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Allostatic Load Biomarker Associations with Depressive Symptoms Vary among US Black and White Women and Men

The prevalence and severity of depression differ in women and men and across racial groups. Psychosocial factors such as chronic stress have been proposed as contributors, but causes of this variation are not fully understood. Allostatic load, a measure of the physiological burden of chronic stress,...

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Autores principales: Bey, Ganga S., Jesdale, Bill M., Ulbricht, Christine M., Mick, Eric O., Person, Sharina D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6163528/
https://www.ncbi.nlm.nih.gov/pubmed/30154326
http://dx.doi.org/10.3390/healthcare6030105
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author Bey, Ganga S.
Jesdale, Bill M.
Ulbricht, Christine M.
Mick, Eric O.
Person, Sharina D.
author_facet Bey, Ganga S.
Jesdale, Bill M.
Ulbricht, Christine M.
Mick, Eric O.
Person, Sharina D.
author_sort Bey, Ganga S.
collection PubMed
description The prevalence and severity of depression differ in women and men and across racial groups. Psychosocial factors such as chronic stress have been proposed as contributors, but causes of this variation are not fully understood. Allostatic load, a measure of the physiological burden of chronic stress, is known to be associated with depression. Using data from the National Health and Nutrition Examination Survey 2005–2010, we examined the associations of nine allostatic load biomarkers with depression among US black and white adults aged 18–64 years (n = 6431). Depressive symptoms were assessed using the Patient Health Questionaire-9; logistic models estimated adjusted odds of depression based on allostatic load biomarkers. High-risk levels of c-reactive protein were significantly associated with increased odds of depression among white women (adjusted odds ratio (aOR) = 1.7, 95% CI: 1.1–2.5) and men (aOR = 1.8, 95% CI: 1.1–2.8) but not black women (aOR = 0.8, 95% CI: 0.6–1.1) or men (aOR = 0.9, 95% CI: 0.5–1.5). Among black men, hypertension (aOR = 1.7, 95% CI: 1.1–2.7) and adverse serum albumin levels (aOR = 1.7, 95% CI: 1.0–2.9) predicted depression, while high total cholesterol was associated with depression among black women (aOR = 1.6, 95% CI: 1.0–2.7). The associations between allostatic load biomarkers and depression varies with gendered race, suggesting that, despite consistent symptomatology, underlying disease mechanisms may differ between these groups.
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spelling pubmed-61635282018-10-10 Allostatic Load Biomarker Associations with Depressive Symptoms Vary among US Black and White Women and Men Bey, Ganga S. Jesdale, Bill M. Ulbricht, Christine M. Mick, Eric O. Person, Sharina D. Healthcare (Basel) Article The prevalence and severity of depression differ in women and men and across racial groups. Psychosocial factors such as chronic stress have been proposed as contributors, but causes of this variation are not fully understood. Allostatic load, a measure of the physiological burden of chronic stress, is known to be associated with depression. Using data from the National Health and Nutrition Examination Survey 2005–2010, we examined the associations of nine allostatic load biomarkers with depression among US black and white adults aged 18–64 years (n = 6431). Depressive symptoms were assessed using the Patient Health Questionaire-9; logistic models estimated adjusted odds of depression based on allostatic load biomarkers. High-risk levels of c-reactive protein were significantly associated with increased odds of depression among white women (adjusted odds ratio (aOR) = 1.7, 95% CI: 1.1–2.5) and men (aOR = 1.8, 95% CI: 1.1–2.8) but not black women (aOR = 0.8, 95% CI: 0.6–1.1) or men (aOR = 0.9, 95% CI: 0.5–1.5). Among black men, hypertension (aOR = 1.7, 95% CI: 1.1–2.7) and adverse serum albumin levels (aOR = 1.7, 95% CI: 1.0–2.9) predicted depression, while high total cholesterol was associated with depression among black women (aOR = 1.6, 95% CI: 1.0–2.7). The associations between allostatic load biomarkers and depression varies with gendered race, suggesting that, despite consistent symptomatology, underlying disease mechanisms may differ between these groups. MDPI 2018-08-28 /pmc/articles/PMC6163528/ /pubmed/30154326 http://dx.doi.org/10.3390/healthcare6030105 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Bey, Ganga S.
Jesdale, Bill M.
Ulbricht, Christine M.
Mick, Eric O.
Person, Sharina D.
Allostatic Load Biomarker Associations with Depressive Symptoms Vary among US Black and White Women and Men
title Allostatic Load Biomarker Associations with Depressive Symptoms Vary among US Black and White Women and Men
title_full Allostatic Load Biomarker Associations with Depressive Symptoms Vary among US Black and White Women and Men
title_fullStr Allostatic Load Biomarker Associations with Depressive Symptoms Vary among US Black and White Women and Men
title_full_unstemmed Allostatic Load Biomarker Associations with Depressive Symptoms Vary among US Black and White Women and Men
title_short Allostatic Load Biomarker Associations with Depressive Symptoms Vary among US Black and White Women and Men
title_sort allostatic load biomarker associations with depressive symptoms vary among us black and white women and men
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6163528/
https://www.ncbi.nlm.nih.gov/pubmed/30154326
http://dx.doi.org/10.3390/healthcare6030105
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