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Effects of pitavastatin versus atorvastatin on the peripheral endothelial progenitor cells and vascular endothelial growth factor in high-risk patients: a pilot prospective, double-blind, randomized study

机译:匹伐他汀与阿托伐他汀对高危患者外周内皮祖细胞和血管内皮生长因子的影响:一项前瞻性,双盲,随机试验

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Background Circulating endothelial progenitor cells (EPCs) reflect endothelial repair capacity and may be a significant marker for the clinical outcomes of cardiovascular disease. While some high-dose statin treatments may improve endothelial function, it is not known whether different statins may have similar effects on EPCs.This study aimed to investigate the potential class effects of different statin treatment including pitavastatin and atorvastatin on circulating EPCs in clinical setting. Methods A pilot prospective, double-blind, randomized study was conducted to evaluate the ordinary dose of pitavastatin (2?mg daily) or atorvastatin (10?mg daily) treatment for 12?weeks on circulating EPCs in patients with cardiovascular risk such as hypercholesterolemia and type 2 diabetes mellitus (T2DM). Additional in vitro study was conducted to clarify the direct effects of both statins on EPCs from the patients. Results A total of 26 patients (19 with T2DM) completed the study. While the lipid-lowering effects were similar in both treatments, the counts of circulating CD34+KDR+EPCs were significantly increased (from 0.021?±?0.015 to 0.054?±?0.044% of gated mononuclear cells, P?P?P?in vitro study, while both statins increased endothelial nitric oxide synthase (eNOS) expression, only pitavastatin increased the phosphorylation of eNOS in EPCs. Pitavastatin but not atorvastatin ameliorated the adhesion ability of early EPCs and the migration and tube formation capacities of late EPCs. Conclusions While both statins similarly reduced plasma lipids, only pitavastatin increased plasma VEGF level and circulating EPCs in high-risk patients, which is probably related to the differential pleiotropic effects of different statins. Trial registration This trial is registered at ClinicalTrials.gov, NCT01386853 webcite .
机译:背景技术循环内皮祖细胞(EPC)反映了内皮修复能力,可能是心血管疾病临床结局的重要标志。尽管一些大剂量他汀类药物治疗可改善内皮功能,但尚不清楚不同的他汀类药物是否对EPC具有相似的作用。本研究旨在研究匹伐他汀和阿托伐他汀在临床环境中对不同的他汀类药物治疗循环EPC的潜在作用。方法进行了一项前瞻性,双盲,随机对照试验,以评估心血管疾病(例如高胆固醇血症)患者中循环血浆EPC的匹伐他汀(每日2?mg)或阿托伐他汀(每日10?mg)的常规剂量治疗12周。和2型糖尿病(T2DM)。进行了进一步的体外研究,以阐明两种他汀类药物对患者EPC的直接作用。结果共有26位患者(19位T2DM)完成了研究。尽管两种治疗方法的降脂作用相似,但循环中CD34 + KDR + EPC的数量均显着增加(从0.021?±?0.015增至0.054?±?)。 0.044%的门控单核细胞,P?P?P?体外研究,两种他汀类药物均可增加内皮细胞一氧化氮合酶(eNOS)的表达,只有匹伐他汀可增加EPC中eNOS的磷酸化,匹伐他汀可改善早期黏附能力,而阿托伐他汀则无此作用。结论尽管两种他汀类药物同样能降低血浆脂质,但只有匹伐他汀能增加高危患者的血浆VEGF水平和循环EPC,这可能与不同他汀类药物的多效性差异有关。注册本临床试验已在ClinicalTrials.gov(NCT01386853网站)上进行了注册。

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