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Y. Milaneschi

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Open access Sep 2026

Longitudinal associations between inflammatory biomarkers, polygenic risk scores and cardiometabolic outcomes in major depressive and anxiety disorders: Findings from the Netherlands Study of Depression and Anxiety (NESDA).

Cardiometabolic dysfunctions are prevalent in individuals with major depressive (MDD) and/or anxiety disorders, yet the longitudinal relationships between inflammation, polygenic susceptibility, and cardiometabolic outcomes remain incompletely understood. We analyzed longitudinal data from 2,716 participants retrieved from the Netherlands Study of Depression and Anxiety (NESDA) across three measurements over six years. Longitudinal associations between inflammatory biomarkers (CRP, IL-6, and TNF-α), polygenic risk scores (PRS), and ten cardiometabolic outcomes were assessed using linear mixed-effects models. Between-group differences were tested via current diagnostic subgroup interaction terms while adjusting for common covariates. Population-level associations were evaluated in the full sample, and PRS-related variance explained was quantified using changes in marginal R2. No interactions between inflammatory biomarkers or PRSes and current MDD and/or anxiety diagnosis survived FDR correction, although several nominally significant interactions were observed. In the full sample, higher CRP, IL-6, and TNF-α levels were consistently associated with higher BMI, waist circumference, and triglyceride levels, and lower HDL cholesterol, while CRP and IL-6 were additionally associated with blood pressure and glucose-related outcomes. PRSCRP was associated with multiple cardiometabolic outcomes, explaining an additional 0.16 % of the variance in systolic blood pressure to 0.72 % in BMI. All eight cardiometabolic PRSes showed positive associations with their corresponding outcomes and explained up to 12.88 % of the variance in LDL cholesterol. Overall, inflammatory biomarkers and polygenic susceptibility to inflammatory and cardiometabolic traits are associated with cardiometabolic outcomes. These findings may help inform future mechanistic and causal studies aimed at improving cardiometabolic risk assessment in people with mental health disorders.

Chen-Xu Zhao, D. Cath, Jens H. van Dalfsen et al. · 0 citations
Open access Jul 2026

Determinants of the plasma metabolome: cross-sectional and longitudinal associations over six years in the NESDA cohort

Summary Background The plasma metabolome represents a valuable molecular readout of a person’s physiological state, yet its relation to health, stress and lifestyle remains underexplored collectively. Methods Here, we conducted an untargeted metabolomics analysis using 3804 paired samples from 1902 participants of the observational Netherlands Study of Depression and Anxiety at baseline and six-year follow-up, quantifying 680 plasma metabolites. We characterised five metabolome principal components, three with distinct biochemical enrichments related to transmembrane transport, sphingolipid, and amino acid metabolism. Findings Metabolite levels showed moderate intrapersonal correlation between baseline and six-year follow-up (ICCmedian = 0.482), and 22% of metabolites showed standardised mean differences >0.2. Multivariate linear modelling on 18 baseline determinants across demographics, psychosocial environment, lifestyle, somatic and mental health explained a maximum of 35% of baseline metabolome PC variance and 12% of six-year change ΔPC variance. Demographic (e.g., sex, age), somatic health (e.g., BMI, medication) and lifestyle factors (e.g., smoking, alcohol intake) demonstrated strong associations both cross-sectionally and longitudinally, while psychosocial factors and mental health contributed minor explained variance in comparison. Interpretation Altogether, our study provides hierarchical insights into the cross-sectional and longitudinal implications of health, stress, and lifestyle exposures for the plasma metabolome. Funding Geestkracht program of the Netherlands Organisation for Health Research and Development, the Dutch Research Council and the Dutch Ministry of Education, Culture and Science, Stress in Action, Amsterdam Neuroscience, ImmunoMIND, the National Institute of Mental Health, National Institute on Ageing and the Foundation for the National Institutes of Health.

D. Klose, Y. Milaneschi, Laura K. M. Han et al. · 0 citations

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