{"title":"外周动脉疾病中的 PCSK9 抑制剂:疗效、安全性和结果综述","authors":"","doi":"10.1016/j.ajpc.2024.100800","DOIUrl":null,"url":null,"abstract":"<div><h3>Therapeutic Area</h3><div>Peripheral Artery Disease</div></div><div><h3>Background</h3><div>Peripheral artery disease (PAD) is a debilitating condition characterized by atherosclerosis in the peripheral arteries, affecting approximately 200 million people worldwide. Current treatment options for PAD, such as statins, have limitations in terms of efficacy and tolerability. Proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors have shown promise in reducing cardiovascular events in hypercholesterolemic patients. This review focuses on the efficacy, safety, and clinical outcomes of PCSK9 inhibitors in PAD based on recent trials and literature.</div></div><div><h3>Methods</h3><div>A comprehensive literature search was conducted using PubMed to identify relevant trials and studies evaluating PCSK9 inhibitors in PAD patients. Key trials including FOURIER and ODYSSEY were analyzed for efficacy in reducing LDL cholesterol levels and cardiovascular events, including myocardial infarction, stroke, coronary revascularization, and major adverse limb events. Safety data was compiled from multiple trials. Cost-effectiveness studies were also reviewed.</div></div><div><h3>Results</h3><div>The FOURIER trial demonstrated that evolocumab significantly reduced LDL cholesterol by 59% (p<0.001) and the risk of cardiovascular events (HR 0.85; 95% CI, 0.79 to 0.92; p<0.001) in PAD patients at 48 weeks. The ODYSSEY trial showed similar LDL reductions of 55% at 4 months and 63% at 48 months with alirocumab. Injection site reactions were the most common adverse event in safety evaluations (evolocumab 2.1% vs placebo 1.6%). Despite high costs (incremental cost-effectiveness ratios >$500,000 per QALY in some analyses), PCSK9 inhibitors may be cost-effective in specific high-risk populations.</div></div><div><h3>Conclusions</h3><div>PCSK9 inhibitors demonstrate significant efficacy in lowering LDL cholesterol and reducing cardiovascular events in PAD patients, with a favorable safety profile. However, cost remains a barrier to widespread utilization. Current PAD treatment guidelines do not yet incorporate PCSK9 inhibitors. Further research is needed on long-term outcomes, cost-effectiveness, and the role of PCSK9 inhibitors in the context of current PAD management. PCSK9 inhibitors represent a promising therapeutic option for select high-risk PAD patients not at goal with statins alone.</div></div>","PeriodicalId":72173,"journal":{"name":"American journal of preventive cardiology","volume":null,"pages":null},"PeriodicalIF":4.3000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"PCSK9 INHIBITORS IN PERIPHERAL ARTERY DISEASE: REVIEW OF EFFICACY, SAFETY, AND OUTCOMES\",\"authors\":\"\",\"doi\":\"10.1016/j.ajpc.2024.100800\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Therapeutic Area</h3><div>Peripheral Artery Disease</div></div><div><h3>Background</h3><div>Peripheral artery disease (PAD) is a debilitating condition characterized by atherosclerosis in the peripheral arteries, affecting approximately 200 million people worldwide. Current treatment options for PAD, such as statins, have limitations in terms of efficacy and tolerability. Proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors have shown promise in reducing cardiovascular events in hypercholesterolemic patients. This review focuses on the efficacy, safety, and clinical outcomes of PCSK9 inhibitors in PAD based on recent trials and literature.</div></div><div><h3>Methods</h3><div>A comprehensive literature search was conducted using PubMed to identify relevant trials and studies evaluating PCSK9 inhibitors in PAD patients. Key trials including FOURIER and ODYSSEY were analyzed for efficacy in reducing LDL cholesterol levels and cardiovascular events, including myocardial infarction, stroke, coronary revascularization, and major adverse limb events. Safety data was compiled from multiple trials. Cost-effectiveness studies were also reviewed.</div></div><div><h3>Results</h3><div>The FOURIER trial demonstrated that evolocumab significantly reduced LDL cholesterol by 59% (p<0.001) and the risk of cardiovascular events (HR 0.85; 95% CI, 0.79 to 0.92; p<0.001) in PAD patients at 48 weeks. The ODYSSEY trial showed similar LDL reductions of 55% at 4 months and 63% at 48 months with alirocumab. Injection site reactions were the most common adverse event in safety evaluations (evolocumab 2.1% vs placebo 1.6%). Despite high costs (incremental cost-effectiveness ratios >$500,000 per QALY in some analyses), PCSK9 inhibitors may be cost-effective in specific high-risk populations.</div></div><div><h3>Conclusions</h3><div>PCSK9 inhibitors demonstrate significant efficacy in lowering LDL cholesterol and reducing cardiovascular events in PAD patients, with a favorable safety profile. However, cost remains a barrier to widespread utilization. Current PAD treatment guidelines do not yet incorporate PCSK9 inhibitors. Further research is needed on long-term outcomes, cost-effectiveness, and the role of PCSK9 inhibitors in the context of current PAD management. PCSK9 inhibitors represent a promising therapeutic option for select high-risk PAD patients not at goal with statins alone.</div></div>\",\"PeriodicalId\":72173,\"journal\":{\"name\":\"American journal of preventive cardiology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.3000,\"publicationDate\":\"2024-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"American journal of preventive cardiology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2666667724001685\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CARDIAC & CARDIOVASCULAR SYSTEMS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"American journal of preventive cardiology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666667724001685","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CARDIAC & CARDIOVASCULAR SYSTEMS","Score":null,"Total":0}
引用次数: 0
摘要
治疗领域外周动脉疾病背景外周动脉疾病(PAD)是一种以外周动脉粥样硬化为特征的使人衰弱的疾病,影响着全球约 2 亿人。他汀类药物等目前治疗 PAD 的方法在疗效和耐受性方面都有局限性。Proprotein convertase subtilisin/kexin type 9 (PCSK9) 抑制剂有望减少高胆固醇血症患者的心血管事件。本综述基于最近的试验和文献,重点讨论 PCSK9 抑制剂在 PAD 中的疗效、安全性和临床结果。方法使用 PubMed 进行了全面的文献检索,以确定评估 PCSK9 抑制剂在 PAD 患者中应用的相关试验和研究。分析了包括 FOURIER 和 ODYSSEY 在内的主要试验在降低低密度脂蛋白胆固醇水平和心血管事件(包括心肌梗死、中风、冠状动脉血运重建和肢体主要不良事件)方面的疗效。安全性数据来自多项试验。结果FOURIER试验表明,48周时,evolocumab能显著降低PAD患者59%的低密度脂蛋白胆固醇(p<0.001)和心血管事件风险(HR 0.85; 95% CI, 0.79 to 0.92; p<0.001)。ODYSSEY试验显示,阿利珠单抗在4个月和48个月时的低密度脂蛋白降幅相似,分别为55%和63%。在安全性评估中,注射部位反应是最常见的不良事件(evolocumab 2.1%,安慰剂 1.6%)。结论PCSK9抑制剂在降低PAD患者低密度脂蛋白胆固醇和减少心血管事件方面疗效显著,且安全性良好。然而,成本仍然是广泛使用的障碍。目前的 PAD 治疗指南尚未纳入 PCSK9 抑制剂。还需要进一步研究PCSK9抑制剂的长期疗效、成本效益以及在当前PAD治疗中的作用。PCSK9 抑制剂是一种很有前景的治疗选择,适用于部分单用他汀类药物达不到治疗目标的高风险 PAD 患者。
PCSK9 INHIBITORS IN PERIPHERAL ARTERY DISEASE: REVIEW OF EFFICACY, SAFETY, AND OUTCOMES
Therapeutic Area
Peripheral Artery Disease
Background
Peripheral artery disease (PAD) is a debilitating condition characterized by atherosclerosis in the peripheral arteries, affecting approximately 200 million people worldwide. Current treatment options for PAD, such as statins, have limitations in terms of efficacy and tolerability. Proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors have shown promise in reducing cardiovascular events in hypercholesterolemic patients. This review focuses on the efficacy, safety, and clinical outcomes of PCSK9 inhibitors in PAD based on recent trials and literature.
Methods
A comprehensive literature search was conducted using PubMed to identify relevant trials and studies evaluating PCSK9 inhibitors in PAD patients. Key trials including FOURIER and ODYSSEY were analyzed for efficacy in reducing LDL cholesterol levels and cardiovascular events, including myocardial infarction, stroke, coronary revascularization, and major adverse limb events. Safety data was compiled from multiple trials. Cost-effectiveness studies were also reviewed.
Results
The FOURIER trial demonstrated that evolocumab significantly reduced LDL cholesterol by 59% (p<0.001) and the risk of cardiovascular events (HR 0.85; 95% CI, 0.79 to 0.92; p<0.001) in PAD patients at 48 weeks. The ODYSSEY trial showed similar LDL reductions of 55% at 4 months and 63% at 48 months with alirocumab. Injection site reactions were the most common adverse event in safety evaluations (evolocumab 2.1% vs placebo 1.6%). Despite high costs (incremental cost-effectiveness ratios >$500,000 per QALY in some analyses), PCSK9 inhibitors may be cost-effective in specific high-risk populations.
Conclusions
PCSK9 inhibitors demonstrate significant efficacy in lowering LDL cholesterol and reducing cardiovascular events in PAD patients, with a favorable safety profile. However, cost remains a barrier to widespread utilization. Current PAD treatment guidelines do not yet incorporate PCSK9 inhibitors. Further research is needed on long-term outcomes, cost-effectiveness, and the role of PCSK9 inhibitors in the context of current PAD management. PCSK9 inhibitors represent a promising therapeutic option for select high-risk PAD patients not at goal with statins alone.