Division of Cardiology, Yokohama City University Medical Center.
YCU Center for Novel and Exploratory Clinical Trials (Y-NEXT), Yokohama City University Hospital.
J Atheroscler Thromb. 2024 Dec 1;31(12):1748-1762. doi: 10.5551/jat.64988. Epub 2024 Jun 15.
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).
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.
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.
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.
在急性冠状动脉综合征(ACS)的二级预防中,早期和强化低密度脂蛋白胆固醇(LDL-C)降低治疗发挥着重要作用,但进一步临床获益的治疗时间仍未确定。本单中心回顾性研究探讨了 ACS 后 LDL-C 轨迹及其与随后心血管事件(CVE)的关系。
在 831 例 ACS 患者中,我们评估了 ACS 后前 2 个月内 LDL-C 降低情况,作为早期干预的指标,并评估了 LDL-C 下 70mg/dl 面积(AOC-70)作为持续强度指标。中位随访时间为 3.0(1.1-5.2)年,随访终点为 CVE,定义为心血管死亡、非致死性心肌梗死、需要血运重建的心绞痛、脑梗死和冠状动脉旁路移植术的复合终点。
通过高强度他汀类药物治疗(91.8%),LDL-C 从基线下降至 ACS 后 2 个月(107±38mg/dl 至 78±25mg/dl,p<0.001),但 LDL-C<70mg/dl 的达标率在 2 个月后仅为 40.2%,此后无显著变化。在随访期间,有 200 例患者发生 CVE。前 2 个月的 LDL-C 降低和接下来 6 个月的 AOC-70 均与随后的 CVE 风险相关(亚 HR [风险比] [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 LDL-C 降低治疗可进一步降低 CVE 风险。
本研究观察到 ACS 后前两个月内实现早期和强化 LDL-C 降低,并在接下来的 6 个月内维持该水平可降低随后的 CVE 风险,提示早期、强化和持续 LDL-C 降低治疗在 ACS 的二级预防中的重要性。