Increased Serum Level of Growth Differentiation Factor 15 (GDF-15) is Associated with Coronary Artery Disease

Xia Wang1, Lei-Lei Chen2, Qing Zhang3

  • 1Department of Clinical laboratory, Huai'an First People's Hospital, Nanjing Medical University, Huai'an, China.

Insights

Elevated serum levels of Growth Differentiation Factor 15 (GDF-15) are significantly associated with coronary artery disease (CAD). GDF-15 shows high accuracy in predicting CAD, suggesting its potential as a diagnostic biomarker.

Area of Science:

  • Cardiology
  • Biomarkers
  • Inflammation

Background:

  • Inflammatory responses are implicated in coronary artery disease (CAD) development.
  • Growth Differentiation Factor 15 (GDF-15), a stress-responsive cytokine, increases during inflammation and is linked to cardiometabolic risk.
  • The specific relationship between GDF-15 and CAD is not well-established.

Purpose of the Study:

  • To evaluate serum GDF-15 levels in patients with CAD.
  • To determine the predictive value of GDF-15 for CAD.
  • To assess the correlation between GDF-15 levels and CAD severity.

Main Methods:

  • Serum GDF-15 levels were measured using enzyme-linked immunosorbent assay in 105 CAD patients and 96 healthy controls.
  • Coronary artery disease severity was assessed using Gensini scores.
  • Spearman's correlation and ROC curve analysis were employed to examine associations and predictive values.

Main Results:

  • Serum GDF-15 levels were significantly higher in the CAD group compared to controls (P < 0.001).
  • A strong positive correlation was found between GDF-15 levels and Gensini scores (r = 0.85, P < 0.001).
  • ROC analysis indicated a high predictive value for GDF-15 in CAD detection (AUC = 0.96), with 80.0% sensitivity and 91.7% specificity.

Conclusions:

  • Increased serum GDF-15 levels are positively associated with the presence and severity of CAD.
  • GDF-15 demonstrates potential as a valuable adjunct biomarker for discriminating CAD.
  • Further research may explore GDF-15's role in CAD pathogenesis and management.
Abstract

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