靶向甘油三酯：载脂蛋白C3和血管生成素样蛋白3抑制剂的兴起。

IF 3 4区医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS

American Journal of Cardiovascular Drugs Pub Date : 2025-07-12 DOI:10.1007/s40256-025-00748-7

Taha Mansoor, Vijay Nambi, Sachin Parikh, Arunima Misra, Mahmoud Ismayl, Claire Sullivan, Laurence Sperling, Salim S Virani, Mahmoud Al Rifai, Santhosh K G Koshy, Dmitry Abramov, Abdul Mannan Khan Minhas

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引用次数: 0

摘要

高甘油三酯血症已被认为是动脉粥样硬化性心血管疾病（ASCVD）的危险因素。甘油三酯（TG）被视为富含甘油三酯的脂蛋白中残余胆固醇的标记物，因为这种残余胆固醇已被确定为ASCVD的因果危险因素。针对高TG的有效治疗方法数量有限，这促使人们寻找新的药物治疗方案，并正在探索多种药物类别。载脂蛋白C3 （APOC3）和血管生成素样蛋白3 （ANGPTL3）是最有希望的靶点。利用这些途径的几种新型药物，包括olezarsen、plozasiran和zodasiran，目前正在开发中，用于治疗TG升高，olezarsen于2024年被批准用于治疗家族性乳糜小铁血症综合征。这篇全面的综述为新型高甘油三酯血症治疗的发展提供了最新的见解。

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Targeting Triglycerides: The Rise of Apolipoprotein C3 and Angiopoietin-Like Protein 3 Inhibitors.

Hypertriglyceridemia has been proposed as a risk factor for atherosclerotic cardiovascular disease (ASCVD). Triglycerides (TG) are viewed as a marker for remnant cholesterol in triglyceride-rich lipoproteins, as this remnant cholesterol has been identified as a causal risk factor for ASCVD. The limited number of effective treatments for elevated TG has fueled the search for novel pharmacotherapy options, and multiple medication classes are being explored. Apolipoprotein C3 (APOC3) and angiopoietin-like protein 3 (ANGPTL3) are among the most promising targets. Several novel agents utilizing these pathways, including olezarsen, plozasiran, and zodasiran, are currently under development for the management of elevated TG, with olezarsen approved in 2024 for the management of familial chylomicronemia syndrome. This comprehensive review provides updated insights into the development of novel hypertriglyceridemia treatments.

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来源期刊

American Journal of Cardiovascular Drugs 医学-心血管系统

CiteScore

6.70

自引率

3.30%

发文量

审稿时长

>12 weeks

期刊介绍： Promoting rational therapy within the discipline of cardiology, the American Journal of Cardiovascular Drugs covers all aspects of the treatment of cardiovascular disorders, particularly the place in therapy of newer and established agents. Via a program of reviews and original clinical research articles, the journal addresses major issues relating to treatment of these disorders, including the pharmacology, efficacy and adverse effects of the major classes of drugs; information on newly developed drugs and drug classes; the therapeutic implications of latest research into the aetiology of cardiovascular disorders; and the practical management of specific clinical situations. The American Journal of Cardiovascular Drugs offers a range of additional enhanced features designed to increase the visibility, readership and educational value of the journal’s content. Each article is accompanied by a Key Points summary, giving a time-efficient overview of the content to a wide readership. Articles may be accompanied by plain language summaries to assist patients, caregivers and others in understanding important medical advances. The journal also provides the option to include various other types of enhanced features including slide sets, videos and animations. All enhanced features are peer reviewed to the same high standard as the article itself. Peer review is conducted using Editorial Manager®, supported by a database of international experts. This database is shared with other Adis journals.