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FTO Genotype and Aging: Pleiotropic Longitudinal Effects on Adiposity, Brain function, Impulsivity and Diet
While overweight and obesity are associated with poor health outcomes in the elderly, the biological bases of obesity-related behaviors during aging are poorly understood. Common variants in the FTO gene are associated with adiposity in children and younger adults as well as with adverse mental heal...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4246032/ https://www.ncbi.nlm.nih.gov/pubmed/24863145 http://dx.doi.org/10.1038/mp.2014.49 |
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author | Chuang, Yi-Fang Tanaka, Toshiko Beason-Held, Lori L. An, Yang Terracciano, Antonio Sutin, Angelina R. Kraut, Michael Singleton, Andrew B. Resnick, Susan M. Thambisetty, Madhav |
author_facet | Chuang, Yi-Fang Tanaka, Toshiko Beason-Held, Lori L. An, Yang Terracciano, Antonio Sutin, Angelina R. Kraut, Michael Singleton, Andrew B. Resnick, Susan M. Thambisetty, Madhav |
author_sort | Chuang, Yi-Fang |
collection | PubMed |
description | While overweight and obesity are associated with poor health outcomes in the elderly, the biological bases of obesity-related behaviors during aging are poorly understood. Common variants in the FTO gene are associated with adiposity in children and younger adults as well as with adverse mental health in older individuals. However, it is unclear whether FTO influences longitudinal trajectories of adiposity and other intermediate phenotypes relevant to mental health during aging. We examined whether a commonly carried obesity risk variant in the FTO gene (rs1421085 single nucleotide polymorphism) influences adiposity and is associated with changes in brain function in participants within the Baltimore Longitudinal Study of Aging (BLSA), one of the longest-running longitudinal aging studies in the United States. Our results show that obesity-related risk allele carriers of FTO gene show dose-dependent increments in body mass index during aging. Moreover, the obesity-related risk allele is associated with reduced medial prefrontal cortical function during aging. Consistent with reduced brain function in regions intrinsic to impulse control and taste responsiveness, risk allele carriers of FTO exhibit dose-dependent increments in both impulsivity and intake of fatty foods. We propose that a common neural mechanism may underlie obesity-associated impulsivity and increased consumption of high calorie foods during aging. |
format | Online Article Text |
id | pubmed-4246032 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
record_format | MEDLINE/PubMed |
spelling | pubmed-42460322015-08-01 FTO Genotype and Aging: Pleiotropic Longitudinal Effects on Adiposity, Brain function, Impulsivity and Diet Chuang, Yi-Fang Tanaka, Toshiko Beason-Held, Lori L. An, Yang Terracciano, Antonio Sutin, Angelina R. Kraut, Michael Singleton, Andrew B. Resnick, Susan M. Thambisetty, Madhav Mol Psychiatry Article While overweight and obesity are associated with poor health outcomes in the elderly, the biological bases of obesity-related behaviors during aging are poorly understood. Common variants in the FTO gene are associated with adiposity in children and younger adults as well as with adverse mental health in older individuals. However, it is unclear whether FTO influences longitudinal trajectories of adiposity and other intermediate phenotypes relevant to mental health during aging. We examined whether a commonly carried obesity risk variant in the FTO gene (rs1421085 single nucleotide polymorphism) influences adiposity and is associated with changes in brain function in participants within the Baltimore Longitudinal Study of Aging (BLSA), one of the longest-running longitudinal aging studies in the United States. Our results show that obesity-related risk allele carriers of FTO gene show dose-dependent increments in body mass index during aging. Moreover, the obesity-related risk allele is associated with reduced medial prefrontal cortical function during aging. Consistent with reduced brain function in regions intrinsic to impulse control and taste responsiveness, risk allele carriers of FTO exhibit dose-dependent increments in both impulsivity and intake of fatty foods. We propose that a common neural mechanism may underlie obesity-associated impulsivity and increased consumption of high calorie foods during aging. 2014-05-27 2015-02 /pmc/articles/PMC4246032/ /pubmed/24863145 http://dx.doi.org/10.1038/mp.2014.49 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Chuang, Yi-Fang Tanaka, Toshiko Beason-Held, Lori L. An, Yang Terracciano, Antonio Sutin, Angelina R. Kraut, Michael Singleton, Andrew B. Resnick, Susan M. Thambisetty, Madhav FTO Genotype and Aging: Pleiotropic Longitudinal Effects on Adiposity, Brain function, Impulsivity and Diet |
title | FTO Genotype and Aging: Pleiotropic Longitudinal Effects on Adiposity, Brain function, Impulsivity and Diet |
title_full | FTO Genotype and Aging: Pleiotropic Longitudinal Effects on Adiposity, Brain function, Impulsivity and Diet |
title_fullStr | FTO Genotype and Aging: Pleiotropic Longitudinal Effects on Adiposity, Brain function, Impulsivity and Diet |
title_full_unstemmed | FTO Genotype and Aging: Pleiotropic Longitudinal Effects on Adiposity, Brain function, Impulsivity and Diet |
title_short | FTO Genotype and Aging: Pleiotropic Longitudinal Effects on Adiposity, Brain function, Impulsivity and Diet |
title_sort | fto genotype and aging: pleiotropic longitudinal effects on adiposity, brain function, impulsivity and diet |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4246032/ https://www.ncbi.nlm.nih.gov/pubmed/24863145 http://dx.doi.org/10.1038/mp.2014.49 |
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