Allostatic Load Biomarker Associations with Depressive Symptoms Vary among US Black and White Women and Men
UMass Chan Affiliations
Department of Quantitative Health SciencesDocument Type
Journal ArticlePublication Date
2018-08-28Keywords
allostatic loadchronic stress
depression
gender
intersectionality
race
Amino Acids, Peptides, and Proteins
Biological Factors
Gender and Sexuality
Health Psychology
Medicine and Health
Psychiatry and Psychology
Race and Ethnicity
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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.Source
Healthcare (Basel). 2018 Aug 28;6(3). pii: E105. doi: 10.3390/healthcare6030105. Link to article on publisher's site
DOI
10.3390/healthcare6030105Permanent Link to this Item
http://hdl.handle.net/20.500.14038/40764PubMed ID
30154326Related Resources
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© 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/).Distribution License
http://creativecommons.org/licenses/by/4.0/ae974a485f413a2113503eed53cd6c53
10.3390/healthcare6030105
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Except where otherwise noted, this item's license is described as © 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/).