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Genome-Wide Association Study of Personality Traits in the Long Life Family Study

Personality traits have been shown to be associated with longevity and healthy aging. In order to discover novel genetic modifiers associated with personality traits as related with longevity, we performed a genome-wide association study (GWAS) on personality factors assessed by NEO-five-factor inve...

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Autores principales: Bae, Harold T., Sebastiani, Paola, Sun, Jenny X., Andersen, Stacy L., Daw, E. Warwick, Terracciano, Antonio, Ferrucci, Luigi, Perls, Thomas T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3647245/
https://www.ncbi.nlm.nih.gov/pubmed/23658558
http://dx.doi.org/10.3389/fgene.2013.00065
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author Bae, Harold T.
Sebastiani, Paola
Sun, Jenny X.
Andersen, Stacy L.
Daw, E. Warwick
Terracciano, Antonio
Ferrucci, Luigi
Perls, Thomas T.
author_facet Bae, Harold T.
Sebastiani, Paola
Sun, Jenny X.
Andersen, Stacy L.
Daw, E. Warwick
Terracciano, Antonio
Ferrucci, Luigi
Perls, Thomas T.
author_sort Bae, Harold T.
collection PubMed
description Personality traits have been shown to be associated with longevity and healthy aging. In order to discover novel genetic modifiers associated with personality traits as related with longevity, we performed a genome-wide association study (GWAS) on personality factors assessed by NEO-five-factor inventory in individuals enrolled in the Long Life Family Study (LLFS), a study of 583 families (N up to 4595) with clustering for longevity in the United States and Denmark. Three SNPs, in almost perfect LD, associated with agreeableness reached genome-wide significance (p < 10(−8)) and replicated in an additional sample of 1279 LLFS subjects, although one (rs9650241) failed to replicate and the other two were not available in two independent replication cohorts, the Baltimore Longitudinal Study of Aging and the New England Centenarian Study. Based on 10,000,000 permutations, the empirical p-value of 2 × 10(−7) was observed for the genome-wide significant SNPs. Seventeen SNPs that reached marginal statistical significance in the two previous GWASs (p-value <10(−4) and 10(−5)), were also marginally significantly associated in this study (p-value <0.05), although none of the associations passed the Bonferroni correction. In addition, we tested age-by-SNP interactions and found some significant associations. Since scores of personality traits in LLFS subjects change in the oldest ages, and genetic factors outweigh environmental factors to achieve extreme ages, these age-by-SNP interactions could be a proxy for complex gene–gene interactions affecting personality traits and longevity.
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spelling pubmed-36472452013-05-08 Genome-Wide Association Study of Personality Traits in the Long Life Family Study Bae, Harold T. Sebastiani, Paola Sun, Jenny X. Andersen, Stacy L. Daw, E. Warwick Terracciano, Antonio Ferrucci, Luigi Perls, Thomas T. Front Genet Genetics Personality traits have been shown to be associated with longevity and healthy aging. In order to discover novel genetic modifiers associated with personality traits as related with longevity, we performed a genome-wide association study (GWAS) on personality factors assessed by NEO-five-factor inventory in individuals enrolled in the Long Life Family Study (LLFS), a study of 583 families (N up to 4595) with clustering for longevity in the United States and Denmark. Three SNPs, in almost perfect LD, associated with agreeableness reached genome-wide significance (p < 10(−8)) and replicated in an additional sample of 1279 LLFS subjects, although one (rs9650241) failed to replicate and the other two were not available in two independent replication cohorts, the Baltimore Longitudinal Study of Aging and the New England Centenarian Study. Based on 10,000,000 permutations, the empirical p-value of 2 × 10(−7) was observed for the genome-wide significant SNPs. Seventeen SNPs that reached marginal statistical significance in the two previous GWASs (p-value <10(−4) and 10(−5)), were also marginally significantly associated in this study (p-value <0.05), although none of the associations passed the Bonferroni correction. In addition, we tested age-by-SNP interactions and found some significant associations. Since scores of personality traits in LLFS subjects change in the oldest ages, and genetic factors outweigh environmental factors to achieve extreme ages, these age-by-SNP interactions could be a proxy for complex gene–gene interactions affecting personality traits and longevity. Frontiers Media S.A. 2013-05-08 /pmc/articles/PMC3647245/ /pubmed/23658558 http://dx.doi.org/10.3389/fgene.2013.00065 Text en Copyright © 2013 Bae, Sebastiani, Sun, Andersen, Daw, Terracciano, Ferrucci and Perls. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Genetics
Bae, Harold T.
Sebastiani, Paola
Sun, Jenny X.
Andersen, Stacy L.
Daw, E. Warwick
Terracciano, Antonio
Ferrucci, Luigi
Perls, Thomas T.
Genome-Wide Association Study of Personality Traits in the Long Life Family Study
title Genome-Wide Association Study of Personality Traits in the Long Life Family Study
title_full Genome-Wide Association Study of Personality Traits in the Long Life Family Study
title_fullStr Genome-Wide Association Study of Personality Traits in the Long Life Family Study
title_full_unstemmed Genome-Wide Association Study of Personality Traits in the Long Life Family Study
title_short Genome-Wide Association Study of Personality Traits in the Long Life Family Study
title_sort genome-wide association study of personality traits in the long life family study
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3647245/
https://www.ncbi.nlm.nih.gov/pubmed/23658558
http://dx.doi.org/10.3389/fgene.2013.00065
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