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Hostility and Cellular Aging in Men from the Whitehall II Cohort

BACKGROUND: Hostility is associated with a significantly increased risk of age-related disease and mortality, yet the pathophysiological mechanisms involved remain unclear. Here we investigated the hypothesis that hostility might impact health by promoting cellular aging. METHODS: We tested the rela...

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Detalles Bibliográficos
Autores principales: Brydon, Lena, Lin, Jue, Butcher, Lee, Hamer, Mark, Erusalimsky, Jorge D., Blackburn, Elizabeth H., Steptoe, Andrew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3657139/
https://www.ncbi.nlm.nih.gov/pubmed/21974787
http://dx.doi.org/10.1016/j.biopsych.2011.08.020
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author Brydon, Lena
Lin, Jue
Butcher, Lee
Hamer, Mark
Erusalimsky, Jorge D.
Blackburn, Elizabeth H.
Steptoe, Andrew
author_facet Brydon, Lena
Lin, Jue
Butcher, Lee
Hamer, Mark
Erusalimsky, Jorge D.
Blackburn, Elizabeth H.
Steptoe, Andrew
author_sort Brydon, Lena
collection PubMed
description BACKGROUND: Hostility is associated with a significantly increased risk of age-related disease and mortality, yet the pathophysiological mechanisms involved remain unclear. Here we investigated the hypothesis that hostility might impact health by promoting cellular aging. METHODS: We tested the relationship between cynical hostility and two known markers of cellular aging, leukocyte telomere length (TL) and leukocyte telomerase activity (TA), in 434 men and women from the Whitehall II cohort. RESULTS: High-hostile men had significantly shorter leukocyte TL than their low-hostile counterparts. They also had elevated leukocyte TA, with a significantly increased likelihood of having both short TL and high TA, compared with low-hostile individuals. CONCLUSIONS: Because telomerase is known to counteract telomere shortening by synthesizing telomeric DNA repeats, particularly in the context of shortened telomeres, heightened TA might represent a compensatory response in high-hostile individuals. The relationship between hostility and disease is stronger in men than in women, and men generally have a shorter life expectancy than women. Our findings suggest that telomere attrition might represent a novel mechanism mediating the detrimental effects of hostility on men's health.
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spelling pubmed-36571392013-05-18 Hostility and Cellular Aging in Men from the Whitehall II Cohort Brydon, Lena Lin, Jue Butcher, Lee Hamer, Mark Erusalimsky, Jorge D. Blackburn, Elizabeth H. Steptoe, Andrew Biol Psychiatry Priority Communication BACKGROUND: Hostility is associated with a significantly increased risk of age-related disease and mortality, yet the pathophysiological mechanisms involved remain unclear. Here we investigated the hypothesis that hostility might impact health by promoting cellular aging. METHODS: We tested the relationship between cynical hostility and two known markers of cellular aging, leukocyte telomere length (TL) and leukocyte telomerase activity (TA), in 434 men and women from the Whitehall II cohort. RESULTS: High-hostile men had significantly shorter leukocyte TL than their low-hostile counterparts. They also had elevated leukocyte TA, with a significantly increased likelihood of having both short TL and high TA, compared with low-hostile individuals. CONCLUSIONS: Because telomerase is known to counteract telomere shortening by synthesizing telomeric DNA repeats, particularly in the context of shortened telomeres, heightened TA might represent a compensatory response in high-hostile individuals. The relationship between hostility and disease is stronger in men than in women, and men generally have a shorter life expectancy than women. Our findings suggest that telomere attrition might represent a novel mechanism mediating the detrimental effects of hostility on men's health. Elsevier 2012-05-01 /pmc/articles/PMC3657139/ /pubmed/21974787 http://dx.doi.org/10.1016/j.biopsych.2011.08.020 Text en © 2012 Elsevier Inc. https://creativecommons.org/licenses/by/3.0/ Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license
spellingShingle Priority Communication
Brydon, Lena
Lin, Jue
Butcher, Lee
Hamer, Mark
Erusalimsky, Jorge D.
Blackburn, Elizabeth H.
Steptoe, Andrew
Hostility and Cellular Aging in Men from the Whitehall II Cohort
title Hostility and Cellular Aging in Men from the Whitehall II Cohort
title_full Hostility and Cellular Aging in Men from the Whitehall II Cohort
title_fullStr Hostility and Cellular Aging in Men from the Whitehall II Cohort
title_full_unstemmed Hostility and Cellular Aging in Men from the Whitehall II Cohort
title_short Hostility and Cellular Aging in Men from the Whitehall II Cohort
title_sort hostility and cellular aging in men from the whitehall ii cohort
topic Priority Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3657139/
https://www.ncbi.nlm.nih.gov/pubmed/21974787
http://dx.doi.org/10.1016/j.biopsych.2011.08.020
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