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A Putatively Functional Polymorphism in the HTR2C Gene is Associated with Depressive Symptoms in White Females Reporting Significant Life Stress

Psychosocial stress is well known to be positively associated with subsequent depressive symptoms. Cortisol response to stress may be one of a number of biological mechanisms that links psychological stress to depressive symptoms, although the precise causal pathway remains unclear. Activity of the...

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Autores principales: Brummett, Beverly H., Babyak, Michael A., Williams, Redford B., Harris, Kathleen Mullan, Jiang, Rong, Kraus, William E., Singh, Abanish, Costa, Paul T., Georgiades, Anastasia, Siegler, Ilene C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4267787/
https://www.ncbi.nlm.nih.gov/pubmed/25514629
http://dx.doi.org/10.1371/journal.pone.0114451
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author Brummett, Beverly H.
Babyak, Michael A.
Williams, Redford B.
Harris, Kathleen Mullan
Jiang, Rong
Kraus, William E.
Singh, Abanish
Costa, Paul T.
Georgiades, Anastasia
Siegler, Ilene C.
author_facet Brummett, Beverly H.
Babyak, Michael A.
Williams, Redford B.
Harris, Kathleen Mullan
Jiang, Rong
Kraus, William E.
Singh, Abanish
Costa, Paul T.
Georgiades, Anastasia
Siegler, Ilene C.
author_sort Brummett, Beverly H.
collection PubMed
description Psychosocial stress is well known to be positively associated with subsequent depressive symptoms. Cortisol response to stress may be one of a number of biological mechanisms that links psychological stress to depressive symptoms, although the precise causal pathway remains unclear. Activity of the x-linked serotonin 5-HTR2C receptor has also been shown to be associated with depression and with clinical response to antidepressant medications. We recently demonstrated that variation in a single nucleotide polymorphism on the HTR2C gene, rs6318 (Ser23Cys), is associated with different cortisol release and short-term changes in affect in response to a series of stress tasks in the laboratory. Based on this observation, we decided to examine whether rs6318 might moderate the association between psychosocial stress and subsequent depressive symptoms. In the present study we use cross-sectional data from a large population-based sample of young adult White men (N = 2,366) and White women (N = 2,712) in the United States to test this moderation hypothesis. Specifically, we hypothesized that the association between self-reported stressful life events and depressive symptoms would be stronger among homozygous Ser23 C females and hemizygous Ser23 C males than among Cys23 G carriers. In separate within-sex analyses a genotype-by-life stress interaction was observed for women (p = .022) but not for men (p = .471). Homozygous Ser23 C women who reported high levels of life stress had depressive symptom scores that were about 0.3 standard deviations higher than female Cys23 G carriers with similarly high stress levels. In contrast, no appreciable difference in depressive symptoms was observed between genotypes at lower levels of stress. Our findings support prior work that suggests a functional SNP on the HTR2C gene may confer an increased risk for depressive symptoms in White women with a history of significant life stress.
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spelling pubmed-42677872014-12-26 A Putatively Functional Polymorphism in the HTR2C Gene is Associated with Depressive Symptoms in White Females Reporting Significant Life Stress Brummett, Beverly H. Babyak, Michael A. Williams, Redford B. Harris, Kathleen Mullan Jiang, Rong Kraus, William E. Singh, Abanish Costa, Paul T. Georgiades, Anastasia Siegler, Ilene C. PLoS One Research Article Psychosocial stress is well known to be positively associated with subsequent depressive symptoms. Cortisol response to stress may be one of a number of biological mechanisms that links psychological stress to depressive symptoms, although the precise causal pathway remains unclear. Activity of the x-linked serotonin 5-HTR2C receptor has also been shown to be associated with depression and with clinical response to antidepressant medications. We recently demonstrated that variation in a single nucleotide polymorphism on the HTR2C gene, rs6318 (Ser23Cys), is associated with different cortisol release and short-term changes in affect in response to a series of stress tasks in the laboratory. Based on this observation, we decided to examine whether rs6318 might moderate the association between psychosocial stress and subsequent depressive symptoms. In the present study we use cross-sectional data from a large population-based sample of young adult White men (N = 2,366) and White women (N = 2,712) in the United States to test this moderation hypothesis. Specifically, we hypothesized that the association between self-reported stressful life events and depressive symptoms would be stronger among homozygous Ser23 C females and hemizygous Ser23 C males than among Cys23 G carriers. In separate within-sex analyses a genotype-by-life stress interaction was observed for women (p = .022) but not for men (p = .471). Homozygous Ser23 C women who reported high levels of life stress had depressive symptom scores that were about 0.3 standard deviations higher than female Cys23 G carriers with similarly high stress levels. In contrast, no appreciable difference in depressive symptoms was observed between genotypes at lower levels of stress. Our findings support prior work that suggests a functional SNP on the HTR2C gene may confer an increased risk for depressive symptoms in White women with a history of significant life stress. Public Library of Science 2014-12-16 /pmc/articles/PMC4267787/ /pubmed/25514629 http://dx.doi.org/10.1371/journal.pone.0114451 Text en © 2014 Brummett et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Brummett, Beverly H.
Babyak, Michael A.
Williams, Redford B.
Harris, Kathleen Mullan
Jiang, Rong
Kraus, William E.
Singh, Abanish
Costa, Paul T.
Georgiades, Anastasia
Siegler, Ilene C.
A Putatively Functional Polymorphism in the HTR2C Gene is Associated with Depressive Symptoms in White Females Reporting Significant Life Stress
title A Putatively Functional Polymorphism in the HTR2C Gene is Associated with Depressive Symptoms in White Females Reporting Significant Life Stress
title_full A Putatively Functional Polymorphism in the HTR2C Gene is Associated with Depressive Symptoms in White Females Reporting Significant Life Stress
title_fullStr A Putatively Functional Polymorphism in the HTR2C Gene is Associated with Depressive Symptoms in White Females Reporting Significant Life Stress
title_full_unstemmed A Putatively Functional Polymorphism in the HTR2C Gene is Associated with Depressive Symptoms in White Females Reporting Significant Life Stress
title_short A Putatively Functional Polymorphism in the HTR2C Gene is Associated with Depressive Symptoms in White Females Reporting Significant Life Stress
title_sort putatively functional polymorphism in the htr2c gene is associated with depressive symptoms in white females reporting significant life stress
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4267787/
https://www.ncbi.nlm.nih.gov/pubmed/25514629
http://dx.doi.org/10.1371/journal.pone.0114451
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