Background: Adults with Down syndrome develop Alzheimer's disease neuropathology in an age-dependent manner. This unique feature provides an opportunity to test interventions targeted for prevention of Alzheimer's disease neuropathology and dementia in Down syndrome. Discussion. In considering clinical trial designs, however, there are several challenges that we believe will be critical to examine further. These include: accuracy in dementia, mild cognitive impairment and preclinical Alzheimer's disease diagnoses in Down syndrome; clinical trial outcome measures appropriate for individuals with Down syndrome; in vivo imaging outcome measures (and practical considerations); and contributions of medical co-morbidities to disease progression. Also, when studies are designed, the molecular target may appear to be obvious (for example, targeting beta-amyloid pathology), but chromosome 21 has over 200 additional genes that could influence both positive and negative clinical trial outcomes. Summary. Observational longitudinal studies of aging in Down syndrome will be critically important as there is a need to establish sensitive clinical outcome measures and understand the consequences of gene overexpression in relation to specific interventions.
|Journal||Alzheimer's Research and Therapy|
|State||Published - Sep 12 2014|
Bibliographical noteFunding Information:
EH and FAS are supported by the Eunice Kennedy Shriver National Institute of Child Health and Development of the National Institutes of Health (award R01HD064993). The content of this article is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
© 2014 Head and Schmitt; licensee BioMed Central.
ASJC Scopus subject areas
- Clinical Neurology
- Cognitive Neuroscience