Circulating progenitor cells and outcomes in patients with coronary artery disease

Devinder S Dhindsa1, Shivang R Desai1, Qingchun Jin2

  • 1Emory Clinical Cardiovascular Research Institute, Division of Cardiology, Department of Medicine, Emory University School of Medicine, Atlanta, Georgia.

Insights

Low circulating progenitor cells (CPCs) indicate poor regenerative capacity. Reduced counts of CD34+/CXCR4+ and CD34+/VEGFR2+ CPCs predict increased mortality and cardiovascular risk in coronary artery disease patients.

Area of Science:

  • Cardiovascular Research
  • Regenerative Medicine
  • Stem Cell Biology

Background:

  • Low circulating progenitor cell (CPC) counts, particularly CD34+ populations, signify impaired intrinsic regenerative capacity.
  • This study explores the association between specific CPC subsets and adverse clinical outcomes.

Purpose of the Study:

  • To investigate the relationship between hematopoietic and endothelial CPC subsets and adverse outcomes in patients with coronary artery disease (CAD).
  • To determine if CPC levels can predict mortality and major adverse cardiovascular events.

Main Methods:

  • 1366 patients undergoing angiography for CAD were analyzed using flow cytometry to identify CPCs (CD45med, CD34+).
  • Hematopoietic CPCs were quantified as CD133+/CXCR4+ and endothelial CPCs as VEGFR2+.
  • Cox or Fine and Gray regression models assessed the association between CPC levels and all-cause death or a composite of cardiovascular death/myocardial infarction.

Main Results:

  • Over a median 3.1-year follow-up, lower counts of CD34+/CXCR4+ and CD34+/VEGFR2+ CPCs independently predicted higher all-cause mortality and cardiovascular death/MI.
  • A combination of low CD34+/CXCR4+ and CD34+/VEGFR2+ CPCs significantly increased the risk of all-cause death and cardiovascular death/MI.

Conclusions:

  • Diminished levels of hematopoietic and endothelial CPCs reflect reduced endogenous regenerative capacity.
  • Lower CPC counts are independently associated with increased mortality and cardiovascular risk in patients with CAD.
Abstract

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