Key result
High-dose lipid-lowering therapy administered 24 hours before percutaneous coronary intervention did not acutely change the levels or functional activity of endothelial progenitor cells and circulating endothelial cells in patients with stable coronary artery disease.
Why the study?
Does high-dose lipid-lowering therapy acutely increase levels or activity of endothelial progenitor cells and circulating endothelial cells in patients with stable coronary artery disease?
RCT (n=38)
Double-blind
randomized
No
Does high-dose lipid-lowering therapy acutely increase levels or activity of endothelial progenitor cells and circulating endothelial cells in patients with stable coronary artery disease?
Pre-procedural high-dose lipid-lowering therapy does not acutely alter the levels or activity of endothelial progenitor cells or circulating endothelial cells in patients with stable CAD.
Suggests acute pleiotropic benefits of pre-PCI lipid-lowering are not mediated by.
RATIONALE AND OBJECTIVE: Endothelial progenitor cells (EPCs) play a role in vascular repair, while circulating endothelial cells (CECs) are biomarkers of vascular damage and regeneration. Statins may promote EPC/CEC mobilization in the peripheral blood. We evaluated whether pre-procedural exposure to different lipid-lowering drugs (statins±ezetimibe) can acutely increase levels/activity of EPCs/CECs in patients with stable coronary artery disease (CAD). METHODS: In a planned sub-analysis of the Rosuvastatin For REduction Of Myocardial DamagE During Coronary AngioplastY (REMEDY) trial, 38 patients with stable CAD on chronic low-dose statin therapy were randomized, in a double-blind, placebo-controlled design, into 4 groups before PCI: i. placebo (n = 11); ii. atorvastatin (80 mg+40 mg, n = 9); iii. rosuvastatin (40 mg twice, n = 9); and iv. rosuvastatin (5 mg) and ezetimibe (10 mg) twice, (n = 9). At baseline and 24 h after treatment-before PCI-, patients underwent blinded analyses of EPCs [colony forming units-endothelial cells (CFU-ECs), endothelial colony-forming cells (ECFCs) and tubulization activity] and CECs in peripheral blood. RESULTS: We found no significant treatment effects on parameters investigated such as number of CECs [Median (IQR): i. 0(0), ii. 4.5(27), iii. 1.9(2.3), iv. 1.9(2.3)], CFU-ECs [Median (IQR): i. 27(11), ii. 19(31), iii. 47(36), iv. 30(98)], and ECFCs [Median (IQR): i. 86(84), ii. 7(84), iii. 8/(42.5), iv. 5(2)], as well as tubulization activity [total tubuli (well), Median (IQR): i. 19(7), ii. 5(4), iii. 25(13), iv. 15(24)]. CONCLUSIONS: In this study, we found no evidence of acute changes in levels or activity of EPCs and CECs after high-dose lipid-lowering therapy in stable CAD patients.
No takes yet. Share an insight, caveat, or question.
Madonna et al. (2017) conducted an RCT in Coronary artery disease (n=38). High-dose lipid-lowering therapy vs. Placebo was evaluated on Changes in levels of circulating endothelial cells (CECs) and levels/functional activities of endothelial progenitor cells (EPCs) (p=>0.05). High-dose lipid-lowering therapy administered 24 hours before percutaneous coronary intervention did not acutely change the levels or functional activity of endothelial progenitor cells and circulating endothelial cells in patients with stable coronary artery disease.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: