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普伐他汀治疗的高胆固醇血症患者血浆脂质、脂蛋白和载脂蛋白的变化

Changes in plasma lipids, lipoproteins and apolipoproteins in hypercholesterolaemic patients treated with pravastatin.

作者信息

Lijnen P, Celis H, Desager J P, Fagard R

机构信息

Department of Molecular and Cardiovascular Research, University of Leuven, Belgium.

出版信息

J Hum Hypertens. 1995 Jul;9(7):557-64.

PMID:7562885
Abstract

Plasma lipids, lipoproteins and apolipoproteins were studied before and during 6 months of pravastatin administration in patients with hypecholesterolaemia. After a 1 month placebo run-in period, the patients were treated double-blind either with placebo (n = 25) or with pravastatin (n = 25) for 6 months. Placebo or pravastatin 10 mg during the first month, 20 mg during the second month and 40 mg during the additional 4 months was administered once daily in the evening. Compared with the placebo group the plasma concentration of total cholesterol and phospholipids, free cholesterol and cholesterol esters as well as the plasma LDL-cholesterol and LDL-phospholipids were decreased during 6 months of pravastation therapy. No changes in plasma VLDL-, HDL-, HDL2-, or HDL3-cholesterol, -phospholipids or -triglycerides were observed in the pravastatin-treated patients. A decrease in the plasma level of apolipoprotein B and of LDL-apo B, but not of VLDL-apo B, was observed during pravastatin therapy; the plasma apolipoprotein AI and AII levels as well as HDL2- and HDL3-apo AI and apo AII levels remained, however, unchanged. Plasma lipoprotein Lp(a) did not change during pravastatin therapy whereas the plasma lecithin cholesterol acyltransferase activity (LCAT) increased. In conclusion, treatment of hypercholesterolaemic patients with pravastatin results in a decrease in the plasma concentration of total and free cholesterol, LDL-cholesterol, apolipoprotein B, LDL-apo B, phospholipids and cholesterol esters and in an increase in plasma LCAT activity. Plasma Lp(a), HDL-cholesterol and triglyceride levels remained, however, unchanged.

摘要

对高胆固醇血症患者在服用普伐他汀前及服用6个月期间的血浆脂质、脂蛋白和载脂蛋白进行了研究。经过1个月的安慰剂导入期后,患者被双盲分为安慰剂组(n = 25)或普伐他汀组(n = 25),治疗6个月。安慰剂或普伐他汀在第1个月为10 mg,第2个月为20 mg,在接下来的4个月为40 mg,均于每晚每日1次给药。与安慰剂组相比,在普伐他汀治疗6个月期间,血浆总胆固醇、磷脂、游离胆固醇和胆固醇酯的浓度以及血浆低密度脂蛋白胆固醇和低密度脂蛋白磷脂均降低。在接受普伐他汀治疗的患者中,未观察到血浆极低密度脂蛋白、高密度脂蛋白、高密度脂蛋白2或高密度脂蛋白3胆固醇、磷脂或甘油三酯的变化。在普伐他汀治疗期间,观察到血浆载脂蛋白B和低密度脂蛋白载脂蛋白B水平降低,但极低密度脂蛋白载脂蛋白B水平未降低;然而,血浆载脂蛋白AI和AII水平以及高密度脂蛋白2和高密度脂蛋白3载脂蛋白AI和载脂蛋白AII水平保持不变。在普伐他汀治疗期间,血浆脂蛋白Lp(a)未发生变化,而血浆卵磷脂胆固醇酰基转移酶活性(LCAT)增加。总之,用普伐他汀治疗高胆固醇血症患者可导致血浆总胆固醇、游离胆固醇、低密度脂蛋白胆固醇、载脂蛋白B、低密度脂蛋白载脂蛋白B、磷脂和胆固醇酯浓度降低,血浆LCAT活性增加。然而,血浆Lp(a)、高密度脂蛋白胆固醇和甘油三酯水平保持不变。

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