Real World Evidence of Bempedoic Acid on Efficacy and Safety in Patients with Uncontrolled LDL-c and at High Risk of CVD

S. Manoj, Jay Shah, Dilip Kumar, A. Pradhan, Amit B. Kinare, A. Sharma, M. S. Aditya, R. Raj, A. Raina, Ashish Patel, B. Das, D. Bathe, Sameer Muchhala, Kunal Jhaveri
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Abstract

Background and Objective: Cardiovascular disease (CVD) is a significant cause of morbidity and mortality worldwide, with high-risk patients requiring effective management to reduce their risk of cardiovascular events. Bempedoic acid is a novel therapeutic agent recently approved as an add-on therapy to statins in patients with uncontrolled LDL-c. Bempedoic acid inhibits cholesterol synthesis in the liver, which ultimately reduces the risk of cardiovascular events. Therefore, the present study aims to assess the efficacy and safety of bempedoic acid in patients with uncontrolled LDL-c (Previously on moderate or high-intensity statins) with a high risk of CVD in real-world settings. Methods: This is a multicenter, retrospective, observational study on the data of high-risk-CVD patients collected from Bempedoic Acid on Efficacy and Safety in patients (BEST) Registry. The clinical data of 140 patients who were already on statin therapy and were receiving Bempedoic acid at a dose of 180 mg, along with measurements of the level of LDL-c, HbA1c, HDL, TG, TC, PPPG, FPG, AST, ALT, serum creatinine was taken into consideration. The primary outcome includes a change in LDL-c level, and secondary outcomes involve a change in the level of HbA1c, HDL, TG, TC, PPPG, FPG, AST, ALT, and serum creatinine at week 12 and 24. Adverse events were reported at both time points. Results: A total of 140 patients were included in the present study with a mean age of 51.8 ± 9.2 years and had primary confirmed diagnosis of dyslipidemia with uncontrolled LDL-c. The mean levels of LDL-c decreased from the mean baseline value of 142.67 ± 46.49 mg/dL, to 106.78 ±33.92 mg/d; a statistically significant reduction by 23.23% (p < 0.01) at week 12. Similarly, at week 24, the mean LDL-c value reduced to 90.39 ± 38.89 mg/dL. A 33.38 % decrease was observed (p < 0.01). Other parameters such as non-HDL, FPG, PPPG, AST and serum creatinine also showed statistically significant reduction at week 12 and week 24.  Conclusion: The present study demonstrates that bempedoic acid is an effective add-on medication in lowering LDL-c levels in high-risk CVD patients with uncontrolled LDL-c.
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苯甲多酸对不受控制的LDL-c和心血管疾病高风险患者的有效性和安全性的真实世界证据
背景与目的:心血管疾病(CVD)是世界范围内发病率和死亡率的重要原因,高危患者需要有效的管理来降低心血管事件的风险。苯戊酸是一种新型的治疗药物,最近被批准作为他汀类药物的附加治疗,用于LDL-c不控制的患者。苯二甲酸抑制肝脏中胆固醇的合成,最终降低心血管事件的风险。因此,本研究旨在评估在现实环境中,对LDL-c不受控制(先前使用中或高强度他汀类药物)且心血管疾病高风险的患者使用苯戊酸的疗效和安全性。方法:这是一项多中心、回顾性、观察性研究,收集了本培多酸在患者中的疗效和安全性(BEST)登记处收集的高风险cvd患者的数据。140例已接受他汀类药物治疗并接受本培多酸180 mg剂量的患者的临床资料,以及LDL-c、HbA1c、HDL、TG、TC、PPPG、FPG、AST、ALT、血清肌酐水平的测量。主要结果包括LDL-c水平的变化,次要结果包括第12周和第24周HbA1c、HDL、TG、TC、PPPG、FPG、AST、ALT和血清肌酐水平的变化。两个时间点均报告了不良事件。结果:本研究共纳入140例患者,平均年龄51.8±9.2岁,初步确诊为血脂异常且LDL-c不受控制。LDL-c的平均水平从基线值142.67±46.49 mg/dL降至106.78±33.92 mg/d;在第12周时,有统计学意义降低23.23% (p < 0.01)。同样,在第24周,平均LDL-c值降至90.39±38.89 mg/dL。下降33.38% (p < 0.01)。其他参数如non-HDL、FPG、PPPG、AST和血清肌酐在第12周和第24周也有统计学意义的降低。结论:本研究表明,在LDL-c未控制的高危CVD患者中,苯戊酸是一种有效的辅助药物。
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