Role of APOE and Age at Enrollment in the Alzheimer’s Disease Anti-Inflammatory Prevention Trial (ADAPT)

Background: The Alzheimer’s Disease Anti-inflammatory Prevention Trial (ADAPT) tested whether non-steroidal anti-inflammatory drugs (NSAIDs) can prevent Alzheimer’s disease (AD). The results were null. We analyzed ADAPT data to examine if the effects of NSAIDs on AD risk differed depending upon APOE...

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Main Authors: Lea T. Drye, Peter P. Zandi
Format: Article
Language:English
Published: Karger Publishers 2012-08-01
Series:Dementia and Geriatric Cognitive Disorders Extra
Subjects:
Age
Online Access:http://www.karger.com/Article/FullText/341783
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spelling doaj-45555a7d8d8a4dbf909188bde04c803b2020-11-25T03:55:54ZengKarger PublishersDementia and Geriatric Cognitive Disorders Extra1664-54642012-08-012130431110.1159/000341783341783Role of APOE and Age at Enrollment in the Alzheimer’s Disease Anti-Inflammatory Prevention Trial (ADAPT)Lea T. DryePeter P. ZandiBackground: The Alzheimer’s Disease Anti-inflammatory Prevention Trial (ADAPT) tested whether non-steroidal anti-inflammatory drugs (NSAIDs) can prevent Alzheimer’s disease (AD). The results were null. We analyzed ADAPT data to examine if the effects of NSAIDs on AD risk differed depending upon APOE genotype or age as has been suggested by previous observational studies. Methods: ADAPT randomized 2,528 cognitively intact older adults to either celecoxib, naproxen sodium or placebo; 2,388 participants provided blood samples for APOE genotyping. Proportional hazards regression was used to estimate the effects of naproxen or celecoxib versus placebo on incident AD by age at enrollment and APOE genotype. Results: The proportion of subjects providing a biological sample did not differ between the treatment groups. In models of AD risk, none of the tests for 2-way interactions between either NSAID and age or APOE genotype were significant (p > 0.05). Conclusions: The data did not support the hypothesis that the association between NSAIDs and AD risk differed by age or APOE genotype.http://www.karger.com/Article/FullText/341783AgePreventionClinical trialAlzheimer’s diseaseApolipoprotein E
collection DOAJ
language English
format Article
sources DOAJ
author Lea T. Drye
Peter P. Zandi
spellingShingle Lea T. Drye
Peter P. Zandi
Role of APOE and Age at Enrollment in the Alzheimer’s Disease Anti-Inflammatory Prevention Trial (ADAPT)
Dementia and Geriatric Cognitive Disorders Extra
Age
Prevention
Clinical trial
Alzheimer’s disease
Apolipoprotein E
author_facet Lea T. Drye
Peter P. Zandi
author_sort Lea T. Drye
title Role of APOE and Age at Enrollment in the Alzheimer’s Disease Anti-Inflammatory Prevention Trial (ADAPT)
title_short Role of APOE and Age at Enrollment in the Alzheimer’s Disease Anti-Inflammatory Prevention Trial (ADAPT)
title_full Role of APOE and Age at Enrollment in the Alzheimer’s Disease Anti-Inflammatory Prevention Trial (ADAPT)
title_fullStr Role of APOE and Age at Enrollment in the Alzheimer’s Disease Anti-Inflammatory Prevention Trial (ADAPT)
title_full_unstemmed Role of APOE and Age at Enrollment in the Alzheimer’s Disease Anti-Inflammatory Prevention Trial (ADAPT)
title_sort role of apoe and age at enrollment in the alzheimer’s disease anti-inflammatory prevention trial (adapt)
publisher Karger Publishers
series Dementia and Geriatric Cognitive Disorders Extra
issn 1664-5464
publishDate 2012-08-01
description Background: The Alzheimer’s Disease Anti-inflammatory Prevention Trial (ADAPT) tested whether non-steroidal anti-inflammatory drugs (NSAIDs) can prevent Alzheimer’s disease (AD). The results were null. We analyzed ADAPT data to examine if the effects of NSAIDs on AD risk differed depending upon APOE genotype or age as has been suggested by previous observational studies. Methods: ADAPT randomized 2,528 cognitively intact older adults to either celecoxib, naproxen sodium or placebo; 2,388 participants provided blood samples for APOE genotyping. Proportional hazards regression was used to estimate the effects of naproxen or celecoxib versus placebo on incident AD by age at enrollment and APOE genotype. Results: The proportion of subjects providing a biological sample did not differ between the treatment groups. In models of AD risk, none of the tests for 2-way interactions between either NSAID and age or APOE genotype were significant (p > 0.05). Conclusions: The data did not support the hypothesis that the association between NSAIDs and AD risk differed by age or APOE genotype.
topic Age
Prevention
Clinical trial
Alzheimer’s disease
Apolipoprotein E
url http://www.karger.com/Article/FullText/341783
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