Abstract

1. Introduction

Down syndrome (DS) is the most common genetic condition in the United States, currently affecting approximately one in 700 live births. In addition to intellectual disability and characteristic physical traits such as small stature and facial dysmorphism, people with DS are at increased risk for cardiac defects and certain blood diseases, such as leukemia during childhood, autoimmune disorders and recurrent infections, and are at a markedly increased risk of Alzheimer's disease (AD). Because life expectancy for people with DS has more than doubled over the past 30 years, their increased risk for AD has become an important concern. Virtually all adults with DS develop neuropathology consistent with AD by their 40s and by age 55–60 years, their current lifespan, at least 70% will develop dementia [1–4]. Unfortunately, as they live longer their risk for developing Alzheimer's will increase for there are no treatments to slow, stop, or prevent AD. Thus, with prevalence varying between 250,000 and 400,000 in the United States and more than 5 million worldwide, DS represents the largest group of individuals with early onset AD (EOAD) (i.e. individual under the age of 65 years).

The high incidence of AD among adults with DS, combined with the ability to identify these individuals at or before birth, suggests that it may be possible to target this population for early intervention or prevention. With this in mind, the Alzheimer's Association, in partnership with the Linda Crnic Institute for Down Syndrome and the Global Down Syndrome Foundation, convened a workshop of AD and DS experts to explore the pathogenic and mechanistic links between the two disorders, discuss whether individuals with DS comprise an appropriate population for AD clinical trials, and strategize about how to advance collaborative research toward the parallel goals of providing effective treatment for individuals with DS and AD and expediting AD drug development. The workshop articulated a set of research priorities to move the field forward, including further exploration of shared pathophysiologic mechanisms, exploration of the course of pathogenesis long before the onset of dementia, identification of additional and possibly unique biomarkers that herald the onset of pathogenesis and/or that differentiate AD + DS from the other types of early or late onset AD, establishment of a national repository of AD + DS brains and other tissues, discovery and validation of novel therapeutic targets, and implementation of clinical trials designed to anticipate and prevent pathogenesis. Since this meeting, this group has gone on to establish a Professional Interest Area for DS-AD under the auspices of the International Society To Advance Alzheimer's Research and Treatments of the Alzheimer's Association (AA). Furthermore, the AA, Linda Crnic Institute for Down Syndrome, and the Global Down Syndrome Foundation have sponsored a grant program to support these efforts.

2. Pathologic and mechanistic links between DS and AD

Post-mortem studies of DS brains reveal both pathological similarities to and differences from AD brains. Amyloid-β (Aβ) protein is deposited into extracellular plaques and blood vessel walls in brain in both AD and DS, however, Aβ deposition occurs decades earlier in DS compared with non-DS individuals with the most common form of AD, late-onset Alzheimer's disease (LOAD) (i.e. individuals over the age of 65) [3–5]. In a study of 29 DS subjects between the ages of 3 and 73, Aβ deposition was seen as early as age 12 in individuals with DS and was universal by age 31 [6], beginning with diffuse Aβ42 deposits and progressing to compacted, fibrillar plaques often containing Aβ40, that was associated with neurodegeneration. Similar to AD, Aβ42 is always more abundant than Aβ40 in DS individuals, and N-terminally truncated Aβ is observed in both conditions [7]. Imaging studies, using the Pittsburgh compound B (PiB) [8], suggest that early accumulation of amyloid follows a fronto-striatal pattern similar to PS-1 mutation carriers, while a study from using [(18)F]FDDNP (2-(1-{6-[(2-[fluorine-18]fluoroethyl)(methyl)amino]-2-naphthyl}-ethylidene)malononitrile) [9] reported early accumulation of AD pathology in the frontal cortex rather than in the temporal cortex, raising the possibility that there may be regional differences in the pathological progression between AD and DS + AD.

Neurofibrillary tangles (NFTs) accumulate later, with the hippocampus, entorhinal cortex, and neocortex among the most affected regions [10]. The distribution of plaques and tangles in DS brains is very similar to AD, although the density is greater in DS [11]. There may also be less robust progression of neuronal loss in DS compared with AD; however, the DS brain starts out with fewer neurons [12], suggesting a lower brain “reserve”, especially in the frontal and temporal cortices.

Other similarities between AD and DS neuropathology include increased build-up of plaque-associated proteins, microglial activation, astrogliosis, inflammation, and oxidative stress [1,13–17]. Although the pathogenesis proceeds over decades in DS, the staging of AD neuropathology is not as clearly established in DS as it is in AD.

The partial overlap in neuropathology of DS and AD suggests that some common pathogenic mechanisms may exist. More than 50 years ago, DS was shown to result from trisomy of chromosome 21, which contains hundreds of genes, including the gene for amyloid precursor protein (APP). Numerous lines of evidence point to the importance of APP in AD; increased copies of the APP gene is sufficient to cause EOAD with cerebral amyloid angiopathy (CAA) [18]. APP promoter polymorphisms that increase protein expression are also associated with EOAD [19] and may increase susceptibility to sporadic AD [20]. In one 78-year-old individual with DS but only partial trisomy 21 (missing APP and several other genes), there was no dementia or AD pathology at autopsy [21], supporting that APP plays a role in DS + AD.

APP overexpression is also linked to endocytic changes that are seen in both AD and DS. Endocytosis is critical for transmission and transport of neurotrophic factors in both the retrograde and anterograde direction. APP is processed by β- and γ-secretases in the endosomes, which are markedly enlarged in the AD brain early in the disease process. In DS, significant endosome enlargement is seen in the fetus at 28 weeks gestation, decades before the development of AD pathology, suggesting a failure of endosomal trafficking and/or recycling [22]. Endosomal dysfunction results in the disruption of many cellular processes essential for neuronal functioning, including protein turnover at synapses, local signaling, and subsequent effects on the cytoskeleton, protein synthesis, and retrograde signaling. In mouse models of AD and DS, APP overexpression resulted in endosomal dysfunction, increased nerve growth factor (NGF), and brain-derived neurotrophic factor (BDNF) signaling, especially at gamma-aminobutyric acid (GABA) synapses, failed retrograde transport of NGF and BDNF, and neurodegeneration of basal forebrain cholinergic neurons (BFCNs) [23].

BFCNs are important for memory function, and are shown to degenerate progressively in humans with DS, in idiopathic AD, and in the Ts65Dn mouse model of DS [24]. Ts65Dn mice are born with a normal density of BFCNs. However, like patients with DS, older Ts65Dn mice show a progressive decline in density of BFCNs in parallel with progressive loss of spatial reference and working memory [25]. Furthermore, reduced staining for the high-affinity NGF receptor, trkA, is observed in BFCNs not only from Ts65Dn mice, but also from individuals with DS and idiopathic AD, suggesting a biological mechanism for the cell loss involving this growth factor. Recently, Iulita et al [26] demonstrated parallel changes in neurotrophin maturation and cleavage mechanisms in the temporal and frontal cortices of both humans with DS + AD, and in Ts65Dn mice, providing potential mechanisms for BFCN degeneration and a target for development of pharmacotherapy for this population. Endosomal dysfunction is related to increased TrkB signaling, especially in inhibitory synapses, which may underlie the progression of AD [27]. Also notable, endosome enlargement and associated abnormal acceleration of endocytosis are mediated specifically by the β-cleaved carboxyl-terminal fragment (β-CTF) of APP, independently of Aβ [28].

Endocytosis is also critical for apoE function. The ApoE ε4 allele is the strongest genetic risk factor for LOAD, and in individuals with DS a doubling of amyloid burden is observed [10], and a significantly higher risk for AD and an earlier age of onset [29,30]. In patients with sporadic AD, the presence of the ApoE ε4 allele leads to significantly larger endosomes [22]. Interestingly, there is some evidence that the ApoE ε2 allele is protective against the development of dementia in individuals with DS [31].

Of course, APP is not the only gene triplicated in DS, for there are thought to be 635 genes according to the European Bioinformatics Institute listing; certainly other genes play important roles in producing the AD phenotype. One of the other genes triplicated in DS is the gene for dual-specificity tyrosine phosphorylated and regulated kinase 1a (DYRK1A), a protein that is overexpressed in both the DS and AD brain [32], with somewhat lower levels of overexpression in the AD brain. DYRK1A affects alternative splicing of tau by phosphorylating several splicing factors [33], priming tau for abnormal hyperphosphorylation by GSK-3 [34]. Overexpression of DYRK1A may also indirectly contribute to the early onset of neurofibrillary degeneration through phosphorylation of alternative splicing factors, leading to an imbalance between 3R-tau and 4R-tau. This imbalance results in a several-fold increase in the number of DYRK1A-positive and 3R-tau-positive NFTs in DS subjects in comparison to subjects with sporadic AD [35]. Moreover, the enhanced phosphorylation of APP at Thr 688 by overexpressed DYRK1A [36] facilitates amyloidogenic APP cleavage, which elevates Aβ40 and 42 levels resulting in possibly higher level of toxic Aβ oligomers that contributes to the earlier onset of Aβ pathology [37]. Hence, the inhibition of DYRK1A activity can be explored as a potential therapeutic approach to treat the developmental defects and the early onset Alzheimer-type pathology in DS.

Another gene encoded on human chromosome 21 (HSA21) is synaptojanin 1 (SYNJ1), a lipid phosphatase that plays an important role in synaptic transmission. SYNJ1 protein negatively regulates the levels of phosphatidylinositol-4,5-biphosphate [PtdIns(4,5)P₍₂₎], a signaling phospholipid involved in many cellular processes. Studies in DS transgenic mice suggest that overexpression of SYNJ1 and the resulting perturbation of PtdIns(4,5) P₍₂₎ metabolism is associated with cognitive impairment [38]. Furthermore, trisomy for SYNJ1 in DS is functionally linked to the enlargement of early endosomes [39]. Conversely, SYNJ1 haploinsufficiency appears to be protective against the synaptotoxic action of Aβ [40], indicating that SYNJ1 protein levels may be relevant both in DS and AD.

Neuroinflammation has also been linked to cognitive deficits, and many inflammatory genes found on chromosome 21 may contribute to neurodegeneration in DS [16]. For example, the astrocyte-derived growth factor S100β has been implicated in the formation of neuritic plaques in AD. In DS, elevated numbers of S100β positive astrocytes are present throughout life and are associated with neuritic dystrophy [41]. Other inflammatory molecules, including ApoE and alpha1-antichymotrypsin, have also been shown to be upregulated in astrocytes and microglia in both AD and DS and are found in amyloid plaques [42]. Interestingly, a recent study demonstrated alterations in the transcriptome between a pair of monozygotic twins, where only one twin had DS [43]. The investigators found widely occurring gene expression dysregulation domains (GEDDs), suggesting that nuclear components of trisomic cells undergo modifications of the chromatin environment that can influence the overall transcriptome and give rise to specific DS-related phenotypes. The investigators also discovered that similar GEDDs were observed along the mouse chromosomes in Ts65Dn mice that were syntenic to HSA21, suggesting that this mouse model may, indeed, be an appropriate mouse model for DS at least in terms of genome wide alterations. Genetic alterations observed in the trisomic twin were related to an inflammatory response and cytokine-cytokine receptor interactions, confirming that neuroinflammation is an important pathological trait in DS brains. Further support is provided by DS mouse models exhibiting age-related and progressive activation of both microglial cells and astrocytes in the hippocampus and other limbic areas, and BFCN loss, and memory loss that can be prevented by treatment with the tetracycline derivative minocycline [44]. Finally, complement proteins, associated with innate immunity, have also been observed in association with amyloid plaques, dystrophic neuritis, and NFTs in AD and DS [45], supporting an important role of neuroinflammation genes in DS and AD pathophysiology.

Trisomy of chromosome 21 in DS also leads to other cellular changes. Cells may respond to changes in gene dose by altering DNA methylation of genes not only on chromosome 21, but on other genes throughout the genome. Methylation can alternatively silence or activate genes, and may be manipulated by drugs and nutrients. Studies of T-lymphocytes from adults with DS showed a characteristic pattern of methylation abnormalities in genes involved in the immune response [46]. In further studies of other tissues, particularly brain tissue from individuals with DS, researchers have begun to identify changes in methylation in neurons and glia that appear early in development. More research will be needed to determine the consequences of these changes and whether they can be modified therapeutically.

There is some evidence that trisomy may contribute to other forms of sporadic and familial AD. Trisomy 21 mosaicism has been found in fibroblasts from people with all forms of AD, both sporadic and familial [47]. In addition, hyperploidy has been demonstrated in neurons of AD brains at mild stages, before neuronal loss, and these neurons appear to be targeted for cell death as the disease progresses [48]. Studies in human cells and Xenopus egg extracts suggest that excess Aβ in hyperploid cells disrupts mitotic spindle formation by inhibiting kinesins (mitotic motor proteins), including Eg5, thus affecting neurogenesis and neuroplasticity [49]. In contrast, enhancement of neurogenesis and neuronal plasticity by treatment with a ciliary neurotrophic factor peptide was found to rescue cognitive impairment in Ts65Dn mice [50]. This suggests a mechanistic link between trisomy 21 and neurodegenerative disease [49], but the specifics of how small proportions of trisomic cells might contribute to brain-wide AD neuropathophysiology remain unclear.

3. DS animal models to understand AD

Mouse models are useful for studying disease processes and identifying potential interventions in genetically well-defined populations that can be manipulated in various ways. Of the several DS mouse models that have been generated, the most widely used is the Ts65Dn model for studying DS, which is trisomic for 88 of 161 of the ortholog protein coding genes on human chromosome 21 [51]. Ts65Dn mice are characterized by a progressive loss of working memory, cholinergic deficit in the basal forebrain, and neuroinflammation; changes observed in AD. Additionally, there is dysregulation of trophic factors and an altered plasmin pathway for neurotrophin cleavage [52,53]. Importantly, there is a striking correspondence between the developmental impact of trisomy in this mouse and humans with DS, resulting in similar phenotypes such as short stature, flat facies, flat nasal bridge, and a small cerebellum [54].

However, two facts regarding the Ts65Dn genetics must be kept in mind in evaluating it as a model for AD in DS. First, the Ts65Dn lacks trisomy of a number of HSA21 genes with functional features that are of compelling relevance to development of AD. These include S100 B (discussed previously), the Small Ubiquitin-like Modifier, SUMO3 and the serine protease inhibitor, CSTB, and other genes [55]. Second, the Ts65Dn is also trisomic for a small centromeric segment of mouse chromosome 17 that is not orthologous to HSA21. It has recently been shown that this segment is more gene rich than previously assumed, and indeed includes 50 protein coding genes [56], among them paralogs of some HSA21 genes, including SYNJ2 (see previously for paralog SYNJ1) and TIAM2, plus several Dynein light chain genes whose increased dosage could influence endosomal transport. Thus, the genetic basis for the phenotype of the Ts65Dn is more complex and may not be identical to DS.

The functions of orthologs of a few HSA21 genes have been studied individually in model organisms including mouse, fruit fly, Caenorhabditis elegans, and yeast. Typically, such studies suggest these orthologs regulate similar developmental pathways [57]. In mouse models overexpressing single HSA21 genes, hippocampal function is often affected, resulting in specific behavioral abnormalities and sometimes in excessive inhibitory input to the hippocampus, resulting in reduced long-term potentiation. In these studies, treatment with drugs that antagonize GABAergic transmission normalized these physiologic and behavioral outcomes [52]. In particular, studies focusing on the hippocampus indicate that down-regulation of GABA-A interneurons holds promise as a therapeutic agent. However, to date many other therapeutic interventions have also proved effective in the Ts65Dn, suggesting that other important mechanisms need to be explored [58].

In addition to the genetic concerns for replicating human trisomy in mice is the concern for the lack of plaques and tangles formation in DS mouse models to replicate the hallmarks of AD. However this may be due to the three amino acid difference in the mouse vs. the human β-amyloid sequence that increases the ability of the protein to aggregate in humans. Additionally, evidence has suggested that β-amyloid aggregation may be a trigger for tau aggregation, limiting the ability to develop tau abnormalities in mice. Therefore the DS models have interesting potential for studying AD by introducing human β-amyloid sequences into DS mouse models, allowing different trisomy models and their corresponding gene expression patterns to reflect on how they affect the pathophysiology of plaque and tangle development. Conversely, the lack of Aβ aggregation may allow the evaluation of other processes contributing to cognitive impairment and brain neurodegeneration independent of Aβ production or aggregation.

A problem with the current AD mouse models is that they do not reproduce the neuronal cell loss observed in humans; in fact, there is little to no neuronal loss. Of interest is the neurodegeneration in the Ts65Dn mouse, which may be due to increased APP production or one of its nonamyloid cleavage products, impaired NGF transport and/or cleavage to its mature form, gliosis in the hippocampus, impaired mitochondrial function, oxidative stress, neuroinflammation, calcium dysregulation or some combination of these changes [55]. The Ts65Dn model or other DS mouse models could therefore be useful to test whether intervening in these pathways, independent of plaques and tangles, is therapeutic to generally address neuronal cell loss. Although these animals do not produce plaques and tangles, these same cell death mechanisms may play an important role in cell loss downstream from these pathological changes. These similarities and differences in the DS and AD animal models have yet to be explored and may point to important aspects of underlying biochemical and structural changes that may drive the development of AD.

DS mouse models have provided a powerful tool for translational research in DS, and these models may also prove similarly useful in evaluating AD treatments, although the differences between mouse models and humans, as discussed previously, raise some concerns about relevance. Nonetheless, these models are enormous untapped areas of research with implications for drug development in both the DS and AD fields, overlapping in areas such as modifying APP levels and its cleavage products, modifiers of the endosomal/lysosomal system, and the interaction between basic metabolic pathways, such as those involving insulin, mTOR, immune signaling, amyloid and growth factor pathways. Along these lines are the several novel mouse models for DS that have been developed (for review, see Kleschevnikov et al. [59], Rueda et al. [60], Figure 1). It will be important in future studies to correlate phenotypes in the novel models with those already described for Ts65Dn mice, to confirm that a higher inclusion of syntenic genes leads to a more accurate behavioral and pathological model for the human condition. A recently developed mouse model [61] carries duplications of many of the gene regions corresponding to human chromosome 21. Initial studies suggest that this model exhibits additional memory impairment and pathological brain development, suggesting that it may serve as a more appropriate model; however, no aging studies or intervention studies have been carried out to date. The workshop participants identified a need to study the aging process in all DS mouse models, with particular concern for different background strains, to determine the most appropriate models to reflect AD progression in humans.

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Fig. 1

Mouse models of Down syndrome (DS). The diagram shows a representation of human chromosome 21, HSA21, and separate mouse chromosomes (10, 16, and 17) that are orthologous to HSA21that have been used to develop mouse models of DS [59,60]. The mouse models diagrammed here represent the triplication of different regions of the various murine chromosomes, except the Tc1 mouse model, that carries a transchromosome with the human HAS21 genes (black boxes are two internal deletions). The most commonly used model is the Ts65DN which represents the triplication of the mouse chromosome (MMU) 16 [79]. Ts1Cje, Ts1Yu and Ts1Rhr are segmental duplications or translocations of different lengths of MMU16 [60].

4. Diagnosing AD in individuals with Down syndrome

AD and DS follow a similar trajectory of decline; however, diagnosis of dementia in individuals with DS presents challenges, the most obvious related to the baseline functioning of individuals with substantial pre-existing intellectual disabilities that vary in type and severity within this population. Universal norms used in assessing the activities of daily living (ADLs) in AD are difficult when assessing individuals with DS, for some tasks may never have been performed previously, such as handling their own finances or driving a car. Thus, changes in ADLs function in DS need to be compared with the individual's baseline abilities as opposed to current standardized tests. Cognitive assessments must also take into account variability in baseline performance across cognitive domains, because some aspects of cognition are more affected than others. For example, a DS cognitive phenotype is characterized by relative weaknesses in morpho-syntax, visual short-term memory, and explicit long-term memory compared with visual-spatial short term memory, associative learning, and implicit long-term memory [62].

The Arizona Cognitive Test Battery (ACTB) was developed to provide a focused instrument for assessing possible improvements in cognition in clinical trials [63]. While this battery was originally designed to tap into aspects of cognition affected by intellectual disability and other cognitive impairments, it contains assessments of cognitive domains expected to be affected in AD. However, the ACTB is not widely used at this point. The challenge of assessing cognition in individuals with DS is complex, especially as we try to assess individuals very early in the disease process. Multiple groups are developing empirically validated methods for assessing AD in adults with DS, which should be done in conjunction with the current initiatives to develop more sensitive tests to address the new diagnostic guidelines for prodromal or earlier stages of AD (http://www.alz.org/research/diagnostic_criteria/). Universal adoption of cognitive assessments would be helpful in developing national or international DS/AD programs, similar to the successful Alzheimer's Disease Neuroimaging Initiative (ADNI) that is providing valuable insights into the development of AD in the general population. ADNI and its global partners, Worldwide ADNI (http://www.alz.org/research/funding/partnerships/WW-ADNI_overview.asp), have together gathered and shared substantial biomarker data aimed at delineating the pathological progression of AD.

Biomarkers have the potential to aid not only in diagnosis of AD in individuals with DS, but more importantly, biomarkers track the progression of the disease in its earliest stages and the effectiveness of different treatments. However, biomarker data are sparse in the DS + AD field, but there is data from amyloid PET imaging suggesting the deposition of amyloid earlier in individuals with DS than late-onset AD [8,64,65], and with tau PET imaging on the horizon this will help in the identification of individuals at risk. Also, linking cognitive studies and functional imaging may allow prediction of cognitive impairment and provide a platform for early intervention [66]. Other techniques may be of value, such as high resolution electroencephalography to determine epileptic activity, because there appears to be a subset of individuals with DS and/or AD that have seizures [66]. Additionally, structural and functional magnetic resonance imaging in DS population, as in the general population, may reflect early AD neuropathophysiology [67,68].

Cerebrospinal fluid (CSF) biomarkers are thought by many investigators to be necessary to detect brain pathology; however they may be difficult to evaluate in DS individuals due to difficulties in performing lumbar punctures for research with “no prospect of direct benefit”, but with new treatments this could possibly change. Alternatively, the possible availability of plasma biomarkers, including telo-mere length as a marker [69], plasma Aβ [70], or new platforms under development such as the SomaLogic technology [71], may greatly increase acceptance and open the doors to dramatically increased study participation and numbers. A combination of these diagnostic tools may be extremely valuable in early assessment for individuals at risk for developing AD, both in individuals with DS and the general population.

A public-private partnership was recently launched by the Alzheimer's Disease Cooperative Study and Michael Rafii, study director, as a means to establish biomarkers of dementia in DS that would support clinical trials of AD preventive therapies [72]. The clinical study, named the Down Syndrome Biomarker Initiative (DSBI), will mirror the efforts of the ADNI, which was established in 2003 to validate imaging and blood/CSF biomarkers for AD treatment trials as a means of speeding drug development [73]. Like ADNI, DSBI is intended to establish an infrastructure that could eventually be used in the development of clinical trials for secondary prevention studies in individuals with DS and AD. Programs and databases to identify individuals and ways to share information is growing for both communities, as seen in the newly created DS-Connect (https://dsconnect. nih.gov) and the Global Alzheimer's Association Interactive Network (GAAIN) (www.gaain.org).

5. AD clinical trials in individuals with DS

The extremely high prevalence of AD in people with DS could provide a unique opportunity to study how to slow, stop or prevent Alzheimer's in these individuals. Given the complexity of AD in the setting of DS, a single drug may not be completely effective, but novel therapeutics under development for AD and other neurodegenerative diseases may be of interest in the AD 1 DS population, particularly when they target mechanisms that appear to be important in DS. For example, almost all individuals with DS and AD, and about one-third of cognitively normal elderly subjects, have Cerebral amyloid angiopathy (CAA). CAA is an independent risk factor for dementia and may need to be factored in regarding treatment options or for stratifying populations in clinical trials. Certainly, this has been a newly emerging aspect of AD where autopsied brains are showing mixed pathologies.

An added complication is the prevalence of Attention Deficit Hyperactivity Disorder (ADHD) in DS individuals, which is as high as 43% [74]. ADHD may, in part, be due to altered norepinephrine (NE) levels because DS individuals exhibit an early and progressive loss of neurons supplying NE, locus coeruleus neurons, also seen in AD. Thus, a novel treatment approach may be using NE enhancing drugs, such as Atomoxetine or Droxidopa [75]. Because NE signaling has been shown to regulate growth factor expression, inflammatory pathways, and amyloid processing, treatment with NE enhancing drugs may be neuroprotective and prevent or slow further neuropathology progression [76]. Other novel treatment options considered included stimulating innate immune system with a Toll-like receptor 9 ligand [77], inhibiting the interaction of apoE with Aβ, which may prevent or slow oligomerization and polymerization of Aβ, thus halting or reducing the pathogenic cascade [42]. It is unclear at this point whether treatment options for DS individuals will be the same as the general population or possibly require additional treatments in combination.

Currently, there are approximately 12 DS trials related to AD in development, recruitment or active/completed. These include anti-amyloid antibodies, myoinositol, epigallocatechin gallate, nicotine, memantine, and vitamin E. The DS efforts have been recently advanced by the NIH Down Syndrome Registry called DS-Connect™ which links individuals with DS to resources and research studies. Clearly the DS and the Alzheimer's communities will benefit from the crosstalk in these clinical trials and the advanced trials being conducted in the AD field, including the Dominantly Inherited Alzheimer's Network Trial Unit (DIAN-TU), the Anti-Amyloid Asymptomatic Alzheimer's Trial (A4), the TOMMORROW trial, and the two trials under Alzheimer's Prevention Initiative [78].

A final important note with regard to clinical trials in individuals with DS: Institutional Review Board (IRB) approval and enrollment can be a barrier, given that adults with DS typically lack the capacity to balance potential benefits against potential risks. Therefore, IRBs may require increased evidence of safety and tolerability. One strategy for gaining IRB approval is to contend that people with DS constitute a health disparity population at exceptionally high risk, and these individuals should have access to the latest interventions and clinical trials. Programs such as these could greatly benefit from a national IRB protocol as proven to be successful in cancer trials.

6. Future directions

As care for individuals with DS has significantly improved, including medical treatments, educational policies, societal attitudes, better support, and advanced services, so has their lifespan which has unfortunately put them at greater risk for developing AD. Even though this risk has been recognized, awareness is still low, and only a relatively small portion of the DS + AD models have been explored and adequately tested. Expanded prospective studies in the DS population are needed to understand the biological processes that drive the disease. Moreover, a strong, unified effort to deconstruct the problems and identify solutions would be of tremendous benefit, not only to the AD field as a whole, but also to the many individuals and families caring for these individuals afflicted with the disease. Because of the high incidence of AD in individuals with DS, and because DS + AD represents a fairly large group of individuals globally, there is a great need to incorporate individuals with DS in the Alzheimer's biobanks. Few brain banks or Alzheimer Centers have included these individuals in their study, and the workshop participants recognized this as an important area of improvement. Clinical trials of Alzheimer's treatments in individuals with DS will be extremely insightful. As an outcome of this DS/AD workshop, meeting participants recommended a number of research priorities for moving the field forward:

Acknowledgments

References