匹伐他汀对高脂血症患者脂联素的影响。

Pathophysiology of Haemostasis and Thrombosis Pub Date : 2007-01-01 Epub Date: 2008-03-06 DOI:10.1159/000112633
N Inami, S Nomura, A Shouzu, S Omoto, Y Kimura, N Takahashi, A Tanaka, M Nanba, Y Shouda, T Iwasaka
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引用次数: 46

摘要

研究匹伐他汀治疗对117例高脂血症患者炎症、血小板活化标志物及脂联素的影响,以确定匹伐他汀是否可预防高脂血症患者动脉粥样硬化改变的进展。合并和不合并糖尿病的高脂血症患者在接受匹伐他汀治疗前的脂联素水平低于正常血脂对照组。服用匹伐他汀后,总胆固醇和低密度脂蛋白胆固醇均显著降低。此外,伴有或不伴有2型糖尿病的高脂血症患者在匹伐他汀治疗6个月后脂联素水平显著升高(糖尿病:3.52 +/- 0.80 vs 4.52 +/- 0.71微克/毫升,p < 0.001;无糖尿病:3.48 +/- 0.71 vs. 4.23 +/- 0.82 μ g/ml, p < 0.05)。然而,高敏感性c反应蛋白、血小板衍生微粒和可溶性p选择素在匹伐他汀给药前后没有表现出任何差异。低可溶性p -选择素组(在匹伐他汀治疗前可溶p -选择素组)脂联素水平在匹伐他汀治疗后显著升高
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of pitavastatin on adiponectin in patients with hyperlipidemia.

The effects of treatment with pitavastatin on inflammatory and platelet activation markers and adiponectin in 117 patients with hyperlipidemia were investigated to determine whether pitavastatin may prevent the progression of atherosclerotic changes in hyperlipidemic patients. Adiponectin levels prior to pitavastatin treatment in hyperlipidemic patients with and without diabetes were lower than levels in normolipidemic controls. Both total cholesterol and the low-density lipoprotein cholesterol decreased significantly after pitavastatin administration. Additionally, hyperlipidemic patients with or without type 2 diabetes exhibited a significant increase in adiponectin levels 6 months after pitavastatin treatment (diabetes: 3.52 +/- 0.80 vs. 4.52 +/- 0.71 microg/ml, p < 0.001; no diabetes: 3.48 +/- 0.71 vs. 4.23 +/- 0.82 microg/ml, p < 0.05). However, high-sensitivity C-reactive protein, platelet-derived microparticle and soluble P-selectin did not exhibit any differences before or after pitavastatin administration. Levels of adiponectin significantly increased after pitavastatin administration in the group of lower soluble P-selectin (soluble P-selectin before pitavastatin treatment <200 ng/ml). These results suggest that pitavastatin possesses an adiponectin-increasing effect in patients with hyperlipidemia and this effect is influenced by intensive platelet activation.

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