Lp (a) Lipoprotein Biochemistry and Potential Role in Atherogenesis

Q4 Biochemistry, Genetics and Molecular Biology
H. Mezdour, A. Yamamoto
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引用次数: 0

Abstract

Atherosclerosis and thrombosis, major causes of heart attacks and strokes, are diseases of multiple and interactive aetiologies. Despite this frequently fatal association, there has been no evidence linking thrombosis to the earlier process of plaque formation. Lipoprotein(a) described by Berg in 19631), may be the first one. Indeed there is a considerable resurgence of interest in Lp(a), since there is strong evidence that the level of circulating Lp(a) represents an independent risk factor for ischemic disease with probably greater predictive potential than other lipoprotein traits2-4). Moreover, there is a remarkable structural homology between apo(a) and a portion of plasminogen molecule5). This unexpected discovery puts Lp(a) forward as a potential bridge between the fields of atherosclerosis and thrombosis6,4). Our purposal is to up-date knowledge on Lp(a) biochemistry and potential atherogenicity according to recent discoveries.
Lp (a)脂蛋白生化及其在动脉粥样硬化中的潜在作用
动脉粥样硬化和血栓形成是心脏病发作和中风的主要原因,是多种病因相互作用的疾病。尽管这种经常致命的关联,没有证据表明血栓形成与斑块形成的早期过程有关。脂蛋白(a)由Berg于19631年描述,可能是第一个。事实上,由于有强有力的证据表明,循环脂蛋白(a)水平代表了缺血性疾病的独立危险因素,可能比其他脂蛋白特征具有更大的预测潜力,因此对脂蛋白(a)的兴趣有了相当大的复苏。此外,载脂蛋白(a)与部分纤溶酶原分子具有显著的结构同源性(5)。这一意想不到的发现使Lp(a)成为动脉粥样硬化和血栓形成领域之间的潜在桥梁6,4)。我们的目的是根据最近的发现更新关于Lp(a)生物化学和潜在的动脉粥样硬化性的知识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Japanese Journal of Clinical Chemistry
Japanese Journal of Clinical Chemistry Biochemistry, Genetics and Molecular Biology-Clinical Biochemistry
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