APOE-related risk of mild cognitive impairment and dementia for prevention trials: An analysis of four cohorts

BackgroundWith the onset of prevention trials for individuals at high risk for Alzheimer disease, there is increasing need for accurate risk prediction to inform study design and enrollment, but available risk estimates are limited. We developed risk estimates for the incidence of mild cognitive impairment (MCI) or dementia among cognitively unimpaired individuals by APOE-e4 dose for the genetic disclosure process of the Alzheimer's Prevention Initiative Generation Study, a prevention trial in cognitively unimpaired APOE-e4/e4 homozygote individuals.Methods and findingsWe included cognitively... Mehr ...

Verfasser: Qian, Jing
Wolters, Frank J
Beiser, Alexa
Haan, Mary
Ikram, M Arfan
Karlawish, Jason
Langbaum, Jessica B
Neuhaus, John M
Reiman, Eric M
Roberts, J Scott
Seshadri, Sudha
Tariot, Pierre N
Woods, Beth McCarty
Betensky, Rebecca A
Blacker, Deborah
Dokumenttyp: Artikel
Erscheinungsdatum: 2017
Reihe/Periodikum: PLOS Medicine, vol 14, iss 3
Verlag/Hrsg.: eScholarship
University of California
Schlagwörter: Health Services and Systems / Health Sciences / Neurosciences / Brain Disorders / Prevention / Alzheimer's Disease / Alzheimer's Disease including Alzheimer's Disease Related Dementias (AD/ADRD) / Acquired Cognitive Impairment / Neurodegenerative / Aging / Clinical Research / Dementia / Neurological / Aged / Apolipoproteins E / Cognitive Dysfunction / Cohort Studies / Female / Gene Frequency / Genotype / Humans / Male / Middle Aged / Netherlands / Risk Factors / United States / Medical and Health Sciences / General & Internal Medicine / Biomedical and clinical sciences
Sprache: unknown
Permalink: https://search.fid-benelux.de/Record/base-27180703
Datenquelle: BASE; Originalkatalog
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Link(s) : https://escholarship.org/uc/item/3dk6r5w2

BackgroundWith the onset of prevention trials for individuals at high risk for Alzheimer disease, there is increasing need for accurate risk prediction to inform study design and enrollment, but available risk estimates are limited. We developed risk estimates for the incidence of mild cognitive impairment (MCI) or dementia among cognitively unimpaired individuals by APOE-e4 dose for the genetic disclosure process of the Alzheimer's Prevention Initiative Generation Study, a prevention trial in cognitively unimpaired APOE-e4/e4 homozygote individuals.Methods and findingsWe included cognitively unimpaired individuals aged 60-75 y, consistent with Generation Study eligibility criteria, from the National Alzheimer's Coordinating Center (NACC) (n = 5,073, 158 APOE-e4/e4), the Rotterdam Study (n = 6,399, 156 APOE-e4/e4), the Framingham Heart Study (n = 4,078, 67 APOE-e4/e4), and the Sacramento Area Latino Study on Aging (SALSA) (n = 1,294, 11 APOE-e4/e4). We computed stratified cumulative incidence curves by age (60-64, 65-69, 70-75 y) and APOE-e4 dose, adjusting for the competing risk of mortality, and determined risk of MCI and/or dementia by genotype and baseline age. We also used subdistribution hazard regression to model relative hazard based on age, APOE genotype, sex, education, family history of dementia, vascular risk, subjective memory concerns, and baseline cognitive performance. The four cohorts varied considerably in age, education, ethnicity/race, and APOE-e4 allele frequency. Overall, cumulative incidence was uniformly higher in NACC than in the population-based cohorts. Among APOE-e4/e4 individuals, 5-y cumulative incidence was as follows: in the 60-64-y age stratum, it ranged from 0% to 5.88% in the three population-based cohorts versus 23.06% in NACC; in the 65-69-y age stratum, from 9.42% to 10.39% versus 34.62%; and in the 70-75-y age stratum, from 18.64% to 33.33% versus 38.34%. Five-year incidence of dementia was negligible except for APOE-e4/e4 individuals and those over 70 y. Lifetime incidence ...