Roh Ji Woong, Park Moon-Hwa, Son Ji-Won, Bae SungA
Division of Cardiology, Department of Internal Medicine, Yonsei University College of Medicine, Yongin Severance Hospital, Yongin, Republic of Korea.
Hanmi Pharmaceutical Co., Ltd., Seoul, Republic of Korea.
Clin Drug Investig. 2025 Sep 16. doi: 10.1007/s40261-025-01482-3.
Dyslipidaemia is a key modifiable risk factor for atherosclerotic cardiovascular disease. However, achieving recommended low-density lipoprotein cholesterol (LDL-C) target levels is challenging owing to dose-dependent adverse effects and limited tolerability of high-dose statins. This study evaluated the real-world efficacy and safety of combining very-low-dose rosuvastatin (2.5 mg) with ezetimibe (10 mg) in adult patients with dyslipidaemia across different cardiovascular risk strata.
This multicentre prospective study in South Korea enrolled 2,388 patients. Participants were stratified into low-, moderate-, or high-risk groups on the basis of the 2019 European Society of Cardiology and European Atherosclerosis Society guidelines. Lipid profiles and safety outcomes were assessed at baseline and after 12 weeks. The primary and secondary outcomes were LDL-C and non-high-density lipoprotein cholesterol (non-HDL-C) target level achievements, respectively, and adverse events were monitored.
After 12 weeks, LDL-C target levels were achieved by 82.6% of low-risk (< 116 mg/dL), 73.9% of moderate-risk (< 100 mg/dL), and 50.4% of high-risk (< 70 mg/dL) patients. Non-HDL-C target level achievement followed a similar trend. Combination therapy with ezetimibe and low-dose statin resulted in significant LDL-C reductions, compared with statins alone. Adverse events were infrequent (0.6%), and only 0.2% of patients discontinued treatment owing to medication-related concerns.
Very-low-dose rosuvastatin-ezetimibe combination therapy significantly lowered LDL-C levels and improved lipid profiles across various risk groups, demonstrating a favourable safety profile. These findings support its use as an effective, well-tolerated option for managing dyslipidaemia. Longer-term studies are warranted to evaluate sustained lipid control and cardiovascular outcomes.
血脂异常是动脉粥样硬化性心血管疾病的一个关键可改变风险因素。然而,由于大剂量他汀类药物存在剂量依赖性不良反应且耐受性有限,要达到推荐的低密度脂蛋白胆固醇(LDL-C)目标水平具有挑战性。本研究评估了极低剂量瑞舒伐他汀(2.5毫克)与依折麦布(10毫克)联合使用在不同心血管风险分层的成年血脂异常患者中的真实疗效和安全性。
这项在韩国开展的多中心前瞻性研究纳入了2388名患者。根据2019年欧洲心脏病学会和欧洲动脉粥样硬化学会指南,参与者被分为低风险、中风险或高风险组。在基线和12周后评估血脂谱和安全性结果。主要和次要结局分别是LDL-C和非高密度脂蛋白胆固醇(非HDL-C)目标水平的达成情况,并监测不良事件。
12周后,低风险(<116毫克/分升)患者中有82.6%、中风险(<100毫克/分升)患者中有73.9%、高风险(<70毫克/分升)患者中有50.4%达到了LDL-C目标水平。非HDL-C目标水平的达成情况也呈现类似趋势。与单独使用他汀类药物相比,依折麦布与低剂量他汀联合治疗导致LDL-C显著降低。不良事件发生率较低(0.6%),仅有0.2%的患者因药物相关问题停药。
极低剂量瑞舒伐他汀-依折麦布联合治疗显著降低了各风险组的LDL-C水平并改善了血脂谱,显示出良好的安全性。这些发现支持将其作为治疗血脂异常的有效且耐受性良好的选择。有必要开展长期研究以评估持续的血脂控制情况和心血管结局。