Huang Yi-Ting, Ho Li-Ting, Hsu Hsin-Yin, Tu Yu-Kang, Chien Kuo-Liong
Institute of Epidemiology and Preventive Medicine, College of Public Health, National Taiwan University, Taipei, Taiwan.
Department of Internal Medicine, National Taiwan University Hospital and College of Medicine, Taipei, Taiwan.
Front Pharmacol. 2022 Apr 4;13:832614. doi: 10.3389/fphar.2022.832614. eCollection 2022.
The proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors are potent LDL-C lowering agents. However, few head-to-head studies evaluated the efficacy on the lowering in other atherogenic apolipoproteins and safety of PCSK9 inhibitors at different dosages as an add-on statins therapy in hypercholesterolemia patients. This study is a systematic review and network meta-analysis of randomized control trials to compare the efficacy of lipid reduction and adverse events of PCSK9 inhibitors in statin-treated hypercholesterolemia patients. PubMed, EMBASE, and Cochrane Library databases were searched till April 20, 2021, for randomized controlled trials. Random-effect network meta-analyses were undertaken to compare the differences in the percent reduction in low-density lipoprotein cholesterol (LDL-C), apolipoprotein B (ApoB), and lipoprotein (a) [Lp(a)] levels and the risk of AEs among different PCSK9 inhibitors. A total of 22 articles with 42,786 patients were included. The lipid reductions in LDL-C, ApoB, and Lp(a) with add-on PCSK9 inhibitors vs. placebo in statin-treated patients across all trials were 50-63%, 43-52%, and 23-31%, respectively. Evolocumab 140 mg Q2W was ranked the best among all treatment strategies for lowering LDL-C, ApoB, and Lp(a) levels, and the treatment difference was 68.05% (95% confidence interval (CI), 62.43% to 73.67) in LDL-C reduction, 54.95% (95% CI, 49.55% to 60.35%) in ApoB reduction, and 34.25% (95% CI, 27.59% to 40.91%) in Lp(a) reduction compared with the placebo. No significant risk difference of adverse events between PCSK9 inhibitors and placebo was found. PCSK9 inhibitors showed a significant effect on the reduction in LDL-C, ApoB, and Lp(a) levels in statin-treated patients. Evolocumab 140 mg Q2W showed significantly larger degrees of LDL-C, ApoB, and Lp(a) reduction.
前蛋白转化酶枯草溶菌素/kexin 9型(PCSK9)抑制剂是强效的降低低密度脂蛋白胆固醇(LDL-C)的药物。然而,很少有直接比较的研究评估PCSK9抑制剂在不同剂量下作为他汀类药物附加治疗对高胆固醇血症患者降低其他致动脉粥样硬化载脂蛋白的疗效及安全性。本研究是一项对随机对照试验的系统评价和网状荟萃分析,旨在比较PCSK9抑制剂在他汀类治疗的高胆固醇血症患者中降低血脂的疗效及不良事件。检索了PubMed、EMBASE和Cochrane图书馆数据库至2021年4月20日的随机对照试验。采用随机效应网状荟萃分析比较不同PCSK9抑制剂在降低低密度脂蛋白胆固醇(LDL-C)、载脂蛋白B(ApoB)和脂蛋白(a)[Lp(a)]水平的百分比差异以及不良事件风险。共纳入22篇文章,涉及42786例患者。在所有试验中,他汀类治疗患者中,与安慰剂相比,附加PCSK9抑制剂后LDL-C、ApoB和Lp(a)的血脂降低率分别为50 - 63%、43 - 52%和23 - 31%。在降低LDL-C、ApoB和Lp(a)水平的所有治疗策略中,依洛尤单抗140 mg每2周一次效果最佳,与安慰剂相比,LDL-C降低的治疗差异为68.05%(95%置信区间(CI),62.43%至73.67),ApoB降低为54.95%(95%CI,49.55%至60.35%),Lp(a)降低为34.25%(95%CI,27.59%至40.91%)。未发现PCSK9抑制剂与安慰剂之间不良事件的显著风险差异。PCSK9抑制剂对他汀类治疗患者降低LDL-C、ApoB和Lp(a)水平有显著效果。依洛尤单抗140 mg每2周一次降低LDL-C、ApoB和Lp(a)的程度显著更大。