Messenger interference RNA therapies targeting apolipoprotein C-III and angiopoietin-like protein 3 for mixed hyperlipidemia: the future of plozasiran and zodasiran

医学 高脂血症 PCSK9 载脂蛋白B 人口 甘油三酯 生物信息学 内科学 胆固醇 脂蛋白 低密度脂蛋白受体 内分泌学 糖尿病 生物 环境卫生
作者
Zonghao Pan,Muhammad Adnan Zaman,Sidra Kalsoom,Yani Zhang
出处
期刊:Expert Review of Clinical Pharmacology [Taylor & Francis]
卷期号:17 (11): 1017-1023 被引量:4
标识
DOI:10.1080/17512433.2024.2423724
摘要

INTRODUCTION: Mixed hyperlipidemia represents a substantial public health issue and a considerable burden on healthcare systems. Although the introduction of statins and LDL-cholesterol lowering agents have significantly reduced the incidence of atherosclerotic cardiovascular diseases (ASCVD), a significant portion of the population continues to exhibit ASCVD progression due to elevated triglyceride-rich lipoprotein (TRL) levels. This persistent risk has catalyzed the development of novel pharmacological interventions targeting these lipoproteins. AREAS COVERED: Our special report commenced with a targeted PubMed search using keywords such as 'plozasiran,' 'zodasiran,' and terms related to APOC3 and ANGPTL3. As the review progressed, emergent research questions guided further searches, allowing for the inclusion of additional relevant articles to comprehensively illustrate the linkage between TRLs and cardiovascular disease, discuss the roles of APOC3, ANGPTL3, and the pharmaceutical agents that target these proteins, and provide a comparison on the ARCHES-2 and MUIR trials. EXPERT OPINION: The ARCHES-2 and MUIR trials demonstrated effective triglyceride reduction by these therapies, yet it is uncertain if this correlates with significant clinical benefits. Advances in antisense oligonucleotide technology, especially the GalNAc delivery platform, show promise for personalized lipid management, though challenges such as cost and safety concerns remain.
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