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低密度脂蛋白受体基因的PvuII多态性与包括LP(a)在内的低密度脂蛋白血浆浓度无关。

A PvuII polymorphism of the low density lipoprotein receptor gene is not associated with plasma concentrations of low density lipoproteins including LP(a).

作者信息

Klausen I C, Hansen P S, Gerdes L U, Rüdiger N, Gregersen N, Faergeman O

机构信息

Department of Internal Medicine and Cardiology A, Aarhus County Hospital, University of Aarhus, Denmark.

出版信息

Hum Genet. 1993 Mar;91(2):193-5. doi: 10.1007/BF00222725.

Abstract

Lipoprotein(a) [Lp(a)] is a low density lipoprotein (LDL), in which apolipoprotein B-100 (apo B-100) is attached to apolipoprotein(a) [apo(a)], a glycoprotein of variable size. Lp(a) may be as atherogenic as LDL. In normal populations, Lp(a) concentrations in plasma are largely determined by the apo(a) gene locus on chromosome 6, but regulation of synthesis and catabolism of Lp(a) is poorly understood. In some studies, a PvuII restriction fragment length polymorphism (RFLP) in the LDL receptor gene seems to affect concentrations of LDL in plasma, and other studies have indicated that Lp(a) catabolism could be mediated by the LDL receptor. We therefore expected that the PvuII polymorphism in the LDL receptor gene might be associated with Lp(a) levels in 170 Caucasian men aged 40 years, selected to have a high representation of low molecular weight apo(a) phenotypes. However, plasma concentrations of cholesterol, LDL-cholesterol, HDL-cholesterol, triglycerides and Lp(a) were all unrelated to the LDL receptor gene PvuII polymorphism both in the group as a whole and when it was subgrouped by apo(a) phenotype. Therefore our data do not support the concept that this particular LDL receptor gene polymorphism is associated with LDL receptor function, and our data therefore neither support nor rule out a role for the LDL receptor in Lp(a) catabolism.

摘要

脂蛋白(a) [Lp(a)] 是一种低密度脂蛋白 (LDL),其中载脂蛋白B-100 (apo B-100) 与载脂蛋白(a) [apo(a)] 相连,apo(a) 是一种大小可变的糖蛋白。Lp(a) 的致动脉粥样硬化作用可能与LDL相同。在正常人群中,血浆中Lp(a) 的浓度在很大程度上由6号染色体上的apo(a) 基因位点决定,但对Lp(a) 合成和分解代谢的调节了解甚少。在一些研究中,LDL受体基因中的PvuII限制性片段长度多态性 (RFLP) 似乎会影响血浆中LDL的浓度,其他研究表明Lp(a) 的分解代谢可能由LDL受体介导。因此,我们预计LDL受体基因中的PvuII多态性可能与170名40岁白人男性的Lp(a) 水平有关,这些男性被选择具有高比例的低分子量apo(a) 表型。然而,无论是在整个组中还是按apo(a) 表型进行亚组分析时,血浆中的胆固醇、LDL胆固醇、HDL胆固醇、甘油三酯和Lp(a) 浓度均与LDL受体基因PvuII多态性无关。因此,我们的数据不支持这一特定的LDL受体基因多态性与LDL受体功能相关的概念,因此我们的数据既不支持也不排除LDL受体在Lp(a) 分解代谢中的作用。

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