Kuivenhoven Jan Albert, de Grooth Greetje J, Kawamura Hitoshi, Klerkx Anke H, Wilhelm Francois, Trip Mieke D, Kastelein John J P
Department of Vascular Medicine, Academic Medical Center, Amsterdam, The Netherlands.
Am J Cardiol. 2005 May 1;95(9):1085-8. doi: 10.1016/j.amjcard.2004.12.064.
The inhibition of cholesteryl ester transfer protein (CETP) has recently been shown to effectively increase high-density lipoprotein (HDL) cholesterol. This study examined the use of the CETP inhibitor JTT-705 combined with pravastatin. In a randomized, double-blind, placebo-controlled trial, 155 patients with type II dyslipidemia using pravastatin 40 mg were treated with placebo or JTT-705 300 or 600 mg. Four weeks of treatment with JTT-705 600 mg led to a 30% decrease in CETP activity (p <0.001), a 28% increase in HDL cholesterol (p <0.001), and a 5% decrease in low-density lipoprotein cholesterol (p <0.03). Combination therapy using JTT-705 and pravastatin effectively increases HDL cholesterol levels and is safe and well tolerated up to 4 weeks of administration.
最近研究表明,抑制胆固醇酯转运蛋白(CETP)可有效提高高密度脂蛋白(HDL)胆固醇水平。本研究探讨了CETP抑制剂JTT-705与普伐他汀联合使用的情况。在一项随机、双盲、安慰剂对照试验中,155例使用40mg普伐他汀的II型血脂异常患者接受了安慰剂、300mg或600mg JTT-705治疗。600mg JTT-705治疗4周后,CETP活性降低30%(p<0.001),HDL胆固醇升高28%(p<0.001),低密度脂蛋白胆固醇降低5%(p<0.03)。JTT-705与普伐他汀联合治疗可有效提高HDL胆固醇水平,给药4周内安全且耐受性良好。