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Genetic Variation in FOXO3 is Associated with Self-Rated Health in a Population-Based Sample of Older Individuals
Self-rated health (SRH) strongly predicts mortality. Twin studies estimate that genetic factors account for a substantial part of the variability in SRH. Variations in the gene FOXO3 (forkhead box O3), and in genes located at the APOE (apoplipoprotein E) locus, are associated with longevity. This st...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6175024/ https://www.ncbi.nlm.nih.gov/pubmed/29415201 http://dx.doi.org/10.1093/gerona/gly021 |
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author | Zettergren, Anna Kern, Silke Rydén, Lina Östling, Svante Blennow, Kaj Zetterberg, Henrik Falk, Hanna Skoog, Ingmar |
author_facet | Zettergren, Anna Kern, Silke Rydén, Lina Östling, Svante Blennow, Kaj Zetterberg, Henrik Falk, Hanna Skoog, Ingmar |
author_sort | Zettergren, Anna |
collection | PubMed |
description | Self-rated health (SRH) strongly predicts mortality. Twin studies estimate that genetic factors account for a substantial part of the variability in SRH. Variations in the gene FOXO3 (forkhead box O3), and in genes located at the APOE (apoplipoprotein E) locus, are associated with longevity. This study explores the relationship between SRH and genetic variation related to longevity, in a population-based cohort of older individuals. SRH was assessed among 1,520 individuals aged 75–87, and five single nucleotide polymorphisms (SNPs), in APOE, TOMM40 (translocase of outer mitochondrial membrane 40 homolog), and FOXO3 were genotyped. Two SNPs (rs10457180 and rs2802292) in FOXO3 were associated with SRH (OR = 2.18 [CI: 1.27–3.76], p = .005 and OR = 1.63 [CI: 1.11–2.40], p = .013), while no associations were found with SNPs in APOE and TOMM40. Several factors, such as depression, cardiovascular disease (CVD), and diabetes, were related to SRH, but the only factor that had any influence on the association with FOXO3 was CVD. Still, after including CVD as a covariate, the associations between FOXO3 SNPs and SRH remained significant. Our results suggest that FOXO3 is related to SRH in older individuals. This relationship seems to be influenced by CVD, but not by mental and cognitive status. |
format | Online Article Text |
id | pubmed-6175024 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61750242018-10-11 Genetic Variation in FOXO3 is Associated with Self-Rated Health in a Population-Based Sample of Older Individuals Zettergren, Anna Kern, Silke Rydén, Lina Östling, Svante Blennow, Kaj Zetterberg, Henrik Falk, Hanna Skoog, Ingmar J Gerontol A Biol Sci Med Sci The Journal of Gerontology: Biological Sciences Self-rated health (SRH) strongly predicts mortality. Twin studies estimate that genetic factors account for a substantial part of the variability in SRH. Variations in the gene FOXO3 (forkhead box O3), and in genes located at the APOE (apoplipoprotein E) locus, are associated with longevity. This study explores the relationship between SRH and genetic variation related to longevity, in a population-based cohort of older individuals. SRH was assessed among 1,520 individuals aged 75–87, and five single nucleotide polymorphisms (SNPs), in APOE, TOMM40 (translocase of outer mitochondrial membrane 40 homolog), and FOXO3 were genotyped. Two SNPs (rs10457180 and rs2802292) in FOXO3 were associated with SRH (OR = 2.18 [CI: 1.27–3.76], p = .005 and OR = 1.63 [CI: 1.11–2.40], p = .013), while no associations were found with SNPs in APOE and TOMM40. Several factors, such as depression, cardiovascular disease (CVD), and diabetes, were related to SRH, but the only factor that had any influence on the association with FOXO3 was CVD. Still, after including CVD as a covariate, the associations between FOXO3 SNPs and SRH remained significant. Our results suggest that FOXO3 is related to SRH in older individuals. This relationship seems to be influenced by CVD, but not by mental and cognitive status. Oxford University Press 2018-10 2018-02-05 /pmc/articles/PMC6175024/ /pubmed/29415201 http://dx.doi.org/10.1093/gerona/gly021 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of The Gerontological Society of America. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | The Journal of Gerontology: Biological Sciences Zettergren, Anna Kern, Silke Rydén, Lina Östling, Svante Blennow, Kaj Zetterberg, Henrik Falk, Hanna Skoog, Ingmar Genetic Variation in FOXO3 is Associated with Self-Rated Health in a Population-Based Sample of Older Individuals |
title | Genetic Variation in FOXO3 is Associated with Self-Rated Health in a Population-Based Sample of Older Individuals |
title_full | Genetic Variation in FOXO3 is Associated with Self-Rated Health in a Population-Based Sample of Older Individuals |
title_fullStr | Genetic Variation in FOXO3 is Associated with Self-Rated Health in a Population-Based Sample of Older Individuals |
title_full_unstemmed | Genetic Variation in FOXO3 is Associated with Self-Rated Health in a Population-Based Sample of Older Individuals |
title_short | Genetic Variation in FOXO3 is Associated with Self-Rated Health in a Population-Based Sample of Older Individuals |
title_sort | genetic variation in foxo3 is associated with self-rated health in a population-based sample of older individuals |
topic | The Journal of Gerontology: Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6175024/ https://www.ncbi.nlm.nih.gov/pubmed/29415201 http://dx.doi.org/10.1093/gerona/gly021 |
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