André Saad Cleto, João Matheus Schirlo, Janete Machozeki, Camila Marinelli Martins
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引用次数: 0
Abstract
Introduction: The PCSK9 enzyme is present mainly in the liver and is responsible for the degradation of LDL-C receptors. Currently, there are some drugs that inhibit this enzyme, such as alirocumab and evolocumab. Consequently, these drugs reduce serum LDL-C levels. Therefore, a systematic review and a meta-analysis were carried out in order to compare alirocumab against evolocumab in reducing cardiovascular outcomes.
Methods: This systematic review was carried out in accordance with PRISMA and was registered in PROSPERO (CRD42024573217). The following databases were searched on July, 9, 2024: Pubmed, Web of Science and Scopus. Randomized clinical trials with a control group were included and meta-analyses were performed to assess relative risk (RR). The random effects model was used in heterogeneous samples. The articles were distributed into 2 subgroups: use of alirocumab and evolocumab.
Results: Initially, 2,213 articles were found, of which 6 were included. In total, 62,119 patients participated. The RR values were significant for alirocumab in the following outcomes: myocardial infarction (MI) 0.85 (95% CI 0.77-0.93), stroke 0.75 (95% CI 0.60-0.94) and hospitalization for unstable angina 0.58 (95% CI 0.39-0.86), while for evolocumab they were significant for MI 0.75 (95% CI 0.68-0.83) and coronary revascularization 0.81 (95 CI % 0.75-0.88). There was a statistically significant difference between the drugs for hospitalization for unstable angina (p=0.02).
Discussion: This study highlights the benefits of PCSK9 inhibitors, especially alirocumab, in reducing major cardiovascular events. Alirocumab significantly lowered hospitalizations for unstable angina, with a 42% reduction, and showed favorable outcomes in reducing myocardial infarction, coronary revascularization, and stroke. These reductions are clinically meaningful, as they lower morbidity, improve patient quality of life, and reduce healthcare costs. Both alirocumab and evolocumab are effective and safe, offering important therapeutic options for high-risk cardiovascular patients.
Conclusion: The use of alirocumab is preferable if the focus is to avoid hospitalizations for unstable angina or stroke, while evolocumab may be an option if one wants to avoid coronary revascularization. Both drugs are effective in reducing cardiovascular outcomes, but alirocumab was superior to evolocumab.
PCSK9酶主要存在于肝脏中,负责LDL-C受体的降解。目前,有一些药物可以抑制这种酶,如alirocumab和evolocumab。因此,这些药物降低了血清LDL-C水平。因此,进行了系统评价和荟萃分析,以比较alirocumab和evolocumab在降低心血管结局方面的作用。方法:本系统评价按照PRISMA进行,注册号为PROSPERO (CRD42024573217)。在2024年7月9日检索了以下数据库:Pubmed, Web of Science和Scopus。随机临床试验纳入对照组,并进行meta分析以评估相对风险(RR)。随机效应模型用于异质样本。文章被分为2个亚组:使用alirocumab和evolocumab。结果:最初共发现2213篇文献,其中6篇被纳入。总共有62119名患者参与了研究。alirocumab在以下结果中的RR值具有显著性:心肌梗死(MI) 0.85 (95% CI 0.77-0.93),卒中0.75 (95% CI 0.60-0.94),不稳定心绞痛住院0.58 (95% CI 0.39-0.86),而evolocumab在MI 0.75 (95% CI 0.68-0.83)和冠状动脉血运重建术0.81 (95 CI % 0.75-0.88)方面具有显著性。不稳定型心绞痛住院用药差异有统计学意义(p=0.02)。讨论:该研究强调了PCSK9抑制剂,特别是alirocumab在减少主要心血管事件方面的益处。Alirocumab显著降低了不稳定心绞痛的住院率,减少了42%,并在减少心肌梗死、冠状动脉血运重建术和卒中方面显示出良好的结果。这些减少具有临床意义,因为它们降低了发病率,提高了患者的生活质量,并降低了医疗保健成本。alirocumab和evolocumab均有效且安全,为高危心血管患者提供了重要的治疗选择。结论:如果重点是避免因不稳定心绞痛或中风住院,使用alirocumab是可取的,而如果希望避免冠状动脉血运重建术,则可以选择evolocumab。两种药物都能有效降低心血管疾病的预后,但alirocumab优于evolocumab。
期刊介绍:
Current Cardiology Reviews publishes frontier reviews of high quality on all the latest advances on the practical and clinical approach to the diagnosis and treatment of cardiovascular disease. All relevant areas are covered by the journal including arrhythmia, congestive heart failure, cardiomyopathy, congenital heart disease, drugs, methodology, pacing, and preventive cardiology. The journal is essential reading for all researchers and clinicians in cardiology.