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氟伐他汀长期治疗家族性高胆固醇血症的临床疗效

Clinical efficacy of fluvastatin in the long-term treatment of familial hypercholesterolemia.

作者信息

Koizumi J, Haraki T, Yagi K, Inazu A, Kajinami K, Miyamoto S, Ueda K, Ohta M, Takegoshi T, Takeda M

机构信息

Second Department of Internal Medicine, Kanazawa University School of Medicine, Japan.

出版信息

Am J Cardiol. 1995 Jul 13;76(2):47A-50A. doi: 10.1016/s0002-9149(05)80016-5.

Abstract

The long-term clinical efficacy of fluvastatin was assessed in 24 patients with familial hypercholesterolemia over a total treatment period of 104 weeks. Patients received an initial fluvastatin dose of 20 mg/day for 8 weeks, which was increased to 30 mg/day for a further 16 weeks. From week 24, if serum total cholesterol remained > or = 230 mg/dL, the fluvastatin dose could be increased to 40 or 60 mg/day, as necessary. By the end of treatment, 4 patients were receiving 30 mg/day fluvastatin, 1 patient was receiving 40 mg/day, and 19 patients were receiving 60 mg/day. Serum total cholesterol and low density lipoprotein cholesterol (LDL-C) levels showed a significant decrease from baseline at week 104 (total cholesterol, -26.8 +/- 2.4%; LDL-C, -33.1 +/- 3.3%; p < 0.001). The reductions in total cholesterol and LDL-C were dose-related. Statistically significant (p < 0.05) increases in serum high density lipoprotein cholesterol (HDL-C) were observed at week 24 (12.1 +/- 5.0%) and at week 76 (11.0 +/- 3.3%), although the effect was variable. Nevertherless, at the end of treatment the LDL-C: HDL-C ratio showed a 35% reduction from baseline. Changes in triglyceride levels failed to achieve statistical significance, with a reduction from baseline of -13.9 +/- 7.3% at week 104. Changes in apolipoprotein A-I were variable, with statistically significant (p < 0.01) increases observed at week 24 (7.6 +/- 2.3%) and week 76 (8.4 +/- 2.7%). By contrast, a significant reduction from baseline in apolipoprotein B was achieved by week 12 (-15.0 +/- 2.3%; p < 0.001) and was maintained throughout the study.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在24例家族性高胆固醇血症患者中评估了氟伐他汀的长期临床疗效,总治疗期为104周。患者最初接受氟伐他汀剂量为20mg/天,持续8周,之后增加至30mg/天,再持续16周。从第24周起,如果血清总胆固醇仍≥230mg/dL,必要时氟伐他汀剂量可增加至40或60mg/天。治疗结束时,4例患者接受30mg/天的氟伐他汀,1例患者接受40mg/天,19例患者接受60mg/天。血清总胆固醇和低密度脂蛋白胆固醇(LDL-C)水平在第104周时较基线水平显著降低(总胆固醇,-26.8±2.4%;LDL-C,-33.1±3.3%;p<0.001)。总胆固醇和LDL-C的降低与剂量相关。在第24周(12.1±5.0%)和第76周(11.0±3.3%)观察到血清高密度脂蛋白胆固醇(HDL-C)有统计学意义(p<0.05)的升高,尽管效果存在差异。然而,治疗结束时LDL-C:HDL-C比值较基线水平降低了35%。甘油三酯水平的变化未达到统计学意义,在第104周时较基线水平降低了-13.9±7.3%。载脂蛋白A-I的变化存在差异,在第24周(7.6±2.3%)和第76周(8.4±2.7%)观察到有统计学意义(p<0.01)的升高。相比之下,载脂蛋白B在第12周时较基线水平显著降低(-15.0±2.3%;p<0.001),并在整个研究过程中保持这一水平。(摘要截断于250字)

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