Key result
Young adults with a history of childhood-onset depression had significantly higher metabolic syndrome composite scores compared to healthy controls (LSM difference 0.35, p<0.01).
Why the study?
It was unclear whether the early-onset depression phenotype among young adults is associated with metabolic syndrome and its components, and whether metabolic syndrome characterizes unaffected high-risk siblings.
Is early-onset depression or high familial risk for depression associated with metabolic syndrome in young adults?
Cross-Sectional (n=737)
Yes
Is early-onset depression or high familial risk for depression associated with metabolic syndrome in young adults?
Young adults with early-onset depression and their unaffected high-risk siblings exhibit higher metabolic syndrome scores compared to controls, suggesting metabolic dysregulation may predate clinical depression.
Answers are grounded in this paper and cite their sources.
May support metabolic monitoring in young adults with childhood depression history; leaves open causality and needs longitudinal confirmation.
BACKGROUND: Our study examined whether the early-onset depression phenotype among young adults (probands) is associated with the metabolic syndrome (MetS) and its components, and if MetS characterizes unaffected but high-risk siblings of probands. METHODS: = 171). Participants completed a full psychiatric interview, physical and laboratory assessments, and self-rating scales. MetS was defined using the criteria of the Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (). RESULTS: Early-onset depression phenotype and being a high-risk sibling were associated with higher MetS composite scores relative to that of controls, but did not differ from one another. With regard to MetS components: Probands and siblings had similarly larger waist circumference and lower HDL than did controls, while siblings and controls had lower triglyceride levels than did probands but did not differ from one another. Groups did not differ on glucose levels and SBP. CONCLUSIONS: Our study extends the literature on the association between MetS and depression and underscores the importance of depression phenotypes: failure to account for the clinical heterogeneity of depression may partly underlie the inconsistent findings regarding its relation to MetS. The results also suggest that, in depression-prone populations, MetS may predate and possibly function as a risk factor for eventual depression.
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Daches et al. (2021) conducted a cross-sectional in Early-onset depression and familial risk for depression (n=737). Early-onset depression phenotype vs. Healthy controls was evaluated on Metabolic syndrome (MetS) composite z-score (LSM difference 0.35, p=<0.01). Young adults with a history of childhood-onset depression had significantly higher metabolic syndrome composite scores compared to healthy controls (LSM difference 0.35, p<0.01).
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