4.7 Article

Growth differentiation factor 15 and cardiovascular risk: individual patient meta-analysis

期刊

EUROPEAN HEART JOURNAL
卷 44, 期 4, 页码 293-+

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OXFORD UNIV PRESS
DOI: 10.1093/eurheartj/ehac577

关键词

GDF-15; Biomarker; ASCVD; MI; Stroke

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Levels of growth differentiation factor 15 (GDF-15) have been associated with various cardiovascular events. This study analyzed data from eight trials and found that higher GDF-15 concentration was independently associated with increased rates of cardiovascular death/hospitalization for heart failure and major adverse cardiovascular events. However, the prognostic association of GDF-15 with future myocardial infarction and stroke remained significant only in patients stabilized after recent acute coronary syndrome or with stable atherosclerotic cardiovascular disease, not in acute coronary syndrome patients.
Aims Levels of growth differentiation factor 15 (GDF-15), a cytokine secreted in response to cellular stress and inflammation, have been associated with multiple types of cardiovascular (CV) events. However, its comparative prognostic performance across different presentations of atherosclerotic cardiovascular disease (ASCVD) remains unknown. Methods and results An individual patient meta-analysis was performed using data pooled from eight trials including 53 486 patients. Baseline GDF-15 concentration was analyzed as a continuous variable and using established cutpoints (<1200 ng/L, 1200-1800 ng/L, > 1800 ng/L) to evaluate its prognostic performance for CV death/hospitalization for heart failure (HHF), major adverse cardiovascular events (MACE), and their components using Cox models adjusted for clinical variables and established CV biomarkers. Analyses were further stratified on ASCVD status: acute coronary syndrome (ACS), stabilized after recent ACS, and stable ASCVD. Overall, higher GDF-15 concentration was significantly and independently associated with an increased rate of CV death/HHF and MACE (P < 0.001 for each). However, while GDF-15 showed a robust and consistent independent association with CV death and HHF across all presentations of ASCVD, its prognostic association with future myocardial infarction (MI) and stroke only remained significant in patients stabilized after recent ACS or with stable ASCVD [hazard ratio (HR): 1.24, 95% confidence interval (CI): 1.17-1.31 and HR: 1.16, 95% CI: 1.05-1.28 for MI and stroke, respectively] and not in ACS (HR: 0.98, 95% CI: 0.90-1.06 and HR: 0.87, 95% CI: 0.39-1.92, respectively). Conclusion Growth differentiation factor 15 consistently adds prognostic information for CV death and HHF across the spectrum of ASCVD. GDF-15 also adds prognostic information for MI and stroke beyond clinical risk factors and cardiac biomarkers but not in the setting of ACS.

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