Małyszko Jolanta, Małyszko Jacek S, Hryszko Tomasz, Pawlak Krystyna, Myśliwiec Michał
Pol Arch Med Wewn. 2002 Jun;107(6):519-24.
Peritoneally dialyzed subjects (CAPD) are prone to dyslipidemia and have a high risk of cardiovascular death. Statins (hydroxy-methylglutaryloCoA reductase inhibitors) show beneficial effects on serum lipids and hemostasis in kidney diseases. The purpose of this study was to assess platelet functions, some hemostatic parameters-extrinsic coagulation pathway-total, truncated, free TFPI (tissue factor pathway inhibitor), TF (tissue factor), TFPI/Xa and TF/VIIa complexes, as well as a marker of endothelial cell injury--von Willebrand factor--vWF and serum lipids in 10 hyperlipidemic CAPD patients treated with simvastatin (Zocor, MSD, at a dose of 10 mg at bedtime) for 3 months. Cholesterol and LDL fell significantly as early as after 1 month and remained lowered during further months of the therapy. No significant changes in von Willebrand factor, free TFPI, TF, TFPI/Xa and TF/VIIa complexes were found during therapy with simvastatin. Truncated TFPI decreased significantly as early as after 1 month and total TFPI decreased after 3 months of the therapy with simvastatin. Simvastatin is an effective hypolipemic agent. It seems that simvastatin have no or only little effect on endothelial function and extrinsic coagulation pathway in peritoneally dialyzed patients.
接受腹膜透析的患者(持续性非卧床腹膜透析)易患血脂异常,并有较高的心血管死亡风险。他汀类药物(羟甲基戊二酰辅酶A还原酶抑制剂)对肾脏疾病患者的血脂和止血有有益作用。本研究的目的是评估10例接受辛伐他汀(舒降之,默克雪兰诺,睡前剂量10mg)治疗3个月的高脂血症腹膜透析患者的血小板功能、一些止血参数——外源性凝血途径——总组织因子途径抑制物、截短型组织因子途径抑制物、游离组织因子途径抑制物、组织因子、组织因子途径抑制物/因子Xa复合物以及组织因子/因子VIIa复合物,以及内皮细胞损伤标志物——血管性血友病因子——vWF和血脂。早在1个月后,胆固醇和低密度脂蛋白就显著下降,并在治疗的后续几个月中持续降低。在辛伐他汀治疗期间,未发现血管性血友病因子、游离组织因子途径抑制物、组织因子、组织因子途径抑制物/因子Xa复合物以及组织因子/因子VIIa复合物有显著变化。早在1个月后,截短型组织因子途径抑制物就显著下降,在辛伐他汀治疗3个月后,总组织因子途径抑制物下降。辛伐他汀是一种有效的降血脂药物。辛伐他汀似乎对腹膜透析患者的内皮功能和外源性凝血途径没有或只有很小的影响。