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April 1, 2026International Journal of Molecular Sciences0 citationsOpen Access

Growth Differentiation Factor 15 as a Biomarker of Cardiovascular Burden and Mortality in a Population-Based Cohort

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BMBeatriz Martín-CarroLNLeticia Nieto-GarcíaCSClara Sánchez-Pablo

Key Points

  • The study aims to investigate the association between plasma GDF15 levels and cardiovascular disease and mortality in the general population.
  • Analyzed 1532 participants with baseline plasma GDF15 levels.
  • Participants stratified using an optimal cutoff (1081 pg/mL) from ROC curve analysis.
  • Used multivariable logistic regression to assess associations with heart disease.
  • Analyzed mortality using Cox proportional hazards models.
  • GDF15 levels > 1081 pg/mL correlated with older age and worse health profiles.
  • Elevated GDF15 linked to ischemic cardiomyopathy, especially in men.
  • Predicted all-cause mortality during 6.2 years of follow-up.
  • Modest incremental predictive value over NT-proBNP with improved model discrimination.

Abstract

Growth differentiation factor 15 (GDF15) is a stress-responsive cytokine strongly associated with aging, multimorbidity, and cardiovascular disease. Although prior studies have established its prognostic value in high-risk populations, its role in the general population remains less defined. The aim of this study was to determine if there is an association between plasma GDF15 levels, heart disease and mortality in a representative population-based cohort. We analyzed 1532 participants (mean age 55 years; 54.6% women) with available baseline plasma GDF15 concentrations. Participants were stratified according to an optimal cutoff of 1081 pg/mL, derived from ROC curve analysis for mortality. Associations with prevalent heart disease were assessed using multivariable logistic regression models adjusted for cardiovascular risk factors and NT-proBNP. Mortality was analyzed using Cox proportional hazards models, with model performance evaluated by C-index and time-dependent ROC curves. Individuals with GDF15 > 1081 pg/mL were older and exhibited a more adverse cardiometabolic profile with higher prevalence of comorbidities. Elevated GDF15 was independently associated with ischemic cardiomyopathy (OR 3.34, 95% CI: 1.38–8.11), particularly in men (OR 4.26, 95% CI: 1.40–12.96), but not in women. No independent associations were observed with arrhythmias, valvulopathy, or heart failure after adjustment for NT-proBNP. During a median follow-up of 6.2 years, 51 deaths occurred. Elevated GDF15 independently predicted all-cause mortality (HR 2.47, 95% CI: 1.19–5.13), though the effect was attenuated after adjustment for NT-proBNP. GDF15 improved model discrimination (ΔC-index = +0.01; LRT p = 0.011) and showed robust time-dependent predictive ability, with AUCs of 0.76, 0.82, and 0.85 at 2, 4, and 6 years, respectively. In this population-based cohort, elevated GDF15 identified individuals with an adverse health profile, was independently associated with ischemic cardiomyopathy in men, and predicted mortality. Although its incremental predictive value over NT-proBNP was modest, GDF15 could provide complementary biological information and may enhance multimarker strategies for cardiovascular risk stratification in the general population.

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Cite This Study

Martín-Carro et al. (2026) studied this question.

synapsesocial.com/papers/69ccb62016edfba7beb87d7dhttps://doi.org/10.3390/ijms27073078
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