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Sex-specific roles of cellular inflammation and cardiometabolism in obesity-associated depressive symptomatology

BACKGROUND: Obesity and depression are complex conditions with stronger comorbid relationships among women than men. Inflammation and cardiometabolic dysfunction are likely mechanistic candidates for increased depression risk, and their prevalence differs by sex. Whether these relationships extend t...

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Autores principales: Kohn, Jordan N., Cabrera, Yesenia, Dimitrov, Stoyan, Guay-Ross, Nicholas, Pruitt, Christopher, Shaikh, Farah D., Hong, Suzi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6774832/
https://www.ncbi.nlm.nih.gov/pubmed/31089263
http://dx.doi.org/10.1038/s41366-019-0375-3
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author Kohn, Jordan N.
Cabrera, Yesenia
Dimitrov, Stoyan
Guay-Ross, Nicholas
Pruitt, Christopher
Shaikh, Farah D.
Hong, Suzi
author_facet Kohn, Jordan N.
Cabrera, Yesenia
Dimitrov, Stoyan
Guay-Ross, Nicholas
Pruitt, Christopher
Shaikh, Farah D.
Hong, Suzi
author_sort Kohn, Jordan N.
collection PubMed
description BACKGROUND: Obesity and depression are complex conditions with stronger comorbid relationships among women than men. Inflammation and cardiometabolic dysfunction are likely mechanistic candidates for increased depression risk, and their prevalence differs by sex. Whether these relationships extend to depressive symptoms is poorly understood. Therefore, we analyzed sex in associations between inflammation and metabolic syndrome (MetS) criteria on depressive symptomatology. Specifically, we examined whether sex positively moderates the relationship between depressive symptoms and inflammation among women, and whether MetS has parallel effects among men. METHODS: Depressive symptoms, MetS, and inflammation were assessed in 129 otherwise healthy adults. Depressive symptoms were assessed using Beck Depression Inventory (BDI-Ia). Monocyte inflammation regulation (BARIC) was quantified using flow cytometry measurement of TNF-α suppression by β-agonist. Moderation effects of sex on associations between BARIC, MetS criteria, and BDI were estimated using two-way ANOVA and linear regression, adjusting for BMI, and by sex subgroup analyses. RESULTS: Obese individuals reported more depressive symptoms. Sex did not formally moderate this relationship, though BDI scores tended to differ by BMI among women, but not men, in subgroup analysis. Poorer inflammation control and higher MetS criteria were correlated with somatic depressive symptoms. Sex moderated associations between MetS criteria and somatic symptoms; among men, MetS criteria predicted somatic symptoms, not among women. Subgroup analysis further indicated that poorer inflammation control tended to be associated with higher somatic symptoms in women. CONCLUSIONS: These results indicate that obesity-related inflammation and MetS factors have sex-specific effects on depressive symptoms in a non-clinical population. Although pathophysiological mechanisms underlying sex differences remain to be elucidated, our findings suggest that distinct vulnerabilities to depressive symptoms exist between women and men, and highlight the need to consider sex as a key biological variable in obesity-depression relationships. Future clinical studies on comorbid obesity and depression should account for sex, which may optimize therapeutic strategies.
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spelling pubmed-67748322019-11-14 Sex-specific roles of cellular inflammation and cardiometabolism in obesity-associated depressive symptomatology Kohn, Jordan N. Cabrera, Yesenia Dimitrov, Stoyan Guay-Ross, Nicholas Pruitt, Christopher Shaikh, Farah D. Hong, Suzi Int J Obes (Lond) Article BACKGROUND: Obesity and depression are complex conditions with stronger comorbid relationships among women than men. Inflammation and cardiometabolic dysfunction are likely mechanistic candidates for increased depression risk, and their prevalence differs by sex. Whether these relationships extend to depressive symptoms is poorly understood. Therefore, we analyzed sex in associations between inflammation and metabolic syndrome (MetS) criteria on depressive symptomatology. Specifically, we examined whether sex positively moderates the relationship between depressive symptoms and inflammation among women, and whether MetS has parallel effects among men. METHODS: Depressive symptoms, MetS, and inflammation were assessed in 129 otherwise healthy adults. Depressive symptoms were assessed using Beck Depression Inventory (BDI-Ia). Monocyte inflammation regulation (BARIC) was quantified using flow cytometry measurement of TNF-α suppression by β-agonist. Moderation effects of sex on associations between BARIC, MetS criteria, and BDI were estimated using two-way ANOVA and linear regression, adjusting for BMI, and by sex subgroup analyses. RESULTS: Obese individuals reported more depressive symptoms. Sex did not formally moderate this relationship, though BDI scores tended to differ by BMI among women, but not men, in subgroup analysis. Poorer inflammation control and higher MetS criteria were correlated with somatic depressive symptoms. Sex moderated associations between MetS criteria and somatic symptoms; among men, MetS criteria predicted somatic symptoms, not among women. Subgroup analysis further indicated that poorer inflammation control tended to be associated with higher somatic symptoms in women. CONCLUSIONS: These results indicate that obesity-related inflammation and MetS factors have sex-specific effects on depressive symptoms in a non-clinical population. Although pathophysiological mechanisms underlying sex differences remain to be elucidated, our findings suggest that distinct vulnerabilities to depressive symptoms exist between women and men, and highlight the need to consider sex as a key biological variable in obesity-depression relationships. Future clinical studies on comorbid obesity and depression should account for sex, which may optimize therapeutic strategies. 2019-05-14 2019-10 /pmc/articles/PMC6774832/ /pubmed/31089263 http://dx.doi.org/10.1038/s41366-019-0375-3 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Kohn, Jordan N.
Cabrera, Yesenia
Dimitrov, Stoyan
Guay-Ross, Nicholas
Pruitt, Christopher
Shaikh, Farah D.
Hong, Suzi
Sex-specific roles of cellular inflammation and cardiometabolism in obesity-associated depressive symptomatology
title Sex-specific roles of cellular inflammation and cardiometabolism in obesity-associated depressive symptomatology
title_full Sex-specific roles of cellular inflammation and cardiometabolism in obesity-associated depressive symptomatology
title_fullStr Sex-specific roles of cellular inflammation and cardiometabolism in obesity-associated depressive symptomatology
title_full_unstemmed Sex-specific roles of cellular inflammation and cardiometabolism in obesity-associated depressive symptomatology
title_short Sex-specific roles of cellular inflammation and cardiometabolism in obesity-associated depressive symptomatology
title_sort sex-specific roles of cellular inflammation and cardiometabolism in obesity-associated depressive symptomatology
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6774832/
https://www.ncbi.nlm.nih.gov/pubmed/31089263
http://dx.doi.org/10.1038/s41366-019-0375-3
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