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长期低密度脂蛋白去除术在难治性高胆固醇血症及其他病症上的临床应用

Clinical applications of long-term LDL-apheresis on and beyond refractory hypercholesterolemia.

作者信息

Mabuchi Hiroshi, Higashikata Toshinori, Kawashiri Masa-Aki

机构信息

Department of Internal Medicine, Division of Cardiovascular Genetics, Graduate School of Medical Science, Kanazawa University, Takahara-machi 13-1, Kanazawa 920-8641, Japan.

出版信息

Transfus Apher Sci. 2004 Jun;30(3):233-43. doi: 10.1016/j.transci.2004.01.006.

Abstract

Premature coronary heart disease (CHD) can result from high LDL cholesterol levels even in the absence of any other risk factors. A striking example is found in children who have the homozygous form of familial hypercholesterolemia (FH) with extremely high levels of LDL-cholesterol, and severe atherosclerosis and CHD often develop during the first decades of life. LDL-apheresis was developed for the treatment of severe type of FH patients who are resistant to lipid-lowering drug therapy. Clinical efficacy and safety of the therapeutic tool which directly removes LDL from circulation have already been established in the treatment for refractory hypercholesterolemia in FH patients. The most recently developed method enables lipoproteins to be adsorbed directly from whole blood, using polyacrylate column. In addition to benefits derived from the stabilization or regression of arterial lesions, we highlight other possible clinical applications of LDL-apheresis. However, most of these clinical benefits came from case reports or retrospective studies. Mechanisms related these clinical improvement remain unclear, and prospective randomized controlled trials should be performed for the new clinical indications of LDL-apheresis.

摘要

即使没有任何其他风险因素,低密度脂蛋白胆固醇(LDL-C)水平升高也可能导致早发性冠心病(CHD)。一个显著的例子是患有纯合子型家族性高胆固醇血症(FH)的儿童,他们的LDL-C水平极高,并且在生命的最初几十年中常常会发展为严重的动脉粥样硬化和CHD。LDL分离术是为治疗对降脂药物治疗耐药的严重FH患者而开发的。这种直接从循环中去除LDL的治疗工具在治疗FH患者的难治性高胆固醇血症方面的临床疗效和安全性已经得到证实。最新开发的方法能够使用聚丙烯酸酯柱从全血中直接吸附脂蛋白。除了动脉病变稳定或逆转带来的益处外,我们还强调了LDL分离术其他可能的临床应用。然而,这些临床益处大多来自病例报告或回顾性研究。与这些临床改善相关的机制仍不清楚,对于LDL分离术的新临床适应症,应进行前瞻性随机对照试验。

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