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Derivation of Cardiac Progenitor Cells from Embryonic Stem Cells
Published on: January 12, 2015
Circulating Progenitor Cells and Racial Differences
Ayman Samman Tahhan1, Muhammad Hammadah1, Heval Mohamed Kelli1
1From the Division of Cardiology, Emory Clinical Cardiovascular Research Institute, Emory University School of Medicine (A.S.T., M.H., H.M.K., J.H.K., P.B.S., A.A., B.K., M.M.G., M.T., S.S.H., W.T.O., M.O., I.H., V.V., A.A.Q.).
Insights
Black individuals exhibit lower circulating progenitor cell (CPC) counts than white individuals, indicating impaired regenerative capacity. These lower CPC levels are linked to increased cardiovascular risk and mortality in Black populations.
Area of Science:
- Cardiovascular Medicine
- Regenerative Medicine
- Hematology
Background:
- Blacks have a higher risk of adverse cardiovascular outcomes compared to whites.
- Impaired regenerative capacity, indicated by lower circulating progenitor cell (CPC) levels, is a novel determinant of adverse outcomes.
- Racial differences in CPC levels are not well understood.
Purpose of the Study:
- To investigate racial differences in CPC counts between Black and White individuals.
- To examine PC-mobilizing factors and PC mobilization during acute myocardial infarction.
- To determine the predictive value of CPC counts in Black versus White populations.
Main Methods:
- Enumerated CPCs using flow cytometry in 1747 subjects (26% Black).
- Measured levels of SDF-1α, VEGF, and MMP-9.
- Followed 623 patients for survival analysis, with separate analysis for 91 acute myocardial infarction patients.
Main Results:
- Blacks had significantly lower counts of CD34+, CD34+/CD133+, CD34+/CXCR4+, and CD34+/VEGF2R+ cells compared to whites.
- Lower CPC counts in Blacks were not affected by traditional risk factors or cardiovascular disease.
- Lower CD34+ counts predicted mortality similarly in both Black and White individuals.
Conclusions:
- Black individuals have lower CPC levels than whites, partly due to lower circulating MMP-9.
- Impaired regenerative capacity in Black individuals may contribute to their increased cardiovascular event risk.
- Lower CPC levels are predictive of adverse outcomes in Black populations.
Rationale:
Blacks compared with whites have a greater risk of adverse cardiovascular outcomes. Impaired regenerative capacity, measured as lower levels of circulating progenitor cells (CPCs), is a novel determinant of adverse outcomes; however, little is known about racial differences in CPCs.
Objective:
To investigate the number of CPCs, PC-mobilizing factors, PC mobilization during acute myocardial infarction and the predictive value of CPC counts in blacks compared with whites.
Methods And Results:
CPCs were enumerated by flow cytometry as CD45med+ blood mononuclear cells expressing CD34+, CD133+, VEGF2R+, and CXCR4+ epitopes in 1747 subjects, mean age 58.4±13, 55% male, and 26% self-reported black. Patients presenting with acute myocardial infarction (n=91) were analyzed separately. Models were adjusted for relevant clinical variables. SDF-1α (stromal cell-derived factor-1α), VEGF (vascular endothelial growth factor), and MMP-9 (matrix metallopeptidase-9) levels were measured (n=561), and 623 patients were followed for median of 2.2 years for survival analysis. Blacks were younger, more often female, with a higher burden of cardiovascular risk, and lower CPC counts. Blacks had fewer CD34+ cells (-17.6%; [95% confidence interval (CI), -23.5% to -11.3%]; P<0.001), CD34+/CD133+ cells (-15.5%; [95% CI, -22.4% to -8.1%]; P<0.001), CD34+/CXCR4+ cells (-17.3%; [95% CI, -23.9% to -10.2%]; P<0.001), and CD34+/VEGF2R+ cells (-27.9%; [95% CI, -46.9% to -2.0%]; P=0.04) compared with whites. The association between lower CPC counts and black race was not affected by risk factors or cardiovascular disease. Results were validated in a separate cohort of 411 patients. Blacks with acute myocardial infarction had significantly fewer CPCs compared with whites ( P=0.02). Blacks had significantly lower plasma MMP-9 levels ( P<0.001) which attenuated the association between low CD34+ and black race by 19% (95% CI, 13%-33%). However, VEGF and SDF-1α levels were not significantly different between the races. Lower CD34+ counts were similarly predictive of mortality in blacks (hazard ratio, 2.83; [95% CI, 1.12-7.20]; P=0.03) and whites (hazard ratio, 1.79; [95% CI, 1.09-2.94]; P=0.02) without significant interaction.
Conclusions:
Black subjects have lower levels of CPCs compared with whites which is partially dependent on lower circulating MMP-9 levels. Impaired regenerative capacity is predictive of adverse outcomes in blacks and may partly account for their increased risk of cardiovascular events.
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