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HMG-CoA还原酶抑制剂对接受血液透析的高胆固醇血症患者的影响。

Effects of HMG-CoA reductase inhibitors in hypercholesterolemic patients on hemodialysis.

作者信息

Wanner C, Hörl W H, Luley C H, Wieland H

机构信息

Department of Medicine, University Hospital of Freiburg, Germany.

出版信息

Kidney Int. 1991 Apr;39(4):754-60. doi: 10.1038/ki.1991.92.

Abstract

The efficacy of lovastatin and simvastatin, competitive inhibitors of 3-hydroxy-3-methyl glutaryl coenzyme A reductase, was investigated in 40 hemodialysis (HD) patients displaying hypercholesterolemia and moderate hypertriglyceridemia (selection of 40 patients required screening of 700 hemodialysis patients). After a four-week placebo period, lovastatin or simvastatin was administered to two groups of 20 patients in increasing doses over a period of three months. Thirty-six patients completed the study. Lovastatin (1st month 20 mg; 2nd and 3rd months 40 mg day-1) and simvastatin (1st month 10 mg, 2nd month 20 mg and 3rd month 40 mg day-1) reduced total serum cholesterol from 280.3 +/- 9.4 to 213.0 +/- 6.7 (-24%) and 295.0 +/- 12.2 to 202.3 +/- 8.9 mg/dl (-31.4%), LDL cholesterol from 161.9 +/- 10.7 to 112.1 +/- 7.9 (-30.8%) and 181.8 +/- 14.7 to 107.4 +/- 8.1 mg/dl (-40.9%), as well as apolipoprotein B (apo B) from 116.0 +/- 6.6 to 83.3 +/- 3.7 (-28.2%) and 134.4 +/- 8.2 to 84.1 +/- 5.3 mg/dl (-37.4%), respectively. Furthermore, the ratio of LDL apo B/LDL cholesterol increased significantly (0.63 +/- 0.02 vs. 0.71 +/- 0.05 and 0.63 +/- 0.02 vs. 0.66 +/- 0.02, respectively). Another remarkable effect was the reduction of cholesterol concentration in VLDL (72.4 +/- 8.9 vs. 47.3 +/- 6.8 [lovastatin] and 78.3 +/- 11.1 vs. 50.7 +/- 8.8 mg/dl [simvastatin], respectively). Therefore, the ratio of triglycerides/cholesterol in VLDL increased (3.2 +/- 0.2 vs. 3.8 +/- 0.3 and 3.2 +/- 0.2 vs. 4.0 +/- 0.2, respectively), indicating VLDL formation poor in cholesterol and rich in triglycerides.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

对40例患有高胆固醇血症和中度高甘油三酯血症的血液透析(HD)患者(从700例血液透析患者中筛选出40例)研究了3-羟基-3-甲基戊二酰辅酶A还原酶竞争性抑制剂洛伐他汀和辛伐他汀的疗效。经过为期4周的安慰剂期后,将洛伐他汀或辛伐他汀以递增剂量给予两组各20例患者,为期3个月。36例患者完成了研究。洛伐他汀(第1个月20mg;第2和3个月40mg/天)和辛伐他汀(第1个月10mg,第2个月20mg,第3个月40mg/天)分别使总血清胆固醇从280.3±9.4降至213.0±6.7(-24%)和从295.0±12.2降至202.3±8.9mg/dl(-31.4%),低密度脂蛋白胆固醇从161.9±10.7降至112.1±7.9(-30.8%)和从181.8±14.7降至107.4±8.1mg/dl(-40.9%),以及载脂蛋白B(apo B)从116.0±6.6降至83.3±3.7(-28.2%)和从134.4±8.2降至84.1±5.3mg/dl(-37.4%)。此外,低密度脂蛋白apo B/低密度脂蛋白胆固醇的比值显著增加(分别为0.63±0.02对0.71±0.05和0.63±0.02对0.66±0.02)。另一个显著效果是极低密度脂蛋白中胆固醇浓度降低(分别为洛伐他汀:72.4±8.9对47.3±6.8,辛伐他汀:78.3±11.1对50.7±8.8mg/dl)。因此,极低密度脂蛋白中甘油三酯/胆固醇的比值增加(分别为3.2±0.2对3.8±0.3和3.2±0.2对4.0±0.2),表明极低密度脂蛋白形成中胆固醇含量低而甘油三酯含量高。(摘要截断于250字)

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