Muhammad Farhan, Gumana Ashraf Hussein, Thuraya Alom, Arghadip Das, Tooba Ahmed Durrani, Zahraa Mohamed Hayani, Abdulrahman Alkassar, Hala Ashraf Oweis, Muhammad Hashir Nazir, Damandeep Kaur Dhillon, Ernst Servil, Tirath Patel
{"title":"评估PCSK9抑制剂在降低他汀不耐受患者心血管事件中的作用:一项系统综述和荟萃分析","authors":"Muhammad Farhan, Gumana Ashraf Hussein, Thuraya Alom, Arghadip Das, Tooba Ahmed Durrani, Zahraa Mohamed Hayani, Abdulrahman Alkassar, Hala Ashraf Oweis, Muhammad Hashir Nazir, Damandeep Kaur Dhillon, Ernst Servil, Tirath Patel","doi":"10.1097/MS9.0000000000002927","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>To assess the efficacy and safety of Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) inhibitors in reducing major adverse cardiovascular events (MACE) in statin-intolerant patients, focusing on low-density lipoprotein cholesterol (LDL-C) reduction and cardiovascular outcomes.</p><p><strong>Methods: </strong>A systematic review and meta-analysis were conducted according to the PRISMA guidelines. Randomised control trails (RCTs) and observational studies from PubMed, Cochrane Library, and Web of Science databases were included. Independent reviewers extracted the data, and the analyses were performed using fixed- and random-effects models. Heterogeneity was evaluated using the I<sup>2</sup> statistic and publication bias was assessed using Egger's test.</p><p><strong>Results: </strong>Fifteen studies involving 69-18 924 participants were included. PCSK9 inhibitors reduced LDL-C levels by 50-70% and lowered the risk of MACE by 12% (OR 0.88). Minimal heterogeneity (I<sup>2</sup> = 0%) indicated consistency across studies. Subgroup analysis showed greater efficacy in high-risk populations (e.g., acute coronary syndrome and familial hypercholesterolemia). Adverse events were mild, with minimal muscle-related side effects.</p><p><strong>Conclusion: </strong>PCSK9 inhibitors are effective and safe alternatives for LDL-C reduction and cardiovascular risk mitigation in patients with statin intolerance. Their efficacy, favorable safety profile, and consistency across studies highlight their potential for managing dyslipidemia, particularly in high-risk groups. Further research on long-term outcomes is required.</p>","PeriodicalId":8025,"journal":{"name":"Annals of Medicine and Surgery","volume":"87 2","pages":"891-899"},"PeriodicalIF":1.7000,"publicationDate":"2025-01-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11918597/pdf/","citationCount":"0","resultStr":"{\"title\":\"Evaluating the role of PCSK9 inhibitors in reducing cardiovascular events among statin-intolerant patients: a systematic review and meta-analysis.\",\"authors\":\"Muhammad Farhan, Gumana Ashraf Hussein, Thuraya Alom, Arghadip Das, Tooba Ahmed Durrani, Zahraa Mohamed Hayani, Abdulrahman Alkassar, Hala Ashraf Oweis, Muhammad Hashir Nazir, Damandeep Kaur Dhillon, Ernst Servil, Tirath Patel\",\"doi\":\"10.1097/MS9.0000000000002927\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>To assess the efficacy and safety of Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) inhibitors in reducing major adverse cardiovascular events (MACE) in statin-intolerant patients, focusing on low-density lipoprotein cholesterol (LDL-C) reduction and cardiovascular outcomes.</p><p><strong>Methods: </strong>A systematic review and meta-analysis were conducted according to the PRISMA guidelines. Randomised control trails (RCTs) and observational studies from PubMed, Cochrane Library, and Web of Science databases were included. Independent reviewers extracted the data, and the analyses were performed using fixed- and random-effects models. Heterogeneity was evaluated using the I<sup>2</sup> statistic and publication bias was assessed using Egger's test.</p><p><strong>Results: </strong>Fifteen studies involving 69-18 924 participants were included. PCSK9 inhibitors reduced LDL-C levels by 50-70% and lowered the risk of MACE by 12% (OR 0.88). Minimal heterogeneity (I<sup>2</sup> = 0%) indicated consistency across studies. Subgroup analysis showed greater efficacy in high-risk populations (e.g., acute coronary syndrome and familial hypercholesterolemia). Adverse events were mild, with minimal muscle-related side effects.</p><p><strong>Conclusion: </strong>PCSK9 inhibitors are effective and safe alternatives for LDL-C reduction and cardiovascular risk mitigation in patients with statin intolerance. Their efficacy, favorable safety profile, and consistency across studies highlight their potential for managing dyslipidemia, particularly in high-risk groups. Further research on long-term outcomes is required.</p>\",\"PeriodicalId\":8025,\"journal\":{\"name\":\"Annals of Medicine and Surgery\",\"volume\":\"87 2\",\"pages\":\"891-899\"},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2025-01-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11918597/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Annals of Medicine and Surgery\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1097/MS9.0000000000002927\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/2/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q2\",\"JCRName\":\"MEDICINE, GENERAL & INTERNAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of Medicine and Surgery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1097/MS9.0000000000002927","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0
摘要
目的:评价Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9)抑制剂降低他汀类药物不耐受患者主要不良心血管事件(MACE)的有效性和安全性,重点关注低密度脂蛋白胆固醇(LDL-C)降低和心血管结局。方法:根据PRISMA指南进行系统评价和荟萃分析。纳入了PubMed、Cochrane图书馆和Web of Science数据库中的随机对照试验(rct)和观察性研究。独立审稿人提取数据,并使用固定效应和随机效应模型进行分析。异质性采用I2统计量评估,发表偏倚采用Egger检验评估。结果:纳入15项研究,涉及69- 18924名受试者。PCSK9抑制剂降低LDL-C水平50-70%,MACE风险降低12% (OR 0.88)。最小异质性(I2 = 0%)表明研究间的一致性。亚组分析显示对高危人群(如急性冠状动脉综合征和家族性高胆固醇血症)更有效。不良事件轻微,与肌肉相关的副作用最小。结论:PCSK9抑制剂是他汀类药物不耐受患者降低LDL-C和心血管风险的有效且安全的替代方案。它们的有效性、良好的安全性和研究的一致性突出了它们在治疗血脂异常方面的潜力,特别是在高危人群中。需要对长期结果进行进一步研究。
Evaluating the role of PCSK9 inhibitors in reducing cardiovascular events among statin-intolerant patients: a systematic review and meta-analysis.
Objective: To assess the efficacy and safety of Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) inhibitors in reducing major adverse cardiovascular events (MACE) in statin-intolerant patients, focusing on low-density lipoprotein cholesterol (LDL-C) reduction and cardiovascular outcomes.
Methods: A systematic review and meta-analysis were conducted according to the PRISMA guidelines. Randomised control trails (RCTs) and observational studies from PubMed, Cochrane Library, and Web of Science databases were included. Independent reviewers extracted the data, and the analyses were performed using fixed- and random-effects models. Heterogeneity was evaluated using the I2 statistic and publication bias was assessed using Egger's test.
Results: Fifteen studies involving 69-18 924 participants were included. PCSK9 inhibitors reduced LDL-C levels by 50-70% and lowered the risk of MACE by 12% (OR 0.88). Minimal heterogeneity (I2 = 0%) indicated consistency across studies. Subgroup analysis showed greater efficacy in high-risk populations (e.g., acute coronary syndrome and familial hypercholesterolemia). Adverse events were mild, with minimal muscle-related side effects.
Conclusion: PCSK9 inhibitors are effective and safe alternatives for LDL-C reduction and cardiovascular risk mitigation in patients with statin intolerance. Their efficacy, favorable safety profile, and consistency across studies highlight their potential for managing dyslipidemia, particularly in high-risk groups. Further research on long-term outcomes is required.