Associations Between Child Maltreatment, Inflammation, and Comorbid Metabolic Syndrome to Depressed Mood in a

Fabienne E M Willemen1, Mirjam van Zuiden1, Jasper B Zantvoord1,2

  • 1Department of Psychiatry, Amsterdam Neuroscience and Amsterdam Public Health, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, Netherlands.

Insights

Child maltreatment increases the risk for depressed mood in adults. However, this study found no significant association between child maltreatment and metabolic syndrome, even in those with depression.

Area of Science:

  • Psychiatry
  • Public Health
  • Epidemiology

Background:

  • Child maltreatment is linked to long-term mental and physical health issues.
  • Inflammation may mediate the link between child maltreatment and poor adult health.
  • The relationship between child maltreatment, major depressive disorder (MDD), and metabolic syndrome requires further investigation.

Purpose of the Study:

  • To investigate if child maltreatment increases the risk for comorbid metabolic syndrome and depressed mood.
  • To examine if C-reactive protein (CRP) mediates this association.
  • To determine if these effects differ between men and women.

Main Methods:

  • Cross-sectional analysis of the multiethnic HELIUS study (N=21,617).
  • Self-reported child maltreatment and current depressed mood (PHQ-9 score ≥ 10).
  • Physical examination for metabolic syndrome and CRP levels assessed in a subset (N=5,998).

Main Results:

  • Higher numbers of maltreatment types, emotional neglect, emotional abuse, and sexual abuse were linked to increased depressed mood risk.
  • Child maltreatment was not significantly associated with metabolic syndrome risk in the general cohort or individuals with depression.
  • No significant mediation by CRP or moderation by sex was observed.

Conclusions:

  • Child maltreatment is associated with a higher risk of depressed mood in this urban cohort.
  • Contrary to hypotheses, child maltreatment was not linked to an increased risk of metabolic syndrome.
  • Longitudinal studies with comprehensive inflammatory marker assessments are needed.
Abstract

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