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高密度脂蛋白:测量技术及心血管疾病风险的潜在生物标志物

High density lipoproteins: Measurement techniques and potential biomarkers of cardiovascular risk.

作者信息

Hafiane Anouar, Genest Jacques

机构信息

McGill University Health Center, Royal Victoria Hospital, 687 Avenue des Pins West, Montreal, QC H3A 1A1, Canada.

出版信息

BBA Clin. 2015 Jan 31;3:175-88. doi: 10.1016/j.bbacli.2015.01.005. eCollection 2015 Jun.

Abstract

Plasma high density lipoprotein cholesterol (HDL) comprises a heterogeneous family of lipoprotein species, differing in surface charge, size and lipid and protein compositions. While HDL cholesterol (C) mass is a strong, graded and coherent biomarker of cardiovascular risk, genetic and clinical trial data suggest that the simple measurement of HDL-C may not be causal in preventing atherosclerosis nor reflect HDL functionality. Indeed, the measurement of HDL-C may be a biomarker of cardiovascular health. To assess the issue of HDL function as a potential therapeutic target, robust and simple analytical methods are required. The complex pleiotropic effects of HDL make the development of a single measurement challenging. Development of laboratory assays that accurately HDL function must be developed validated and brought to high-throughput for clinical purposes. This review discusses the limitations of current laboratory technologies for methods that separate and quantify HDL and potential application to predict CVD, with an emphasis on emergent approaches as potential biomarkers in clinical practice.

摘要

血浆高密度脂蛋白胆固醇(HDL)由一组异质性的脂蛋白种类组成,它们在表面电荷、大小以及脂质和蛋白质组成方面存在差异。虽然HDL胆固醇(C)质量是心血管风险的一个强有力、分级且连贯的生物标志物,但遗传和临床试验数据表明,简单测量HDL-C在预防动脉粥样硬化方面可能并非因果关系,也不能反映HDL的功能。实际上,HDL-C的测量可能只是心血管健康的一个生物标志物。为了评估HDL功能作为潜在治疗靶点的问题,需要强大且简单的分析方法。HDL复杂的多效性使得开发单一测量方法具有挑战性。必须开发、验证并实现用于准确测定HDL功能的实验室检测方法的高通量,以用于临床目的。本综述讨论了当前用于分离和定量HDL的实验室技术的局限性以及预测心血管疾病的潜在应用,重点是作为临床实践中潜在生物标志物的新兴方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/713a/4661556/259f1150d663/gr1.jpg

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