Madan Mina, Vira Tasnim, Rampakakis Emmanouil, Gupta Anup, Khithani Anil, Balleza Lyn, Vaillancourt Julie, Boukas Stella, Sampalis John, de Carolis Emidio
Schulich Heart Centre, Sunnybrook Health Sciences Centre, D380-2075 Bayview, Avenue, Toronto, ON, Canada M4N 3M5.
Adv Prev Med. 2012;2012:103728. doi: 10.1155/2012/103728. Epub 2012 Dec 6.
Background. There is a paucity of data regarding the effectiveness and safety of lipid-lowering treatments among South-Asian patients. Methods. Sixty-four South-Asian Canadians with coronary artery disease or diabetes and persistent hypercholesterolemia on statin therapy, were randomized to ezetimibe 10 mg/day co-administered with statin therapy (EZE + Statin) or doubling their current statin dose (STAT(2)). Primary outcome was the proportion of patients achieving target LDL-C (<2.0 mmol/L) after 6 weeks. Secondary outcomes included the change in lipid profile and the incidence of treatment-emergent adverse events through 12 weeks. Exploratory markers for vascular inflammation were assessed at baseline and 12 weeks. Results. At 6 weeks, the primary outcome was significantly higher among the EZE + Statin patients (68% versus 36%; P = 0.031) with an OR (95% CI) of 3.97 (1.19, 13.18) upon accounting for baseline LDL-C and adjusting for age. At 12 weeks, 76% of EZE + Statin patients achieved target LDL-C compared to 48% (P = 0.047) of the STAT(2) patients (adjusted OR (95% CI) = 3.31 (1.01,10.89)). No significant between-group differences in exploratory markers were observed with the exception of CRP. Conclusions. Patients receiving ezetimibe and statin were more likely to achieve target LDL-C after 6 and 12 weeks compared to patients doubling their statin dose. Ezetimibe/statin combination therapy was well tolerated among this cohort of South-Asian Canadians, without safety concerns.
背景。关于南亚患者降脂治疗的有效性和安全性的数据匮乏。方法。64名患有冠状动脉疾病或糖尿病且在接受他汀类药物治疗时持续存在高胆固醇血症的南亚裔加拿大患者,被随机分为两组,一组每天服用10毫克依折麦布并联合他汀类药物治疗(依折麦布+他汀类药物组),另一组将当前他汀类药物剂量加倍(他汀类药物加倍组)。主要结局是6周后达到低密度脂蛋白胆固醇目标值(<2.0毫摩尔/升)的患者比例。次要结局包括12周内血脂谱的变化以及治疗中出现的不良事件发生率。在基线和12周时评估血管炎症的探索性标志物。结果。6周时,依折麦布+他汀类药物组患者的主要结局显著更高(68%对36%;P=0.031),在考虑基线低密度脂蛋白胆固醇并对年龄进行校正后,优势比(95%置信区间)为3.97(1.19,13.18)。12周时,76%的依折麦布+他汀类药物组患者达到了低密度脂蛋白胆固醇目标值,而他汀类药物加倍组为48%(P=0.047)(校正优势比(95%置信区间)=3.31(1.01,10.89))。除了C反应蛋白外,未观察到探索性标志物在组间有显著差异。结论。与将他汀类药物剂量加倍的患者相比,接受依折麦布和他汀类药物治疗的患者在6周和12周后更有可能达到低密度脂蛋白胆固醇目标值。依折麦布/他汀类药物联合治疗在这组南亚裔加拿大患者中耐受性良好,没有安全问题。