Soluble CD146, a new endothelial biomarker of acutely decompensated heart failure

Etienne Gayat1, Anaïs Caillard1, Saïd Laribi2

  • 1Department of Anesthesiology and Critical Care Medicine, Saint Louis Lariboisière University Hospital, Assistance Publique - Hôpitaux de Paris, Paris, France; UMR-S 942, INSERM, Paris, France; Université Paris Diderot, Paris, France.

Insights

Soluble CD146 (sCD146) shows diagnostic power for acutely decompensated heart failure (ADHF), comparable to NT-proBNP. Combining sCD146 with NT-proBNP may improve ADHF diagnosis, especially in ambiguous cases.

Area of Science:

  • Cardiology
  • Biomarker Research
  • Endothelial Function

Background:

  • Acutely decompensated heart failure (ADHF) diagnosis relies on sensitive markers.
  • Endothelial dysfunction is implicated in ADHF pathophysiology.
  • Soluble CD146 (sCD146) is a potential biomarker of endothelial function.

Purpose of the Study:

  • Evaluate sCD146 as a diagnostic marker for ADHF.
  • Assess the influence of patient characteristics on sCD146 performance.
  • Explore CD146's role in ADHF pathophysiology.

Main Methods:

  • Human cohort study with 391 patients presenting with acute dyspnea.
  • Measurement of NT-proBNP and sCD146 levels.
  • Receiver Operating Characteristic (ROC) curve analysis.
  • Animal experiments using a rat model of ADHF.

Main Results:

  • sCD146 demonstrated an AUC of 0.86 for ADHF diagnosis.
  • NT-proBNP showed an AUC of 0.90.
  • Combining sCD146 and NT-proBNP improved diagnostic performance in the NT-proBNP "gray zone" (p=0.02).
  • CD146 expression in rat arteries correlated with left ventricular function and organ congestion.

Conclusions:

  • sCD146 is a potent biomarker for detecting cardiac origin of acute dyspnea, similar to NT-proBNP.
  • The combination of sCD146 and NT-proBNP offers improved diagnostic accuracy, particularly for ruling out ADHF in ambiguous cases.
  • CD146 is linked to systolic left ventricular function and organ congestion in both human and experimental models.
Abstract

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