Lee Bom, Hong Sung-Jin, Rha Seung-Woon, Heo Jung Ho, Hur Seung-Ho, Choi Hyun Hee, Kim Kyung-Jin, Kim Ju Han, Kim Hyun Kuk, Kim Ung, Choi Yu Jeong, Lee Yong-Joon, Lee Seung-Jun, Ahn Chul-Min, Ko Young-Guk, Kim Byeong-Keuk, Choi Donghoon, Hong Myeong-Ki, Jang Yangsoo, Kim Jung-Sun
CHA Bundang Medical Center, CHA University College of Medicine, Seongnam, South Korea.
Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.
Atherosclerosis. 2023 Dec;386:117373. doi: 10.1016/j.atherosclerosis.2023.117373. Epub 2023 Nov 10.
Whether the effect of a combination strategy rather than increasing doses of one drug to lower low-density lipoprotein cholesterol (LDL-C) levels is consistent across baseline LDL-C levels remains uncertain.
In the RACING trial, which showed a non-inferiority of moderate-intensity statin with ezetimibe (rosuvastatin 10 mg with ezetimibe 10 mg) to high-intensity statin (rosuvastatin 20 mg) for the primary outcome (3-year composite of cardiovascular death, major cardiovascular event, or stroke), the heterogeneity in treatment effect according to baseline LDL-C levels was assessed for the primary and secondary outcomes (clinical efficacy and safety).
Of 3780 participants, 2817 participants (74.5%) had LDL-C <100 mg/dL, and 963 participants (25.5%) had LDL-C ≥100 mg/dL. The treatment effect of combination therapy versus high-intensity statin monotherapy was similar among the lower LDL-C subset (8.8% vs. 10.2%; hazard ratio [HR] 0.85, 95% confidence interval [CI] 0.67 to 1.08, p = 0.19) and the higher LDL-C subset (10.8% vs. 9.6 %; HR 1.14, 95% CI 0.76 to 1.7, p = 0.53) without a significant interaction (interaction p = 0.22). Of the secondary outcomes, the 1-, 2-, and 3-year achievement of LDL-C <70 mg/dL was greater in the combination therapy group regardless of baseline LDL-C levels.
Among ASCVD patients, there was no heterogeneity in the effect of moderate-intensity statin plus ezetimibe combination therapy in the higher and lower baseline LDL-C levels for the 3-year composite of cardiovascular outcomes.
联合治疗策略而非增加单一药物剂量来降低低密度脂蛋白胆固醇(LDL-C)水平的效果在不同基线LDL-C水平下是否一致仍不确定。
在RACING试验中,主要结局(心血管死亡、主要心血管事件或中风的3年复合结局)显示中等强度他汀类药物联合依折麦布(瑞舒伐他汀10毫克联合依折麦布10毫克)不劣于高强度他汀类药物(瑞舒伐他汀20毫克),根据基线LDL-C水平评估主要和次要结局(临床疗效和安全性)的治疗效果异质性。
在3780名参与者中,2817名参与者(74.5%)的LDL-C<100mg/dL,963名参与者(25.5%)的LDL-C≥100mg/dL。在较低LDL-C亚组(8.8%对10.2%;风险比[HR]0.85,95%置信区间[CI]0.67至1.08,p=0.19)和较高LDL-C亚组(10.8%对9.6%;HR 1.14,95%CI 0.76至1.7,p=0.53)中,联合治疗与高强度他汀类药物单药治疗的效果相似,无显著交互作用(交互作用p=0.22)。在次要结局中,无论基线LDL-C水平如何,联合治疗组1年、2年和3年达到LDL-C<70mg/dL的比例更高。
在动脉粥样硬化性心血管疾病(ASCVD)患者中,中等强度他汀类药物联合依折麦布治疗在较高和较低基线LDL-C水平下对3年心血管复合结局的影响无异质性。