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PCSK9 抑制——治疗脂质代谢紊乱的新机制?

PCSK9 inhibition - a novel mechanism to treat lipid disorders?

机构信息

Department of Hypertension, Medical University of Lodz, Poland.

出版信息

Curr Pharm Des. 2013;19(21):3869-77. doi: 10.2174/13816128113199990303.

Abstract

Plasma low-density lipoprotein cholesterol (LDL-C) is one of the biomarkers of cardiovascular disease (CVD) risk. LDL is cleared from the circulation preferentially through the LDL receptor (LDLR) pathway. Proprotein convertase subtilisin/kexin 9 (PCSK9) promotes the degradation of the LDLR. PCSK9 inhibition is attractive as a new strategy for lowering LDL-C levels, especially in combination with lipid lowering drugs such as statins. We review data from the available studies which focus on PCSK9 as a potential target in the treatment of hyperlipidemia. Further studies are still necessary to investigate the potential underlying mechanisms involved.

摘要

血浆低密度脂蛋白胆固醇(LDL-C)是心血管疾病(CVD)风险的生物标志物之一。LDL 通过 LDL 受体(LDLR)途径从循环中优先清除。前蛋白转化酶枯草溶菌素/柯萨奇蛋白酶 9(PCSK9)促进 LDLR 的降解。PCSK9 抑制作为降低 LDL-C 水平的新策略很有吸引力,尤其是与降脂药物如他汀类药物联合使用时。我们回顾了现有研究的数据,这些研究集中在 PCSK9 作为治疗高血脂的潜在靶点。仍需要进一步研究以探讨潜在的相关机制。

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