IF 2.6 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Undral Munkhsaikhan, Karima Ait-Aissa, Amal M Sahyoun, Ehsanul Hoque Apu, Ammaar H Abidi, Adam Kassan, Modar Kassan
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引用次数: 0

摘要

血脂异常是心血管疾病(CVDs)最重要的风险因素 继发性血脂异常:其治疗方法及其与动脉粥样硬化的关系。全球健康医学》(Glob Health Med),《沙格列扎治疗血脂异常的疗效和安全性》(Saroglitazar for the management of dyslipidemia):对干预性研究的系统回顾和荟萃分析。目前控制血脂异常的治疗策略主要是降低低密度脂蛋白胆固醇(LDL-C),以尽量减少动脉粥样硬化和心肌梗死(MI)的风险。洛米他匹对 LDLr(-/-)肥胖小鼠心血管系统的有益影响,微粒体甘油三酯转移蛋白抑制剂洛米他匹可改善肥胖小鼠的血管功能。虽然他汀类药物治疗一直是血脂异常的主要治疗方法,但HoFH患者对他汀类药物反应不佳,需要替代疗法。抑制微粒体甘油三酯转移蛋白(MTP)已成为治疗HoFH的潜在治疗靶点。微粒体甘油三酯转移蛋白主要负责在肝脏组装极低密度脂蛋白(VLDL)颗粒的过程中将甘油三酯和其他脂类转移到载脂蛋白 B(ApoB)中。洛米他匹是一种 MTP 抑制剂,已被批准用于治疗 HoFH 成人。与他汀类药物不同,洛米他匹不作用于 LDLr 以降低胆固醇。相反,洛米他匹降低含载脂蛋白 B 蛋白(主要是 VLDL)的水平,最终降低 LDL-C 水平。研究表明,对于其他治疗方法无效的 HoFH 患者,洛米他匹可将低密度脂蛋白胆固醇水平降低 50%以上。降低低密度脂蛋白胆固醇水平对于预防动脉粥样硬化、降低心血管风险、改善内皮功能和促进整体心血管健康非常重要,尤其是对于HoFH患者。微粒体甘油三酯转移蛋白抑制剂洛米他匹能改善肥胖症小鼠的血管功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lomitapide: navigating cardiovascular challenges with innovative therapies.

Dyslipidemia is the most significant risk factor for cardiovascular diseases (CVDs) Secondary dyslipidemia: its treatments and association with atherosclerosis. Glob Health Med, Efficacy and safety of saroglitazar for the management of dyslipidemia: A systematic review and meta-analysis of interventional studies. The current treatment strategies for managing dyslipidemia focus on reducing low-density lipoprotein cholesterol (LDL-C) to minimize the risks of atherosclerosis and myocardial infarction (MI). Homozygous Familial Hypercholesterolemia (HoFH) is an inherited autosomal dominant disease caused by a mutation in the LDL receptor (LDLr), which can lead to extremely high levels of LDL-C The Beneficial Effect of Lomitapide on the Cardiovascular System in LDLr(-/-) Mice with Obesity, The microsomal triglyceride transfer protein inhibitor lomitapide improves vascular function in mice with obesity. Although statin therapy has been the primary treatment for dyslipidemia, HoFH patients do not respond well to statins, requiring alternative therapies. Microsomal triglyceride transfer protein (MTP) inhibition has emerged as a potential therapeutic target for treating HoFH. MTP is primarily responsible for transferring triglyceride and other lipids into apolipoprotein B (ApoB) during the assembly of very low-density lipoprotein (VLDL) particles in the liver. Lomitapide, an inhibitor of MTP, has been approved for treatingof HoFH adults. Unlike statins, lomitapide does not act on the LDLr to reduce cholesterol. Instead, lomitapide lowers the levels of ApoB-containing proteins, primarily VLDL, eventually decreasing LDL-C levels. Studies have shown that lomitapide can reduce LDL-C levels by more than 50% in patients with HoFH who have failed to respond adequately to other treatments. Lowering LDL-C levels is important for preventing atherosclerosis, reducing cardiovascular risk, improving endothelial function, and promoting overall cardiovascular health, especially for patients with HoFH Efficacy and safety of a microsomal triglyceride transfer protein inhibitor in patients with homozygous familial hypercholesterolaemia: a single-arm, open-label, phase 3 study. This review paper focuses on research findings regarding the therapeutic benefits of lomitapide, highlighting its effectiveness in lowering cholesterol levels and reducing the risk of CVDs The microsomal triglyceride transfer protein inhibitor lomitapide improves vascular function in mice with obesity.

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来源期刊
Molecular Biology Reports
Molecular Biology Reports 生物-生化与分子生物学
CiteScore
5.00
自引率
0.00%
发文量
1048
审稿时长
5.6 months
期刊介绍: Molecular Biology Reports publishes original research papers and review articles that demonstrate novel molecular and cellular findings in both eukaryotes (animals, plants, algae, funghi) and prokaryotes (bacteria and archaea).The journal publishes results of both fundamental and translational research as well as new techniques that advance experimental progress in the field and presents original research papers, short communications and (mini-) reviews.
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