Mahmoud Abdelrahman, Mohamed Salamah Hazem, Rezq Hazem, Al-Mohtasib Yazan, Ashraf Salah Ahmed Ali, Abdelraouf Mohamed R, Amin Ahmed Mazen, Ibrahim Ahmed A, Adel Mohammed Yasmine, Abdelwahab Omar Ahmed, AlBarakat Majd M, Elshenawy Salem, Abu Suilik Husam, Abdelazeem Basel
Faculty of Medicine, Minia University, Minia, Egypt.
Faculty of Medicine, Zagazig University, Zagazig, Egypt.
Proc (Bayl Univ Med Cent). 2025 Apr 25;38(4):474-483. doi: 10.1080/08998280.2025.2487966. eCollection 2025.
Dyslipidemia is a major risk factor for atherosclerotic cardiovascular disease (ASCVD). Oral regimens to achieve blood lipid targets include increasing the statin dose or adding ezetimibe to statin therapy. The optimal strategy remains debated. This study evaluated the efficacy and safety of ezetimibe plus statin versus a double dose of the same statin in patients with ASCVD risk.
We conducted a systematic review and meta-analysis of randomized controlled trials from PubMed, Embase, Cochrane, Scopus, and Web of Science through December 2023. A random-effects model was used to analyze outcomes, reporting risk ratio and mean difference with 95% confidence intervals.
Forty-seven randomized controlled trials involving 18,592 patients were included. Ezetimibe plus statin significantly reduced low-density lipoprotein (LDL) cholesterol ( < 0.001), triglyceride ( = 0.019), and total cholesterol levels ( < 0.001) and increased target LDL achievement ( < 0.0001) compared to double-dose statin. No significant differences were observed in high-density lipoprotein levels, any adverse events, all-cause mortality, myocardial infarction, angina, or nonfatal stroke. The incidence of severe adverse events was higher with ezetimibe plus statin ( = 0.03).
Ezetimibe plus statin therapy demonstrated superior lipid-lowering efficacy compared with double-dose statin therapy, with no additional clinical benefit. There was no difference in overall adverse events. There was a higher incidence of severe adverse events with combination therapy compared to double-dose statin therapy, although these events were rare and not believed to be attributable to medication.
血脂异常是动脉粥样硬化性心血管疾病(ASCVD)的主要危险因素。实现血脂目标的口服治疗方案包括增加他汀类药物剂量或在他汀类药物治疗基础上加用依折麦布。最佳策略仍存在争议。本研究评估了依折麦布联合他汀类药物与双倍剂量相同他汀类药物在有ASCVD风险患者中的疗效和安全性。
我们对截至2023年12月从PubMed、Embase、Cochrane、Scopus和Web of Science检索到的随机对照试验进行了系统评价和荟萃分析。采用随机效应模型分析结果,报告风险比和平均差以及95%置信区间。
纳入了47项涉及18592例患者的随机对照试验。与双倍剂量他汀类药物相比,依折麦布联合他汀类药物显著降低了低密度脂蛋白(LDL)胆固醇(<0.001)、甘油三酯(=0.019)和总胆固醇水平(<0.001),并提高了LDL达标率(<0.0001)。在高密度脂蛋白水平、任何不良事件、全因死亡率、心肌梗死、心绞痛或非致死性卒中方面未观察到显著差异。依折麦布联合他汀类药物组严重不良事件的发生率更高(=0.03)。
与双倍剂量他汀类药物治疗相比,依折麦布联合他汀类药物治疗显示出更优的降脂疗效,但无额外的临床益处。总体不良事件无差异。与双倍剂量他汀类药物治疗相比,联合治疗组严重不良事件的发生率更高,尽管这些事件很少见,且认为与药物无关。