Publication

Circulating Progenitor Cells in Patients With Coronary Artery Disease and Renal Insufficiency

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Last modified
  • 05/20/2025
Type of Material
Authors
    Anurag Mehta, Emory UniversityAyman S. Tahhan, Emory UniversityChang Liu, Emory UniversityDevinder S. Dhindsa, Emory UniversityAditi Nayak, Emory UniversityAnanya Hooda, Emory UniversityKasra Moazzami, Emory UniversityShabatun J. Islam, Emory UniversitySteven C. Rogers, Emory UniversityZakaria Almuwaqqat, Emory UniversityAli Mokhtari, Emory UniversityIraj Hesaroieh, Emory UniversityYi-An Ko, Emory UniversityEdmund Waller, Emory UniversityArshed Quyyumi, Emory University
Language
  • English
Date
  • 2020-08-01
Publisher
  • Elsevier
Publication Version
Copyright Statement
  • © 2020 The Authors
License
Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 5
Issue
  • 8
Start Page
  • 770
End Page
  • 782
Grant/Funding Information
  • Dr. Quyyumi is supported by National Institutes of Health grants 1P20HL113451-01, 1R61HL138657-02, 1P30DK111024-03S1, 5R01HL095479-08, 3RF1AG051633-01S2, 5R01AG042127-06, 2P01HL086773-08, U54AG062334-01, 1R01HL141205-01, 5P01HL101398-02, 1P20HL113451-01, 5P01HL086773-09 1RF1AG051633-01, R01 NS064162-01, R01 HL89650-01, HL095479-01, 1DP3DK094346-01, and 2P01HL086773 and American Heart Association grant 15SFCRN23910003.
  • Dr. Mehta is supported by American Heart Association postdoctoral fellowship award 19POST34400057.
  • Drs. Mehta, Tahhan, Dhindsa have been supported by the Abraham J. and Phyllis Katz Foundation (Atlanta, Georgia).
Supplemental Material (URL)
Abstract
  • 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.
Author Notes
  • Address for correspondence: Dr. Arshed A. Quyyumi, Division of Cardiology, Emory University School of Medicine, Emory Clinical Cardiovascular Research Institute, 1462 Clifton Road Northeast, Suite 507, Atlanta, Georgia 30322. aquyyum@emory.edu
Keywords
Research Categories
  • Health Sciences, Medicine and Surgery

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