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PCSK‐9 Inhibitors Can Significantly Improve the Coronary Slow Flow Caused by Elevated Lipoprotein (a) in ST‐Elevation Myocardial Infarction Patients With Chronic Kidney Disease

医学 传统PCI 内科学 经皮冠状动脉介入治疗 心脏病学 心肌梗塞 肾脏疾病 脂蛋白(a) 冠状动脉疾病 脂蛋白 胆固醇
作者
Hao Xu,Ziqing Wang,Dan Chen,H Zhang,Junhua Ge,Jian Li
出处
期刊:Catheterization and Cardiovascular Interventions [Wiley]
标识
DOI:10.1002/ccd.31543
摘要

ABSTRACT Background Coronary slow flow and no reflow significantly predict poor prognosis in acute myocardial infarction (AMI) patients, especially those with chronic kidney disease (CKD). Early identification of factors contributing to these conditions can mitigate ischemic events and improve outcomes. Aims This study aimed to investigate the association between elevated lipoprotein (a) [Lp(a)] levels and proprotein convertase subtilisin/kexin Type 9 (PCSK‐9) inhibitor therapy with coronary slow flow or no reflow after percutaneous coronary intervention (PCI) in AMI patients with CKD. Methods A total of 323 ST‐elevation myocardial infarction (STEMI) patients who underwent PCI between October 2017 and June 2023 were included. Patients were divided into CKD ( n = 132) and non‐CKD ( n = 191) groups. Lp(a) levels and the prevalence of coronary slow flow or no reflow after PCI were evaluated. STEMI patients with CKD were further categorized into elevated Lp(a) ( n = 81) and normal Lp(a) ( n = 51) subgroups. Logistic analysis identified risk factors for coronary slow flow/no reflow after PCI. The impact of PCSK‐9 inhibitors on outcomes was also assessed in the elevated Lp(a) subgroup. Results STEMI patients with CKD had significantly higher Lp(a) levels compared to those without CKD (median 36.75 vs. 15.90 mg/dL, p = 0.0001). CKD patients with elevated Lp(a) had a higher prevalence of coronary slow flow/no reflow after PCI than those with normal Lp(a) (38.3% vs. 13.7%, p = 0.002). Logistic regression analysis identified elevated Lp(a) as an independent risk factor for slow flow/no reflow after PCI in STEMI patients with CKD (OR = 2.985, p = 0.027). In CKD patients with elevated Lp(a), PCSK‐9 inhibitors significantly improved post‐PCI coronary flow and reduced composite cardiovascular events during 1‐year follow‐up (22.2% vs. 51.1%, p = 0.008). Conclusions Elevated Lp(a) is an independent risk factor for coronary slow flow or no reflow after PCI in STEMI patients with CKD. PCSK‐9 inhibitors improve coronary blood flow and reduce cardiovascular events in these patients.
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