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Modulating factors of progenitor stem cell kinetics in STEMI patients undergoing primary angioplasty - a pilot study
Miruna Mihaela Micheu1, Nicoleta Oprescu, Lucian Câlmâc
1Department of Cardiology, Clinical Emergency Hospital of Bucharest, Romania; mirunamicheu@yahoo.com.
Insights
Circulating progenitor stem cells (cPCs) increase after ST-segment elevation myocardial infarction (STEMI), with distinct patterns for mature and immature cells. Angiographic factors predict cPCs mobilization post-STEMI.
Area of Science:
- Cardiovascular Medicine
- Stem Cell Biology
- Regenerative Medicine
Background:
- ST-segment elevation myocardial infarction (STEMI) involves significant cardiac damage and inflammation.
- Circulating progenitor stem cells (cPCs) play a crucial role in tissue repair following myocardial injury.
- Understanding cPCs dynamics post-STEMI is vital for developing novel therapeutic strategies.
Purpose of the Study:
- To track the changes in circulating progenitor stem cells (cPCs) counts over seven days in STEMI patients.
- To correlate cPCs count evolution with clinical and angiographic parameters after primary percutaneous coronary intervention (PCI).
Main Methods:
- Twelve STEMI patients undergoing primary PCI were enrolled.
- Blood samples were collected daily for seven days post-STEMI.
- Flow cytometry was used to quantify four main cPCs phenotypes (CD34+, CD133+, KDR+ markers).
Main Results:
- All four cPCs phenotypes showed a statistically significant increase in the days following STEMI.
- Mature cPCs exhibited two peaks (day 3 and day 7), while immature cPCs peaked on day 3 and then diminished.
- Preprocedural Thrombolysis In Myocardial Infarction (TIMI) flow, postprocedural myocardial blush, and Left Ventricular Ejection Fraction (LVEF) were independent predictors of cPCs variation.
Conclusions:
- Circulating progenitor stem cells (cPCs) significantly increase after STEMI, with distinct temporal patterns based on cell phenotype.
- Clinical and angiographic factors, including TIMI flow, myocardial blush, and LVEF, are independent predictors of cPCs mobilization post-STEMI.
Aims:
To investigate the circulating progenitor stem cells (cPCs) count evolution during seven days hospitalization period in ST segment elevation myocardial infarction (STEMI) patients, and to correlate their evolution with some clinical and angiographic parameters.
Materials And Methods:
Twelve Caucasian patients with STEMI undergoing primary percutaneous coronary intervention (PCI) were enrolled. Blood samples were obtained in the emergency room and then daily, for seven days, we evaluated the number of cPCs (CD34+CD45+, CD133+CD34+CD45+, KDR+CD34+CD45+ and KDR+CD133+CD34+CD45+) by flow cytometry using fluorochrome-marked specific monoclonal antibodies.
Results:
There is a statistically significant increase in cPCs counts in the following days after STEMI, with a different behavior depending on their phenotype. Mature cPCs (CD34+CD45dim, KDR+CD34+CD45dim) have two fairly similar peaks, first around the third day of evolution followed by a short decrease and a new raise in the seventh day, the more immature cPCs (CD133+CD34+CD45dim, KDR+CD133+CD34+CD45dim) have just one spike on the third day, and then almost disappear from the peripheral circulation. In a multivariate regression analysis, preprocedural TIMI (Thrombolysis In Myocardial Infarction) flow, postprocedural myocardial blush and LVEF (Left Ventricular Ejection Fraction) proved to be independent predictors for cPCs variation in the first week after STEMI.
Conclusions:
In our study, we demonstrated that all four main phenotypes of circulating progenitor stem cells boosted up in the next days after STEMI, with different patterns depending on cell type; preprocedural TIMI flow, postprocedural myocardial blush and LVEF proved to be independent predictors for cPCs mobilization in the first days after STEMI.
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