用于急性冠状动脉综合征二级预防的早期、强化和持续降脂疗法。

IF 3 2区 医学 Q2 PERIPHERAL VASCULAR DISEASE Journal of atherosclerosis and thrombosis Pub Date : 2024-06-15 DOI:10.5551/jat.64988
Kozo Okada, Tatsuya Haze, Shinnosuke Kikuchi, Hidekuni Kirigaya, Yohei Hanajima, Katsuhiko Tsutsumi, Jin Kirigaya, Hidefumi Nakahashi, Masaomi Gohbara, Yuichiro Kimura, Masami Kosuge, Toshiaki Ebina, Teruyasu Sugano, Kiyoshi Hibi
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引用次数: 0

摘要

目的:早期强化降低低密度脂蛋白(LDL-C)治疗在急性冠状动脉综合征(ACS)的二级预防中发挥着重要作用,但进一步临床获益的治疗期仍未确定。这项单中心回顾性研究探讨了急性冠状动脉综合征后低密度脂蛋白胆固醇的变化轨迹及其与后续心血管事件(CVE)的关系:在 831 名 ACS 患者中,我们评估了 ACS 后前 2 个月的 LDL-C 降幅,以此作为早期干预的指标,并评估了未来 6 个月以 70 mg/dl 为临界值的 LDL-C 曲线面积(AOC-70),以此作为持续强度指标。对患者进行了中位数为 3.0(1.1-5.2)年的 CVE 随访,CVE 被定义为心血管死亡、非致死性心肌梗死、需要血管重建的心绞痛、脑梗死和冠状动脉旁路移植术的综合结果:通过高强度他汀类药物处方(91.8%),低密度脂蛋白胆固醇从基线降至 ACS 后 2 个月(107±38 mg/dl 至 78±25 mg/dl,p<0.001),而 2 个月时低密度脂蛋白胆固醇<70 mg/dl 的达标率仅为 40.2%,此后无显著变化。在随访期间,200 名患者出现了 CVE。头 2 个月的低密度脂蛋白胆固醇降低率和随后 6 个月的 AOC-70 均与随后的 CVE 风险相关(亚 HR [危险比] [95% 置信区间]:1.48 [1.16-1.89] 和 1.22 [1.05-1.44])。此外,早期干预后持续强化降低低密度脂蛋白胆固醇治疗可进一步降低CVE风险:本研究观察到,在 ACS 后的头两个月内实现早期强化降低 LDL-C,并在接下来的 6 个月内保持这一目标,可抑制随后的 CVE 风险,这表明早期、强化和持续降低 LDL-C 治疗在 ACS 二级预防中的重要性。
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Early, Intensive and Persistent Lipid-Lowering Therapy for Secondary Prevention of Acute Coronary Syndrome.

Aim: Early and intensive low-density lipoprotein (LDL-C)-lowering therapy plays important roles in secondary prevention of acute coronary syndrome (ACS), but the treatment period for further clinical benefit remains undefined. This single-center, retrospective study explored LDL-C trajectory after ACS and its associations with subsequent cardiovascular events (CVE).

Methods: In 831 patients with ACS, we evaluated LDL-C reduction during the first 2 months post-ACS as an index of early intervention and the area over the curve for LDL-C using 70 mg/dl as the threshold in the next 6 months (AOC-70) as a persistent intensity index. Patients were followed for a median of 3.0 (1.1-5.2) years for CVE, defined as the composite of cardiovascular death, non-fatal myocardial infarction, angina pectoris requiring revascularization, cerebral infarction, and coronary bypass grafting.

Results: LDL-C decreased from baseline to 2 months post-ACS (107±38 mg/dl to 78±25 mg/dl, p<0.001) through high-intensity statin prescription (91.8%), while achieving rates of LDL-C <70 mg/dl at 2 months remained only 40.2% with no significant changes thereafter. During the follow-up period, CVE occurred in 200 patients. LDL-C reduction during the first 2 months and AOC-70 in the next 6 months were both associated with subsequent CVE risk (sub-HR [hazard ratio] [95% confidence interval]: 1.48 [1.16-1.89] and 1.22 [1.05-1.44]). Furthermore, early intervention followed by persistently intensive LDL-C-lowering therapy resulted in further CVE risk reduction.

Conclusions: The present study observed that achieving early and intensive LDL-C reduction within the first two months after ACS and maintaining it for the next six months suppressed subsequent CVE risk, suggesting the importance of early, intensive, and persistent LDL-C-lowering therapy in the secondary prevention of ACS.

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来源期刊
CiteScore
6.60
自引率
15.90%
发文量
271
审稿时长
1 months
期刊介绍: JAT publishes articles focused on all aspects of research on atherosclerosis, vascular biology, thrombosis, lipid and metabolism.
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