Alunno Alessia, Carubbi Francesco, Campanozzi Elena, Bellisario Federico, Schoones Jan W, Mariani Francesco Maria, Di Ruscio Evy, Altieri Piera, Ferri Claudio
Department of Clinical Medicine, Life, Health & Environmental Sciences, Internal Medicine and Nephrology Division, ASL1 Avezzano-Sulmona-L'Aquila, San Salvatore Hospital, University of L'Aquila, L'Aquila, Italy.
Directorate of Research Policy, Leiden University Medical Center, Leiden, Netherlands.
Front Cardiovasc Med. 2023 Oct 25;10:1234601. doi: 10.3389/fcvm.2023.1234601. eCollection 2023.
Bempedoic acid (BA) is a small-molecule first-in-class of inhibitor of ATP citrate lyase that significantly lowers low-density lipoproteins cholesterol (LDL-c) in statin-intolerant and inadequate responders. Increased serum uric acid (SUA) levels and gout incidence have been described in BA-treated patients. The aim of this systematic review was to investigate the safety of BA regarding SUA levels and gout in randomised controlled trials (RCTs).
A search on 7 databases was performed from inception to May 4, 2023. RCTs of BA monotherapy or combination with other lipid-lowering treatment (LLT) in patients with increased LDL-c were included. Dual data extraction was performed with disagreements resolved through consensus. Due to the methodological purpose of this review risk-of-bias assessment of studies was not performed.
6 Phase 3 RCTs ( = 17,975 patients of which 9,635 received BA) 9 Phase 2 RCTs ( = 362 patients of which 170 received BA) and an open-label extension of a Phase 3 RCT were included. Gout and/or hyperuricemia were not mentioned as exclusion criteria, previous/current use of urate-lowering therapies (ULT) and/or colchicine and/or dietary patterns were not reported. Phase 3 RCTs: 2 studies specified the number of patients experiencing hyperuricemia over the study period (BA: 4.9%-11%; placebo: 1.9%-5.6%) and the effect size was significant only in 1 study (OR = 2.0, 95% CI 1.8-2.3). Four RCTs reported a higher incidence of gout in the BA arm however, when we calculated the effect size, it was small and often not significant. Two studies reported 0 cases of gout. The paucity of information about SUA levels at baseline and/or at the end of follow-up do not allow us to quantify the effect sizes for BA-induced SUA elevation. Data on gout from Phase 2 RCTs is scant.
Data from phase 2 and 3 RCTs do not allow for confirming a clear association between BA and gout. It is conceivable that a careful assessment of SUA levels/history of gout at baseline and the concomitant use of urate-lowering agents may be instrumental to minimise the risk of new-onset gout/gout flares in patients treated with BA.
贝派地酸(BA)是一种小分子的首创ATP柠檬酸裂解酶抑制剂,可显著降低他汀类药物不耐受和反应不足患者的低密度脂蛋白胆固醇(LDL-c)水平。已有报道称,接受BA治疗的患者血清尿酸(SUA)水平升高且痛风发病率增加。本系统评价的目的是在随机对照试验(RCT)中研究BA在SUA水平和痛风方面的安全性。
从数据库创建至2023年5月4日在7个数据库进行检索。纳入LDL-c升高患者接受BA单药治疗或与其他降脂治疗(LLT)联合治疗的RCT。采用双人数据提取,分歧通过共识解决。由于本评价的方法学目的,未对研究进行偏倚风险评估。
纳入了6项3期RCT(n = 17975例患者,其中9635例接受BA治疗)、9项2期RCT(n = 362例患者,其中170例接受BA治疗)以及1项3期RCT的开放标签扩展研究。痛风和/或高尿酸血症未被列为排除标准,未报告既往/当前使用降尿酸治疗(ULT)和/或秋水仙碱和/或饮食模式。3期RCT:2项研究明确了研究期间发生高尿酸血症的患者数量(BA组:4.9%-11%;安慰剂组:1.9%-5.6%),效应量仅在其中1项研究中具有统计学意义(OR = 2.0,95%CI 1.8-2.3)。4项RCT报告BA组痛风发病率较高,然而,当我们计算效应量时,其较小且通常无统计学意义。2项研究报告痛风病例数为0。关于基线和/或随访结束时SUA水平的信息匮乏,使我们无法量化BA诱导的SUA升高的效应量。2期RCT中关于痛风的数据较少。
2期和3期RCT的数据无法证实BA与痛风之间存在明确关联。可以设想,在基线时仔细评估SUA水平/痛风病史以及同时使用降尿酸药物可能有助于将接受BA治疗患者新发痛风/痛风发作的风险降至最低。