Saklamaz Ali, Comlekci Abdurrahman, Temiz Aysegul, Caliskan Sezer, Ceylan Cengiz, Alacacioglu Ahmet, Yesil Sena
Division of Endocrinology, Dokuz Eylul University Medical School, Inciralti, Izmir 35340, Turkey.
Metabolism. 2005 May;54(5):677-81. doi: 10.1016/j.metabol.2004.12.012.
Hyperlipidemia is an important risk factor for atherosclerosis. Hemorheological factors contribute to morbidity and mortality in patients with dyslipidemia. We evaluated the effects of 3 antihyperlipidemic drugs (pravastatin, atorvastatin, and fenofibrate), which have different mechanisms of action and different patterns of action on lipid profiles, on erythrocyte deformability and fibrinogen levels in patients with type IIa and type IIb hyperlipidemia. Twenty-one patients ( 4 men and 17 women) with type IIa and IIb hyperlipidemia were randomized to 3 drugs (pravastatin 20 mg/d, atorvastatin 10 mg/d, fenofibrate 250 mg/d) for 8 weeks. Plasma glucose, total cholesterol, triglyceride, high-density lipoprotein cholesterol (HDL-C), and low-density lipoprotein cholesterol (LDL-C) analysis were performed on a BM-Hitachi 747-200 autoanalyzer (Hitachi-Roche, Tokyo, Japan). Fibrinogen analysis was performed according to Clauss method. Erythrocyte deformability was assessed with cell transit analysis device. There was no significant difference in body mass index, lipid profile, fibrinogen level, and erythrocyte deformability index values among the groups before treatment ( P > .05). In all groups, there were statistically significant reductions in total LDL-C levels ( P < .05). The triglyceride levels were significantly reduced in the atorvastatin and fenofibrate groups ( P < .05), but not in the pravastatin group ( P > .05). There was no significant change in HDL-C levels during the treatment with statins ( P > .05), but there was a significant increase in the fenofibrate group ( P < .05). Mean erythrocyte deformability index was improved in all the groups ( P < .05). There was no significant change in fibrinogen levels during the treatment of pravastatin and atorvastatin ( P > .05), but in fenofibrate group, fibrinogen levels were significantly decreased ( P < .05). The 3 groups of antihyperlipidemic drugs have beneficial effects on the erythrocyte deformability index. Only fenofibrate has significant beneficial effects on the fibrinogen levels.
高脂血症是动脉粥样硬化的重要危险因素。血液流变学因素在血脂异常患者的发病和死亡中起作用。我们评估了3种抗高脂血症药物(普伐他汀、阿托伐他汀和非诺贝特)对IIa型和IIb型高脂血症患者红细胞变形性和纤维蛋白原水平的影响,这3种药物作用机制不同,对血脂谱的作用模式也不同。21例IIa型和IIb型高脂血症患者(4例男性和17例女性)被随机分为3组,分别服用普伐他汀20mg/d、阿托伐他汀10mg/d、非诺贝特250mg/d,为期8周。采用BM-日立747-200自动分析仪(日立-罗氏,东京,日本)进行血浆葡萄糖、总胆固醇、甘油三酯、高密度脂蛋白胆固醇(HDL-C)和低密度脂蛋白胆固醇(LDL-C)分析。纤维蛋白原分析采用克劳斯法。用细胞通过分析装置评估红细胞变形性。治疗前各组间体重指数、血脂谱、纤维蛋白原水平和红细胞变形性指数值无显著差异(P>.05)。所有组的总LDL-C水平均有统计学显著降低(P<.05)。阿托伐他汀组和非诺贝特组的甘油三酯水平显著降低(P<.05),而普伐他汀组无显著变化(P>.05)。他汀类药物治疗期间HDL-C水平无显著变化(P>.05),而非诺贝特组有显著升高(P<.05)。所有组的平均红细胞变形性指数均有改善(P<.05)。普伐他汀和阿托伐他汀治疗期间纤维蛋白原水平无显著变化(P>.05),而非诺贝特组纤维蛋白原水平显著降低(P<.05)。3组抗高脂血症药物对红细胞变形性指数均有有益作用。只有非诺贝特对纤维蛋白原水平有显著有益作用。