Department of Medicine Baylor College of Medicine Houston TX.
Louisville Metabolic and Atherosclerosis Research Center Louisville KY.
J Am Heart Assoc. 2022 Aug 2;11(15):e024531. doi: 10.1161/JAHA.121.024531.
Background Bempedoic acid (BA) inhibits ATP-citrate lyase in the cholesterol synthesis pathway and lowers low-density lipoprotein cholesterol (LDL-C). As with other lipid-lowering therapies, interindividual variation in response to BA was observed in clinical trials. We characterized LDL-C response to BA using guideline-defined statin intensity categories and identified clinical factors associated with enhanced LDL-C lowering with BA. Methods and Results This post hoc analysis used pooled data from 4 phase 3 studies. Patients were randomized 2:1 to once-daily BA 180 mg (n=2321) or placebo (n=1167) for 12 to 52 weeks and grouped based on percent change in LDL-C from baseline to week 12 according to guideline-established statin intensity categories. Factors associated with ≥30% reduction in LDL-C were identified using logistic regression analyses. From baseline to week 12, BA lowered LDL-C levels comparable to a moderate- or high-intensity statin (≥30%) in 28.9% of patients; this degree of LDL-C lowering was observed in 50.9% of patients not receiving background statin therapy. In a multivariable analysis, the absence of statins, female sex, a history of diabetes, ezetimibe use, and higher high-sensitivity C-reactive protein level were associated with increased rates of achieving ≥30% LDL-C reduction with BA (<0.01 for each). Conclusions A large percentage of patients receiving BA achieved LDL-C reductions comparable to a moderate- or high-intensity statin. Factors including statin absence, female sex, diabetes history, ezetimibe use, and a higher high-sensitivity C-reactive protein level may be useful to identify patients who may have a greater LDL-C reduction with BA. Registration URL: https://www.clinicaltrials.gov; Unique identifiers: NCT02666664, NCT02991118, NCT02988115, NCT03001076.
背景 贝匹地酸(BA)抑制胆固醇合成途径中的 ATP-柠檬酸裂解酶,降低低密度脂蛋白胆固醇(LDL-C)。与其他降脂治疗一样,临床试验中观察到 BA 的个体反应存在差异。我们使用指南定义的他汀类药物强度类别来描述 BA 对 LDL-C 的反应,并确定与 BA 降低 LDL-C 作用增强相关的临床因素。
方法和结果 本事后分析使用了 4 项 3 期研究的汇总数据。患者随机以 2:1 的比例接受每日一次 BA 180mg(n=2321)或安慰剂(n=1167)治疗 12 至 52 周,并根据指南确定的他汀类药物强度类别,根据基线至第 12 周 LDL-C 的百分比变化进行分组。使用逻辑回归分析确定与 LDL-C 降低≥30%相关的因素。从基线到第 12 周,BA 降低 LDL-C 水平与中高强度他汀类药物(≥30%)相当,在 28.9%的患者中;在未接受背景他汀类药物治疗的患者中,有 50.9%的患者观察到这种程度的 LDL-C 降低。在多变量分析中,无他汀类药物、女性、糖尿病史、依折麦布的使用以及更高的高敏 C 反应蛋白水平与 BA 降低 LDL-C≥30%的比例增加相关(<0.01)。
结论 接受 BA 治疗的患者中有很大比例的 LDL-C 降低幅度与中高强度他汀类药物相当。包括他汀类药物缺失、女性、糖尿病史、依折麦布的使用以及高敏 C 反应蛋白水平较高等因素,可能有助于识别可能通过 BA 获得更大 LDL-C 降低的患者。
https://www.clinicaltrials.gov;唯一标识符:NCT02666664、NCT02991118、NCT02988115、NCT03001076。