Estrogen receptor polymorphisms and incident dementia: the prospective 3C study.
Identifieur interne : 003A16 ( PubMed/Corpus ); précédent : 003A15; suivant : 003A17Estrogen receptor polymorphisms and incident dementia: the prospective 3C study.
Auteurs : Joanne Ryan ; Isabelle Carrière ; Laure Carcaillon ; Jean-Francois Dartigues ; Sophie Auriacombe ; Olivier Rouaud ; Claudine Berr ; Karen Ritchie ; Pierre-Yves Scarabin ; Marie-Laure AncelinSource :
- Alzheimer's & dementia : the journal of the Alzheimer's Association [ 1552-5279 ] ; 2014.
English descriptors
- KwdEn :
- Aged, Aged, 80 and over, Apolipoproteins E (genetics), Cohort Studies, Dementia (genetics), Estrogen Receptor alpha (genetics), Estrogen Receptor beta (genetics), Female, Gene Frequency, Genetic Predisposition to Disease, Genotype, Humans, Male, Polymorphism, Single Nucleotide (genetics), Proportional Hazards Models, Risk Factors, Time Factors.
- MESH :
- chemical , genetics : Apolipoproteins E, Estrogen Receptor alpha, Estrogen Receptor beta.
- genetics : Dementia, Polymorphism, Single Nucleotide.
- Aged, Aged, 80 and over, Cohort Studies, Female, Gene Frequency, Genetic Predisposition to Disease, Genotype, Humans, Male, Proportional Hazards Models, Risk Factors, Time Factors.
Abstract
Genetic variation in the estrogen receptor (ESR) may be associated with the incidence of Alzheimer's disease (AD), but this association could be modified by genetic and environmental factors.
DOI: 10.1016/j.jalz.2012.12.008
PubMed: 23491264
Links to Exploration step
pubmed:23491264Le document en format XML
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<author><name sortKey="Carriere, Isabelle" sort="Carriere, Isabelle" uniqKey="Carriere I" first="Isabelle" last="Carrière">Isabelle Carrière</name>
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<series><title level="j">Alzheimer's & dementia : the journal of the Alzheimer's Association</title>
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<term>Apolipoproteins E (genetics)</term>
<term>Cohort Studies</term>
<term>Dementia (genetics)</term>
<term>Estrogen Receptor alpha (genetics)</term>
<term>Estrogen Receptor beta (genetics)</term>
<term>Female</term>
<term>Gene Frequency</term>
<term>Genetic Predisposition to Disease</term>
<term>Genotype</term>
<term>Humans</term>
<term>Male</term>
<term>Polymorphism, Single Nucleotide (genetics)</term>
<term>Proportional Hazards Models</term>
<term>Risk Factors</term>
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<term>Estrogen Receptor alpha</term>
<term>Estrogen Receptor beta</term>
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<term>Polymorphism, Single Nucleotide</term>
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<term>Aged, 80 and over</term>
<term>Cohort Studies</term>
<term>Female</term>
<term>Gene Frequency</term>
<term>Genetic Predisposition to Disease</term>
<term>Genotype</term>
<term>Humans</term>
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<front><div type="abstract" xml:lang="en">Genetic variation in the estrogen receptor (ESR) may be associated with the incidence of Alzheimer's disease (AD), but this association could be modified by genetic and environmental factors.</div>
</front>
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<Issue>1</Issue>
<PubDate><Year>2014</Year>
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<Title>Alzheimer's & dementia : the journal of the Alzheimer's Association</Title>
<ISOAbbreviation>Alzheimers Dement</ISOAbbreviation>
</Journal>
<ArticleTitle>Estrogen receptor polymorphisms and incident dementia: the prospective 3C study.</ArticleTitle>
<Pagination><MedlinePgn>27-35</MedlinePgn>
</Pagination>
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<ELocationID EIdType="pii" ValidYN="Y">S1552-5260(13)00011-3</ELocationID>
<Abstract><AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">Genetic variation in the estrogen receptor (ESR) may be associated with the incidence of Alzheimer's disease (AD), but this association could be modified by genetic and environmental factors.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">The association between five ESR α (ESR1) and β (ESR2) polymorphisms with 7-year dementia incidence was examined among 6959 older men and women from the Three City Study using multivariate-adjusted Cox regression models with delayed entry. Gender, the apolipoprotein E (APOE) ε4 allele, and hormone treatment were considered as potential effect modifiers of this association.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">Among women, the CC genotype of ESR1rs2234693 was specifically associated with a small increased risk of AD (adjusted hazard ratio [HR]: 1.54, 95% confidence interval [CI]: 1.03-2.28, P = .03). However, women with this genotype had a substantially increased risk of AD associated with the APOE ε4 allele (adjusted HR: 3.24, 95% CI: 1.81-5.79 for women rs2234693 CC; compared with HR: 1.87, 95% CI: 1.37-2.56 for all women). There was also evidence of a nominally significant interaction between the ESR1 and ESR2 polymorphisms on the risk of all dementias (P = .04). Hormone treatment did not modify these associations, and there were no significant associations in men.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">Although there was only weak support for a gender-specific association between the common ESR1rs2234693 polymorphism and AD, this polymorphism may act as an effect modifier, modifying the association between an ESR2 polymorphism and dementia, as well as the risk of AD associated with the APOE ε4 allele.</AbstractText>
<CopyrightInformation>Copyright © 2014 The Alzheimer's Association. Published by Elsevier Inc. All rights reserved.</CopyrightInformation>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Ryan</LastName>
<ForeName>Joanne</ForeName>
<Initials>J</Initials>
<AffiliationInfo><Affiliation>Inserm, U1061, Neuropsychiatry: Epidemiological and Clinical Research, Montpellier, France; Université Montpellier1, Montpellier, France; Murdoch Children's Research Institute, Royal Children's Hospital, Victoria, Australia. Electronic address: joanne.ryan@inserm.fr.</Affiliation>
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<AffiliationInfo><Affiliation>CHRU Dijon, Centre Mémoire Ressources et Recherche, Dijon, France.</Affiliation>
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<AffiliationInfo><Affiliation>Inserm, U1018, Université Paris Sud 11, Villejuif, France.</Affiliation>
</AffiliationInfo>
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<Author ValidYN="Y"><LastName>Ancelin</LastName>
<ForeName>Marie-Laure</ForeName>
<Initials>ML</Initials>
<AffiliationInfo><Affiliation>Inserm, U1061, Neuropsychiatry: Epidemiological and Clinical Research, Montpellier, France; Université Montpellier1, Montpellier, France.</Affiliation>
</AffiliationInfo>
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