Suzuki Hiromichi, Watanabe Yusuke, Kumagai Hiroo, Shuto Hiroshi
Department of Nephrology, Saitama Medical University.
Ther Adv Cardiovasc Dis. 2013 Dec;7(6):306-15. doi: 10.1177/1753944713513222. Epub 2013 Nov 26.
The recent SHARP trial clearly demonstrated that a reduction in low-density lipoprotein (LDL) cholesterol with a daily regimen of simvastatin plus ezetimibe safely reduced the incidence of major atherosclerotic events in patients with chronic kidney disease (CKD). We aimed to compare the efficacy of and adverse effects from statin uptitration versus statin in combination with ezetimibe since only a few studies have addressed this question.
This was a randomized, open-label, multicenter trial that included 286 patients with CKD whose LDL cholesterol levels were not reduced below 120 mg/dl despite a minimum dose of statin therapy. Patients received double doses of statin or usual statin dose with the addition of ezetimibe 10 mg daily. The observation period was 1 year during which time patients were checked regularly in clinic for adverse effects as well as for usual laboratory examinations. The key prespecified outcome was the incidence of adverse effects, which included skeletal muscle complaints, myalgia, muscle weakness, and muscle cramps with and without elevated CK levels. Increases in alanine transaminase (ALT) or aspartate transaminase (AST) levels >2 times the upper limit of normal (ULN) were considered clinically significant adverse effects.
Adverse events occurred in 9/145 in the combination group and in 24/141 in the statin uptitration group (p < 0.01). Moreover, in patients with CKD of stages 3-5, rates were 6/58 in the combination group versus 20/52 in the statin uptitration group (p < 0.01). No serious adverse effects such as rhabdomyolysis were noted in either group. Serum creatinine levels remained essentially unchanged in both groups except in CKD stages 4 and 5. Reductions in LDL cholesterol were similar between the two groups at the start of and at the end of the study. During the study, no atherosclerotic events were reported in either group.
When statin uptitration produces adverse effects such as myopathy, combination therapy with ezetimibe is recommended instead of statin alone.
近期的SHARP试验清楚地表明,慢性肾病(CKD)患者每日服用辛伐他汀加依泽替米贝降低低密度脂蛋白(LDL)胆固醇水平可安全降低主要动脉粥样硬化事件的发生率。由于仅有少数研究涉及此问题,我们旨在比较他汀类药物增量与他汀类药物联合依泽替米贝的疗效及不良反应。
这是一项随机、开放标签、多中心试验,纳入了286例CKD患者,尽管接受了最低剂量的他汀类药物治疗,其LDL胆固醇水平仍未降至120mg/dl以下。患者接受双倍剂量的他汀类药物或常规他汀类药物剂量并每日加用10mg依泽替米贝。观察期为1年,在此期间定期在诊所检查患者的不良反应以及进行常规实验室检查。预先设定的关键结局是不良反应的发生率,包括骨骼肌不适、肌痛、肌肉无力以及有无肌酸激酶(CK)水平升高的肌肉痉挛。丙氨酸转氨酶(ALT)或天冬氨酸转氨酶(AST)水平升高超过正常上限(ULN)2倍被视为具有临床意义的不良反应。
联合治疗组145例中有9例发生不良事件,他汀类药物增量组141例中有24例发生不良事件(p<0.01)。此外,在3 - 5期CKD患者中,联合治疗组发生率为6/58,他汀类药物增量组为20/52(p<0.01)。两组均未观察到诸如横纹肌溶解等严重不良反应。除CKD 4期和5期外,两组血清肌酐水平基本保持不变。研究开始时和结束时两组LDL胆固醇的降低情况相似。研究期间,两组均未报告动脉粥样硬化事件。
当他汀类药物增量产生如肌病等不良反应时,推荐使用依泽替米贝联合治疗而非单独使用他汀类药物。