The Apolipoprotein E Antagonistic Pleiotropy Hypothesis: Review and Recommendations

Research on apolipoprotein E (APOE) has consistently revealed a relationship between the gene's ε4 allele and risk for development of Alzheimer's disease (AD). However, research with younger populations of ε4 carriers has suggested that the APOE ε4 allele may in fact be beneficial in earli...

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Main Authors: Elizabeth R. Tuminello, S. Duke Han
Format: Article
Language:English
Published: Hindawi Limited 2011-01-01
Series:International Journal of Alzheimer's Disease
Online Access:http://dx.doi.org/10.4061/2011/726197
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spelling doaj-8b8fe8f091c94a9d8b479d9645e4e53a2020-11-25T00:52:31ZengHindawi LimitedInternational Journal of Alzheimer's Disease2090-02522011-01-01201110.4061/2011/726197726197The Apolipoprotein E Antagonistic Pleiotropy Hypothesis: Review and RecommendationsElizabeth R. Tuminello0S. Duke Han1Department of Psychology, Loyola University Chicago, Chicago, IL 60660, USADepartment of Behavioral Sciences, Rush University Medical Center, 1645 W. Jackson Boulevard, Suite 400, Chicago, IL 60612, USAResearch on apolipoprotein E (APOE) has consistently revealed a relationship between the gene's ε4 allele and risk for development of Alzheimer's disease (AD). However, research with younger populations of ε4 carriers has suggested that the APOE ε4 allele may in fact be beneficial in earlier ages and may only confer risk of cognitive decline later in life. Accordingly, we and others have proposed that APOE may represent an example of antagonistic pleiotropy. Antagonistic pleiotropy is an evolutionary biology concept that proposes certain genes or alleles that may differentially impact fitness during different life stages. We critically review this hypothesis in light of new research of the impact of APOE on cognition and neural integrity across the lifespan. We provide recommendations for the revision of the antagonistic pleiotropy hypothesis of APOE and suggest important avenues for future research in this area.http://dx.doi.org/10.4061/2011/726197
collection DOAJ
language English
format Article
sources DOAJ
author Elizabeth R. Tuminello
S. Duke Han
spellingShingle Elizabeth R. Tuminello
S. Duke Han
The Apolipoprotein E Antagonistic Pleiotropy Hypothesis: Review and Recommendations
International Journal of Alzheimer's Disease
author_facet Elizabeth R. Tuminello
S. Duke Han
author_sort Elizabeth R. Tuminello
title The Apolipoprotein E Antagonistic Pleiotropy Hypothesis: Review and Recommendations
title_short The Apolipoprotein E Antagonistic Pleiotropy Hypothesis: Review and Recommendations
title_full The Apolipoprotein E Antagonistic Pleiotropy Hypothesis: Review and Recommendations
title_fullStr The Apolipoprotein E Antagonistic Pleiotropy Hypothesis: Review and Recommendations
title_full_unstemmed The Apolipoprotein E Antagonistic Pleiotropy Hypothesis: Review and Recommendations
title_sort apolipoprotein e antagonistic pleiotropy hypothesis: review and recommendations
publisher Hindawi Limited
series International Journal of Alzheimer's Disease
issn 2090-0252
publishDate 2011-01-01
description Research on apolipoprotein E (APOE) has consistently revealed a relationship between the gene's ε4 allele and risk for development of Alzheimer's disease (AD). However, research with younger populations of ε4 carriers has suggested that the APOE ε4 allele may in fact be beneficial in earlier ages and may only confer risk of cognitive decline later in life. Accordingly, we and others have proposed that APOE may represent an example of antagonistic pleiotropy. Antagonistic pleiotropy is an evolutionary biology concept that proposes certain genes or alleles that may differentially impact fitness during different life stages. We critically review this hypothesis in light of new research of the impact of APOE on cognition and neural integrity across the lifespan. We provide recommendations for the revision of the antagonistic pleiotropy hypothesis of APOE and suggest important avenues for future research in this area.
url http://dx.doi.org/10.4061/2011/726197
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