Department of Medical and Surgical Sciences, Sant'Orsola-Malpighi University Hospital, University of Bologna, Via Albertoni, 15, 40138, Bologna, Italy.
Department of Internal Medicine, Università degl Studi and IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
Drug Saf. 2020 Aug;43(8):727-736. doi: 10.1007/s40264-020-00931-6.
Bempedoic acid (ETC-1002) is a first-in-class lipid-lowering agent recently approved by the United States (US) Food and Drug Administration (FDA) and the European Medicines Agency (EMA) for commercialization.
The aim was to assess, through a systematic review of the literature and a meta-analysis of the available phase 2 and phase 3 clinical studies, the effect of treatment with bempedoic acid on serum uric acid (SUA) concentration. Secondary outcomes were treatment-related variations in creatinine serum level and incidence of gout.
A systematic literature search in SCOPUS, PubMed Medline, ISI Web of Science and Google Scholar databases was conducted up to November 13th, 2019, in order to identify clinical trials potentially eligible for the meta-analysis. Effect sizes were expressed as absolute mean differences (MDs) and 95% confidence intervals (CIs).
Data were pooled from four clinical studies comprising ten arms, which included overall 3369 subjects, with 2213 in the active-treatment arm and 1156 in the control one. Meta-analysis of data suggested that treatment with bempedoic acid is related to a significant increase in SUA (MD 0.73, 95% CI 0.54-0.91, P < 0.001), serum creatinine (MD 0.04, 95% CI 0.03-0.05, P < 0.001) and the incidence of gout (odds ratio 3.56, 95% CI 1.24-10.19, P = 0.018). The relatively small number of subjects involved in the studies and the exclusion of patients with renal impairment from the clinical trials are important limitations of the meta-analysis. However, our data indicate potential safety issues with bempedoic acid and suggest that further studies are performed both to elucidate the pathogenetic mechanisms underlying these associations and to verify the long-term safety of this treatment.
Bempedoic acid seems to have unfavourable effects on SUA, creatinine level and the incidence of gout. The ongoing Cardiovascular Outcomes Trial (CVOT) will explore the longer-term safety of treatment with bempedoic acid and clarify its effect on cardiovascular events and mortality.
CRD42019146126.
贝匹达酸(ETC-1002)是一种新型降脂药物,最近被美国食品和药物管理局(FDA)和欧洲药品管理局(EMA)批准商业化。
通过对现有 2 期和 3 期临床试验的文献系统评价和荟萃分析,评估贝匹达酸治疗对血清尿酸(SUA)浓度的影响。次要结局为治疗相关的肌酐血清水平变化和痛风发生率。
在 SCOPUS、PubMed Medline、ISI Web of Science 和 Google Scholar 数据库中进行系统文献检索,截至 2019 年 11 月 13 日,以确定可能适合荟萃分析的临床试验。效应大小表示为绝对平均差异(MD)和 95%置信区间(CI)。
数据来自四项临床试验,共纳入 10 个试验组,共 3369 例患者,其中活性治疗组 2213 例,对照组 1156 例。荟萃分析结果表明,贝匹达酸治疗与 SUA(MD0.73,95%CI0.54-0.91,P<0.001)、血清肌酐(MD0.04,95%CI0.03-0.05,P<0.001)和痛风发生率(比值比 3.56,95%CI1.24-10.19,P=0.018)显著升高相关。研究中纳入的受试者数量相对较少,以及临床试验排除了肾功能受损患者,这是荟萃分析的重要局限性。然而,我们的数据表明贝匹达酸可能存在安全性问题,并建议进一步研究,以阐明这些关联的发病机制,并验证这种治疗的长期安全性。
贝匹达酸似乎对 SUA、肌酐水平和痛风的发生率有不利影响。正在进行的心血管结局试验(CVOT)将探讨贝匹达酸治疗的长期安全性,并阐明其对心血管事件和死亡率的影响。
PROSPERO 数据库注册:CRD42019146126。