The Second Affiliated Hospital of Chongqing, Chongqing, China.
Kardiol Pol. 2019;77(2):207-216. doi: 10.5603/KP.a2019.0013. Epub 2019 Feb 11.
Due to the myopathic adverse events of statins, safer alternatives are being studied. Bempedoic acid (ETC-1002) is a novel low-density lipoprotein cholesterol (LDL-C)-lowering agent, currently under trial in hypercholesterolaemic patients.
To investigate the tolerability and efficacy of ETC-1002 in hypercholesterolaemic patients through a systematic review of published randomised controlled trials (RCTs).
Five databases were searched for RCTs that investigated the safety and efficacy of ETC-1002 in hypercholesterol-aemic patients. The retrieved search results were screened, and then data were extracted and analysed (as mean difference [MD] or odds ratio [OR]) using the RevMan software.
Five RCTs (625 hypercholesterolaemic patients) were identified. ETC-1002 was superior to placebo in terms of percent-age changes from baseline in serum levels of LDL-C (MD -26.58, 95% confidence interval [CI] -35.50 to -17.66, p < 0.0001), non-high-density lipoprotein cholesterol (MD -21.54, 95% CI -28.48 to -14.6, p < 0.00001), and apolipoprotein-B (MD -15.97, 95% CI -19.36 to -12.57, p < 0.0001). When compared to ezetimibe, ETC-1002 was superior in reducing LDL-C (-30.1 ± 1.3 vs. -21.1 ± 1.3). Regarding safety, ETC-1002 did not increase the risk of all adverse events (OR 0.58, 95% CI 0.37-0.91, p = 0.02) and arthralgia (OR 0.32, 95% CI 0.13-0.81, p = 0.02) compared to placebo. All other adverse events including myalgia, headache, and urinary tract infections were similar between ETC-1002 and placebo groups. The evidence certainty in the assessed outcomes was moderate to high except for lipoprotein(a), free fatty acids, and very low-density lipoprotein particle number (very low certainty).
ETC-1002 is a safe and effective lipid-lowering agent and may be a suitable alternative in statin-intolerant pa-tients. Well-designed studies are needed to explore the long-term safety and efficacy of ETC-1002 in these patients.
由于他汀类药物的肌病不良反应,正在研究更安全的替代药物。贝匹地酸(ETC-1002)是一种新型的降低低密度脂蛋白胆固醇(LDL-C)的药物,目前正在高脂血症患者中进行临床试验。
通过系统评价已发表的随机对照试验(RCT),研究贝匹地酸在高脂血症患者中的耐受性和疗效。
在五个数据库中搜索了调查贝匹地酸治疗高胆固醇血症患者的安全性和疗效的 RCT。筛选检索结果,然后使用 RevMan 软件提取和分析数据(均为均数差[MD]或比值比[OR])。
共纳入 5 项 RCT(625 例高脂血症患者)。与安慰剂相比,ETC-1002 可更显著降低血清 LDL-C(MD -26.58,95%置信区间[CI] -35.50 至 -17.66,p < 0.0001)、非高密度脂蛋白胆固醇(MD -21.54,95%CI -28.48 至 -14.6,p < 0.00001)和载脂蛋白 B(MD -15.97,95%CI -19.36 至 -12.57,p < 0.0001)水平。与依折麦布相比,ETC-1002 降低 LDL-C 的效果更优(-30.1 ± 1.3 vs. -21.1 ± 1.3)。关于安全性,与安慰剂相比,ETC-1002 并未增加所有不良反应(OR 0.58,95%CI 0.37-0.91,p = 0.02)和关节痛(OR 0.32,95%CI 0.13-0.81,p = 0.02)的风险。ETC-1002 组与安慰剂组的其他所有不良反应(包括肌痛、头痛和尿路感染)均相似。除脂蛋白(a)、游离脂肪酸和极低密度脂蛋白颗粒数(极低确定性)外,评估结局的证据确定性为中至高。
ETC-1002 是一种安全有效的降脂药物,可能是他汀类药物不耐受患者的合适替代药物。需要设计良好的研究来探索 ETC-1002 在这些患者中的长期安全性和疗效。