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胆固醇降低的联合治疗:聚焦依折麦布与他汀类药物

Combination therapy in cholesterol reduction: focus on ezetimibe and statins.

作者信息

Grigore Liliana, Norata Giuseppe Danilo, Catapano Alberico L

机构信息

Department of Pharmacological Sciences, University of Milan, Milan, Italy.

出版信息

Vasc Health Risk Manag. 2008;4(2):267-78. doi: 10.2147/vhrm.s1204.

DOI:10.2147/vhrm.s1204
PMID:18561502
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2496970/
Abstract

Although widely used in lipid lowering therapy, HMG CoA reductase inhibitors (even when administered at high doses) are frequently insufficient to achieve guideline-recommended LDL-C goals for many patients with hypercholesterolemia in everyday clinical practice. Many patients do not achieve LDL-C goal on the initial dose of statin and the majority of these patients does not reach their goal after 6 months. As a consequence, a wide therapeutic gap exists between target LDL-C levels and those typically achieved in clinical practice. A recent and more effective therapeutic hypocholesterolemic strategy is to treat the two main sources of cholesterol simultaneously (production of cholesterol, mainly in the liver, and absorption of cholesterol in the intestine) with a complementary mechanism of action, by co-administering ezetimibe, a novel agent inhibiting cholesterol absorption, with a statin, which inhibits cholesterol production in the liver. Ezetimibe can be effectively and safely co-administered with any dose of any statin and, compared with the single inhibition of cholesterol production, afforded by statins alone, provides consistently greater reductions in LDL-C through dual inhibition of both cholesterol production and absorption. We summarize the pivotal role of both the liver and intestine in the overall balance of cholesterol in the body and describe the clinical impact and relevance of using ezetimibe either alone or co-administered with statins in controlling elevated levels of plasma LDL cholesterol.

摘要

尽管HMG CoA还原酶抑制剂在降脂治疗中广泛应用,但在日常临床实践中,对于许多高胆固醇血症患者,即便大剂量使用该抑制剂,往往也不足以达到指南推荐的低密度脂蛋白胆固醇(LDL-C)目标。许多患者在初始剂量他汀治疗时未达到LDL-C目标,且这些患者中的大多数在6个月后仍未达标。因此,目标LDL-C水平与临床实践中通常达到的水平之间存在很大的治疗差距。一种最新且更有效的治疗性降胆固醇策略是,通过联合使用依折麦布(一种新型胆固醇吸收抑制剂)和他汀类药物(抑制肝脏中胆固醇生成),以互补的作用机制同时治疗胆固醇的两个主要来源(主要在肝脏中生成胆固醇以及在肠道中吸收胆固醇)。依折麦布可与任何剂量的任何他汀类药物有效且安全地联合使用,并且与仅由他汀类药物单独抑制胆固醇生成相比,通过对胆固醇生成和吸收的双重抑制,依折麦布能持续更大程度地降低LDL-C。我们总结了肝脏和肠道在体内胆固醇总体平衡中的关键作用,并描述了单独使用依折麦布或与他汀类药物联合使用在控制血浆LDL胆固醇水平升高方面的临床影响及相关性。

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Co-administration of ursodeoxycholic acid with rosuvastatin/ezetimibe in a non-alcoholic fatty liver disease model.在非酒精性脂肪性肝病模型中熊去氧胆酸与瑞舒伐他汀/依折麦布的联合应用。
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