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Updated: Jul 14, 2026

Analysis of Hematopoietic Stem Progenitor Cell Metabolism
Published on: November 9, 2019
Glucose tolerance is negatively associated with circulating progenitor cell levels
G P Fadini1, L Pucci, R Vanacore
1Department of Clinical and Experimental Medicine, Medical School, University of Padua, Via Giustiniani 2, 35100, Padua, Italy. gianpaolo.fadini@unipd.it
Lower levels of circulating progenitor cells, including endothelial progenitor cells (EPCs), are linked to impaired glucose tolerance and increased cardiovascular risk in middle-aged adults. This suggests a potential mechanism for cardiovascular damage in pre-diabetes.
Area of Science:
- Cardiovascular biology
- Metabolic health
- Stem cell research
Background:
- Circulating progenitor cells are vital for cardiovascular homeostasis.
- Endothelial progenitor cell (EPC) depletion is linked to elevated cardiovascular risk.
- EPC levels decrease with traditional risk factors like diabetes mellitus.
Purpose of the Study:
- To investigate progenitor cell levels in individuals with varying glucose tolerance.
- To assess the relationship between glucose metabolism and circulating progenitor cells.
Main Methods:
- Evaluated cardiovascular parameters and CD34(+) and CD34(+)KDR(+) cell counts in 219 middle-aged individuals.
- Assessed glucose tolerance via fasting and 2-hour post-challenge glucose levels.
- Defined impaired fasting glucose (IFG) and impaired glucose tolerance (IGT) as pre-diabetic states.
Main Results:
- CD34(+) and CD34(+)KDR(+) cells were significantly lower in individuals with diabetes mellitus.
- Progenitor cell levels showed a negative correlation with fasting and post-challenge glucose across the population.
- Pre-diabetic individuals had reduced CD34(+) cells, and post-challenge glucose independently affected both CD34(+) and CD34(+)KDR(+) cell levels.
Conclusions:
- Glucose tolerance is inversely associated with progenitor cell counts in healthy middle-aged adults.
- Reduced endothelial progenitor cells due to elevated glucose may contribute to cardiovascular damage in pre-diabetes.
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