Cited by 171Down syndrome and intellectual disability researchDementia and Cognitive Impairment ResearchWilliams Syndrome Research

Normal ageing in adults with Down's syndrome: a longitudinal study

Devenny, D. A., Silverman, W. P., Hill, A. L., Jenkins, E., Sersen, E. A., Wisniewski, K. E.·1996·Journal of Intellectual Disability Research

Abstract

The ubiquitous presence of the neuropathology of Alzheimer disease (AD) in individuals with Down's syndrome (DS) over 40 years of age suggests that this group of people will exhibit a high prevalence of dementia of the Alzheimer type (DAT) as they age. The present study indicates that there is a clear discrepancy between the presumed presence of AD neuropathology and the clinical expression of DAT among older people with DS. In the first 6 years of a longitudinal study, the present authors compared 91 adults (31-63 years of age) with DS and mild or moderate mental retardation to 64 adults (31-76 years of age) with other forms of mental retardation (MR) on yearly measures of mental status, short- and long-term memory, speeded psychomotor function, and visuospatial organization. The results indicated that, over repeated testing on the verbal long-term memory test, younger participants with DS showed small increases in their scores, while older participants with DS showed very slight decreases. Overall performance scores on this test and a speeded psychomotor task were poorer for both diagnostic groups in individuals aged 50 years and older. The magnitude and type of these selective changes in performance were consistent with performance profiles observed in older healthy adults without mental retardation on tests measuring similar cognitive functions. Only four out of the 91 people with DS in the present sample showed changes in functioning that have led to a diagnosis of possi…

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Crossref · 10.1111/j.1365-2788.1996.tb00624.x

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  • Virtually all people with full trisomy 21 are expected to develop the pathophysiological changes of Alzheimer's disease by their early to mid-40s.

    “Because virtually all people with full trisomy 21 are expected to develop the pathophysiological changes of AD by their earyl to mid‐40's, this longitudinal design provides a unique opportunity to track physiological and cognitive changes through the clinically asymptomatic preclinical to the clinical stages of dementia.”
  • Most adults with Down syndrome will have the neuropathologies characteristic of Alzheimer's disease by their early to mid-40s.

    “In fact, most adults with DS will have the neuropathologies characteristic of AD by the time they reach their early to mid‐40s that anticipates further progression some years or decades later. 3 , 4 , 5 , 6”

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Authors
Devenny, D. A., Silverman, W. P., Hill, A. L., Jenkins, E., Sersen, E. A., & Wisniewski, K. E.
Venue
Journal of Intellectual Disability Research
Publisher
Wiley
Published
1996-06
Volume
40
Issue
3
Pages
208-221
ISSN
  • 0964-2633 (ISSN-L)
  • 1365-2788
OpenAlex
W2043270657
Cited by
171
References
0
Citations by year
2026: 1 · 2025: 4 · 2024: 2 · 2023: 1 · 2022: 1 · 2021: 7 · 2020: 6 · 2019: 5 · 2018: 6 · 2017: 5 · 2016: 4 · 2015: 7 · 2014: 5 · 2013: 6 · 2012: 5
FWCI
8.07
Type
journal article
Language
en
Open access
closed
Locations
  • Journal of Intellectual Disability Research (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health (5p01ag011531-10, 5p01hd022634-05)
  • National Institute on Aging (P01-AG1 1531)
  • Eunice Kennedy Shriver National Institute of Child Health and Human Development (P01 HD22634)
Topics
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Down syndrome and intellectual disability research
  • Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
  • Life Sciences › Neuroscience › Developmental Neuroscience › Williams Syndrome Research
Keywords
Down syndrome, normal aging, Alzheimer's disease, dementia risk, intellectual disability, long-term memory, psychomotor speed, age-related cognitive decline, thyroid dysfunction
MeSH terms
Adult, Age Factors, Aged, Alzheimer Disease, Down Syndrome, Humans, Intelligence, Longitudinal Studies, Mental Status Schedule, Middle Aged, Neuropsychological Tests, Mental Recall, Reference Values, Risk, Wechsler Scales

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