院内埃沃洛单抗治疗对急性心肌梗死患者脂蛋白(a)的影响:一项回顾性队列研究和倾向评分匹配分析。

Q4 Medicine
Cardiology Plus Pub Date : 2023-01-01 Epub Date: 2023-04-27 DOI:10.1097/CP9.0000000000000036
Ge Gao, Tao Zheng, Beidi Lan, Weiying Hui, Shi Chen, Zuyi Yuan, Yue Wu, John Y L Chiang, Tao Chen
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引用次数: 1

摘要

脂蛋白(a)升高与动脉粥样硬化性心血管疾病的风险增加有关。Evolocumab是一种前蛋白转化酶枯草杆菌蛋白酶/kexin 9型抑制剂,已被证明可降低脂蛋白(a)。然而,埃沃洛单抗对急性心肌梗死(AMI)患者脂蛋白(a)的影响研究很少。本研究旨在研究急性心肌梗死患者在依沃洛单抗治疗下脂蛋白(a)的变化 mg每2周)加他汀类药物(20 mg阿托伐他汀或10 mg瑞舒伐他汀/天),其余335人仅接受他汀类药物治疗。比较两组在随访1个月时的血脂情况。基于年龄、性别和基线脂蛋白(A),使用0.02卡尺以1:1的比例进行倾向评分匹配分析。结果:在1个月的随访中,埃沃洛单抗联合他汀类药物组的脂蛋白(a)水平从27.0(17.5,50.6)mg/dL降至20.9(9.4,52.5)mg/dL,但仅他汀类药物的组从24.5(13.2,41.1)mg/d升至27.9(14.8,58.6)mg/d。倾向评分匹配分析包括262名患者(每组131名)。在倾向评分匹配队列的亚组分析中,根据基线脂蛋白(a)在20和50的临界值进行分层 脂蛋白(a)的绝对变化为-4.9(-8.5,-1.3),-5.0(-13.9,1.9),-0.2(-9.9,16.9)mg/dL,在埃沃洛单抗加他汀类药物组的三个亚组中,以及在仅他汀类药物的组中,0.9(-1.7,5.5),10.7(4.6,21.9),12.2(2.9,35.6)mg/dL。与仅他汀类药物组相比,埃沃洛单抗联合他汀类药物在所有亚组中1个月时的脂蛋白(a)水平均较低(P<0.05)。无论基线脂蛋白(a)水平如何,Evolocumab联合他汀类药物治疗均可抑制仅他汀类药物疗法中脂蛋白(a)的增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Effect of in-hospital evolocumab therapy on lipoprotein(a) in patients with acute myocardial infarction: a retrospective cohort study and a propensity score matching analysis.

Effect of in-hospital evolocumab therapy on lipoprotein(a) in patients with acute myocardial infarction: a retrospective cohort study and a propensity score matching analysis.

Effect of in-hospital evolocumab therapy on lipoprotein(a) in patients with acute myocardial infarction: a retrospective cohort study and a propensity score matching analysis.

Effect of in-hospital evolocumab therapy on lipoprotein(a) in patients with acute myocardial infarction: a retrospective cohort study and a propensity score matching analysis.

Elevated lipoprotein(a) is associated with an increased risk of atherosclerotic cardiovascular disease. Evolocumab, a proprotein convertase subtilisin/kexin type 9 inhibitor, has been shown to reduce lipoprotein(a). However, the effect of evolocumab on lipoprotein(a) in patients with acute myocardial infarction (AMI) is poorly studied. This study aims to investigate the change in lipoprotein(a) under evolocumab therapy in patients with AMI.

Methods: This retrospective cohort analysis included a total of 467 AMI patients with LDL-C level >2.6 mmol/L upon admission, among whom 132 received in-hospital evolocumab (140 mg every 2 weeks) plus statin (20 mg atorvastatin or 10 mg rosuvastatin per day) and the remaining 335 received statin only. Lipid profiles at 1-month follow-up were compared between the two groups. A propensity score matching analysis was also conducted based on age, sex, and baseline lipoprotein(a) at a 1:1 ratio using a 0.02 caliper.

Results: At the 1-month follow-up, the lipoprotein(a) level decreased from 27.0 (17.5, 50.6) mg/dL to 20.9 (9.4, 52.5) mg/dL in evolocumab plus statin group, but increased from 24.5 (13.2, 41.1) mg/dL to 27.9 (14.8, 58.6) mg/dL in statin only group. The propensity score matching analysis included 262 patients (131 in each group). In subgroup analysis of the propensity score matching cohort stratified by the baseline lipoprotein(a) at cutoff values of 20 and 50 mg/dL, the absolute change in lipoprotein(a) was -4.9 (-8.5, -1.3), -5.0 (-13.9, 1.9), -0.2 (-9.9, 16.9) mg/dL in three subgroups in evolocumab plus statin group, and 0.9 (-1.7, 5.5), 10.7 (4.6, 21.9), 12.2 (2.9, 35.6) mg/dL in three subgroups in statin only group. In comparison to statin only group, evolocumab plus statin group had lower lipoprotein(a) level at 1 month in all subgroups (P < 0.05).

Conclusions: In-hospital initiation of evolocumab on a background statin therapy reduced lipoprotein(a) level at 1-month follow-up in patients with AMI. Evolocumab plus statin therapy inhibited the increase in lipoprotein(a) in statin only therapy, regardless of the baseline lipoprotein(a) level.

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