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Coronary Progenitor Cells and Soluble Biomarkers in Cardiovascular Prognosis after Coronary Angioplasty
Published on: January 28, 2020
Circulating proangiogenic cell activity is associated with cardiovascular disease risk
Kreton Mavromatis1, Konstantinos Aznaouridis, Ibhar Al Mheid
1Department of Medicine, Emory University, Atlanta, GA, USA. kmavro@emory.edu
Insights
Circulating proangiogenic cell activity, measured by angiogenic colony-forming units (CFU-A), increases with cardiovascular disease (CVD) risk factors and established CVD. Higher CFU-A levels are linked to poorer clinical outcomes in CVD patients.
Area of Science:
- Cardiovascular Research
- Regenerative Medicine
- Biomarker Discovery
Background:
- Vascular injury triggers bone marrow-derived cells for repair.
- Proangiogenic cell activity is crucial for vascular health.
- A new biomarker for circulating proangiogenic cell activity was investigated.
Purpose of the Study:
- To assess the relationship between a novel biomarker of circulating proangiogenic cell activity and cardiovascular disease (CVD).
- To determine associations with CVD risk factors and clinical outcomes.
Main Methods:
- Utilized an angiogenic colony-forming unit (CFU-A) assay to measure proangiogenic cell activity.
- Studied 532 subjects across the CVD risk spectrum.
- Followed up on 232 subjects with established CVD.
Main Results:
- CFU-A counts significantly correlated with the burden of CVD risk factors (p < 0.001).
- Subjects with symptomatic CVD exhibited higher CFU-A counts than those without (p < 0.001).
- Higher CFU-A levels in CVD patients predicted adverse events like death, myocardial infarction, or stroke (p = 0.01).
Conclusions:
- Circulating proangiogenic cell activity, assessed by CFU-A, rises with CVD risk factor accumulation and presence of established CVD.
- Elevated proangiogenic cell activity is associated with worse clinical outcomes in individuals with CVD.
Abstract:
Vascular injury mobilizes bone marrow-derived proangiogenic cells into the circulation, where these cells can facilitate vascular repair and new vessel formation. We sought to determine the relationship between a new biomarker of circulating bone marrow-derived proangiogenic cell activity, the presence of atherosclerotic cardiovascular disease (CVD) and its risk factors, and clinical outcomes. Circulating proangiogenic cell activity was estimated using a reproducible angiogenic colony-forming unit (CFU-A) assay in 532 clinically stable subjects aged 20 to 90 years and ranging in the CVD risk spectrum from those who are healthy without risk factors to those with active CVD. CFU-A counts increased with the burden of CVD risk factors (p < 0.001). CFU-A counts were higher in subjects with symptomatic CVD than in those without (p < 0.001). During follow-up of 232 subjects with CVD, CFU-A counts were higher in those with death, myocardial infarction, or stroke than in those without (110 [70-173] vs 84 [51-136], p = 0.01). Therefore, we conclude that circulating proangiogenic cell activity, as estimated by CFU-A counts, increases with CVD risk factor burden and in the presence of established CVD. Furthermore, higher circulating proangiogenic cell activity is associated with worse clinical outcome in those with CVD.
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