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


Journal

International journal of obesity (2005)
ISSN: 1476-5497
Titre abrégé: Int J Obes (Lond)
Pays: England
ID NLM: 101256108

Informations de publication

Date de publication:
10 2019
Historique:
received: 14 06 2018
accepted: 29 03 2019
revised: 06 02 2019
pubmed: 16 5 2019
medline: 19 5 2020
entrez: 16 5 2019
Statut: ppublish

Résumé

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. 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. 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. 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.

Sections du résumé

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.

Identifiants

pubmed: 31089263
doi: 10.1038/s41366-019-0375-3
pii: 10.1038/s41366-019-0375-3
pmc: PMC6774832
mid: NIHMS1525852
doi:

Substances chimiques

C-Reactive Protein 9007-41-4

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

2045-2056

Subventions

Organisme : NCATS NIH HHS
ID : UL1 TR001442
Pays : United States
Organisme : NCATS NIH HHS
ID : TL1 TR001443
Pays : United States
Organisme : ARRA NIH HHS
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL090975
Pays : United States
Organisme : NCRR NIH HHS
ID : UL1 RR031980
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR000100
Pays : United States

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Auteurs

Jordan N Kohn (JN)

Department of Psychiatry, University of California San Diego, La Jolla, 92093, California, United States.

Yesenia Cabrera (Y)

Neuroscience Interdepartmental PhD Program, University of California, Los Angeles, CA, 90095, USA.

Stoyan Dimitrov (S)

Institute of Medical Psychology and Behavioral Neurobiology, University of Tübingen, 72076, Tübingen, Germany.

Nicholas Guay-Ross (N)

Department of Psychiatry, University of California San Diego, La Jolla, 92093, California, United States.

Christopher Pruitt (C)

Department of Family Medicine and Public Health, University of California San Diego, La Jolla, 92093, CA, USA.

Farah D Shaikh (FD)

Department of Psychiatry, University of California San Diego, La Jolla, 92093, California, United States.

Suzi Hong (S)

Department of Psychiatry, University of California San Diego, La Jolla, 92093, California, United States. s1hong@ucsd.edu.
Department of Family Medicine and Public Health, University of California San Diego, La Jolla, 92093, CA, USA. s1hong@ucsd.edu.

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