Association of participants who screened positive for night eating syndrome with physical health, sleep problems, and weight status in an Australian adult population.
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Abstract
Background
Night eating syndrome (NES) is a unique eating disorder characterised by evening hyperphagia and nocturnal ingestions which cause significant distress and/or impairment in functioning. Despite the growing literature, NES remains poorly understood and under diagnosed. As such, this study aims to compare the prevalence of physical health conditions in participants with NES when compared to participants without an eating disorder (ED) and participants with other eating disorders (including anorexia nervosa (AN), binge eating disorder (BED) and bulimia nervosa (BN)) in a general population Australian sample of adults.Methods
The data for this study were obtained from the 2017 Health Omnibus Survey (HOS) a multi-stage, cross-sectional survey, conducted by Harrison Research in South Australia. This current study focused on 2547 participants over 18 years of age and specific questions from this population survey including those related to participant demographics and health.Results
This study identified that participants who screened positive for night eating syndrome (spNES) when compared to participants with other eating disorders (ED) or no ED diagnosis, were significantly more likely to have an increased age, be female, have lower levels of education and have lower household income. Additionally, the spNES group was significantly associated with sleep apnoea (p = 0.031), insomnia or other sleep problems (p < 0.0001), increased BMI (p < 0.0001), increased levels of pain/discomfort and lower physical health-related quality of life. Hypertension, hypercholesterolemia, and diabetes were not significantly associated with the spNES group or the "other ED" group which included participants with AN, BED, BN.Conclusions
Several physical health problems were found to be significantly associated with the spNES group including sleep problems, increased BMI, increased levels of pain and lower self-reported physical health-related quality of life. Consequently, future research exploring the complex interaction between NES and these medical conditions may provide further insight into the diagnosis, screening tools and management of NES. Additionally, this study highlights the need for future studies which use larger population-based samples.Level of evidence
Level III. Evidence obtained from well-designed cohort or case-control analytic studies.Free full text
Association of participants who screened positive for night eating syndrome with physical health, sleep problems, and weight status in an Australian adult population
1Abstract
Background
Night eating syndrome (NES) is a unique eating disorder characterised by evening hyperphagia and nocturnal ingestions which cause significant distress and/or impairment in functioning. Despite the growing literature, NES remains poorly understood and under diagnosed. As such, this study aims to compare the prevalence of physical health conditions in participants with NES when compared to participants without an eating disorder (ED) and participants with other eating disorders (including anorexia nervosa (AN), binge eating disorder (BED) and bulimia nervosa (BN)) in a general population Australian sample of adults.
Methods
The data for this study were obtained from the 2017 Health Omnibus Survey (HOS) a multi-stage, cross-sectional survey, conducted by Harrison Research in South Australia. This current study focused on 2547 participants over 18 years of age and specific questions from this population survey including those related to participant demographics and health.
Results
This study identified that participants who screened positive for night eating syndrome (spNES) when compared to participants with other eating disorders (ED) or no ED diagnosis, were significantly more likely to have an increased age, be female, have lower levels of education and have lower household income. Additionally, the spNES group was significantly associated with sleep apnoea (p
=0.031), insomnia or other sleep problems (p<0.0001), increased BMI (p<0.0001), increased levels of pain/discomfort and lower physical health-related quality of life. Hypertension, hypercholesterolemia, and diabetes were not significantly associated with the spNES group or the “other ED” group which included participants with AN, BED, BN.
Conclusions
Several physical health problems were found to be significantly associated with the spNES group including sleep problems, increased BMI, increased levels of pain and lower self-reported physical health-related quality of life. Consequently, future research exploring the complex interaction between NES and these medical conditions may provide further insight into the diagnosis, screening tools and management of NES. Additionally, this study highlights the need for future studies which use larger population-based samples.
Level of evidence
Level III. Evidence obtained from well-designed cohort or case–control analytic studies.
Introduction
Eating disorders (ED) are physically, physiologically, financially, and socially incapacitating, contributing to a significant burden for individuals and society [1, 2]. ED affects ~ 4% of the Australian population, however, the actual prevalence may be significantly higher [2]. These disorders include anorexia nervosa (AN), binge eating disorder (BED), bulimia nervosa (BN), other specified and unspecified feeding and eating disorders (OS/UFED. Night eating syndrome (NES) is classified as a type of OSFED [3].
NES is characterised by recurrent episodes of night eating (NE), described by excessive food consumption after the evening meal (evening hyperphagia) or eating after awakening from sleep (nocturnal ingestions) [3, 4]. Individuals with NES are aware and can recall these episodes [3, 5]. Additionally, Allison et al. proposed that this pattern of disordered eating must be maintained for 3 months or more and with specific features such as at least 25% of food intake consumed after the evening meal and at least 2 episodes of nocturnal eating per week [5]. Although the aetiology of NES is poorly understood, the syndrome is thought to result from a desynchronisation of mood, sleep, satiety, and circadian rhythms of food ingestion [4, 6, 7]. Additionally, NES has a significant association with concurrent psychiatric diagnoses and comorbidities including BED, BN, generalised anxiety disorder and substance use disorder [4, 8]. Consequently, individuals with NES often experience significant distress and/or impairments in normal functioning [3, 4, 6]. With a prevalence of 1.5% in the general population of the United States [9], NES creates a substantial burden to the healthcare system, detrimentally impacting quality of life and increasing morbidity [4, 6, 8, 10, 11].
Currently, inconsistent evidence exists regarding the impact of NES on body mass index (BMI; kg/m2), physical health and sleep [4, 6–8, 11–13]. Additionally, a majority of the research on NES has been conducted within clinical settings [14–16] or in adolescent populations [17–19]. As such, there is a lack of knowledge regarding NES within general and adult population groups [14, 20, 21]. A study, reported in 2012, conducted in an adult Swedish twin population by Lundgren et al. reported no association between a lifetime history of any physical health variable (specifically blood pressure, cholesterol, gastrointestinal problems, heart burn and diabetes) and evening hyperphagia as well as nocturnal ingestions of food [22]. It is likely that the inconsistencies have occurred due to the use of different samples and age groups and highlights the importance of replication of studies. In contrast, this study primarily aims to investigate the prevalence of physical health conditions (specifically; hypertension, hypercholesterolemia, diabetes/ high BSL, and sleep apnoea), sleep problems, low physical health-related quality of life [23] and increased weight status [24] in people who screened positive for night eating syndrome (spNES) compared to people without an eating disorder and people with BED or BN or AN in a general population Australian sample of adults.
Methods
Study design and weighting
The data for this study were obtained from the 2017 Health Omnibus Survey (HOS) [25, 26], a multi-stage, cross-sectional, face-to-face survey, conducted by Harrison Research in association with South Australia Health. This 25-page structured interview was conducted annually and included questions related to demographics and participant health (medical conditions, weight control, etc.). Between September and December 2017, personal interviews were conducted with households throughout South Australia. Additionally, cities and towns were initially stratified into Metropolitan and Country statistical areas based on the Australian Bureau of Statistics (ABS) census. From the Statistical Areas Level 1 (SA1) used in the ABS 2016 census, 398 metropolitan and 132 regionals were selected through a probability of selection proportional to their size procedure. Furthermore, a skip pattern of every fourth household, was utilised to select ten households within each level 1 SA and only one interview with a participant 15 or over was conducted per household. In instances where more than one person aged 15 years or over resided within the household, the respondent was the participant with the most recent birthday. Verbal consent was obtained for adult participants and written consent was obtained from parents or guardians of participants under the age of 18 years. Additionally, missing data were obtained by telephone interview and weighted by ABS 2016 Census data on age, sex, educational level, country of birth, marital status and household income.
Participants
From the 5300 households selected in 2017, 2977 interviews were conducted between September and December 2017, with a response rate (i.e. included vacant houses, holiday homes, businesses and non-permanent tenants) of 57.0% and a participation rate (i.e. the number of people eligible to participate excluding those not able to be contacted after six attempts (i.e. house was vacant at the time of survey) was 65.3% [25, 26]. This study reports only data collected in adult participants (i.e. data from all participants under 18 years of age were excluded).
Ethics
The 2017 HOS [25, 26] was approved by the University of Adelaide Human Research Ethics Committee (HREC). Ethics Approval ID: H-097-2010. An exemption from further Human Research Ethics Review was obtained from the Western Sydney University HREC as data may be analysed and published beyond 2019 on the condition that the datasets are fully de-identified prior to being shared with researchers that were not included on the original ethics approval and analysis aligns with consent provided by participants.
Measures
Demographics
Sociodemographic data were collected by face-to-face interview. During the initial interview, participants self-reported their height and weight, and BMI (kg/m2) was calculated and classified in accordance with the Centers for Disease Control and Prevention (CDC) [24].
Eating disorder symptoms
Questions on eating disorder symptoms were derived from the Eating Disorder Examination Interview (EDE) [27], to ensure participants were accurately allocated into the BN, BED and spNES groups. Participants were also interviewed with questions clarifying components of DSM-5 [3]. Participants were asked to respond based on the 3 months immediately preceding the interview, to screen for NE, BN, BED, AN or no eating disorders. These questions included episodes of night eating, episodes of binge eating, purging, the presence of distress and other emotions associated with these episodes, dietary restriction, presence of inappropriate compensatory behaviours and level of weight/shape over-valuation. Frequency of binge eating, and night eating episodes were characterised by, “Not at all”, “less than weekly”, “once a week”, “two or more times a week”, “don’t know” or “refused”. The presence of inappropriate compensatory measures (e.g., laxatives, diuretics, etc.) was categorised by “yes”, “no” and “refused”. The question to determine night eating was: “In the past 3 months have you had any episodes of night eating? By night eating I mean waking from sleep and eating (i.e. you were not sleep walking and eating, you were awake), OR episodes of eating a very large amount after your evening meal. (This does not include eating at night because of social or other circumstances e.g., you are travelling overseas on a night flight or because of work shifts)”. Participants responded to questions regarding distress associated with binge eating and night eating with the following responses: “not at all”, “yes—a little”, or “yes—a lot” or with “refused”. For this study, the spNES variable was defined by participants with any episodes of night eating with “a lot” of distress experienced over the last 3 months.
Physical health questions
Participants self-reported a medical diagnosis of hypertension, hypercholesterolemia, high blood sugar level (BSL) or diabetes, insomnia, and obstructive sleep apnoea, with the question, “Has a doctor ever told you that you have …”. These questions were answered with “yes”, “no”, “don’t know” or “refused”. Additionally, participants could answer, “No, not told have any of these conditions”. Participants who responded with “don’t know” or “refused” were reported as “missing”. Furthermore, pain and discomfort were rated on a scale from 1 to 5, described as “no”, “slight”, “moderate”, “severe” and “extreme”.
Physical health-related quality of life (HRQoL)
Participant health status was assessed with the validated Short Form 12 Health-Related Quality of Life (SF12) tool [28]. The SF-12 [28] is a 12-item questionnaire which contains 8 subscales: physical functioning, role limitation due to physical problems, bodily pain, general health perceptions, vitality, social functioning, role limitations due to emotional problems and mental health. These subscales are weighted in 2 separate scales, a Physical Component Summary Scale (PCS) and a Mental Component Summary Scale (MCS) [28]. Each scale has a mean score of 50 and standard deviation of 10, with higher scores indicating an increased health status. This current study utilised only the PCS to identify the impact of physical health problems on quality of life [28].
Data analysis
The data were inspected for normal distribution and cleaned. Participants below the age of 18 years were removed. All data analyses were performed using “Statistical Packages For Social Sciences” (SPSS Version 27) and “Statistical Analysis System” (SAS version 9.4). Adjusted prevalence estimates and their respective 95% confidence intervals (CI) were predicted and reported as percentages. For this study, the spNES variable was defined as participants experiencing “a lot” of distress associated with any episodes of night eating which had occurred for the last 3 months. Additionally, participants were divided into the “other ED group” if they currently satisfied DSM-5 diagnostic criteria [3] for AN, BED or BN using the EDE-Q [27]. The “no known ED group” consisted of the remaining participants above 18 years of age.
Descriptive data were expressed in percentage of total participants who responded to the question, means, medians, standard deviations, and interquartile ranges. Chi-squared (χ2) test, Kruskal–Wallis test and F test were used as appropriate, to assess differences between the 3 groups and their associations with demographic and physical features. Physical characteristics such as BMI [24], physical component of the SF12 [28] [utilised to represent physical health-related quality of life (HRQoL)] and medical conditions (including increased BMI, hypercholesterolemia, hypertension, hyperglycaemia or diabetes mellitus, sleep apnoea, insomnia and other problems) were examined whilst controlling for confounding variables (i.e. age and sex). Regression analyses which adjusted for age and sex were utilised to examine the relationship between the dependent outcome (physical features) and the independent variables (spNES, other ED or no ED). Linear regression was used for continuous data whilst ordinal logistic regression was used for ordinal data.
Outcomes
There were 23 people (0.90%) with spNES, 44 (1.73%) with other EDs and the remaining 2480 (97.37%) with no ED. Table Table11 presents this and the association between the spNES, other ED and no ED groups and socio-demographic features including age, sex, marital status, education, and household income. The spNES variable was significantly associated with the female sex, increased age, reduced highest education level and lower household income. Additionally, the “other ED” group had increased participants in the certificate, trade or apprenticeship groups when compared to the “no ED” group.
Table 1
Demographic and clinical features of study participants over the age of 18 years
| Characteristic (n) | Total n =2547 | spNES n =23 | BN, AN, BED (other ED) n =44 | No ED known n =2480 | Statistics | Post Hoc |
|---|---|---|---|---|---|---|
| Mean (SE) n | ANOVA (p) | |||||
| Age (2547) | 49.02 (0.36) 2547 | 45.32 (2.70) 23 | 38.18 (1.97) 44 | 49.25 (0.38) 2480 | F df (p | No ED>NE>Other ED |
| Characteristic (n) | N (%) | χ2 (p) | Post Hoc | |||
|---|---|---|---|---|---|---|
| Sex (2548) | ||||||
| Female | 1307 (51.30) | 18 (78.26) | 31 (70.45) | 1258 (50.72) | χ2 df (p | NE and Other ED more likely to be female than no ED |
| Male | 1241 (48.70) | 5 (21.74) | 13 (29.55) | 1223 (49.31) | ||
| Marital status (2543) | ||||||
| Married/De facto | 1617 (63.59) | 10 (43.48) | 24 (54.54) | 1583 (63.83) | χ2 df | N/A |
| Never married | 540 (21.23) | 7 (30.43) | 15 (34.09) | 518 (20.89) | ||
| Separated/divorced/widowed | 386 (15.18) | 6 (26.09) | 5 (11.36) | 375 (15.12) | ||
| Highest Education level (2544) | ||||||
| Secondary school | 921 (36.20) | 11(47.83) | 11 (25.00) | 899 (36.25) | χ2 df | Other ED more certificate and trade and apprenticeship than no ED |
| Certificate/trade/Apprenticeship | 962 (37.81) | 8 (34.78) | 26 (59.09) | 928 (37.42) | ||
| Bachelor or higher | 661 (25.98) | 4 (17.39) | 7 (15.91) | 650 (26.21) | ||
| Household Income (2006) | ||||||
| Up to $40,000 | 574 (28.61) | 11(47.83) | 11 (25.00) | 552 (22.26) | χ2 df (p | NE lower income (<40 K) than no ED |
| $40,001–$100,000 | 775 (38.63) | 8 (34.78) | 21 (47.73) | 746 (30.08) | ||
| $100,001–$140,000 | 307 (15.30) | 1 (4.35) | 7 (15.91) | 299 (12.06) | ||
| $140,001 or more | 350 (17.45) | 1 (4.35) | 2 (4.55) | 347 (13.99) | ||
Four cases of BN also have NE and were included with the “Other ED” group
“spNES” group=participants with night eating and experienced distress, “Other ED” group=participants with Anorexia nervosa (AN), Binge eating disorder (BED) and Bulimia nervosa (BN), “No ED” group = participants who are not categorised into the “NE group” or “Other ED” groups
F is calculated by dividing two mean squares, Df is degrees of freedom
Table Table22 reports the associations between self-reported physical health conditions and spNES, other ED and no ED groups. Sleep apnoea was significantly associated with the spNES variable (p=0.031). Similarly, insomnia or other sleep problems and the spNES group had a significant relationship (p<0.0001). The mean BMI for participants who spNES was 33.45 kg/m2, which is higher than participants in the other ED group and significantly higher than participants without a known ED. Hypertension, hypercholesterolemia and diabetes were not significantly associated with an ED diagnosis. However, near significance was reached when exploring the association between diabetes, high BSL and in participant who spNES.
Table 2
Comparison of physical health problems between people with NES and other groups
| Characteristic | spNES n=23 (0.90%) | BN, AN, BED (other ED) n =44 (1.73%) | No ED known n =2480 (97.33%) | Statistic | Post hoc |
|---|---|---|---|---|---|
| Characteristic (n) | N (%) | χ2 (p) | |||
| Hypertension (1807) | 12 (52.17) | 10 (22.73) | 687 (27.70) | χ2 df (p | N/A |
| Hypercholesterolemia (1807) | 7 (30.43) | 14 (31.82) | 563 (22.70) | χ2 df (p | N/A |
| Diabetes or high BSL (1808) | 8 (34.78) | 7 (15.91) | 278 (11.21) | χ2 df (p | N/A |
| Characteristic (n) | N (%) | Binary logistic regression (p) | Post hoc | ||
|---|---|---|---|---|---|
| Sleep apnoea (1808) | 5 (21.74) | 3 (6.82) | 123 (4.96) | OR SE B (p | NE>other ED>no ED |
| Insomnia or other sleep problems (1807) | 11 (47.83) | 10 (22.73) | 219 (8.83) | OR SE B (p | NE>other ED>no ED |
| Characteristic (n) | Median (IQR) n | Statistic K-W | Post hoc | ||
|---|---|---|---|---|---|
| Pain/discomfort (2545) | 2 (2–4) 23 | 1 (1–2) 44 | 1 (1–2) 2477 | c index=0.628 | NE>other ED>No ED |
| Characteristic (n) | Mean (SD) n | ANOVA (p) | Post hoc | ||
|---|---|---|---|---|---|
| BMI (kg/m2) (2403) | 33.45 (9.41) 22 | 31.37 (7.90) 44 | 26.75 (5.55) 2337 | F df B 95%CI (p | NE>other ED>No ED |
| Physical component (SF12) (2533) | 42.90 (12.98) 22 | 45.94 (10.34) 44 | 48.07 (10.60) 2467 | F df B 95%CI (p | NE<other ED<No ED |
Four cases of BN also have NE and were included with the “other ED” group
“spNES” group=participants with night eating and experienced distress, “other ED” group=participants with anorexia nervosa (AN), binge eating disorder (BED) and bulimia nervosa (BN), “No ED” group: participants who are not categorised into the “NE group” or “other ED” groups
F is calculated by dividing two mean squares, Df is degrees of freedom
Higher levels of self-reported pain and discomfort were significantly associated with the spNES variable, with an interquartile range of 2–4. In comparison, participants in the other ED and no ED groups had an interquartile range of 1–2. Participants who spNES were found to have 3.21 times higher odds of low pain compared with no pain, 2.39 times higher odds of moderate pain compared with no pain and 6.16 times higher odds of extreme pain compared with no pain. As such, the odds of the spNES group were highest when participants reported extreme pain. These finding were all statistically significant. When compared with no pain, participants in the “other ED” group were found to have 1.16 times higher odds of low pain, 1.91 times higher odds of moderate pain and 2.46 times higher odds of extreme pain. Thus, for participants with AN, BED or BN, the odds of the self-reported pain increased with the severity of pain reported. The findings for the “other ED” group were all statistically significant except for when participants reported “low pain”.
This study also identified a significant association between participants who spNES and poorer scores for the summary physical component of the SF-12 [27]. The Physical Component Summary Scale (PCS) [27] involves several questions categorised into limitations to physical functioning, limitations to usual role activities, presence of bodily pain and general health perceptions. This suggested that participants in the “spNES” group had statistically significantly lower HRQoL than participants within the “No ED” group.
Discussion
This study investigated the complex interaction between participants who spNES and physical health features within a representative adult Australian population, to provide insight regarding the pathophysiology and thus, the management of NES and other ED. The respondents were contacted independently of health service contact in distinction to previous studies. This current study found that participants who spNES were more likely to be female, less likely to have obtained higher education levels and had lower household income when compared to those with no ED. This reiterates the findings of a previous epidemiological study conducted in 2014, which speculated this higher prevalence of NES in women was attributable to the lack of distress reported by men, although more men endorsed night eating symptoms [29]. Additionally, this study identified that those who spNES much like other EDs such as BED had notable physical health comorbidities [30, 31].
Sleep apnoea and insomnia or other sleep problems were identified to have a significant relationship with participants who spNES. This echoed current literature [32–36] which revealed significant relationships between poor sleep quality and NES when utilising self-reported questionnaires. This contrasted with Cleator et al. [32] and Geliebter et al. [16] who reported no significant association between OSA and NES. Although objective data were obtained using polysomnography which objectively evaluated the Apnoea–Hypopnoea Index (AHI), Geliebter et al. [16] were limited in providing further information addressed through questionnaires such as sleep duration, daytime sleepiness, and impact of quality of life. Confirming the current literature, a narrative review [37] identified an association with nocturnal feeding and impaired sleep when observing shift workers, suggesting nocturnal feeding mimicked NES and that this disturbance in circadian rhythm resulted in metabolic disorders.
Although limited studies have been written on this specific topic, Karp et al. [38] suggests that this may be associated with increased BMI which is often linked with NES. Furthermore, literature suggests that repeated ingestion of large amounts of food may be associated with gastric distension and subsequently pain [39, 40]. A more speculative explanation is that people who have chronic pain may experience night awakenings from such pain and begin a pattern of overeating when aroused from sleep with pain [39, 40]. This is consistent with Beauchamp et al. who suggested pain was associated with poor sleep quality, which was more central to the NES symptom network than nocturnal ingestions and evening hyperphagia when using a network analysis of the diagnostic criteria for NES [41].
Literature concerning the relationship between NES and BMI provided inconclusive and contradictory findings [16, 32, 36, 42, 43]. This current study identified a significantly positive relationship between participants who spNES and BMI when using self-reported height and weight. Several studies hypothesised that the incongruent results when exploring the association between NES and BMI may result from the use of different measurement methods and the presence of confounding variables such as age, sex, socio-economic status, and symptoms variability [43]. The present sample controls for such confounding factors as selection bias is lower in representative community populations, lending more confidence to the finding of an association with BMI.
This study identified that the spNES group was significantly associated with lower scores on the physical component of the SF12 [28] (i.e. physical health-related quality of life (HRQoL). This questionnaire explored several facets of physical health including patient reported limitations to physical functioning, limitations to usual role activities. Current literature [17, 36, 42] exploring the relationship between NES and physical activity reported incongruous findings. It was suggested that this may result from the use of different tools when assessing activity or use of small sample sizes. Several studies have suggested multifactorial causes for participant reported poorer health-related quality of life, including sleep quality, age and stress levels [17, 44]. This was particularly evident when observing university participants [17, 44]. The poorer sleep quality reported in participants with NES, as well as the presence of other physical health problems such as pain, may therefore explain the poorer physical HRQoL we found.
The current data suggested that the spNES variable was not significantly associated with diabetes mellitus or hyperglycaemia, hypercholesterolemia, or hypertension. This supported existing studies [32, 33, 35] which reported no significant relation between NES and type two diabetes mellitus, as well as other concomitant disease including hypertension, hypercholesterolemia, and cardiovascular disease. Hood et al. however, reported a significant correlation between NEQ scores and haemoglobin A1c (HbA1C) [34], an indicator of glycaemic control. Current literature [32–35] regarding the impact of NES on these conditions have largely been conducted within clinical environments, as such these studies may not be representative of the general population, with participants more likely to have comorbidities [32, 34, 35].
This study has several clinical implications. NES is an emerging area for clinical investigation, evaluation, and intervention, due to its substantial impact on individuals and the healthcare system [3, 4, 6, 8, 10, 11]. The findings of this study highlight the need for health professionals to be aware of the extensive impacts of NES and other eating disorders on patient health and their associations with comorbidities. Screening for specific comorbidities such as sleep apnoea will allow for earlier diagnosis and management of these conditions, thus improving patient reported quality of life.
Strengths and limitations
The study has several strengths and limitations. It reported on participants who were representative of the general population, with males and females evenly distributed, and with a wide range of ages. The validity of this current study was increased through the use of a representative sample, which reduced the likelihood of bias and confounding variables which may occur from selection bias and bias in clinical samples. Additionally, the use of face-to-face interviews enabled participants to clarify any survey questions to obtain the most accurate data. Similarly, categorisation into spNES, other ED and no ED groups was achieved through interview items which closely matched the DSM-5 [3] and ICD-11 [45] criteria, thus increasing the validity of this study. However, the proposed diagnostic criteria suggested by Allison et al. is often used in current literature [5], which categorises NES into evening hyperphagia and nocturnal ingestions. This study would be improved with use of food records over a period to assess evening hyperphagia and the inclusion of questions regarding the frequency of nocturnal ingestions. Additionally, due to the variety of criteria utilised in current literature to diagnose NES [11], this study may have included participants in the spNES group who may not meet the “full diagnostic criteria”.
The data set relied heavily upon self-reported data to lay (albeit trained) interviewers, which may have over-estimated number of participants with each medical condition. Furthermore, this study did not investigate the cases of self-reported diabetes or high BSL to identify type of diabetes or severity. Potential bias of self-reported data could not be excluded; however, the validity of self-reported data for these medical conditions has been proven by several studies [46, 47] and is commonly utilised in screening and surveillance programmes [48, 49]. Participant height and weight were self-reported to calculate BMI, so clinician-measured anthropometric may have yielded more accurate results [50]. However, the direction and magnitude of findings have face validity, and most people are likely to report with the same degree of skewness—i.e. under-reporting. The use of estimated anthropometric measures in place of accurate measures reduced the accuracy of results and consequently, the validity of diagnoses.
What is already known on this subject?
Existing literature regarding the association of NES on components of physical health is inconsistent and has been conducted largely in clinical settings [14–16] or within adolescent populations [17–19]. As such, further research is imperative to understand the impact of NES within general representative and adult population samples [14, 20, 21].
What this study adds?
This current study aims to investigate the prevalence of physical health problems in spNES when compared to individuals without an eating disorder or those with other eating disorders (BED or BN or AN) in a general population Australian sample of adults.
Conclusion
NES is an emerging area for clinical investigation, evaluation, and intervention, due to its substantial impact on individuals and the healthcare system [3, 4, 6, 8, 11]. This study identified significant associations between the spNES variable and multiple facets of physical health including higher BMI, increased levels of pain/ discomfort, poorer scores of the physical component of the SF-12, sleep apnoea, insomnia or other sleep problems. The spNES group was not found to be significantly associated with diabetes mellitus or hyperglycaemia, hypercholesterolemia, or hypertension in this study. Future longitudinal studies on general population samples are essential to clarify the impact of NES on physical and mental health to improve the assessment, identification of comorbidities and management of NES.
Acknowledgements
We acknowledge the Harrison Research for conducting the Health Omnibus survey.
Author contribution
SJS performed the descriptive analysis, contributed to writing and editing of the manuscript; PH conceptualised the study, contributed to writing and editing of the manuscript including clinical implications of findings; ST provided comments to the final draft; DC provided comments to the final draft; HM led the study design, regression analysis, interpretation and implications of findings, writing and editing of the manuscript. All authors read and approved the final draft.
Funding
Open Access funding enabled and organized by CAUL and its Member Institutions. The research was funded by a Shire Pharmaceuticals (Zug, Switzerland, now a member of the Takeda group of companies) Investigator (noncommissioned) grant to ST IIR-AUS-001151 and an internal Western Sydney University School of Medicine fund held by PH.
Declarations
HM declares no conflict of interest. PH received royalties from Hogrefe, and Huber and McGraw-Hill publishers for contributions on eating disorders. PH received royalties from Oxford University Press and receives sessional fees and lecture fees from the Australian Medical Council, Therapeutic Guidelines publication, and New South Wales Institute of Psychiatry. She is the joint Editor in Chief of the Journal of Eating Disorders. PH was a member of the World Health Organisation Working Group on Feeding and Eating Disorders for the Revision of ICD-10 Mental and Behavioural Disorders. PH has received an honorarium from Shire (now Takeda) Pharmaceuticals for a commissioned report and is an advisor to Takeda. ST receives royalties from Taylor and Francis, Hogrefe and Huber and McGraw-Hill for published book chapters. He has received honoraria from Shire/Takeda Group of Companies for chairing the Australian Clinical Advisory Board for Binge Eating Disorder, public speaking engagements, commissioned reports as well as investigator-initiated research grants. He is the Editor in Chief of the Journal of Eating Disorders, an inaugural committee member of the National Eating Disorders Collaboration, a Member of the Technical Advisory Group (TAG) on Eating Disorders (Commonwealth of Australia) and a member of the governing council of the Australian Eating Disorders Research and Translation Centre. DC declares no conflict of interest.
The study was approved by the University of Adelaide Human Research Ethics Committee Protocol Number H-097-2010 and participants provided informed consent. We received Ethics exemption to conduct later analyses on de-identified data from Western Sydney HREC.
Not applicable.
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