Patients with coronary artery disease and renal insufficiency (RI) (estimated glomerular filtration rate <60 ml/min/1.73 m2) are at an increased risk of cardiovascular events. The contribution of regenerative capacity, measured as circulating progenitor cell (CPC) counts, to this increased risk is unclear. CPCs were enumerated as cluster of differentiation (CD) 45med+ mononuclear cells expressing CD34+, CD133+, CXCR4+ (chemokine [C-X-C motif] receptor 4), and VEGF2R+ (vascular endothelial growth factor receptor 2) epitopes in 1,281 subjects with coronary artery disease (35% with RI). Patients with RI and low (<median) hematopoietic CPCs (CD34+, CD34+/CD133+, and CD34+/CXCR4+) were at an increased risk of cardiovascular death or myocardial infarction events (hazard ratios: 1.75 to 1.80) during 3.5-year follow-up, while those with RI and high CPCs (>median) were at a similar risk as those without RI.
Keywords: BNP, B-type natriuretic peptide; CAD, coronary artery disease; CD, cluster of differentiation; CI, confidence interval; CPC, circulating progenitor cell; CV, cardiovascular; CXCR4, chemokine (C-X-C motif) receptor 4; HR, hazard ratio; IDI, integrated discrimination index; MI, myocardial infarction; VEGF2R, vascular endothelial growth factor receptor 2; coronary artery disease; eGFR, estimated glomerular filtration rate; hsTnI, high-sensitivity troponin I; outcomes; progenitor cells; regenerative capacity; renal insufficiency.
© 2020 The Authors.