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The sex-dependent response to psychosocial stress and ischaemic heart disease
Stress is an important risk factor for modern chronic diseases, with distinct influences in males and females. The sex specificity of the mammalian stress response contributes to the sex-dependent development and impacts of coronary artery disease (CAD). Compared to men, women appear to have greater...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10160413/ https://www.ncbi.nlm.nih.gov/pubmed/37153459 http://dx.doi.org/10.3389/fcvm.2023.1072042 |
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author | Helman, Tessa J. Headrick, John P. Stapelberg, Nicolas J. C. Braidy, Nady |
author_facet | Helman, Tessa J. Headrick, John P. Stapelberg, Nicolas J. C. Braidy, Nady |
author_sort | Helman, Tessa J. |
collection | PubMed |
description | Stress is an important risk factor for modern chronic diseases, with distinct influences in males and females. The sex specificity of the mammalian stress response contributes to the sex-dependent development and impacts of coronary artery disease (CAD). Compared to men, women appear to have greater susceptibility to chronic forms of psychosocial stress, extending beyond an increased incidence of mood disorders to include a 2- to 4-fold higher risk of stress-dependent myocardial infarction in women, and up to 10-fold higher risk of Takotsubo syndrome—a stress-dependent coronary-myocardial disorder most prevalent in post-menopausal women. Sex differences arise at all levels of the stress response: from initial perception of stress to behavioural, cognitive, and affective responses and longer-term disease outcomes. These fundamental differences involve interactions between chromosomal and gonadal determinants, (mal)adaptive epigenetic modulation across the lifespan (particularly in early life), and the extrinsic influences of socio-cultural, economic, and environmental factors. Pre-clinical investigations of biological mechanisms support distinct early life programming and a heightened corticolimbic-noradrenaline-neuroinflammatory reactivity in females vs. males, among implicated determinants of the chronic stress response. Unravelling the intrinsic molecular, cellular and systems biological basis of these differences, and their interactions with external lifestyle/socio-cultural determinants, can guide preventative and therapeutic strategies to better target coronary heart disease in a tailored sex-specific manner. |
format | Online Article Text |
id | pubmed-10160413 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101604132023-05-06 The sex-dependent response to psychosocial stress and ischaemic heart disease Helman, Tessa J. Headrick, John P. Stapelberg, Nicolas J. C. Braidy, Nady Front Cardiovasc Med Cardiovascular Medicine Stress is an important risk factor for modern chronic diseases, with distinct influences in males and females. The sex specificity of the mammalian stress response contributes to the sex-dependent development and impacts of coronary artery disease (CAD). Compared to men, women appear to have greater susceptibility to chronic forms of psychosocial stress, extending beyond an increased incidence of mood disorders to include a 2- to 4-fold higher risk of stress-dependent myocardial infarction in women, and up to 10-fold higher risk of Takotsubo syndrome—a stress-dependent coronary-myocardial disorder most prevalent in post-menopausal women. Sex differences arise at all levels of the stress response: from initial perception of stress to behavioural, cognitive, and affective responses and longer-term disease outcomes. These fundamental differences involve interactions between chromosomal and gonadal determinants, (mal)adaptive epigenetic modulation across the lifespan (particularly in early life), and the extrinsic influences of socio-cultural, economic, and environmental factors. Pre-clinical investigations of biological mechanisms support distinct early life programming and a heightened corticolimbic-noradrenaline-neuroinflammatory reactivity in females vs. males, among implicated determinants of the chronic stress response. Unravelling the intrinsic molecular, cellular and systems biological basis of these differences, and their interactions with external lifestyle/socio-cultural determinants, can guide preventative and therapeutic strategies to better target coronary heart disease in a tailored sex-specific manner. Frontiers Media S.A. 2023-04-21 /pmc/articles/PMC10160413/ /pubmed/37153459 http://dx.doi.org/10.3389/fcvm.2023.1072042 Text en © 2023 Helman, Headrick, Stapelberg and Braidy. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (https://creativecommons.org/licenses/by/4.0/) . The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cardiovascular Medicine Helman, Tessa J. Headrick, John P. Stapelberg, Nicolas J. C. Braidy, Nady The sex-dependent response to psychosocial stress and ischaemic heart disease |
title | The sex-dependent response to psychosocial stress and ischaemic heart disease |
title_full | The sex-dependent response to psychosocial stress and ischaemic heart disease |
title_fullStr | The sex-dependent response to psychosocial stress and ischaemic heart disease |
title_full_unstemmed | The sex-dependent response to psychosocial stress and ischaemic heart disease |
title_short | The sex-dependent response to psychosocial stress and ischaemic heart disease |
title_sort | sex-dependent response to psychosocial stress and ischaemic heart disease |
topic | Cardiovascular Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10160413/ https://www.ncbi.nlm.nih.gov/pubmed/37153459 http://dx.doi.org/10.3389/fcvm.2023.1072042 |
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