Literature DB >> 34117182

Efficacy and Safety of Evinacumab for the Treatment of Hypercholesterolemia: A Meta-Analysis.

Menglong Jin1, Fanhua Meng2, Wenwen Yang1, Liyan Liang1, Hao Wang1, Zhenyan Fu2.   

Abstract

ABSTRACT: Angiopoietin-like protein 3 is essential in lipid metabolism regulation. However, the efficacy and safety of evinacumab (angiopoietin-like protein 3 inhibition drug) for hypercholesterolemia treatment is unknown. In this study, a meta-analysis of randomized controlled trials (RCTs) was conducted to assess the efficacy and safety of evinacumab. RCTs published between January 1, 2000, and November 1, 2020, were obtained from PubMed, Embase, and Cochrane Library. All RCTs evaluating the efficacy and safety of evinacumab were included without language restrictions. Our primary end points included the percent change of low-density lipoprotein cholesterol (LDL-C) from baseline and the incidence of at least one treatment emergent adverse events including nasopharyngitis, influenza-like illness, headache, dizziness, injection-site reaction, increased aspartate aminotransferase, increased alanine aminotransferase, and any other discomfort during treatments. Percentage changes of triglycerides and high-density lipoprotein cholesterol (HDL-C) from baseline indicated secondary end points. A random-effects model was used to assess pooled data if there was moderate to high heterogeneity between studies. Four studies with 5 RCTs (568 participants) were identified. Evinacumab significantly reduced LDL-C [mean difference (MD) -33.123%, 95% confidence interval (CI), -48.639% to -17.606%, P < 0.0001], triglycerides (MD -50.959%, 95% CI, -56.555% to -45.362%, P < 0.0001), and HDL-C (MD -12.773%, 95% CI, -16.359% to -9.186%, P < 0.0001) compared with placebo. The incidence of at least 1 treatment emergent adverse events was not significantly different between evinacumab and placebo groups (relative risk 1.080, 95% CI, 0.901-1.296, P = 0.405). Evinacumab decreased triglycerides, LDL-C, and HDL-C without significant adverse effects, indicating that it can be a therapeutic strategy for hypercholesterolemia.
Copyright © 2021 Wolters Kluwer Health, Inc. All rights reserved.

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Year:  2021        PMID: 34117182     DOI: 10.1097/FJC.0000000000001073

Source DB:  PubMed          Journal:  J Cardiovasc Pharmacol        ISSN: 0160-2446            Impact factor:   3.105


  2 in total

1.  A novel nanobody-heavy chain antibody against Angiopoietin-like protein 3 reduces plasma lipids and relieves nonalcoholic fatty liver disease.

Authors:  Xiaozhi Hu; Jiajun Fan; Qianqian Ma; Lei Han; Zhonglian Cao; Caili Xu; Jingyun Luan; Guangjun Jing; Yanyang Nan; Tao Wu; Yuting Zhang; Hanqi Wang; Yuanzhen Zhang; Dianwen Ju
Journal:  J Nanobiotechnology       Date:  2022-05-19       Impact factor: 9.429

Review 2.  Angiopoietin-Like Protein 3 (ANGPTL3) Inhibitors in the Management of Refractory Hypercholesterolemia.

Authors:  Constantine E Kosmas; Maria D Bousvarou; Andreas Sourlas; Evangelia J Papakonstantinou; Edilberto Peña Genao; Rogers Echavarria Uceta; Eliscer Guzman
Journal:  Clin Pharmacol       Date:  2022-07-16
  2 in total

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