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在心血管代谢疾病中平衡极低密度脂蛋白(VLDL)水平

Walking the VLDL tightrope in cardiometabolic diseases.

作者信息

Kim Mindy, Zheng Ze

机构信息

Medical Scientist Training Program, Medical College of Wisconsin, Milwaukee, 53226, USA; Department of Physiology, Medical College of Wisconsin, Milwaukee, 53226, USA.

Department of Physiology, Medical College of Wisconsin, Milwaukee, 53226, USA; Department of Medicine, Medical College of Wisconsin, Milwaukee, 53226, USA; Cardiovascular Center, Medical College of Wisconsin, Milwaukee, 53226, USA; Thrombosis & Hemostasis Program, Versiti Blood Research Institute, Milwaukee, 53226, USA.

出版信息

Trends Endocrinol Metab. 2025 Mar;36(3):278-291. doi: 10.1016/j.tem.2024.07.020. Epub 2024 Aug 26.

Abstract

Very-low-density lipoprotein (VLDL), a triglyceride-rich lipoprotein secreted by hepatocytes, is pivotal for supplying peripheral tissues with fatty acids for energy production. As if walking on a tightrope, perturbations in the balance of VLDL metabolism contribute to cardiometabolic dysfunction, promoting pathologies such as cardiovascular disease (CVD) or metabolic dysfunction-associated steatotic liver disease (MASLD). Despite the advent of lipid-lowering therapies, including statins and proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors, risks for cardiovascular events persist. With limitations to currently available CVD therapeutics and no US Food and Drug Administration (FDA)-approved treatment for MASLD, this review summarizes the current understanding of VLDL metabolism that sheds light on novel therapeutic avenues to pursue for cardiometabolic disorders.

摘要

极低密度脂蛋白(VLDL)是一种由肝细胞分泌的富含甘油三酯的脂蛋白,对于为外周组织提供脂肪酸以进行能量产生至关重要。就像在走钢丝一样,VLDL代谢平衡的扰动会导致心脏代谢功能障碍,促进心血管疾病(CVD)或代谢功能障碍相关脂肪性肝病(MASLD)等疾病的发生。尽管出现了包括他汀类药物和前蛋白转化酶枯草溶菌素/kexin 9型(PCSK9)抑制剂在内的降脂疗法,但心血管事件的风险仍然存在。鉴于目前可用的CVD治疗方法存在局限性,且尚无美国食品药品监督管理局(FDA)批准的MASLD治疗方法,本综述总结了目前对VLDL代谢的认识,为探索心脏代谢疾病的新治疗途径提供了思路。

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Walking the VLDL tightrope in cardiometabolic diseases.在心血管代谢疾病中平衡极低密度脂蛋白(VLDL)水平
Trends Endocrinol Metab. 2025 Mar;36(3):278-291. doi: 10.1016/j.tem.2024.07.020. Epub 2024 Aug 26.

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