) and human herpesvirus 6 (HHV-6) among others^17,18,21,22; impacts of SARS-CoV-2 on the microbiota, including the virome^17,23–25; autoimmunity^17,26–28 and priming of the immune system from molecular mimicry¹⁷; microvascular blood clotting with endothelial dysfunction^17,29–31; and dysfunctional signalling in the brainstem and/or vagus nerve^17,32 (Fig. 3). Mechanistic studies are generally at an early stage, and although work that builds on existing research from postviral illnesses such as ME/CFS has advanced some theories, many questions remain and are a priority to address. Risk factors potentially include female sex, type 2 diabetes, EBV reactivation, the presence of specific autoantibodies²⁷, connective tissue disorders³³, attention deficit hyperactivity disorder, chronic urticaria and allergic rhinitis³⁴, although a third of people with long COVID have no identified pre-existing conditions⁶. A higher prevalence of long Covid has been reported in certain ethnicities, including people with Hispanic or Latino heritage³⁵. Socio-economic risk factors include lower income and an inability to adequately rest in the early weeks after developing COVID-19 (refs. ^36,37). Before the emergence of SARS-CoV-2, multiple viral and bacterial infections were known to cause postinfectious illnesses such as ME/CFS^17,38, and there are indications that long COVID shares their mechanistic and phenotypic characteristics^17,39. Further, dysautonomia has been observed in other postviral illnesses and is frequently observed in long COVID⁷.

Fig. 3

Hypothesized mechanisms of long COVID pathogenesis.

There are several hypothesized mechanisms for long COVID pathogenesis, including immune dysregulation, microbiota disruption, autoimmunity, clotting and endothelial abnormality, and dysfunctional neurological signalling. EBV, Epstein–Barr virus; HHV-6, human herpesvirus 6; SARS-CoV-2, severe acute respiratory syndrome coronavirus 2.

In this Review, we explore the current knowledge base of long COVID as well as misconceptions surrounding long COVID and areas where additional research is needed. Because most patients with long COVID were not hospitalized for their initial SARS-CoV-2 infection⁶, we focus on research that includes patients with mild acute COVID-19 (meaning not hospitalized and without evidence of respiratory disease). Most of the studies we discuss refer to adults, except for those in Box 1.

Box 1 Long COVID in children

Long COVID impacts children of all ages. One study found that fatigue, headache, dizziness, dyspnoea, chest pain, dysosmia, dysgeusia, reduced appetite, concentration difficulties, memory issues, mental exhaustion, physical exhaustion and sleep issues were more common in individuals with long COVID aged 15–19 years compared with controls of the same age²⁰³. A nationwide study in Denmark comparing children with a positive PCR test result with control individuals found that the former had a higher chance of reporting at least one symptom lasting more than 2 months²⁰⁴. Similarly to adults with long COVID, children with long COVID experience fatigue, postexertional malaise, cognitive dysfunction, memory loss, headaches, orthostatic intolerance, sleep difficulty and shortness of breath^204,205. Liver injury has been recorded in children who were not hospitalized during acute severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infections²⁰⁶, and although rare, children who had COVID-19 have increased risks of acute pulmonary embolism, myocarditis and cardiomyopathy, venous thromboembolic events, acute and unspecified renal failure, and type 1 diabetes²⁰⁷. Infants born to women who had COVID-19 during pregnancy were more likely to receive a neurodevelopmental diagnosis in the first year after delivery²⁰⁸. A paediatric long COVID centre’s experience treating patients suggests that adolescents with a moderate to severe form of long COVID have features consistent with myalgic encephalomyelitis/chronic fatigue syndrome²⁰⁵. Children experiencing long COVID have hypometabolism in the brain similar to the patterns found in adults with long COVID²⁰⁹. Long-term pulmonary dysfunction is found in children with long COVID and those who have recovered from COVID-19 (ref. ²¹⁰). Children with long COVID were more likely to have had attention deficit hyperactivity disorder, chronic urticaria and allergic rhinitis before being infected³⁴.

More research on long COVID in children is needed, although there are difficulties in ensuring a proper control group due to testing issues. Several studies have found that children infected with SARS-CoV-2 are considerably less likely to have a positive PCR test result than adults despite seroconverting weeks later, with up to 90% of cases being missed^189,190. Additionally, children are much less likely to seroconvert and, if they develop antibodies, are more likely to have a waning response months after infection compared with adults¹⁹³.

Go to:

Major findings

Immunology and virology

Studies looking at immune dysregulation in individuals with long COVID who had mild acute COVID-19 have found T cell alterations, including exhausted T cells¹⁸, reduced CD4⁺ and CD8⁺ effector memory cell numbers^18,19 and elevated PD1 expression on central memory cells, persisting for at least 13 months¹⁹. Studies have also reported highly activated innate immune cells, a lack of naive T and B cells and elevated expression of type I and type III interferons (interferon-β (IFNβ) and IFNλ1), persisting for at least 8 months²⁰. A comprehensive study comparing patients with long COVID with uninfected individuals and infected individuals without long COVID found increases in the numbers of non-classical monocytes, activated B cells, double-negative B cells, and IL-4- and IL-6-secreting CD4⁺ T cells and decreases in the numbers of conventional dendritic cells and exhausted T cells and low cortisol levels in individuals with long COVID at a median of 14 months after infection¹⁸. The expansion of cytotoxic T cells has been found to be associated with the gastrointestinal presentation of long COVID²⁷. Additional studies have found elevated levels of cytokines, particularly IL-1β, IL-6, TNF and IP10 (refs. ^40,41), and a recent preprint has reported persistent elevation of the level of CCL11, which is associated with cognitive dysfunction⁴². It remains to be seen whether the pattern of cytokines in ME/CFS, where the levels of certain cytokines are elevated in the first 2–3 years of illness but decrease over time without a corresponding decrease in symptoms⁴³, is similar in long COVID.

Multiple studies have found elevated levels of autoantibodies in long COVID²⁷, including autoantibodies to ACE2 (ref. ²⁸) (the receptor for SARS-CoV-2 entry), β₂-adrenoceptor, muscarinic M2 receptor, angiotensin II AT₁ receptor and the angiotensin 1–7 MAS receptor²⁶. High levels of other autoantibodies have been found in some patients with COVID-19 more generally, including autoantibodies that target the tissue (such as connective tissue, extracellular matrix components, vascular endothelium, coagulation factors and platelets), organ systems (including the lung, central nervous system, skin and gastrointestinal tract), immunomodulatory proteins (cytokines, chemokines, complement components and cell-surface proteins)⁴⁴. A major comprehensive study, however, did not find autoantibodies to be a major component of long COVID¹⁸.

Reactivated viruses, including EBV and HHV-6, have been found in patients with long COVID^18,21,22,27 (and have been identified in ME/CFS⁴⁵), and lead to mitochondrial fragmentation and severely affect energy metabolism⁴⁶. A recent preprint has reported that EBV reactivation is associated with fatigue and neurocognitive dysfunction in patients with long COVID²².

Several studies have shown low or no SARS-CoV-2 antibody production and other insufficient immune responses in the acute stage of COVID-19 to be predictive of long COVID at 6–7 months, in both hospitalized patients and non-hospitalized patients^47,48. These insufficient immune responses include a low baseline level of IgG⁴⁸, low levels of receptor-binding domain and spike-specific memory B cells, low levels of nucleocapsid IgG⁴⁹ and low peaks of spike-specific IgG⁴⁷. In a recent preprint, low or absent CD4⁺ T cell and CD8⁺ T cell responses were noted in patients with severe long COVID⁴⁹, and a separate study found lower levels of CD8⁺ T cells expressing CD107a and a decline in nucleocapsid-specific interferon-γ-producing CD8⁺ T cells in patients with long COVID compared with infected controls without long COVID⁵⁰. High levels of autoantibodies in long COVID have been found to be inversely correlated with protective COVID-19 antibodies, suggesting that patients with high autoantibody levels may be more likely to have breakthrough infections²⁷. SARS-CoV-2 viral rebound in the gut, possibly resulting from viral persistence, has also been associated with lower levels and slower production of receptor-binding domain IgA and IgG antibodies⁵¹. There are major differences in antibody creation, seroreversion and antibody titre levels across the sexes, with women being less likely to seroconvert, being more likely to serorevert and having lower antibody levels overall^52,53, even affecting antibody waning after vaccination⁵⁴.

Several reports have pointed towards possible viral persistence as a driver of long COVID symptoms; viral proteins and/or RNA has been found in the reproductive system, cardiovascular system, brain, muscles, eyes, lymph nodes, appendix, breast tissue, hepatic tissue, lung tissue, plasma, stool and urine^55–60. In one study, circulating SARS-CoV-2 spike antigen was found in 60% of a cohort of 37 patients with long COVID up to 12 months after diagnosis compared with 0% of 26 SARS-CoV-2-infected individuals, likely implying a reservoir of active virus or components of the virus¹⁶. Indeed, multiple reports following gastrointestinal biopsies have indicated the presence of virus, suggestive of a persistent reservoir in some patients^58,61.

Vascular issues and organ damage

Although COVID-19 was initially recognized as a respiratory illness, SARS-CoV-2 has capability to damage many organ systems. The damage that has been demonstrated across diverse tissues has predominantly been attributed to immune-mediated response and inflammation, rather than direct infection of cells by the virus. Circulatory system disruption includes endothelial dysfunction and subsequent downstream effects, and increased risks of deep vein thrombosis, pulmonary embolism and bleeding events^29,30,62. Microclots detected in both acute COVID-19 and long COVID contribute to thrombosis⁶³ and are an attractive diagnostic and therapeutic target. Long-term changes to the size and stiffness of blood cells have also been found in long COVID, with the potential to affect oxygen delivery⁶⁴. A long-lasting reduction in vascular density, specifically affecting small capillaries, was found in patients with long COVID compared with controls, 18 months after infection⁶⁵. A study finding elevated levels of vascular transformation blood biomarkers in long COVID also found that the angiogenesis markers ANG1 and P-selectin both had high sensitivity and specificity for predicting long COVID status⁶⁶.

An analysis of the US Department of Veterans Affairs databases (VA data) including more than 150,000 individuals 1 year after SARS-CoV-2 infection indicated a significantly increased risk of a variety of cardiovascular diseases, including heart failure, dysrhythmias and stroke, independent of the severity of initial COVID-19 presentation⁸ (Fig. 2). Cardiac MRI studies revealed cardiac impairment in 78% of 100 individuals who had a prior COVID-19 episode (investigated an average of 71 days after infection⁶⁷) and in 58% of participants with long COVID (studied 12 months after infection⁶⁸), reinforcing the durability of cardiac abnormalities.

Multiple studies have revealed multi-organ damage associated with COVID-19. One prospective study of low-risk individuals, looking at the heart, lungs, liver, kidneys, pancreas and spleen, noted that 70% of 201 patients had damage to at least one organ and 29% had multi-organ damage⁶⁹. In a 1-year follow-up study, conducted by the same research group with 536 participants, the study authors found that 59% had single-organ damage and 27% multi-organ damage⁷⁰. A dedicated kidney study of VA data including more than 89,000 individuals who had COVID-19 noted an increased risk of numerous adverse kidney outcomes⁷¹. Another VA data analysis, including more than 181,000 individuals who had COVID-19, found that infection also increases the risk of type 2 diabetes⁹ (Fig. 2). The organ damage experienced by patients with long COVID appears durable, and long-term effects remain unknown.

Neurological and cognitive systems

Neurological and cognitive symptoms are a major feature of long COVID, including sensorimotor symptoms, memory loss, cognitive impairment, paresthesia, dizziness and balance issues, sensitivity to light and noise, loss of (or phantom) smell or taste, and autonomic dysfunction, often impacting activities of daily living^7,32. Audiovestibular manifestations of long COVID include tinnitus, hearing loss and vertigo^7,72.

In a meta-analysis, fatigue was found in 32% and cognitive impairment was found in 22% of patients with COVID-19 at 12 weeks after infection³. Cognitive impairments in long COVID are debilitating, at the same magnitude as intoxication at the UK drink driving limit or 10 years of cognitive ageing⁷³, and may increase over time, with one study finding occurrence in 16% of patients at 2 months after infection and 26% of patients at 12 months after infection⁷⁴. Activation of the kynurenine pathway, particularly the presence of the metabolites quinolinic acid, 3-hydroxyanthranilic acid and kynurenine, has been identified in long COVID, and is associated with cognitive impairment⁷⁴. Cognitive impairment has also been found in individuals who recovered from COVID-19 (ref. ⁷⁵), and at higher rates when objective versus subjective measures were used³, suggesting that a subset of those with cognitive impairment may not recognize and/or report their impairment. Cognitive impairment is a feature that manifests itself independently of mental health conditions such as anxiety and depression^74,76, and occurs at similar rates in hospitalized and non-hospitalized patients^74,76. A report of more than 1.3 million people who had COVID-19 showed mental health conditions such as anxiety and depression returned to normal over time, but increased risks of cognitive impairment (brain fog), seizures, dementia, psychosis and other neurocognitive conditions persisted for at least 2 years⁷⁷.

Possible mechanisms for these neuropathologies include neuroinflammation, damage to blood vessels by coagulopathy and endothelial dysfunction, and injury to neurons³². Studies have found Alzheimer disease-like signalling in patients with long COVID⁷⁸, peptides that self-assemble into amyloid clumps which are toxic to neurons⁷⁹, widespread neuroinflammation⁸⁰, brain and brainstem hypometabolism correlated with specific symptoms^81,82 and abnormal cerebrospinal fluid findings in non-hospitalized individuals with long COVID along with an association between younger age and a delayed onset of neurological symptoms⁸³. Multilineage cellular dysregulation and myelin loss were reported in a recent preprint in patients with long COVID who had mild infections, with microglial reactivity similar to that seen in chemotherapy, known as ‘chemo-brain’⁴². A study from the UK Biobank, including brain imaging in the same patients before and after COVID-19 as well as control individuals, showed a reduction in grey matter thickness in the orbitofrontal cortex and parahippocampal gyrus (markers of tissue damage in areas connected to the primary olfactory cortex), an overall reduction in brain size and greater cognitive decline in patients after COVID-19 compared with controls, even in non-hospitalized patients. Although that study looked at individuals with COVID-19 compared with controls, not specifically long COVID, it may have an implication for the cognitive component of long COVID⁸⁴. Abnormal levels of mitochondrial proteins as well as SARS-CoV-2 spike and nucleocapsid proteins have been found in the central nervous system⁸⁵. Tetrahydrobiopterin deficiencies and oxidative stress are found in long COVID as well⁸⁶.

In the eyes, corneal small nerve fibre loss and increased dendritic cell density have been found in long COVID^87,88, as well as significantly altered pupillary light responses⁸⁹ and impaired retinal microcirculation⁹⁰. SARS-CoV-2 can infect and replicate in retinal⁵⁹ and brain⁹¹ organoids. Other manifestations of long COVID include retinal haemorrhages, cotton wool spots and retinal vein occlusion⁹².

Mouse models of mild SARS-CoV-2 infection demonstrated microglial reactivity and elevated levels of CCL11, which is associated with cognitive dysfunction and impaired neurogenesis⁴². Hamster models exhibited an ongoing inflammatory state, involving T cell and myeloid activation, production of pro-inflammatory cytokines and an interferon response that was correlated with anxiety and depression-like behaviours in the hamsters, with similar transcriptional signatures found in the tissue of humans who had recovered from COVID-19 (ref. ⁹³). Infected non-human primates with mild illness showed neuroinflammation, neuronal injury and apoptosis, brain microhaemorrhages, and chronic hypoxaemia and brain hypoxia⁹⁴.

Recent reports indicate low blood cortisol levels in patients with long COVID as compared with control individuals, more than 1 year into symptom duration^18,27. Low cortisol production by the adrenal gland should be compensated by an increase in adrenocorticotropic hormone (ACTH) production by the pituitary gland, but this was not the case, supporting hypothalamus–pituitary–adrenal axis dysfunction¹⁸. This may also reflect an underlying neuroinflammatory process. Low cortisol levels have previously been documented in individuals with ME/CFS.

ME/CFS, dysautonomia and related conditions

ME/CFS is a multisystem neuroimmune illness with onset often following a viral or bacterial infection. Criteria include a “substantial reduction or impairment in the ability to engage in pre-illness levels of occupational, educational, social, or personal activities” for at least 6 months, accompanied by a profound fatigue that is not alleviated by rest, along with postexertional malaise, unrefreshing sleep and cognitive impairment or orthostatic intolerance (or both)⁹⁵. Up to 75% of people with ME/CFS cannot work full-time and 25% have severe ME/CFS, which often means they are bed-bound, have extreme sensitivity to sensory input and are dependent on others for care⁹⁶. There is a vast collection of biomedical findings in ME/CFS^97,98, although these are not well known to researchers and clinicians in other fields.

Many researchers have commented on the similarity between ME/CFS and long COVID⁹⁹; around half of individuals with long COVID are estimated to meet the criteria for ME/CFS^10,11,29,100, and in studies where the cardinal ME/CFS symptom of postexertional malaise is measured, a majority of individuals with long COVID report experiencing postexertional malaise^7,100. A study of orthostatic stress in individuals with long COVID and individuals with ME/CFS found similar haemodynamic, symptomatic and cognitive abnormalities in both groups compared with healthy individuals¹⁰¹. Importantly, it is not surprising that ME/CFS should stem from SARS-CoV-2 infection as 27.1% of SARS-CoV infection survivors in one study met the criteria for ME/CFS diagnosis 4 years after onset¹⁰². A wide range of pathogens cause ME/CFS onset, including EBV, Coxiella burnetii (which causes Q fever), Ross River virus and West Nile virus³⁸.

Consistent abnormal findings in ME/CFS include diminished natural killer cell function, T cell exhaustion and other T cell abnormalities, mitochondrial dysfunction, and vascular and endothelial abnormalities, including deformed red blood cells and reduced blood volume. Other abnormalities include exercise intolerance, impaired oxygen consumption and a reduced anaerobic threshold, and abnormal metabolic profiles, including altered usage of fatty acids and amino acids. Altered neurological functions have also been observed, including neuroinflammation, reduced cerebral blood flow, brainstem abnormalities and elevated ventricular lactate level, as well as abnormal eye and vision findings. Reactivated herpesviruses (including EBV, HHV-6, HHV-7 and human cytomegalovirus) are also associated with ME/CFS^{97,98,103,104}.

Many of these findings have been observed in long COVID studies in both adults and children (Box 1). Long COVID research has found mitochondrial dysfunction including loss of mitochondrial membrane potential¹⁰⁵ and possible dysfunctional mitochondrial metabolism¹⁰⁶, altered fatty acid metabolism and dysfunctional mitochondrion-dependent lipid catabolism consistent with mitochondrial dysfunction in exercise intolerance¹⁰⁷, redox imbalance¹⁰⁸, and exercise intolerance and impaired oxygen extraction^100,109,110. Studies have also found endothelial dysfunction²⁹, cerebral blood flow abnormalities and metabolic changes^81,111–113 (even in individuals with long COVID whose POTS symptoms abate¹¹⁴), extensive neuroinflammation^42,80, reactivated herpesviruses^18,21,27, deformed red blood cells⁶⁴ and many findings discussed elsewhere. Microclots and hyperactivated platelets are found not only in individuals with long COVID but also in individuals with ME/CFS¹¹⁵.

Dysautonomia, particularly POTS, is commonly comorbid with ME/CFS¹¹⁶ and also often has a viral onset¹¹⁷. POTS is associated with G protein-coupled adrenergic receptor and muscarinic acetylcholine receptor autoantibodies, platelet storage pool deficiency, small fibre neuropathy and other neuropathologies¹¹⁸. Both POTS and small fibre neuropathy are commonly found in long COVID^111,119, with one study finding POTS in 67% of a cohort with long COVID¹²⁰.

Mast cell activation syndrome is also commonly comorbid with ME/CFS. The number and severity of mast cell activation syndrome symptoms substantially increased in patients with long COVID compared with pre-COVID and control individuals¹²¹, with histamine receptor antagonists resulting in improvements in the majority of patients¹⁹.

Other conditions that are commonly comorbid with ME/CFS include connective tissue disorders including Ehlers–Danlos syndrome and hypermobility, neuro-orthopaedic spinal and skull conditions, and endometriosis^33,122,123. Evidence is indicating these conditions may be comorbid with long COVID as well. The overlap of postviral conditions with these conditions should be explored further.

Reproductive system

Impacts on the reproductive system are often reported in long COVID, although little research has been done to document the extent of the impact and sex-specific pathophysiology. Menstrual alterations are more likely to occur in women and people who menstruate with long COVID than in women and people who menstruate with no history of COVID and those who had COVID-19 but not long COVID¹²⁴. Menstruation and the week before menstruation have been identified by patients as triggers for relapses of long COVID symptoms⁷. Declined ovarian reserve and reproductive endocrine disorder have been observed in people with COVID-19 (ref. ¹²⁵), and initial theories suggest that SARS-CoV-2 infection affects ovary hormone production and/or the endometrial response due to the abundance of ACE2 receptors on ovarian and endometrial tissue¹²⁶. Individuals with both COVID-19 and menstrual changes were more likely to experience fatigue, headache, body ache and pain, and shortness of breath than those who did not have menstrual changes, and the most common menstrual changes were irregular menstruation, increased premenstrual symptoms and infrequent menstruation¹²⁷.

Research on ME/CFS shows associations between ME/CFS and premenstrual dysphoric disorder, polycystic ovarian syndrome, menstrual cycle abnormalities, ovarian cysts, early menopause and endometriosis^128–130. Pregnancy, postpartum changes, perimenopause and menstrual cycle fluctuations affect ME/CFS and influence metabolic and immune system changes¹²⁹. Long COVID research should focus on these relationships to better understand the pathophysiology.

Viral persistence in the penile tissue has been documented, as has an increased risk of erectile dysfunction, likely resulting from endothelial dysfunction¹³¹. In one study, impairments to sperm count, semen volume, motility, sperm morphology and sperm concentration were reported in individuals with long COVID compared with control individuals, and were correlated with elevated levels of cytokines and the presence of caspase 8, caspase 9 and caspase 3 in seminal fluid¹³².

Respiratory system

Respiratory conditions are a common phenotype in long COVID, and in one study occurred twice as often in COVID-19 survivors as in the general population². Shortness of breath and cough are the most common respiratory symptoms, and persisted for at least 7 months in 40% and 20% of patients with long COVID, respectively⁷. Several imaging studies that included non-hospitalized individuals with long COVID demonstrated pulmonary abnormalities including in air trapping and lung perfusion^133,134. An immunological and proteomic study of patients 3–6 months after infection indicated apoptosis and epithelial damage in the airway but not in blood samples¹³⁵. Further immunological characterization comparing individuals with long COVID with individuals who had recovered from COVID-19 noted a correlation between decreased lung function, systemic inflammation and SARS-CoV-2-specific T cells¹³⁶.

Gastrointestinal system

Long COVID gastrointestinal symptoms include nausea, abdominal pain, loss of appetite, heartburn and constipation¹³⁷. The gut microbiota composition is significantly altered in patients with COVID-19 (ref. ²³), and gut microbiota dysbiosis is also a key component of ME/CFS¹³⁸. Higher levels of Ruminococcus gnavus and Bacteroides vulgatus and lower levels of Faecalibacterium prausnitzii have been found in people with long COVID compared with non-COVID-19 controls (from before the pandemic), with gut dysbiosis lasting at least 14 months; low levels of butyrate-producing bacteria are strongly correlated with long COVID at 6 months²⁴. Persisting respiratory and neurological symptoms are each associated with specific gut pathogens²⁴. Additionally, SARS-CoV-2 RNA is present in stool samples of patients with COVID-19 (ref. ¹³⁹), with one study indicating persistence in the faeces of 12.7% of participants 4 months after diagnosis of COVID-19 and in 3.8% of participants at 7 months after diagnosis⁶¹. Most patients with long COVID symptoms and inflammatory bowel disease 7 months after infection had antigen persistence in the gut mucosa¹⁴⁰. Higher levels of fungal translocation, from the gut and/or lung epithelium, have been found in the plasma of patients with long COVID compared with those without long COVID or SARS-CoV-2-negative controls, possibly inducing cytokine production¹⁴¹. Transferring gut bacteria from patients with long COVID to healthy mice resulted in lost cognitive functioning and impaired lung defences in the mice, who were partially treated with the commensal probiotic bacterium Bifidobacterium longum²⁵.

Timelines

The onset and time course of symptoms differ across individuals and by symptom type. Neurological symptoms often have a delayed onset of weeks to months: among participants with cognitive symptoms, 43% reported a delayed onset of cognitive symptoms at least 1 month after COVID-19, with the delay associated with younger age⁸³. Several neurocognitive symptoms worsen over time and tend to persist longer, whereas gastrointestinal and respiratory symptoms are more likely to resolve^7,74,142. Additionally, pain in joints, bones, ears, neck and back are more common at 1 year than at 2 months, as is paresthesia, hair loss, blurry vision and swelling of the legs, hands and feet¹⁴³. Parosmia has an average onset of 3 months after the initial infection¹⁴⁴; unlike other neurocognitive symptoms, it often decreases over time¹⁴³.

Few people with long COVID demonstrate full recovery, with one study finding that 85% of patients who had symptoms 2 months after the initial infection reported symptoms 1 year after symptom onset¹⁴³. Future prognosis is uncertain, although diagnoses of ME/CFS and dysautonomia are generally lifelong.

Go to:

Diagnostic tools and treatments

Although diagnostic tools exist for some components of long COVID (for example, tilt table tests for POTS¹⁴⁵ and MRI scans to detect cardiovascular impairment⁶⁸), diagnostic tools for long COVID are mostly in development, including imaging to detect microclots⁶³, corneal microscopy to identify small fibre neuropathy⁸⁷, new fragmentation of QRS complex on electrocardiograms as indicative of cardiac injury¹⁴⁶ and use of hyperpolarized MRI to detect pulmonary gas exchange abnormalities¹⁴⁷. On the basis of the tests that are offered as standard care, the results for patients with long COVID are often normal; many providers are unaware of the symptom-specific testing and diagnostic recommendations from the ME/CFS community¹⁴⁸. Early research into biomarkers suggests that levels of extracellular vesicles⁸⁵ and/or immune markers indicating high cytotoxicity¹⁴⁹ could be indicative of long COVID. Intriguingly, dogs can identify individuals with long COVID on the basis of sweat samples¹⁵⁰. Biomarker research in ME/CFS may also be applicable to long COVID, including electrical impedance blood tests, saliva tests, erythrocyte deformation, sex-specific plasma lipid profiles and variables related to isocapnic buffering^151–154. The importance of developing and validating biomarkers that can be used for the diagnosis of long COVID cannot be adequately emphasized — they will not only be helpful in establishing the diagnosis but will also be helpful for objectively defining treatment responses.

Although there are currently no broadly effective treatments for long COVID, treatments for certain components have been effective for subsets of populations (Table 1). Many strategies for ME/CFS are effective for individuals with long COVID, including pacing^7,37 and symptom-specific pharmacological options (for example, β-blockers for POTS, low-dose naltrexone for neuroinflammation¹⁵⁵ and intravenous immunoglobulin for immune dysfunction) and non-pharmacological options (including increasing salt intake for POTS, cognitive pacing for cognitive dysfunction and elimination diets for gastrointestinal symptoms)⁹⁶. Low-dose naltrexone has been used in many diseases, including ME/CFS¹⁵⁵, and has also shown promise in treating long COVID¹⁵⁶. H₁ and H₂ antihistamines, often following protocols for mast cell activation syndrome and particularly involving famotidine, are used to alleviate a wide range of symptoms^19,157, although they are not a cure. Another drug, BC007, potentially addresses autoimmunity by neutralizing G protein-coupled receptor autoantibody levels¹⁵⁸. Anticoagulant regimens are a promising way to address abnormal clotting¹⁵⁹; in one study, resolution of symptoms was seen in all 24 patients receiving triple anticoagulant therapy³¹. Apheresis has also shown promise to alleviate long COVID symptoms; it has been theorized to help remove microclots¹⁶⁰ and has been shown to reduce autoantibodies in ME/CFS¹⁶¹. However, it is quite expensive, and its benefits are uncertain. Some supplements have shown promise in treating both long COVID and ME/CFS, including coenzyme Q₁₀ and d-ribose¹⁶², and may deserve further study.

Table 1

Summary of candidate treatments and supporting evidence

Symptoms and/or biological mechanism	Treatments	Supporting evidence	Comments
Postexertional malaise	Pacing	ME/CFS literature	Exercise, cognitive behavioural therapy and graded exercise therapy are contraindicated
POTS	Pharmacological: β-blockers, pyridostigmine, fludrocortisone, midodrine	POTS and ME/CFS literature	Options can be prioritized on the basis of a specific constellation of symptoms
POTS	Non-pharmacological: increase salt and fluid intake, intravenously administered salt, compression stockings	POTS and ME/CFS literature	–
Immune dysfunction	Intravenous immunoglobulin	ME/CFS literature	Consider consulting an immunologist on implementation
Cognitive dysfunction	Cognitive pacing	ME/CFS literature	Consider implementation alongside pacing physical exertion
Cognitive dysfunction	Postconcussion syndrome protocols	ME/CFS and postconcussion syndrome literature	–
Fatigue	Coenzyme Q₁₀, d-ribose	ME/CFS literature	–
Pain, fatigue, neurological symptoms	Low-dose naltrexone	ME/CFS and other literature	Substantial anecdotal reports of success within the patient community
Fatigue, unrefreshing sleep, brain fog	Low-dose aripiprazole	ME/CFS literature	–
Autoimmunity	BC007	Long COVID case report	Neutralizes G protein-coupled receptor autoantibodies
Abnormal clotting	Anticoagulants	Long COVID pilot study	Additional trials in progress
Abnormal clotting	Apheresis	ME/CFS literature, long COVID pilot study	–
Viral persistence and antivirals (COVID-19)	Paxlovid	Long COVID case reports	No active trials, despite strong evidence for viral persistence
Viral persistence and antivirals (reactivations such as of EBV, HCMV and VZV)	Valaciclovir, famciclovir, valganciclovir and other antivirals	ME/CFS literature	–
Endothelial dysfunction	Sulodexide	Long COVID pilot study	–
Gastrointestinal symptoms	Probiotics	Long COVID pilot study	Resolved gastrointestinal and other symptoms
Dysautonomia	Stellate ganglion block	Long COVID case report	Effects may wane over time and require repeated procedures
Endothelial function, microcirculation, inflammatory markers and oxidative stress	Pycnogenol	COVID-19 pilot study	–
MCAS	H₁ and H₂ antihistamines, particularly famotidine	Long COVID case reports, MCAS literature	Expected to treat symptoms, not underlying mechanism
Autonomic dysfunction	Transcutaneous vagal stimulation	Long COVID pilot study	–

Open in a separate window

EBV, Epstein–Barr virus; HCMV, human cytomegalovirus; MCAS, mast cell activation syndrome; ME/CFS, myalgic encephalomyelitis/chronic fatigue syndrome; POTS, postural orthostatic tachycardia syndrome; VZV, varicella zoster virus.

Of note, exercise is harmful for patients with long COVID who have ME/CFS or postexertional malaise^110,163 and should not be used as a treatment^164–166; one study of people with long COVID noted that physical activity worsened the condition of 75% of patients, and less than 1% saw improvement¹⁰⁹.

Pilot studies and case reports have revealed additional treatment options worth exploring. A case report noted resolution of long COVID following treatment with the antiviral Paxlovid¹⁶⁷, and a study investigating the treatment of acute COVID-19 with Paxlovid showed a 25% reduction in the incidence of long COVID¹⁶⁸; Paxlovid should be investigated further for prevention and treatment of long COVID. A small trial of sulodexide in individuals with endothelial dysfunction saw a reduction in symptom severity¹⁶⁹. Pilot studies of probiotics indicated potential in alleviating gastrointestinal and non-gastrointestinal symptoms^170,171. Two patients with long COVID experienced substantial alleviation of dysautonomia symptoms following stellate ganglion block¹⁷². An early study noted that Pycnogenol statistically significantly improved physiological measurements (for example, reduction in oxidative stress) and quality of life (indicated by higher Karnofsky Performance Scale Index scores)^173,174, as hypothesized on the basis of success in other clinical studies.

Taken together, the current treatment options are based on small-scale pilot studies in long COVID or what has been effective in other diseases; several additional trials are in progress¹⁷⁵. There is a wide range of possible treatment options from ME/CFS covering various mechanisms, including improving natural killer cell function, removing autoantibodies, immunosuppressants, antivirals for reactivated herpesviruses, antioxidants, mitochondrial support and mitochondrial energy generation^176,177; most need to be clinically trialled, which should happen urgently. Many newer treatment options remain underexplored, including anticoagulants and SARS-CoV-2-specific antivirals, and a lack of funding is a significant limitation to robust trials.

Go to:

Impact of vaccines, variants and reinfections

The impact of vaccination on the incidence of long COVID differs across studies, in part because of differing study methods, time since vaccination and definitions of long COVID. One study indicated no significant difference in the development of long COVID between vaccinated individuals and unvaccinated individuals¹⁷⁸; other studies indicate that vaccines provide partial protection, with a reduced risk of long COVID between 15% and 41%^4,5, with long COVID continuing to impact 9% of people with COVID-19.

The different SARS-CoV-2 variants and level of (and time since) vaccination may impact the development of long COVID. The UK’s Office for National Statistics found that long COVID was 50% less common in double-vaccinated participants with Omicron BA.1 than in double-vaccinated participants Delta, but that there was no significant difference between triple-vaccinated participants; it also found long COVID was more common after Omicron BA.2 infection than after BA.1 infection in triple-vaccinated participants, with 9.3% developing long COVID from infection with the BA.2 variant¹⁷⁹.

The impact of vaccination on long COVID symptoms in people who had already developed long COVID differs among patients, with 16.7% of patients experiencing a relief of symptoms, 21.4% experiencing a worsening of symptoms and the remainder experiencing unchanged symptoms¹⁸⁰.

Reinfections are increasingly common¹⁸¹. The impact of multiple instances of COVID-19, including the rate of long COVID in those who recovered from a first infection but developed long COVID following reinfection, and the impact of reinfection on those with pre-existing long COVID is crucial to understand to inform future policy decisions. Early research shows an increasing risk of long COVID sequelae after the second and third infection, even in double-vaccinated and triple-vaccinated people¹⁸². Existing literature suggests multiple infections may cause additional harm or susceptibility to the ME/CFS-type presentation^33,183.

There is also early evidence that certain immune responses in people with long COVID, including low levels of protective antibodies and elevated levels of autoantibodies, may suggest an increased susceptibility to reinfection²⁷.

Go to:

Challenges and recommendations

Issues with PCR and antibody testing throughout the pandemic, inaccurate pandemic narratives and widespread lack of postviral knowledge have caused downstream issues and biases in long COVID research and care.

Testing issues

Most patients with COVID-19 from the first waves did not have laboratory-confirmed infection, with PCR tests being difficult to access unless individuals were hospitalized. Only 1–3% of cases to March 2020 were likely detected¹⁸⁴, and the CDC estimates that only 25% of cases in the USA were reported from February 2020 to September 2021 (ref. ¹⁸⁵); that percentage has likely decreased with the rise in use of at-home rapid tests.

Although PCR tests are our best tool for detecting SARS-CoV-2 infections, their false negative rates are still high¹⁸⁶. Further bias is caused by false negative rates being higher in women and adults younger than 40 years¹⁸⁷, those with a low viral load¹⁸⁸ and children (Box 1), with several studies showing 52–90% of cases in children missed by PCR tests^189,190. The high false negative PCR rate results in symptomatic patients with COVID-19, who seek a COVID-19 test but receive a false negative result, being included as a control in many studies. Those who have a positive PCR test result (who are more likely to be included in research) are more likely to be male or have a higher viral load. Additionally, the lack of test accessibility as well as the false negative rates has created a significant barrier to care, as many long COVID clinics require PCR tests for admission.

Similarly, there is a broad misconception that everyone makes and retains SARS-CoV-2 antibodies, and many clinicians and researchers are unaware of the limited utility of antibody tests to determine prior infection. Between 22% and 36% of people infected with SARS-CoV-2 do not seroconvert, and many others lose their antibodies over the first few months, with both non-seroconversion and seroreversion being more likely in women, children and individuals with mild infections^{52,53,191–193}. At 4 and 8 months after infection, 19% and 61% of patients, respectively, who had mild infections and developed antibodies were found to have seroreverted, compared with 2% and 29% of patients, respectively who had severe infections¹⁹¹. Still, many clinicians and researchers use antibody tests to include or exclude patients with COVID-19 from control groups.

Furthermore, during periods of test inaccessibility, tests were given on the basis of patients having COVID-19-specific symptoms such as loss of smell and taste, fever, and respiratory symptoms, resulting in a bias towards people with those symptoms.

Misinformation on PCR and antibody tests has resulted in the categorization of patients with long COVID into non-COVID-19 control groups, biasing the research output. Because low or no antibody levels and viral load may be related to long COVID pathophysiology, including a clinically diagnosed cohort will strengthen the research.

Important miscues

The narrative that COVID-19 had only respiratory sequelae led to a delayed realization of the neurological, cardiovascular and other multisystem impacts of COVID-19. Many long COVID clinics and providers still disproportionately focus on respiratory rehabilitation, which results in skewed electronic health record data. Electronic health record data are also more comprehensive for those who were hospitalized with COVID-19 than for those who were in community care, leading to a bias towards the more traditional severe respiratory presentation and less focus on non-hospitalized patients, who tend to have neurological and/or ME/CFS-type presentations.

The narrative that initially mild COVID-19 cases, generally defined as not requiring hospitalization in the acute phase, would not have long-term consequences has also had downstream effects on research. These so-called mild cases that result in long COVID often have an underlying biology different from acute severe cases, but the same types of tests are being used to evaluate patients. This is despite basic tests such as D-dimer, C-reactive protein (CRP) and antinuclear antibody tests and complete blood count being known to often return normal results in patients with long COVID. Tests that return abnormal results in patients with ME/CFS and dysautonomia, such as total immunoglobulin tests, natural killer cell function tests, the tilt table or NASA lean test, the four-point salivary cortisol test, reactivated herpesvirus panels, small fibre neuropathy biopsy, and tests looking for abnormal brain perfusion⁹⁶, should instead be prioritized. Other recurring issues include studies failing to include the full range of symptoms, particularly neurological and reproductive system symptoms, and not asking patients about symptom frequency, severity and disability. Cardinal symptoms such as postexertional malaise are not widely known, and therefore are rarely included in study designs.

Widespread lack of postviral knowledge and misinformation

The widespread lack of knowledge of viral-onset illnesses, especially ME/CFS and dysautonomia, as well as often imperfect coding, prevents these conditions from being identified and documented by clinicians; this means that they are frequently absent from electronic health record data. Further, because ME/CFS and dysautonomia research is not widely known or comprehensively taught in medical schools¹⁹⁴, long COVID research is often not built on past findings, and tends to repeat old hypotheses. Additionally, long COVID research studies and medical histories tend to document only the risk factors for severe acute COVID-19, which are different from the risk factors for conditions that overlap with long COVID such as ME/CFS and dysautonomia (for example, connective tissue disorders such as Ehlers–Danlos syndrome, prior illnesses such as infectious mononucleosis and mast cell involvement)^33,195,196.

Clinicians who are not familiar with ME/CFS and dysautonomia often misdiagnose mental health disorders in patients; four in five patients with POTS receive a diagnosis with a psychiatric or psychological condition before receiving a POTS diagnosis, with only 37% continuing to have the psychiatric or psychological diagnosis once they have received their POTS diagnosis¹¹⁷. Researchers who are unfamiliar with ME/CFS and dysautonomia often do not know to use specific validated tools when conducting mental health testing, as anxiety scales often include autonomic symptoms such as tachycardia, and depression scales often include symptoms such as fatigue, both of which overestimate mental health disorder prevalence in these conditions^197,198.

Recommendations

Although research into long COVID has been expansive and has accelerated, the existing research is not enough to improve outcomes for people with long COVID. To ensure an adequate response to the long COVID crisis, we need research that builds on existing knowledge and is inclusive of the patient experience, training and education for the health-care and research workforce, a public communication campaign, and robust policies and funding to support research and care in long COVID.

Research

We need a comprehensive long COVID research agenda that builds on the existing knowledge from ME/CFS, dysautonomia and other viral-onset conditions, including but not limited to brain and brainstem inflammation, appropriate neuroimaging techniques, neuroimmunology, metabolic profiling, impaired endothelial function, mitochondrial fragmentation, antiviral and metabolic phenotypes, hypoperfusion/cerebral blood flow, nanoneedle diagnostic testing, overlaps with connective tissue disorders, autoimmunity and autoantibodies, viral/microbial persistence, intracranial hypertension, hypermobility, craniocervical obstructions, altered T and B cells, metabolomics and proteomics, elevated blood lactate level, herpesvirus reactivations, immune changes in the early versus late postviral years, and changes to the gut microbiota. The mechanisms of and overlaps between long COVID and connective tissue involvement, mast cells and inflammatory conditions such as endometriosis are particularly understudied and should be focused on. Because of the high prevalence of ME/CFS, POTS and other postinfectious illnesses in patients with long COVID, long COVID research should include people who developed ME/CFS and other postinfectious illnesses from a trigger other than SARS-CoV-2 in comparator groups to improve understanding of the onset and pathophysiology of these illnesses¹¹³. Additionally, there is a known immune exhaustion process that occurs between the second and third year of illness in ME/CFS, with test results for cytokines being different between patients who have been sick for shorter durations (less than 2 years) than for those who have been sick for longer durations⁴³. Because of this, studies should implement subanalyses based on the length of time participants have been ill. Because ME/CFS and dysautonomia research is not widely known across the biomedical field, long COVID research should be led by experts from these areas to build on existing research and create new diagnostic and imaging tools.

Robust clinical trials must be a priority moving forward as patients currently have few treatment options. In the absence of validated treatment options, patients and physicians conduct individual experiments, which result in the duplication of efforts without generalizable knowledge and pose undue risks to patients. Robust study design and knowledge sharing must be prioritized by both funding institutions and clinician-researchers.

It is critical that research on long COVID be representative of (or oversample) the populations who had COVID-19 and are developing long COVID at high rates, which is disproportionately people of colour³⁵. Medical research has historically under-represented these populations, and over-representation of white and socio-economically privileged patients has been common in long COVID research. Researchers must work within communities of colour, LGBTQ+ communities and low-income communities to build trust and conduct culturally competent studies that will provide insights and treatments for long COVID for marginalized populations.

As a subset of patients will improve over time, and others will have episodic symptoms, care should be taken to incorporate the possibility of alleviation of symptoms into the study design, and care should be taken not to ascribe improvement to a particular cause without proper modelling.

Finally, it is critical that communities of patients with long COVID and associated conditions are meaningfully engaged in long COVID research and clinical trials. The knowledge of those who experience an illness is crucial in identifying proper study design and key research questions and solutions, improving the speed and direction of research.

Training and education of the health-care and research workforce

To prepare the next generation of health-care providers and researchers, medical schools must improve their education on pandemics, viruses and infection-initiated illnesses such as long COVID and ME/CFS, and competency evaluations should include these illnesses. As of 2013, only 6% of medical schools fully cover ME/CFS across the domains of treatment, research and curricula, which has created obstacles to care, accurate diagnosis, research and treatment¹⁹⁴. To ensure people with long COVID and associated conditions can receive adequate care now, professional societies and government agencies must educate the health-care and research workforce on these illnesses, including the history of and current best practices for ME/CFS to not repeat mistakes of the past, which have worsened patients’ prognoses. The research community has made a misstep in its efforts to treat ME/CFS¹⁹⁹, and some physicians, poorly educated in the aetiology and pathophysiology of the disorder, still advise patients to pursue harmful interventions such as graded exercise therapy and cognitive behavioural therapy, despite the injury that these interventions cause²⁰⁰ and the fact that they are explicitly not advised as treatments^163,164,166.

Public communications campaign

In addition to providing education on long COVID to the biomedical community, we need a public communications campaign that informs the public about the risks and outcomes of long COVID.

Policies and funding

Finally, we need policies and funding that will sustain long COVID research and enable people with long COVID to receive adequate care and support. For instance, in the USA, the creation of a national institute for complex chronic conditions within the NIH would go a long way in providing a durable funding mechanism and a robust research agenda. Further, we need to create and fund centres of excellence, which would provide inclusive, historically informed and culturally competent care, as well as conduct research and provide medical education to primary care providers. Additionally, research and clinical care do not exist in silos. It is critical to push forward policies that address both the social determinants of health and the social support that is needed for disabled people.

Go to:

Conclusions

Long COVID is a multisystemic illness encompassing ME/CFS, dysautonomia, impacts on multiple organ systems, and vascular and clotting abnormalities. It has already debilitated millions of individuals worldwide, and that number is continuing to grow. On the basis of more than 2 years of research on long COVID and decades of research on conditions such as ME/CFS, a significant proportion of individuals with long COVID may have lifelong disabilities if no action is taken. Diagnostic and treatment options are currently insufficient, and many clinical trials are urgently needed to rigorously test treatments that address hypothesized underlying biological mechanisms, including viral persistence, neuroinflammation, excessive blood clotting and autoimmunity.

Go to:

Acknowledgements

We would like to thank the long COVID and associated conditions patient and research community and the entire team at Patient-Led Research Collaborative. E.J.T. was supported by National Center for Advancing Translational Sciences (NCATS) grant UL1TR002550.

Go to:

Author contributions

The authors contributed equally to all aspects of the article.

Go to:

Peer review

Go to:

Peer review information

Nature Reviews Microbiology thanks Akiko Iwasaki, Ziyad Al-Aly and the other, anonymous, reviewer(s) for their contribution to the peer review of this work.

Go to:

Competing interests

The authors declare no competing interests.

Go to:

Footnotes

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Change history

4/17/2023

A Correction to this paper has been published: 10.1038/s41579-023-00896-0

Go to:

References

1. Ballering AV, van Zon SKR, Hartman TCO, Rosmalen JGM. Persistence of somatic symptoms after COVID-19 in the Netherlands: an observational cohort study. Lancet. 2022;400:452–461. 10.1016/S0140-6736(22)01214-4. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

2. Bull-Otterson L. Post–COVID conditions among adult COVID-19 survivors aged 18–64 and ≥65 years — United States, March 2020–November 2021. MMWR Morb. Mortal. Wkly Rep. 2022;71:713. 10.15585/mmwr.mm7121e1. [CrossRef] [Google Scholar]

3. Ceban F, et al. Fatigue and cognitive impairment in post-COVID-19 syndrome: a systematic review and meta-analysis. Brain Behav. Immun. 2022;101:93–135. 10.1016/j.bbi.2021.12.020. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

4. Al-Aly Z, Bowe B, Xie Y. Long COVID after breakthrough SARS-CoV-2 infection. Nat. Med. 2022 10.1038/s41591-022-01840-0. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

5. Ayoubkhani, D. et al. Risk of Long Covid in people infected with SARS-CoV-2 after two doses of a COVID-19 vaccine: community-based, matched cohort study. Preprint at medRxiv10.1101/2022.02.23.22271388 (2022).

6. FAIR Health. Patients Diagnosed with Post-COVID Conditions: An Analysis of Private Healthcare Claims Using the Official ICD-10 Diagnostic Code (FAIR Health, 2022).

7. Davis HE, et al. Characterizing long COVID in an international cohort: 7 months of symptoms and their impact. eClinicalMedicine. 2021;38:101019. 10.1016/j.eclinm.2021.101019. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

8. Xie Y, Xu E, Bowe B, Al-Aly Z. Long-term cardiovascular outcomes of COVID-19. Nat. Med. 2022;28:583–590. 10.1038/s41591-022-01689-3. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

9. Xie Y, Al-Aly Z. Risks and burdens of incident diabetes in long COVID: a cohort study. Lancet Diabetes Endocrinol. 2022;10:311–321. 10.1016/S2213-8587(22)00044-4. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

10. Mancini DM, et al. Use of cardiopulmonary stress testing for patients with unexplained dyspnea post–coronavirus disease. JACC Heart Fail. 2021;9:927–937. 10.1016/j.jchf.2021.10.002. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

11. Kedor C, et al. A prospective observational study of post-COVID-19 chronic fatigue syndrome following the first pandemic wave in Germany and biomarkers associated with symptom severity. Nat. Commun. 2022;13:5104. 10.1038/s41467-022-32507-6. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

12. Larsen NW, et al. Characterization of autonomic symptom burden in long COVID: a global survey of 2314 adults. Front. Neurol. 2022;13:1012668. 10.3389/fneur.2022.1012668. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

13. Demko, Z. O. et al. Post-acute sequelae of SARS-CoV-2 (PASC) impact quality of life at 6, 12 and 18 months post-infection. Preprint at medRxiv10.1101/2022.08.08.22278543 (2022).

14. Cairns R, Hotopf M. A systematic review describing the prognosis of chronic fatigue syndrome. Occup. Med. Oxf. Engl. 2005;55:20–31. 10.1093/occmed/kqi013. [Abstract] [CrossRef] [Google Scholar]

15. Bach, K. Is ‘long Covid’ worsening the labor shortage? Brookingshttps://www.brookings.edu/research/is-long-covid-worsening-the-labor-shortage/ (2022).

16. Swank Z, et al. Persistent circulating severe acute respiratory syndrome coronavirus 2 spike is associated with post-acute coronavirus disease 2019 sequelae. Clin. Infect. Dis. 2022 10.1093/cid/ciac722. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

17. Proal AD, VanElzakker MB. Long COVID or post-acute sequelae of COVID-19 (PASC): an overview of biological factors that may contribute to persistent symptoms. Front. Microbiol. 2021;12:698169. 10.3389/fmicb.2021.698169. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

18. Klein, J. et al. Distinguishing features of Long COVID identified through immune profiling. Preprint at medRxiv10.1101/2022.08.09.22278592 (2022). [Europe PMC free article] [Abstract]

19. Glynne P, Tahmasebi N, Gant V, Gupta R. Long COVID following mild SARS-CoV-2 infection: characteristic T cell alterations and response to antihistamines. J. Investig. Med. 2022;70:61–67. 10.1136/jim-2021-002051. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

20. Phetsouphanh C, et al. Immunological dysfunction persists for 8 months following initial mild-to-moderate SARS-CoV-2 infection. Nat. Immunol. 2022;23:210–216. 10.1038/s41590-021-01113-x. [Abstract] [CrossRef] [Google Scholar]

21. Zubchenko S, Kril I, Nadizhko O, Matsyura O, Chopyak V. Herpesvirus infections and post-COVID-19 manifestations: a pilot observational study. Rheumatol. Int. 2022 10.1007/s00296-022-05146-9. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

22. Peluso MJ, et al. Evidence of recent Epstein-Barr virus reactivation in individuals experiencing Long COVID. Preprint at medRxiv. 2022 10.1101/2022.06.21.22276660. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

23. Yeoh YK, et al. Gut microbiota composition reflects disease severity and dysfunctional immune responses in patients with COVID-19. Gut. 2021;70:698–706. 10.1136/gutjnl-2020-323020. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

24. Liu Q, et al. Gut microbiota dynamics in a prospective cohort of patients with post-acute COVID-19 syndrome. Gut. 2022;71:544–552. 10.1136/gutjnl-2021-325989. [Abstract] [CrossRef] [Google Scholar]

25. Mendes de Almeida V. Gut microbiota from patients with mild COVID-19 cause alterations in mice that resemble post-COVID syndrome. Res. Sq. 2022 10.21203/rs.3.rs-1756189/v1. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

26. Wallukat G, et al. Functional autoantibodies against G-protein coupled receptors in patients with persistent long-COVID-19 symptoms. J. Transl Autoimmun. 2021;4:100100. 10.1016/j.jtauto.2021.100100. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

27. Su Y, et al. Multiple early factors anticipate post-acute COVID-19 sequelae. Cell. 2022;185:881–895.e20. 10.1016/j.cell.2022.01.014. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

28. Arthur JM, et al. Development of ACE2 autoantibodies after SARS-CoV-2 infection. PLoS ONE. 2021;16:e0257016. 10.1371/journal.pone.0257016. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

29. Haffke M, et al. Endothelial dysfunction and altered endothelial biomarkers in patients with post-COVID-19 syndrome and chronic fatigue syndrome (ME/CFS) J. Transl Med. 2022;20:138. 10.1186/s12967-022-03346-2. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

30. Charfeddine S. Long COVID 19 syndrome: is it related to microcirculation and endothelial dysfunction? Insights from TUN-EndCOV study. Front. Cardiovasc. Med. 2021 10.3389/fcvm.2021.745758. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

31. Pretorius E, et al. Prevalence of symptoms, comorbidities, fibrin amyloid microclots and platelet pathology in individuals with Long COVID/post-acute sequelae of COVID-19 (PASC) Cardiovasc. Diabetol. 2022;21:148. 10.1186/s12933-022-01579-5. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

32. Spudich S, Nath A. Nervous system consequences of COVID-19. Science. 2022;375:267–269. 10.1126/science.abm2052. [Abstract] [CrossRef] [Google Scholar]

33. Renz-Polster H, Tremblay M-E, Bienzle D, Fischer JE. The pathobiology of myalgic encephalomyelitis/chronic fatigue syndrome: the case for neuroglial failure. Front. Cell. Neurosci. 2022;16:888232. 10.3389/fncel.2022.888232. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

34. Merzon E, et al. Clinical and socio-demographic variables associated with the diagnosis of long COVID syndrome in youth: a population-based study. Int. J. Environ. Res. Public Health. 2022;19:5993. 10.3390/ijerph19105993. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

35. CDC. Long COVID - household pulse survey - COVID-19. CDChttps://www.cdc.gov/nchs/covid19/pulse/long-covid.htm (2022).

36. Williamson AE, Tydeman F, Miners A, Pyper K, Martineau AR. Short-term and long-term impacts of COVID-19 on economic vulnerability: a population-based longitudinal study (COVIDENCE UK) BMJ Open. 2022;12:e065083. 10.1136/bmjopen-2022-065083. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

37. Ziauddeen N, et al. Characteristics and impact of Long Covid: findings from an online survey. PLoS ONE. 2022;17:e0264331. 10.1371/journal.pone.0264331. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

38. Choutka J, Jansari V, Hornig M, Iwasaki A. Unexplained post-acute infection syndromes. Nat. Med. 2022;28:911–923. 10.1038/s41591-022-01810-6. [Abstract] [CrossRef] [Google Scholar]

39. Komaroff AL, Lipkin WI. Insights from myalgic encephalomyelitis/chronic fatigue syndrome may help unravel the pathogenesis of postacute COVID-19 syndrome. Trends Mol. Med. 2021;27:895–906. 10.1016/j.molmed.2021.06.002. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

40. Schultheiß C, et al. From online data collection to identification of disease mechanisms: the IL-1ß, IL-6 and TNF-α cytokine triad is associated with post-acute sequelae of COVID-19 in a digital research cohort. SSRN. 2021 10.2139/ssrn.3963839. [CrossRef] [Google Scholar]

41. Peluso MJ, et al. Markers of immune activation and inflammation in individuals with postacute sequelae of severe acute respiratory syndrome coronavirus 2 infection. J. Infect. Dis. 2021;224:1839–1848. 10.1093/infdis/jiab490. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

42. Fernández-Castañeda A, et al. Mild respiratory SARS-CoV-2 infection can cause multi-lineage cellular dysregulation and myelin loss in the brain. bioRxiv. 2022 10.1101/2022.01.07.475453. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

43. Hornig M, et al. Distinct plasma immune signatures in ME/CFS are present early in the course of illness. Sci. Adv. 2015;1:e1400121. 10.1126/sciadv.1400121. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

44. Wang EY, et al. Diverse functional autoantibodies in patients with COVID-19. Nature. 2021;595:283–288. 10.1038/s41586-021-03631-y. [Abstract] [CrossRef] [Google Scholar]

45. Shikova E, et al. Cytomegalovirus, Epstein-Barr virus, and human herpesvirus-6 infections in patients with myalgic еncephalomyelitis/chronic fatigue syndrome. J. Med. Virol. 2020;92:3682–3688. 10.1002/jmv.25744. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

46. Schreiner P, et al. Human herpesvirus-6 reactivation, mitochondrial fragmentation, and the coordination of antiviral and metabolic phenotypes in myalgic encephalomyelitis/chronic fatigue syndrome. Immunohorizons. 2020;4:201–215. 10.4049/immunohorizons.2000006. [Abstract] [CrossRef] [Google Scholar]

47. García-Abellán J, et al. Antibody response to SARS-CoV-2 is associated with long-term clinical outcome in patients with COVID-19: a longitudinal study. J. Clin. Immunol. 2021;41:1490–1501. 10.1007/s10875-021-01083-7. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

48. Augustin M, et al. Post-COVID syndrome in non-hospitalised patients with COVID-19: a longitudinal prospective cohort study. Lancet Reg. Health Eur. 2021;6:100122. 10.1016/j.lanepe.2021.100122. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

49. Talla A, et al. Longitudinal immune dynamics of mild COVID-19 define signatures of recovery and persistence. bioRxiv. 2022 10.1101/2021.05.26.442666. [CrossRef] [Google Scholar]

50. Peluso MJ, et al. Long-term SARS-CoV-2-specific immune and inflammatory responses in individuals recovering from COVID-19 with and without post-acute symptoms. Cell Rep. 2021;36:109518. 10.1016/j.celrep.2021.109518. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

51. Hu F, et al. A compromised specific humoral immune response against the SARS-CoV-2 receptor-binding domain is related to viral persistence and periodic shedding in the gastrointestinal tract. Cell. Mol. Immunol. 2020;17:1119–1125. 10.1038/s41423-020-00550-2. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

52. Korte W, et al. SARS-CoV-2 IgG and IgA antibody response is gender dependent; and IgG antibodies rapidly decline early on. J. Infect. 2021;82:e11–e14. 10.1016/j.jinf.2020.08.032. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

53. Jo W, et al. A two-phase, single cohort study of COVID-19 antibody sera-surveillance. Ann. Epidemiol. Public Health. 2021;4:1055. 10.33582/2639-4391/1055. [CrossRef] [Google Scholar]

54. Nomura Y, et al. Attenuation of antibody titers from 3 to 6 months after the second dose of the BNT162b2 vaccine depends on sex, with age and smoking risk factors for lower antibody titers at 6 months. Vaccines. 2021;9:1500. 10.3390/vaccines9121500. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

55. Tejerina F, et al. Post-COVID-19 syndrome. SARS-CoV-2 RNA detection in plasma, stool, and urine in patients with persistent symptoms after COVID-19. BMC Infect. Dis. 2022;22:211. 10.1186/s12879-022-07153-4. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

56. Goh, D. et al. Persistence of residual SARS-CoV-2 viral antigen and RNA in tissues of patients with long COVID-19. Preprint at https://www.researchsquare.com/article/rs-1379777/v1 (2022).

57. Ceulemans LJ, et al. Persistence of SARS-CoV-2 RNA in lung tissue after mild COVID-19. Lancet Respir. Med. 2021;9:e78–e79. 10.1016/S2213-2600(21)00240-X. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

58. Gaebler C, et al. Evolution of antibody immunity to SARS-CoV-2. Nature. 2021;591:639–644. 10.1038/s41586-021-03207-w. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

59. Menuchin-Lasowski Y, et al. SARS-CoV-2 infects and replicates in photoreceptor and retinal ganglion cells of human retinal organoids. Stem Cell Rep. 2022;17:789–803. 10.1016/j.stemcr.2022.02.015. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

60. Cheung CCL, et al. Residual SARS-CoV-2 viral antigens detected in GI and hepatic tissues from five recovered patients with COVID-19. Gut. 2022;71:226–229. 10.1136/gutjnl-2021-324280. [Abstract] [CrossRef] [Google Scholar]

61. Natarajan A, et al. Gastrointestinal symptoms and fecal shedding of SARS-CoV-2 RNA suggest prolonged gastrointestinal infection. Med. 2022;3:371–387.e9. 10.1016/j.medj.2022.04.001. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

62. Katsoularis I, et al. Risks of deep vein thrombosis, pulmonary embolism, and bleeding after covid-19: nationwide self-controlled cases series and matched cohort study. BMJ. 2022;377:e069590. 10.1136/bmj-2021-069590. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

63. Pretorius E, et al. Persistent clotting protein pathology in Long COVID/post-acute sequelae of COVID-19 (PASC) is accompanied by increased levels of antiplasmin. Cardiovasc. Diabetol. 2021;20:172. 10.1186/s12933-021-01359-7. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

64. Kubánková M, et al. Physical phenotype of blood cells is altered in COVID-19. Biophys. J. 2021;120:2838–2847. 10.1016/j.bpj.2021.05.025. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

65. Osiaevi I, et al. Persistent capillary rarefication in long COVID syndrome. Angiogenesis. 2022 10.1007/s10456-022-09850-9. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

66. Patel MA, et al. Elevated vascular transformation blood biomarkers in long-COVID indicate angiogenesis as a key pathophysiological mechanism. Mol. Med. 2022;28:122. 10.1186/s10020-022-00548-8. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

67. Puntmann VO, et al. Outcomes of cardiovascular magnetic resonance imaging in patients recently recovered from coronavirus disease 2019 (COVID-19) JAMA Cardiol. 2020;5:1265–1273. 10.1001/jamacardio.2020.3557. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

68. Roca-Fernández A, et al. Cardiac impairment in Long Covid 1-year post-SARS-CoV-2 infection. Eur. Heart J. 2022;43:ehac544.219. 10.1093/eurheartj/ehac544.219. [CrossRef] [Google Scholar]

69. Dennis A, et al. Multiorgan impairment in low-risk individuals with post-COVID-19 syndrome: a prospective, community-based study. BMJ Open. 2021;11:e048391. 10.1136/bmjopen-2020-048391. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

70. Dennis, A. et al. Multi-organ impairment and Long COVID: a 1-year prospective, longitudinal cohort study. Preprint at medRxiv10.1101/2022.03.18.22272607 (2022). [Europe PMC free article] [Abstract]

71. Bowe B, Xie Y, Xu E, Al-Aly Z. Kidney outcomes in Long COVID. J. Am. Soc. Nephrol. 2021;32:2851–2862. 10.1681/ASN.2021060734. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

72. Almufarrij I, Munro KJ. One year on: an updated systematic review of SARS-CoV-2, COVID-19 and audio-vestibular symptoms. Int. J. Audiol. 2021;60:935–945. 10.1080/14992027.2021.1896793. [Abstract] [CrossRef] [Google Scholar]

73. Holdsworth DA, et al. Comprehensive clinical assessment identifies specific neurocognitive deficits in working-age patients with long-COVID. PLoS ONE. 2022;17:e0267392. 10.1371/journal.pone.0267392. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

74. Cysique, L. A. et al. Post-acute COVID-19 cognitive impairment and decline uniquely associate with kynurenine pathway activation: a longitudinal observational study. Preprint at medRxiv10.1101/2022.06.07.22276020 (2022).

75. Crivelli L, et al. Changes in cognitive functioning after COVID-19: a systematic review and meta-analysis. Alzheimers Dement. 2022;18:1047–1066. 10.1002/alz.12644. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

76. Woo MS, et al. Frequent neurocognitive deficits after recovery from mild COVID-19. Brain Commun. 2020;2:fcaa205. 10.1093/braincomms/fcaa205. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

77. Taquet M, et al. Neurological and psychiatric risk trajectories after SARS-CoV-2 infection: an analysis of 2-year retrospective cohort studies including 1 284 437 patients. Lancet Psychiatry. 2022;9:815–827. 10.1016/S2215-0366(22)00260-7. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

78. Reiken S, et al. Alzheimer’s-like signaling in brains of COVID-19 patients. Alzheimers Dement. 2022;18:955–965. 10.1002/alz.12558. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

79. Charnley M, et al. Neurotoxic amyloidogenic peptides in the proteome of SARS-COV2: potential implications for neurological symptoms in COVID-19. Nat. Commun. 2022;13:3387. 10.1038/s41467-022-30932-1. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

80. Visser, D. et al. Long COVID is associated with extensive in-vivo neuroinflammation on [18F]DPA-714 PET. Preprint at medRxiv10.1101/2022.06.02.22275916 (2022).

81. Guedj E, et al. 18F-FDG brain PET hypometabolism in patients with long COVID. Eur. J. Nucl. Med. Mol. Imaging. 2021;48:2823–2833. 10.1007/s00259-021-05215-4. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

82. Hugon J, et al. Cognitive decline and brainstem hypometabolism in long COVID: a case series. Brain Behav. 2022;12:e2513. 10.1002/brb3.2513. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

83. Apple AC, et al. Risk factors and abnormal cerebrospinal fluid associate with cognitive symptoms after mild COVID-19. Ann. Clin. Transl Neurol. 2022;9:221–226. 10.1002/acn3.51498. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

84. Douaud G, et al. SARS-CoV-2 is associated with changes in brain structure in UK Biobank. Nature. 2022;604:697–707. 10.1038/s41586-022-04569-5. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

85. Peluso MJ, et al. SARS-CoV-2 and mitochondrial proteins in neural-derived exosomes of COVID-19. Ann. Neurol. 2022;91:772–781. 10.1002/ana.26350. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

86. Villaume WA. Marginal BH4 deficiencies, iNOS, and self-perpetuating oxidative stress in post-acute sequelae of Covid-19. Med. Hypotheses. 2022;163:110842. 10.1016/j.mehy.2022.110842. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

87. Bitirgen G, et al. Corneal confocal microscopy identifies corneal nerve fibre loss and increased dendritic cells in patients with long COVID. Br. J. Ophthalmol. 2021 10.1136/bjophthalmol-2021-319450. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

88. Barros A, et al. Small fiber neuropathy in the cornea of Covid-19 patients associated with the generation of ocular surface disease. Ocul. Surf. 2022;23:40–48. 10.1016/j.jtos.2021.10.010. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

89. Bitirgen G, et al. Abnormal quantitative pupillary light responses following COVID-19. Int. Ophthalmol. 2022 10.1007/s10792-022-02275-9. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

90. Mardin CY, et al. Possible impact of functional active GPCR-autoantibodies on retinal microcirculation in long-COVID. Invest. Ophthalmol. Vis. Sci. 2022;63:3315–F0124. [Google Scholar]

91. Zhang B-Z, et al. SARS-CoV-2 infects human neural progenitor cells and brain organoids. Cell Res. 2020;30:928–931. 10.1038/s41422-020-0390-x. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

92. Sen S, et al. Retinal manifestations in patients with SARS-CoV-2 infection and pathogenetic implications: a systematic review. Int. Ophthalmol. 2022;42:323–336. 10.1007/s10792-021-01996-7. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

93. Frere JJ, et al. SARS-CoV-2 infection in hamsters and humans results in lasting and unique systemic perturbations post recovery. Sci. Transl Med. 2022;14:eabq3059. 10.1126/scitranslmed.abq3059. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

94. Rutkai I, et al. Neuropathology and virus in brain of SARS-CoV-2 infected non-human primates. Nat. Commun. 2022;13:1745. 10.1038/s41467-022-29440-z. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

95. Committee on the Diagnostic Criteria for Myalgic Encephalomyelitis/Chronic Fatigue Syndrome, Board on the Health of Select Populations, & Institute of Medicine. Beyond Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: Redefining an Illness (National Academies Press, 2015). [Abstract]

96. Bateman L, et al. Myalgic encephalomyelitis/chronic fatigue syndrome: essentials of diagnosis and management. Mayo Clin. Proc. 2021;96:2861–2878. 10.1016/j.mayocp.2021.07.004. [Abstract] [CrossRef] [Google Scholar]

97. The ME Association. Index of ME/CFS published research - Nov 2022. 224 Index of ME/CFS Published Research. The ME Associationhttps://meassociation.org.uk/ (2022).

98. Seltzer, J. & Thomas, J. ME Research Summary 2019 (The ME Association, 2019).

99. Wong TL, Weitzer DJ. Long COVID and myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS)-a systemic review and comparison of clinical presentation and symptomatology. Med. (Kaunas.) 2021;57:418. [Europe PMC free article] [Abstract] [Google Scholar]

100. Twomey R, et al. Chronic fatigue and postexertional malaise in people living with Long COVID: an observational study. Phys. Ther. 2022;102:pzac005. 10.1093/ptj/pzac005. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

101. Vernon SD, et al. Orthostatic challenge causes distinctive symptomatic, hemodynamic and cognitive responses in Long COVID and myalgic encephalomyelitis/chronic fatigue syndrome. Front. Med. 2022;9:917019. 10.3389/fmed.2022.917019. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

102. Lam MH-B, et al. Mental morbidities and chronic fatigue in severe acute respiratory syndrome survivors: long-term follow-up. Arch. Intern. Med. 2009;169:2142–2147. 10.1001/archinternmed.2009.384. [Abstract] [CrossRef] [Google Scholar]

103. Keller BA, Pryor JL, Giloteaux L. Inability of myalgic encephalomyelitis/chronic fatigue syndrome patients to reproduce VO2peak indicates functional impairment. J. Transl Med. 2014;12:104. 10.1186/1479-5876-12-104. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

104. Saha AK, et al. Erythrocyte deformability as a potential biomarker for chronic fatigue syndrome. Blood. 2018;132:4874. 10.1182/blood-2018-99-117260. [CrossRef] [Google Scholar]

105. Díaz-Resendiz KJG, et al. Loss of mitochondrial membrane potential (ΔΨm) in leucocytes as post-COVID-19 sequelae. J. Leukoc. Biol. 2022;112:23–29. 10.1002/JLB.3MA0322-279RRR. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

106. Pozzi A. COVID-19 and mitochondrial non-coding RNAs: new insights from published data. Front. Physiol. 2022;12:805005. 10.3389/fphys.2021.805005. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

107. Guntur VP, et al. Signatures of mitochondrial dysfunction and impaired fatty acid metabolism in plasma of patients with post-acute sequelae of COVID-19 (PASC) Metabolites. 2022;12:1026. 10.3390/metabo12111026. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

108. Paul BD, Lemle MD, Komaroff AL, Snyder SH. Redox imbalance links COVID-19 and myalgic encephalomyelitis/chronic fatigue syndrome. Proc. Natl Acad. Sci. USA. 2021;118:e2024358118. 10.1073/pnas.2024358118. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

109. Wright J, Astill SL, Sivan M. The relationship between physical activity and Long COVID: a cross-sectional study. Int. J. Environ. Res. Public Health. 2022;19:5093. 10.3390/ijerph19095093. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

110. Heerdt PM, Shelley B, Singh I. Impaired systemic oxygen extraction long after mild COVID-19: potential perioperative implications. Br. J. Anaesth. 2022;128:e246–e249. 10.1016/j.bja.2021.12.036. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

111. Novak P, et al. Multisystem involvement in post-acute sequelae of coronavirus disease 19. Ann. Neurol. 2022;91:367–379. 10.1002/ana.26286. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

112. Holmes E, et al. Incomplete systemic recovery and metabolic phenoreversion in post-acute-phase nonhospitalized COVID-19 patients: implications for assessment of post-acute COVID-19 syndrome. J. Proteome Res. 2021;20:3315–3329. 10.1021/acs.jproteome.1c00224. [Abstract] [CrossRef] [Google Scholar]

113. van Campen CLMC, Visser FC. Orthostatic intolerance in long-haul COVID after SARS-CoV-2: a case-control comparison with post-EBV and insidious-onset myalgic encephalomyelitis/chronic fatigue syndrome patients. Healthcare. 2022;10:2058. 10.3390/healthcare10102058. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

114. van Campen CLMC, Visser FC. Long-Haul COVID patients: prevalence of POTS are reduced but cerebral blood flow abnormalities remain abnormal with longer disease duration. Healthcare. 2022;10:2105. 10.3390/healthcare10102105. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

115. Nunes JM, Kruger A, Proal A, Kell DB, Pretorius E. The occurrence of hyperactivated platelets and fibrinaloid microclots in myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) Pharmaceuticals. 2022;15:931. 10.3390/ph15080931. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

116. Hoad A, Spickett G, Elliott J, Newton J. Postural orthostatic tachycardia syndrome is an under-recognized condition in chronic fatigue syndrome. QJM. 2008;101:961–965. 10.1093/qjmed/hcn123. [Abstract] [CrossRef] [Google Scholar]

117. Shaw BH, et al. The face of postural tachycardia syndrome – insights from a large cross‐sectional online community‐based survey. J. Intern. Med. 2019;286:438–448. 10.1111/joim.12895. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

118. Raj SR, et al. Postural orthostatic tachycardia syndrome (POTS): priorities for POTS care and research from a 2019 National Institutes of Health expert consensus meeting - part 2. Auton. Neurosci. Basic. Clin. 2021;235:102836. 10.1016/j.autneu.2021.102836. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

119. Oaklander AL, et al. Peripheral neuropathy evaluations of patients with prolonged Long COVID. Neurol. Neuroimmunol. Neuroinflamm. 2022;9:e1146. 10.1212/NXI.0000000000001146. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

120. Larsen NW, et al. Characterization of autonomic symptom burden in long COVID: a global survey of 2,314 adults. Front. Neurol. 2022;13:1012668. 10.3389/fneur.2022.1012668. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

121. Weinstock LB, et al. Mast cell activation symptoms are prevalent in Long-COVID. Int. J. Infect. Dis. 2021;112:217–226. 10.1016/j.ijid.2021.09.043. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

122. Boneva RS, et al. Endometriosis as a comorbid condition in chronic fatigue syndrome (CFS): secondary analysis of data from a CFS case-control study. Front. Pediatr. 2019;7:195. 10.3389/fped.2019.00195. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

123. Bragée, B. et al. Signs of intracranial hypertension, hypermobility, and craniocervical obstructions in patients with myalgic encephalomyelitis/chronic fatigue syndrome. Front. Neurol. 11, (2020). [Europe PMC free article] [Abstract]

124. Medina-Perucha L, et al. Self-reported menstrual alterations during the COVID-19 syndemic in Spain: a cross-sectional study. Int. J. Womens Health. 2022;14:529–544. 10.2147/IJWH.S354655. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

125. Ding T, et al. Analysis of ovarian injury associated with COVID-19 disease in reproductive-aged women in Wuhan, China: an observational study. Front. Med. 2021;8:635255. 10.3389/fmed.2021.635255. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

126. Sharp GC, et al. The COVID-19 pandemic and the menstrual cycle: research gaps and opportunities. Int. J. Epidemiol. 2021 10.1093/ije/dyab239. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

127. Khan SM, et al. SARS-CoV-2 infection and subsequent changes in the menstrual cycle among participants in the Arizona CoVHORT study. Am. J. Obstet. Gynecol. 2022;226:270–273. 10.1016/j.ajog.2021.09.016. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

128. Harlow BL, Signorello LB, Hall JE, Dailey C, Komaroff AL. Reproductive correlates of chronic fatigue syndrome. Am. J. Med. 1998;105:94S–99S. 10.1016/S0002-9343(98)00173-9. [Abstract] [CrossRef] [Google Scholar]

129. Thomas N, Gurvich C, Huang K, Gooley PR, Armstrong CW. The underlying sex differences in neuroendocrine adaptations relevant to myalgic encephalomyelitis chronic fatigue syndrome. Front. Neuroendocrinol. 2022;66:100995. 10.1016/j.yfrne.2022.100995. [Abstract] [CrossRef] [Google Scholar]

130. Boneva RS, Lin J-MS, Unger ER. Early menopause and other gynecologic risk indicators for chronic fatigue syndrome in women. Menopause. 2015;22:826–834. 10.1097/GME.0000000000000411. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

131. Kresch E, et al. COVID-19 endothelial dysfunction can cause erectile dysfunction: histopathological, immunohistochemical, and ultrastructural study of the human penis. World J. Mens Health. 2021;39:466–469. 10.5534/wjmh.210055. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

132. Maleki BH, Tartibian B. COVID-19 and male reproductive function: a prospective, longitudinal cohort study. Reproduction. 2021;161:319–331. 10.1530/REP-20-0382. [Abstract] [CrossRef] [Google Scholar]

133. Yu JZ, et al. Lung perfusion disturbances in nonhospitalized post-COVID with dyspnea — a magnetic resonance imaging feasibility study. J. Intern. Med. 2022;292:941–956. 10.1111/joim.13558. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

134. Cho JL, et al. Quantitative chest CT assessment of small airways disease in post-acute SARS-CoV-2 infection. Radiology. 2022;304:185–192. 10.1148/radiol.212170. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

135. Vijayakumar B, et al. Immuno-proteomic profiling reveals aberrant immune cell regulation in the airways of individuals with ongoing post-COVID-19 respiratory disease. Immunity. 2022;55:542–556.e5. 10.1016/j.immuni.2022.01.017. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

136. Littlefield KM, et al. SARS-CoV-2-specific T cells associate with inflammation and reduced lung function in pulmonary post-acute sequalae of SARS-CoV-2. PLOS Pathog. 2022;18:e1010359. 10.1371/journal.ppat.1010359. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

137. Meringer H, Mehandru S. Gastrointestinal post-acute COVID-19 syndrome. Nat. Rev. Gastroenterol. Hepatol. 2022;19:345–346. 10.1038/s41575-022-00611-z. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

138. König RS, et al. The gut microbiome in myalgic encephalomyelitis (ME)/chronic fatigue syndrome (CFS) Front. Immunol. 2022;12:628741. 10.3389/fimmu.2021.628741. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

139. Zuo T, et al. Depicting SARS-CoV-2 faecal viral activity in association with gut microbiota composition in patients with COVID-19. Gut. 2021;70:276–284. [Europe PMC free article] [Abstract] [Google Scholar]

140. Zollner A, et al. Postacute COVID-19 is characterized by gut viral antigen persistence in inflammatory bowel diseases. Gastroenterology. 2022;163(495):506.e8. [Europe PMC free article] [Abstract] [Google Scholar]

141. Giron, L. B. et al. Markers of fungal translocation are elevated during post-acute sequelae of SARS-CoV-2 and induce NF-κB signaling. JCI Insight10.1172/jci.insight.160989 (2022). [Europe PMC free article] [Abstract]

142. Jason LA, et al. COVID-19 symptoms over time: comparing long-haulers to ME/CFS. Fatigue Biomed. Health Behav. 2021;9:59–68. 10.1080/21641846.2021.1922140. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

143. Tran V-T, Porcher R, Pane I, Ravaud P. Course of post COVID-19 disease symptoms over time in the ComPaRe long COVID prospective e-cohort. Nat. Commun. 2022;13:1812. 10.1038/s41467-022-29513-z. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

144. Walker A, Kelly C, Pottinger G, Hopkins C. Parosmia — a common consequence of covid-19. BMJ. 2022;377:e069860. 10.1136/bmj-2021-069860. [Abstract] [CrossRef] [Google Scholar]

145. Jamal SM, et al. Prospective evaluation of autonomic dysfunction in post-acute sequela of COVID-19. J. Am. Coll. Cardiol. 2022;79:2325–2330. 10.1016/j.jacc.2022.03.357. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

146. Stavileci B, Özdemir E, Özdemir B, Ereren E, Cengiz M. De-novo development of fragmented QRS during a six-month follow-up period in patients with COVID-19 disease and its cardiac effects. J. Electrocardiol. 2022;72:44–48. 10.1016/j.jelectrocard.2022.02.012. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

147. Grist JT, et al. Lung abnormalities depicted with hyperpolarized ¹²⁹Xe MRI in patients with long COVID. Radiology. 2022;305:709–717. 10.1148/radiol.220069. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

148. US ME/CFS Clinician Coalition. Testing Recommendations for Suspected ME/CFS (US ME/CFS Clinician Coalition, 2021).

149. Galán M, et al. Persistent overactive cytotoxic immune response in a Spanish cohort of individuals with long-COVID: identification of diagnostic biomarkers. Front. Immunol. 2022;13:848886. 10.3389/fimmu.2022.848886. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

150. Grandjean D, et al. Screening for SARS-CoV-2 persistence in Long COVID patients using sniffer dogs and scents from axillary sweats samples. Clin. Trials. 2022;12:2. [Google Scholar]

151. Pifarré F, et al. The use of oxygen as a possible screening biomarker for the diagnosis of chronic fatigue. Apunt. Sports Med. 2022;57:100379. 10.1016/j.apunsm.2022.100379. [CrossRef] [Google Scholar]

152. Jason LA, Kalns J, Richarte A, Katz BZ, Torres C. Saliva fatigue biomarker index as a marker for severe myalgic encephalomyelitis/chronic fatigue syndrome in a community based sample. Fatigue Biomed. Health Behav. 2021;9:189–195. 10.1080/21641846.2021.1994222. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

153. Esfandyarpour R, Kashi A, Nemat-Gorgani M, Wilhelmy J, Davis RW. A nanoelectronics-blood-based diagnostic biomarker for myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) Proc. Natl Acad. Sci. USA. 2019;116:10250–10257. 10.1073/pnas.1901274116. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

154. Nkiliza A, et al. Sex-specific plasma lipid profiles of ME/CFS patients and their association with pain, fatigue, and cognitive symptoms. J. Transl Med. 2021;19:370. 10.1186/s12967-021-03035-6. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

155. Bolton MJ, Chapman BP. & Van Marwijk, H. Low-dose naltrexone as a treatment for chronic fatigue syndrome. BMJ Case Rep. 2020;13:e232502. 10.1136/bcr-2019-232502. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

156. Pitt B, Tate AM, Gluck D, Rosenson RS, Goonewardena SN. Repurposing low-dose naltrexone (LDN) for the prevention and treatment of immunothrombosis in COVID-19. Eur. Heart J. Cardiovasc. Pharmacother. 2022 10.1093/ehjcvp/pvac014. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

157. Alper K. Case report: famotidine for neuropsychiatric symptoms in COVID-19. Front. Med. 2020;7:614393. 10.3389/fmed.2020.614393. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

158. Hohberger B, et al. Case report: neutralization of autoantibodies targeting G-protein-coupled receptors improves capillary impairment and fatigue symptoms after COVID-19 infection. Front. Med. 2021;8:754667. 10.3389/fmed.2021.754667. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

159. Wang C, et al. Long COVID: the nature of thrombotic sequelae determines the necessity of early anticoagulation. Front. Cell. Infect. Microbiol. 2022;12:861703. 10.3389/fcimb.2022.861703. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

160. The ME Association. A new treatment for Long Covid? The ME Associationhttps://meassociation.org.uk/2021/10/a-new-treatment-for-long-covid/ (2021).

161. Tölle M, et al. Myalgic encephalomyelitis/chronic fatigue syndrome: efficacy of repeat immunoadsorption. J. Clin. Med. 2020;9:E2443. 10.3390/jcm9082443. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

162. Wood E, Hall KH, Tate W. Role of mitochondria, oxidative stress and the response to antioxidants in myalgic encephalomyelitis/chronic fatigue syndrome: a possible approach to SARS-CoV-2 ‘long-haulers’? Chronic Dis. Transl Med. 2020;7:14–26. [Europe PMC free article] [Abstract] [Google Scholar]

163. NICE. Myalgic encephalomyelitis (or encephalopathy)/chronic fatigue syndrome: diagnosis and management. NICEhttps://www.nice.org.uk/guidance/NG206 (2021). [Abstract]

164. World Health Organization. Support for Rehabilitation Self-Management After COVID-19 Related Illness (WHO, 2021).

165. CDC. Treatment of ME/CFS | Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). CDChttps://www.cdc.gov/me-cfs/treatment/index.html (2021).

166. Long COVID Physio. Exercise. Long COVID Physiohttps://longcovid.physio/exercise (2022).

167. Geng, L. N., Bonilla, H. F., Shafer, R. W., Miglis, M. G. & Yang, P. C. Case report of breakthrough long COVID and the use of nirmatrelvir-ritonavir. Preprint at https://www.researchsquare.com/article/rs-1443341/v1 (2022).

168. Xie, Y., Choi, T. & Al-Aly, Z. Nirmatrelvir and the risk of post-acute sequelae of COVID-19. Preprint at medRxiv10.1101/2022.11.03.22281783 (2022).

169. Charfeddine S, et al. Sulodexide in the treatment of patients with long COVID 19 symptoms and endothelial dysfunction: the results of TUN-EndCOV study. Arch. Cardiovasc. Dis. Suppl. 2022;14:127. [Google Scholar]

170. Thomas R, et al. A randomised, double-blind, placebo-controlled trial evaluating concentrated phytochemical-rich nutritional capsule in addition to a probiotic capsule on clinical outcomes among individuals with COVID-19 — the UK Phyto-V study. COVID. 2022;2:433–449. 10.3390/covid2040031. [CrossRef] [Google Scholar]

171. Zhang L, et al. Gut microbiota-derived synbiotic formula (SIM01) as a novel adjuvant therapy for COVID-19: an open-label pilot study. J. Gastroenterol. Hepatol. 2022;37:823–831. 10.1111/jgh.15796. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

172. Liu LD, Duricka DL. Stellate ganglion block reduces symptoms of Long COVID: a case series. J. Neuroimmunol. 2022;362:577784. 10.1016/j.jneuroim.2021.577784. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

173. Belcaro G, et al. Preventive effects of Pycnogenol® on cardiovascular risk factors (including endothelial function) and microcirculation in subjects recovering from coronavirus disease 2019 (COVID-19) Minerva Med. 2022;113:300–308. 10.23736/S0026-4806.21.07650-3. [Abstract] [CrossRef] [Google Scholar]

174. Crooks V, Waller S, Smith T, Hahn TJ. The use of the Karnofsky Performance Scale in determining outcomes and risk in geriatric outpatients. J. Gerontol. 1991;46:M139–M144. 10.1093/geronj/46.4.M139. [Abstract] [CrossRef] [Google Scholar]

175. Ledford H. Long-COVID treatments: why the world is still waiting. Nature. 2022;608:258–260. 10.1038/d41586-022-02140-w. [Abstract] [CrossRef] [Google Scholar]

176. Toogood PL, Clauw DJ, Phadke S, Hoffman D. Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS): where will the drugs come from? Pharmacol. Res. 2021;165:105465. 10.1016/j.phrs.2021.105465. [Abstract] [CrossRef] [Google Scholar]

177. US ME/CFS Clinician Coalition. ME/CFS Treatment Recommendations (US ME/CFS Clinician Coalition, 2021).

178. Taquet M, Dercon Q, Harrison PJ. Six-month sequelae of post-vaccination SARS-CoV-2 infection: a retrospective cohort study of 10,024 breakthrough infections. Brain Behav. Immun. 2022;103:154–162. 10.1016/j.bbi.2022.04.013. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

179. Office for National Statistics. Self-reported long COVID after infection with the Omicron variant in the UK: 6 May 2022. Office for National Statisticshttps://www.ons.gov.uk/peoplepopulationandcommunity/healthandsocialcare/conditionsanddiseases/bulletins/selfreportedlongcovidafterinfectionwiththeomicronvariant/6may2022 (2022).

180. Tsuchida T, et al. Relationship between changes in symptoms and antibody titers after a single vaccination in patients with Long COVID. J. Med. Virol. 2022;94:3416–3420. 10.1002/jmv.27689. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

181. VA COVID-19 Observational Research Collaboratory. Burden of PCR-confirmed SARS-CoV-2 reinfection in the U.S. Veterans Administration, March 2020 – January 2022. Preprint at medRxiv10.1101/2022.03.20.22272571 (2022).

182. Bowe, B., Xie, Y. & Al-Aly, Z. Acute and postacute sequelae associated with SARS-CoV-2 reinfection. Nat. Med. 10.1038/s41591-022-02051-3 (2022). [Europe PMC free article] [Abstract]

183. Blomberg J, Gottfries C-G, Elfaitouri A, Rizwan M, Rosén A. Infection elicited autoimmunity and myalgic encephalomyelitis/chronic fatigue syndrome: an explanatory model. Front. Immunol. 2018;9:229. 10.3389/fimmu.2018.00229. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

184. Cauchemez S, Bosetti P. A reconstruction of early cryptic COVID spread. Nature. 2021;600:40–41. 10.1038/d41586-021-02989-3. [Abstract] [CrossRef] [Google Scholar]

185. CDC. Estimated COVID-19 burden. Centers for Disease Control and Preventionhttps://www.cdc.gov/coronavirus/2019-ncov/cases-updates/burden.html (2020).

186. Kucirka LM, Lauer SA, Laeyendecker O, Boon D, Lessler J. Variation in false-negative rate of reverse transcriptase polymerase chain reaction–based SARS-CoV-2 tests by time since exposure. Ann. Intern. Med. 2020;173:262–267. 10.7326/M20-1495. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

187. Levine-Tiefenbrun M, et al. SARS-CoV-2 RT-qPCR test detection rates are associated with patient age, sex, and time since diagnosis. J. Mol. Diagn. 2022;24:112–119. 10.1016/j.jmoldx.2021.10.010. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

188. Jarvis KF, Kelley JB. Temporal dynamics of viral load and false negative rate influence the levels of testing necessary to combat COVID-19 spread. Sci. Rep. 2021;11:9221. 10.1038/s41598-021-88498-9. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

189. Dattner I, et al. The role of children in the spread of COVID-19: using household data from Bnei Brak, Israel, to estimate the relative susceptibility and infectivity of children. PLoS Comput. Biol. 2021;17:e1008559. 10.1371/journal.pcbi.1008559. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

190. Langeland N, Cox RJ. Are low SARS-CoV-2 viral loads in infected children missed by RT-PCR testing? Lancet Reg. Health Eur. 2021;5:100138. 10.1016/j.lanepe.2021.100138. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

191. Van Elslande J, et al. Longitudinal follow-up of IgG anti-nucleocapsid antibodies in SARS-CoV-2 infected patients up to eight months after infection. J. Clin. Virol. 2021;136:104765. 10.1016/j.jcv.2021.104765. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

192. Liu W, et al. Predictors of nonseroconversion after SARS-CoV-2 infection. Emerg. Infect. Dis. 2021;27:2454–2458. 10.3201/eid2709.211042. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

193. Toh ZQ, et al. Comparison of seroconversion in children and adults with mild COVID-19. JAMA Netw. Open. 2022;5:e221313. [Europe PMC free article] [Abstract] [Google Scholar]

194. Peterson TM, et al. Coverage of CFS within U.S. medical schools. Univers. J. Public Health. 2013;1:177–179. 10.13189/ujph.2013.010404. [CrossRef] [Google Scholar]

195. Rowe PC, et al. Orthostatic intolerance and chronic fatigue syndrome associated with Ehlers-Danlos syndrome. J. Pediatr. 1999;135:494–499. 10.1016/S0022-3476(99)70173-3. [Abstract] [CrossRef] [Google Scholar]

196. Nguyen T, et al. Novel characterisation of mast cell phenotypes from peripheral blood mononuclear cells in chronic fatigue syndrome/myalgic encephalomyelitis patients. Asian Pac. J. Allergy Immunol. 2017;35:75–81. [Abstract] [Google Scholar]

197. Wagner C, Isenmann S, Ringendahl H, Haensch C-A. Anxiety in patients with postural tachycardia syndrome (POTS) Fortschr. Neurol. Psychiatr. 2012;80:458–462. [Abstract] [Google Scholar]

198. Grayson DA, Mackinnon A, Jorm AF, Creasey H, Broe GA. Item bias in the center for epidemiologic studies depression scale: effects of physical disorders and disability in an elderly community sample. J. Gerontol. Ser. B. 2000;55:P273–P282. 10.1093/geronb/55.5.P273. [Abstract] [CrossRef] [Google Scholar]

199. Twisk FNM, Maes M. A review on cognitive behavorial therapy (CBT) and graded exercise therapy (GET) in myalgic encephalomyelitis (ME) / chronic fatigue syndrome (CFS): CBT/GET is not only ineffective and not evidence-based, but also potentially harmful for many patients with ME/CFS. Neuro Endocrinol. Lett. 2009;30:284–299. [Abstract] [Google Scholar]

200. Vink M, Vink-Niese F. Is it useful to question the recovery behaviour of patients with ME/CFS or Long COVID? Healthcare. 2022;10:392. 10.3390/healthcare10020392. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

201. Dysautonomia International. What is dysautonomia? Dysautonomia Internationalhttp://www.dysautonomiainternational.org/page.php?ID=34 (2022).

202. CDC. Epidemiology | Presentation and clinical course | Healthcare providers | Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS). CDChttps://www.cdc.gov/me-cfs/healthcare-providers/presentation-clinical-course/epidemiology.html (2021).

203. Sørensen AIV, et al. A nationwide questionnaire study of post-acute symptoms and health problems after SARS-CoV-2 infection in Denmark. Nat. Commun. 2022;13:4213. 10.1038/s41467-022-31897-x. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

204. Berg SK, et al. Long COVID symptoms in SARS-CoV-2-positive children aged 0–14 years and matched controls in Denmark (LongCOVIDKidsDK): a national, cross-sectional study. Lancet Child Adolesc. Health. 2022;6:614–623. 10.1016/S2352-4642(22)00154-7. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

205. Morrow AK, et al. Long-term COVID 19 sequelae in adolescents: the overlap with orthostatic intolerance and ME/CFS. Curr. Pediatr. Rep. 2022;10:31–44. 10.1007/s40124-022-00261-4. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

206. Cooper S, et al. Long COVID-19 liver manifestation in children. J. Pediatr. Gastroenterol. Nutr. 2022 10.1097/MPG.0000000000003521. [Abstract] [CrossRef] [Google Scholar]

207. Kompaniyets L. Post–COVID-19 symptoms and conditions among children and adolescents — United States, March 1, 2020–January 31, 2022. MMWR Morb. Mortal. Wkly Rep. 2022;71:993–999. 10.15585/mmwr.mm7131a3. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

208. Edlow AG, Castro VM, Shook LL, Kaimal AJ, Perlis RH. Neurodevelopmental outcomes at 1 year in infants of mothers who tested positive for SARS-CoV-2 during pregnancy. JAMA Netw. Open. 2022;5:e2215787. 10.1001/jamanetworkopen.2022.15787. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

209. Morand A, et al. Similar patterns of [18F]-FDG brain PET hypometabolism in paediatric and adult patients with long COVID: a paediatric case series. Eur. J. Nucl. Med. Mol. Imaging. 2022;49:913–920. 10.1007/s00259-021-05528-4. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

210. Heiss R, et al. Pulmonary dysfunction after pediatric COVID-19. Radiology. 2022 10.1148/radiol.221250. [Europe PMC free article] [Abstract] [CrossRef] [Google Scholar]

Full text links

Read article at publisher's site: https://doi.org/10.1038/s41579-022-00846-2

Read article for free, from open access legal sources, via Unpaywall: https://www.nature.com/articles/s41579-022-00846-2.pdf

Citations & impact

Impact metrics

1,105

Citations

Jump to Citations

Citations of article over time

Alternative metrics

Altmetric item for https://www.altmetric.com/details/141252064

Altmetric
Discover the attention surrounding your research
https://www.altmetric.com/details/141252064

Smart citations by scite.ai
Explore citation contexts and check if this article has been supported or disputed.
https://scite.ai/reports/10.1038/s41579-022-00846-2

Supporting

Mentioning

Contrasting

1472

Article citations

Cost-effectiveness of an online supervised group physical and mental health rehabilitation programme for adults with post-COVID-19 condition after hospitalisation for COVID-19: the REGAIN RCT.
Nwankwo H, Mason J, Underwood M, Bruce J, Lall R, Ji C, Ratna M, McGregor G
BMC Health Serv Res, 24(1):1326, 31 Oct 2024
Cited by: 0 articles | PMID: 39482691 | PMCID: PMC11528998
This article is in the Europe PMC Open access subset. Refer to the copyright information in the article for licensing details.
Free full text in Europe PMC
A worldwide look into long COVID-19 management: an END-COVID survey.
Nigro M, Valenzuela C, Arancibia F, Cohen M, Lam DCL, Maves RC, Rath B, Simpson SQ, Song Y, Tsiodras S, Chalmers JD, Aliberti S
ERJ Open Res, 10(6):96-2024, 11 Nov 2024
Cited by: 0 articles | PMID: 39534773 | PMCID: PMC11551856
This article is in the Europe PMC Open access subset. Refer to the copyright information in the article for licensing details.
Free full text in Europe PMC
Overlapping conditions in Long COVID at a multisite academic center.
Grach SL, Dudenkov DV, Pollack B, Fairweather D, Aakre CA, Munipalli B, Croghan IT, Mueller MR, Overgaard JD, Bruno KA, Collins NM, Li Z, Hurt RT, Tal MC, Ganesh R, Knight DTR
Front Neurol, 15:1482917, 25 Oct 2024
Cited by: 0 articles | PMID: 39524912
Is there a rationale for hyperbaric oxygen therapy in the patients with Post COVID syndrome? : A critical review.
Pawlik MT, Rinneberg G, Koch A, Meyringer H, Loew TH, Kjellberg A
Eur Arch Psychiatry Clin Neurosci, 15 Nov 2024
Cited by: 0 articles | PMID: 39545965
Review
A worldwide perspective of long COVID management: how can we END-COVID?
Choi H
ERJ Open Res, 10(6):500-2024, 11 Nov 2024
Cited by: 0 articles | PMID: 39534771 | PMCID: PMC11551858
This article is in the Europe PMC Open access subset. Refer to the copyright information in the article for licensing details.
Free full text in Europe PMC

Go to all (1,105) article citations

Funding

Funders who supported this work.

NCATS NIH HHS (1)

Grant ID: UL1 TR002550
208 publications

Search life-sciences literature (45,100,050 articles, preprints and more)

Long COVID: major findings, mechanisms and recommendations.

Author information

Affiliations

Authors

Authors

Authors

ORCIDs linked to this article

Abstract

Free full text

Long COVID: major findings, mechanisms and recommendations

Hannah E. Davis

Lisa McCorkell

Julia Moore Vogel

Eric J. Topol

Abstract

Introduction

Box 1 Long COVID in children

Major findings

Immunology and virology

Vascular issues and organ damage

Neurological and cognitive systems

ME/CFS, dysautonomia and related conditions

Reproductive system

Respiratory system

Gastrointestinal system

Timelines

Diagnostic tools and treatments

Table 1

Impact of vaccines, variants and reinfections

Challenges and recommendations

Testing issues

Important miscues

Widespread lack of postviral knowledge and misinformation

Recommendations

Research

Training and education of the health-care and research workforce

Public communications campaign

Policies and funding

Conclusions

Acknowledgements

Author contributions

Peer review

Peer review information

Competing interests

Footnotes

References

Full text links

Citations & impact

Impact metrics

Citations of article over time

Alternative metrics

Article citations

Similar Articles

Funding

NCATS NIH HHS (1)﻿

Partnerships & funding

NCATS NIH HHS (1)