The APOE epsilon 4 polymorphism does not predict late onset depression: the Three-City Study.
Identifieur interne : 001649 ( Main/Exploration ); précédent : 001648; suivant : 001650The APOE epsilon 4 polymorphism does not predict late onset depression: the Three-City Study.
Auteurs : Phillip J. Tully [France] ; Karine Péres [France] ; Claudine Berr [France] ; Christophe Tzourio [France]Source :
- Neurobiology of aging [ 1558-1497 ] ; 2016.
Descripteurs français
- KwdFr :
- Apolipoprotéine E4 (génétique), Caractères sexuels, Démence (génétique), Dépression (génétique), Facteurs de risque, Femelle, Humains, Mâle, Phénotype, Polymorphisme génétique (génétique), Sujet âgé, Sujet âgé de 80 ans ou plus, Valeur prédictive des tests, Vieillissement (génétique), Études d'associations génétiques.
- MESH :
English descriptors
- KwdEn :
- MESH :
- chemical , genetics : Apolipoprotein E4.
- genetics : Aging, Dementia, Depression, Polymorphism, Genetic.
- Aged, Aged, 80 and over, Female, Genetic Association Studies, Humans, Male, Phenotype, Predictive Value of Tests, Risk Factors, Sex Characteristics.
Abstract
The apolipoprotein E ε4 allele (APOE4) is an established risk factor for dementia; however, conflicting findings have been reported as to whether this phenotype confers a heightened risk for late onset depression (LOD) independent of dementia. We examined 2242 persons for incident LOD who also underwent genotyping for APOE4. Major LOD was associated with female sex (odds ratio, 3.61; 95% confidence interval, 1.89-6.90). APOE4 was not associated with major LOD regardless of whether dementia was excluded. In conclusion, we showed that the APOE4 phenotype holds no predictive value for major LOD.
DOI: 10.1016/j.neurobiolaging.2015.12.018
PubMed: 26785975
Affiliations:
- France
- Aquitaine, Languedoc-Roussillon, Nouvelle-Aquitaine, Occitanie (région administrative)
- Bordeaux, Montpellier
- Université Montpellier 1
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Le document en format XML
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<term>Aging (genetics)</term>
<term>Apolipoprotein E4 (genetics)</term>
<term>Dementia (genetics)</term>
<term>Depression (genetics)</term>
<term>Female</term>
<term>Genetic Association Studies</term>
<term>Humans</term>
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<term>Démence (génétique)</term>
<term>Dépression (génétique)</term>
<term>Facteurs de risque</term>
<term>Femelle</term>
<term>Humains</term>
<term>Mâle</term>
<term>Phénotype</term>
<term>Polymorphisme génétique (génétique)</term>
<term>Sujet âgé</term>
<term>Sujet âgé de 80 ans ou plus</term>
<term>Valeur prédictive des tests</term>
<term>Vieillissement (génétique)</term>
<term>Études d'associations génétiques</term>
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<term>Depression</term>
<term>Polymorphism, Genetic</term>
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<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Apolipoprotéine E4</term>
<term>Démence</term>
<term>Dépression</term>
<term>Polymorphisme génétique</term>
<term>Vieillissement</term>
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<term>Aged, 80 and over</term>
<term>Female</term>
<term>Genetic Association Studies</term>
<term>Humans</term>
<term>Male</term>
<term>Phenotype</term>
<term>Predictive Value of Tests</term>
<term>Risk Factors</term>
<term>Sex Characteristics</term>
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<term>Humains</term>
<term>Mâle</term>
<term>Phénotype</term>
<term>Sujet âgé</term>
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<front><div type="abstract" xml:lang="en">The apolipoprotein E ε4 allele (APOE4) is an established risk factor for dementia; however, conflicting findings have been reported as to whether this phenotype confers a heightened risk for late onset depression (LOD) independent of dementia. We examined 2242 persons for incident LOD who also underwent genotyping for APOE4. Major LOD was associated with female sex (odds ratio, 3.61; 95% confidence interval, 1.89-6.90). APOE4 was not associated with major LOD regardless of whether dementia was excluded. In conclusion, we showed that the APOE4 phenotype holds no predictive value for major LOD.</div>
</front>
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