Tomlinson B, Mak T W, Tsui J Y, Woo J, Shek C C, Critchley J A, Masarei J R
Department of Clinical Pharmacology, Chinese University of Hong Kong, Prince of Wales Hospital, Shatin.
Am J Cardiol. 1995 Jul 13;76(2):136A-139A. doi: 10.1016/s0002-9149(05)80036-0.
The effects of fluvastatin treatment on lipid profile and apolipoproteins were assessed in a group of 31 Chinese patients with hypercholesterolemia, maintained on a constant low-fat diet. Some patients had the additional cardiovascular risk factors of hypertension and non-insulin-dependent diabetes mellitus, and 6 patients had familial hypercholesterolemia. Baseline lipid levels were measured after a 4-week placebo period, and these were repeated after 4 weeks of treatment with fluvastatin 20 mg daily, and after 4 weeks of treatment with fluvastatin 40 mg daily. Total cholesterol, low density lipoprotein cholesterol, and apolipoprotein (apo) B were each reduced to the same extent with the 2 doses of fluvastatin (-20%, -26%, and -20%, respectively). Triglycerides and very low density lipoprotein cholesterol were also reduced by about 12% with the 2 doses of fluvastatin. Apo A-I was increased by 7% and high density lipoprotein cholesterol (HDL-C) was increased by 10% with the 40 mg dose. The increase in HDL-C was due to increases in both HDL2-C (18%) and HDL3-C (7%). Lipoprotein(a) levels did not show any significant change with the 2 doses of fluvastatin in this short-term study. One patient developed reversible asymptomatic elevation of liver enzymes with the higher dose of fluvastatin; otherwise the drug was well tolerated and no patients had to be withdrawn from the study.
对31名中国高胆固醇血症患者进行了一项研究,评估氟伐他汀治疗对血脂谱和载脂蛋白的影响,这些患者维持恒定的低脂饮食。部分患者伴有高血压和非胰岛素依赖型糖尿病等额外心血管危险因素,6名患者患有家族性高胆固醇血症。在4周安慰剂期后测量基线血脂水平,之后每日服用20mg氟伐他汀治疗4周后以及每日服用40mg氟伐他汀治疗4周后再次测量。两种剂量的氟伐他汀均使总胆固醇、低密度脂蛋白胆固醇和载脂蛋白(apo)B降低至相同程度(分别降低20%、26%和20%)。两种剂量的氟伐他汀还使甘油三酯和极低密度脂蛋白胆固醇降低约12%。40mg剂量使apo A-I升高7%,高密度脂蛋白胆固醇(HDL-C)升高10%。HDL-C的升高是由于HDL2-C(升高18%)和HDL3-C(升高7%)均升高。在这项短期研究中,两种剂量的氟伐他汀均未使脂蛋白(a)水平出现任何显著变化。一名患者在服用较高剂量氟伐他汀后出现可逆性无症状肝酶升高;除此之外,该药物耐受性良好,没有患者必须退出研究。