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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

Effects of Ezetimibe on Endothelial Progenitor Cells and Microparticles in High-Risk Patients

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Autor(es):
Amaral Lins, Livia Campos [1] ; Franca, Carolina Nunes [1] ; Helfenstein Fonseca, Francisco Antonio [1] ; Melo Barbosa, Simone Pinto [1] ; Matos, Livia Nascimento [1] ; Aguirre, Ana Carolina [1] ; Bianco, Henrique Tria [1] ; do Amaral, Jonatas Bussador [1] ; Izar, Maria Cristina [1]
Número total de Autores: 9
Afiliação do(s) autor(es):
[1] Univ Fed Sao Paulo, Dept Med, Div Cardiol, Lipids Atherosclerosis & Vasc Biol Sect, BR-04039030 Sao Paulo - Brazil
Número total de Afiliações: 1
Tipo de documento: Artigo Científico
Fonte: Cell Biochemistry and Biophysics; v. 70, n. 1, p. 687-696, SEP 2014.
Citações Web of Science: 12
Resumo

Imbalance on endothelial turnover can predict cardiovascular outcomes. We aimed at evaluating the effects of lipid-modifying therapies on circulating endothelial progenitor cells (EPCs), endothelial microparticles (EMPs), and platelet microparticles (PMPs) in high cardiovascular risk subjects with elevated C-reactive protein (CRP). Sixty-three individuals with coronary heart disease (CHD) or CHD risk equivalent on stable statin therapy, with LDL-cholesterol < 100 mg/dL and CRP a parts per thousand yen2.0 mg/L were selected. After a 4-week run-in period with atorvastatin 10 mg, those with persistent CRP a parts per thousand yen2.0 mg/L were randomized to another 4-week treatment period with atorvastatin 40 mg, ezetimibe 10 mg or atorvastatin 40 mg/ezetimibe 10 mg. EPC (CD34(+)/CD133(+)/KDR+), EMP (CD51(+)), and PMP (CD42(+)/CD31(+)) were quantified by flow cytometry. Atorvastatin 40 mg and atorvastatin 40 mg/ezetimibe 10 mg reduced LDL-cholesterol (P < 0.001, paired T test, vs. baseline). Combined therapy, but not ezetimibe reduced CRP. CD34(+)/KDR+ EPC were reduced after ezetimibe alone (P = 0.011 vs. baseline, Wilcoxon test) or combined with atorvastatin (P = 0.016 vs. baseline, Wilcoxon test). In addition, ezetimibe increased CD51(+) EMP (P = 0.017 vs. baseline, Wilcoxon test). No correlations between these markers and LDL-cholesterol or CRP were observed. These results contribute to understand the link between inflammation and vascular homeostasis and highlight the broader benefit of statins decreasing inflammation and preventing microparticles release, an effect not observed with ezetimibe alone. (AU)

Processo FAPESP: 09/50052-1 - Como o tratamento hipolipemiante modifica a expressão e níveis séricos da proteína C reativa e possíveis implicações clínicas
Beneficiário:Maria Cristina de Oliveira Izar
Modalidade de apoio: Auxílio à Pesquisa - Regular