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不同强度和剂量他汀类药物对急性心肌梗死患者致糖尿病作用的差异:一项全国性队列研究。

Different diabetogenic effect of statins according to intensity and dose in patients with acute myocardial infarction: a nationwide cohort study.

机构信息

Division of Cardiology, Department of Internal Medicine, Korea University Guro Hospital, 148, Gurodong-Ro, Guro-Gu, Seoul, 08308, South Korea.

Chonnam National University Hospital, Gwangju, South Korea.

出版信息

Sci Rep. 2024 Aug 21;14(1):19438. doi: 10.1038/s41598-024-67585-7.

DOI:10.1038/s41598-024-67585-7
PMID:39169014
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11339444/
Abstract

Statin is crucial for acute myocardial infarction (AMI) patients. However, the risk of new-onset diabetes mellitus (NODM) associated with statin is a concern. This study aimed to determine the incremental diabetogenic effects of statins according to their intensity and dose in AMI patients undergoing percutaneous coronary intervention (PCI). Among 13,104 patients enrolled in the Korea AMI Registry between 2011 and 2015, 6152 patients without diabetes mellitus (DM) who underwent PCI and received moderate-to-high-intensity atorvastatin and rosuvastatin were selected for the study. The endpoints were NODM and major adverse cardiovascular events (MACE), composite of all-cause mortality, recurrent MI, and revascularization up to 3 years. Among the participants, 3747 and 2405 received moderate- and high-intensity statins, respectively. The Kaplan-Meier curves demonstrated a higher incidence of NODM in patients with high-intensity statins than those with moderate-intensity. High-intensity statin was a significant predictor of NODM after adjusting for other co-variables (HR = 1.316, 95% CI 1.024-1.692; P < 0.032). Higher dose of rosuvastatin was associated with a higher cumulative incidence of NODM, but this dose-dependency was not apparent with atorvastatin. Cumulative incidence of MACE decreased dose-dependently only with atorvastatin. High-intensity statin was associated with a higher cumulative incidence of NODM in AMI patients, and this association was more evident in rosuvastatin. The different diabetogenic effects of the two statins provide supporting evidence for understanding the nuanced nature of statin treatment in relation to NODM.

摘要

他汀类药物对急性心肌梗死(AMI)患者至关重要。然而,与他汀类药物相关的新发糖尿病(NODM)风险令人担忧。本研究旨在确定经皮冠状动脉介入治疗(PCI)的 AMI 患者中,根据他汀类药物的强度和剂量,他汀类药物的致糖尿病作用的增量。在 2011 年至 2015 年间纳入韩国 AMI 登记处的 13104 名患者中,选择了 6152 名无糖尿病(DM)且接受中等至高强度阿托伐他汀和瑞舒伐他汀治疗并接受 PCI 的患者进行研究。终点为 NODM 和主要不良心血管事件(MACE),复合终点为全因死亡率、复发性 MI 和 3 年内血运重建。在参与者中,分别有 3747 人和 2405 人接受了中等强度和高强度他汀类药物治疗。Kaplan-Meier 曲线显示,高强度他汀类药物治疗的患者 NODM 发生率高于中强度他汀类药物治疗的患者。在校正其他协变量后,高强度他汀类药物是 NODM 的显著预测因子(HR=1.316,95%CI 1.024-1.692;P<0.032)。更高剂量的瑞舒伐他汀与 NODM 的累积发生率增加相关,但阿托伐他汀则不然。只有阿托伐他汀的累积 MACE 发生率呈剂量依赖性降低。高强度他汀类药物与 AMI 患者的 NODM 累积发生率增加相关,而这种关联在瑞舒伐他汀中更为明显。两种他汀类药物的不同致糖尿病作用为理解他汀类药物治疗与 NODM 之间的细微差别提供了支持性证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7ef/11339444/e923e0a86ab5/41598_2024_67585_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7ef/11339444/cf1e79c42746/41598_2024_67585_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7ef/11339444/be9d581b416d/41598_2024_67585_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7ef/11339444/52af00b8cb84/41598_2024_67585_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7ef/11339444/e923e0a86ab5/41598_2024_67585_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7ef/11339444/cf1e79c42746/41598_2024_67585_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7ef/11339444/be9d581b416d/41598_2024_67585_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7ef/11339444/52af00b8cb84/41598_2024_67585_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7ef/11339444/e923e0a86ab5/41598_2024_67585_Fig4_HTML.jpg

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BMJ. 2023 Oct 18;383:e075837. doi: 10.1136/bmj-2023-075837.
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New onset diabetes mellitus and cardiovascular outcomes according to statin intensity in patients after drug-eluting stent implantation in Asian patients.亚洲患者药物洗脱支架置入术后依他汀类药物强度发生新发糖尿病与心血管结局
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2019 ESC/EAS Guidelines for the management of dyslipidaemias: lipid modification to reduce cardiovascular risk.
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Arterioscler Thromb Vasc Biol. 2019 Feb;39(2):e38-e81. doi: 10.1161/ATV.0000000000000073.
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