他伐昔单抗治疗中国家族性高胆固醇血症患者的疗效和安全性:随机对照试验的系统评价和荟萃分析

IF 1.6 Q2 MEDICINE, GENERAL & INTERNAL
Annals of Medicine and Surgery Pub Date : 2025-07-22 eCollection Date: 2025-09-01 DOI:10.1097/MS9.0000000000003623
Alaa Ramadan, Ravindra Reddy Gangavarapu, Hina Aziz, Akshat Sinha, Shubh Mehta, Nathan Ezie Kengo
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引用次数: 0

摘要

背景:家族性高胆固醇血症(FH)是一种普遍的遗传性疾病,其特征是低密度脂蛋白胆固醇(LDL-C)水平升高,使个体易患过早的心血管疾病和相关疾病。在许多患者中,传统的治疗方法往往不能达到目标LDL-C水平,因此需要新的治疗方法。Tafolecimab是一种靶向PCSK9的单克隆抗体,通过增强LDL受体循环和LDL- c清除,有望治疗HeFH。目的:通过系统评价和荟萃分析,评价他伐昔单抗治疗中国FH患者的疗效和安全性。方法:本荟萃分析遵循PRISMA指南,并在前瞻性系统评价登记册上注册。在PubMed/MEDLINE、Web of Science、Scopus和Embase数据库中进行了全面的搜索。纳入标准集中于随机对照试验(rct),涉及18-75岁高胆固醇血症和心血管高危患者。数据提取和质量评估由两名审稿人独立完成。采用随机效应模型进行统计分析。结果:纳入4项随机对照试验,共841例中国患者。他伐昔单抗显著降低LDL-C(平均差异[MD]: -2.05; 95% CI: -2.19至-1.90)、载脂蛋白水平(MD: -0.53; 95% CI: -0.56至-0.50)、非hdl - c (MD: -2.19; 95% CI: -2.32至-2.06)和脂蛋白(a)水平(MD: -0.09; 95% CI: -0.11至-0.07)。他伐昔单抗组的不良事件发生率较高(风险比:0.68;95% CI: 0.61, 0.75),但与安慰剂组相比,在严重不良事件、因不良事件而中断治疗、死亡、过敏、肌肉相关问题、上呼吸道问题或肝损害方面没有发现显著差异。结论:他伐昔单抗可有效降低各种脂质参数,提示其在治疗高胆固醇血症和降低心血管风险方面的潜力。虽然不良事件更频繁,但其严重程度与安慰剂没有显著差异。这些发现的普遍性仅限于中国人群,强调需要在不同人群中进行进一步的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Efficacy and safety of tafolecimab in Chinese patients with familial hypercholesterolemia: a systematic review and meta-analysis of randomized controlled trials.

Efficacy and safety of tafolecimab in Chinese patients with familial hypercholesterolemia: a systematic review and meta-analysis of randomized controlled trials.

Efficacy and safety of tafolecimab in Chinese patients with familial hypercholesterolemia: a systematic review and meta-analysis of randomized controlled trials.

Efficacy and safety of tafolecimab in Chinese patients with familial hypercholesterolemia: a systematic review and meta-analysis of randomized controlled trials.

Background: Familial hypercholesterolemia (FH) is a prevalent inherited disorder marked by elevated low-density lipoprotein cholesterol (LDL-C) levels, predisposing individuals to premature cardiovascular disease and related morbidities. Traditional treatments often fail to achieve target LDL-C levels in many patients, necessitating novel therapies. Tafolecimab, a monoclonal antibody targeting PCSK9, shows promise in managing HeFH by enhancing LDL receptor recycling and LDL-C clearance.

Objective: To evaluate the efficacy and safety of tafolecimab in Chinese patients with FH through a systematic review and meta-analysis.

Methods: This meta-analysis followed PRISMA guidelines and was registered in Prospective Register of Systematic Reviews. A comprehensive search was conducted across PubMed/MEDLINE, Web of Science, Scopus, and Embase databases. Inclusion criteria focused on randomized controlled trials (RCTs) involving patients aged 18-75 with hypercholesterolemia and high cardiovascular risk. Data extraction and quality assessment were performed independently by two reviewers. Statistical analyses were conducted using random-effects models.

Results: Four RCTs involving 841 Chinese patients were included. Tafolecimab significantly reduced LDL-C (mean difference [MD]: -2.05; 95% CI: -2.19 to -1.90), apolipoprotein levels (MD: -0.53; 95% CI: -0.56 to -0.50), non-HDL-C (MD: -2.19; 95% CI: -2.32 to -2.06), and lipoprotein(a) levels (MD: -0.09; 95% CI: -0.11 to -0.07). The incidence of adverse events was higher in the tafolecimab group (risk ratio: 0.68; 95% CI: 0.61, 0.75), but no significant differences were found in serious adverse events, treatment discontinuation due to adverse events, deaths, hypersensitivity, muscle-related problems, upper respiratory issues, or liver damage compared to placebo.

Conclusion: Tafolecimab effectively reduces various lipid parameters, suggesting its potential in managing hypercholesterolemia and reducing cardiovascular risk. Although adverse events were more frequent, their severity did not significantly differ from placebo. The generalizability of these findings is limited to Chinese populations, highlighting the need for further research in diverse cohorts.

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Annals of Medicine and Surgery
Annals of Medicine and Surgery MEDICINE, GENERAL & INTERNAL-
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