Department of Cardiology, Affiliated Hospital of Chengde Medical College, Chengde, Hebei China.
Am J Cardiol. 2012 Nov 1;110(9):1296-301. doi: 10.1016/j.amjcard.2012.06.050. Epub 2012 Jul 27.
Addition of fenofibrate to statin therapy might represent a viable treatment option for patients whose high risk for coronary heart disease is not controlled by a statin alone. However, safety of coadministration of statin with fenofibrate has been a great concern. The present study tested the safety of coadministration of statin with fenofibrate. We systematically searched the literature to identify randomized controlled trials examining safety of coadministration of statin with fenofibrate. A meta-analysis was performed to estimate safety of coadministration of statin with fenofibrate using fixed-effects models. There were 1,628 subjects in the identified 6 studies. Discontinuation attributed to any adverse events (4.5% vs 3.1%, p = 0.20), any adverse events (42% vs 41%, p = 0.82), adverse events related to study drug (10.9% vs 11.0%, p = 0.95), and serious adverse events (2.0% vs 1.5%, p = 0.71) were not significantly different in the 2 arms. Incidence of alanine aminotransferase and/or aspartate aminotransferase ≥3 times upper limit of normal in the combination therapy arm was significantly higher than in the statin monotherapy arm (3.1% vs 0.2%, p = 0.0009). In the 6 trials with 1,628 subjects no case of myopathy or rhabdomyolysis was reported. In conclusion, statin-fenofibrate combination therapy was tolerated as well as statin monotherapy. Physicians should consider statin-fenofibrate combination therapy to treat patients with mixed dyslipidemia.
在他汀类药物治疗的基础上加用心伐他汀可能是一种可行的治疗选择,适用于那些仅用他汀类药物不能有效控制冠心病风险的患者。然而,他汀类药物与非诺贝特联合应用的安全性一直是一个很大的关注点。本研究旨在检验他汀类药物与非诺贝特联合应用的安全性。我们系统地检索了文献,以确定评估他汀类药物与非诺贝特联合应用安全性的随机对照试验。采用固定效应模型进行荟萃分析,以评估他汀类药物与非诺贝特联合应用的安全性。在确定的 6 项研究中,共有 1628 名受试者。因任何不良事件(4.5% vs 3.1%,p = 0.20)、任何不良事件(42% vs 41%,p = 0.82)、与研究药物相关的不良事件(10.9% vs 11.0%,p = 0.95)和严重不良事件(2.0% vs 1.5%,p = 0.71)而停药的比例在两组间无显著差异。联合治疗组丙氨酸氨基转移酶和/或天冬氨酸氨基转移酶升高至正常值上限 3 倍以上的发生率显著高于他汀类药物单药治疗组(3.1% vs 0.2%,p = 0.0009)。在这 6 项包含 1628 名受试者的试验中,均未报告肌病或横纹肌溶解症病例。总之,他汀类药物与非诺贝特联合治疗的耐受性与他汀类药物单药治疗相当。医生应考虑使用他汀类药物与非诺贝特联合治疗来治疗混合性血脂异常患者。