Evaluating the role of PCSK9 inhibitors in reducing cardiovascular events among statin-intolerant patients: a systematic review and meta-analysis

被引:0
作者
Farhan, Muhammad [1 ]
Hussein, Gumana Ashraf [2 ]
Alom, Thuraya [2 ]
Das, Arghadip [3 ]
Durrani, Tooba Ahmed [2 ]
Hayani, Zahraa Mohamed [2 ]
Alkassar, Abdulrahman [1 ]
Oweis, Hala Ashraf [2 ]
Nazir, Muhammad Hashir [4 ]
Dhillon, Damandeep Kaur [5 ]
Servil, Ernst [5 ]
Patel, Tirath [6 ]
机构
[1] Ajman Univ, Coll Med, Ajman, U Arab Emirates
[2] Dubai Med Coll Girls, Dubai, U Arab Emirates
[3] Nilratan Sircar Med Coll & Hosp, Kolkata, India
[4] King Edward Med Univ, Lahore, Pakistan
[5] St James Sch Med, Arnos Vale, St Vincent
[6] Trinity Med Sci Univ, Sch Med, Ribishi, St Vincent
关键词
cardiovascular risk; LDL-C reduction; lipid-lowering therapy; major adverse cardiovascular events (MACE); PCSK9; inhibitors; statin intolerance; MONOCLONAL-ANTIBODY; PATIENTS DESIGN; RISK-FACTORS; DOUBLE-BLIND; ALIROCUMAB; RATIONALE; EFFICACY; EVOLOCUMAB; EZETIMIBE; SAFETY;
D O I
10.1097/MS9.0000000000002927
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:891 / 899
页数:9
相关论文
共 50 条
[31]   Effect of a Monoclonal Antibody to PCSK9 on Low-Density Lipoprotein Cholesterol Levels in Statin-Intolerant Patients The GAUSS Randomized Trial [J].
Sullivan, David ;
Olsson, Anders G. ;
Scott, Rob ;
Kim, Jae B. ;
Xue, Allen ;
Gebski, Val ;
Wasserman, Scott M. ;
Stein, Evan A. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2012, 308 (23) :2497-2506
[32]   Efficacy and Safety of PCSK9 Monoclonal Antibodies in Patients at High Cardiovascular Risk: An Updated Systematic Review and Meta-Analysis of 32 Randomized Controlled Trials [J].
Mu, Guangyan ;
Xiang, Qian ;
Zhou, Shuang ;
Liu, Zhiyan ;
Qi, Litong ;
Jiang, Jie ;
Gong, Yanjun ;
Xie, Qiufen ;
Wang, Zining ;
Zhang, Hanxu ;
Huo, Yong ;
Cui, Yimin .
ADVANCES IN THERAPY, 2020, 37 (04) :1496-1521
[33]   Cost-effectiveness analysis of PCSK9 inhibitors in cardiovascular diseases: a systematic review [J].
Azari, Samad ;
Rezapour, Aziz ;
Omidi, Negar ;
Alipour, Vahid ;
Behzadifar, Masoud ;
Safari, Hossein ;
Tajdini, Masih ;
Bragazzi, Nicola Luigi .
HEART FAILURE REVIEWS, 2020, 25 (06) :1077-1088
[34]   Neurocognitive Impairment in Cardiovascular Disease Patients Taking Statins Versus Proprotein Convertase Subtilisin/Kexin Type 9 (PCSK9) Inhibitors: A Systematic Review [J].
Shahid, Rabia ;
Naik, Shaili S. ;
Ramphall, Shivana ;
Rijal, Swarnima ;
Prakash, Vishakh ;
Ekladios, Heba ;
Saju, Jiya Mulayamkuzhiyil ;
Mandal, Naishal ;
Kham, Nang I. ;
Hamid, Pousette .
CUREUS JOURNAL OF MEDICAL SCIENCE, 2022, 14 (10)
[35]   Early administration of proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors in patients with acute coronary syndrome: a systematic review and meta-analysis [J].
Hosseini, Kaveh ;
Soleimani, Hamidreza ;
Maleki, Saba ;
Nasrollahizadeh, Amir ;
Tayebi, Sima ;
Nelson, John ;
Heffron, Sean P. .
BMC CARDIOVASCULAR DISORDERS, 2024, 24 (01)
[36]   Therapeutic efficacy and safety of PCSK9-monoclonal antibodies on familial hypercholesterolemia and statin-intolerant patients: A meta-analysis of 15 randomized controlled trials [J].
Qian, Li Jun ;
Gao, Yao ;
Zhang, Yan Mei ;
Chu, Ming ;
Yao, Jing ;
Xu, Di .
SCIENTIFIC REPORTS, 2017, 7
[37]   A Bayesian network meta-analysis of PCSK9 inhibitors, statins and ezetimibe with or without statins for cardiovascular outcomes [J].
Khan, Safi U. ;
Talluri, Swapna ;
Riaz, Haris ;
Rahman, Hammad ;
Nasir, Fahad ;
Bin Riaz, Irbaz ;
Sattur, Sudhakar ;
Ahmed, Haitham ;
Kaluski, Edo ;
Krasuski, Richard .
EUROPEAN JOURNAL OF PREVENTIVE CARDIOLOGY, 2018, 25 (08) :844-853
[38]   Efficacy and safety of alirocumab, a monoclonal antibody to PCSK9, in statin-intolerant patients: Design and rationale of ODYSSEY ALTERNATIVE, a randomized phase 3 trial [J].
Moriarty, Patrick M. ;
Jacobson, Terry A. ;
Bruckert, Eric ;
Thompson, Paul D. ;
Guyton, John R. ;
Baccara-Dinet, Marie T. ;
Gipe, Daniel .
JOURNAL OF CLINICAL LIPIDOLOGY, 2014, 8 (06) :554-561
[39]   Effects of PCSK9 inhibitors on LDL cholesterol, cardiovascular morbidity and all-cause mortality: a systematic review and meta-analysis of randomized controlled trials [J].
Dicembrini, I. ;
Giannini, S. ;
Ragghianti, B. ;
Mannucci, E. ;
Monami, M. .
JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, 2019, 42 (09) :1029-1039
[40]   Meta-analysis of clinical outcomes of PCSK9 modulators in patients with established ASCVD [J].
Talasaz, Azita H. ;
Ho, Ai-Chen ;
Bhatty, Fawzia ;
Koenig, Rachel A. ;
Dixon, Dave L. ;
Baker, William L. ;
Van Tassell, Benjamin W. .
PHARMACOTHERAPY, 2021, 41 (12) :1009-1023