Austin M A, King M C, Vranizan K M, Krauss R M
Research Medicine and Radiation Biophysics, University of California, Berkeley.
Circulation. 1990 Aug;82(2):495-506. doi: 10.1161/01.cir.82.2.495.
In a community-based study of 301 subjects from 61 nuclear families, two distinct phenotypes (denoted A and B) were identified by nondenaturing gradient gel electrophoretic analysis of low density lipoprotein (LDL) subclasses. Phenotype A was characterized by predominance of large, buoyant LDL particles, and phenotype B consisted of a major peak of small, dense LDL particles. Previous analysis of the family data by complex segregation analysis demonstrated that these phenotypes appear to be inherited as a single-gene trait. In the present study, the phenotypes were found to be closely associated with variations in plasma levels of other lipid, lipoprotein, and apolipoprotein measurements. Specifically, phenotype B was associated with increases in plasma levels of triglyceride and apolipoprotein B, with mass of very low and intermediate density lipoproteins, and with decreases in high density lipoprotein (HDL) cholesterol, HDL2 mass, and plasma levels of apolipoprotein A-I. Thus, the proposed genetic locus responsible for LDL subclass phenotypes also results in an atherogenic lipoprotein phenotype.
在一项针对来自61个核心家庭的301名受试者的社区研究中,通过对低密度脂蛋白(LDL)亚类进行非变性梯度凝胶电泳分析,确定了两种不同的表型(分别记为A和B)。表型A的特征是大的、漂浮性LDL颗粒占主导,而表型B则以小的、致密的LDL颗粒的一个主要峰为特征。先前通过复杂分离分析对家族数据进行的分析表明,这些表型似乎作为单基因性状遗传。在本研究中,发现这些表型与其他脂质、脂蛋白和载脂蛋白测量的血浆水平变化密切相关。具体而言,表型B与甘油三酯和载脂蛋白B的血浆水平升高、极低密度和中间密度脂蛋白的质量增加以及高密度脂蛋白(HDL)胆固醇、HDL2质量和载脂蛋白A-I的血浆水平降低有关。因此,所提出的负责LDL亚类表型的基因座也导致了一种致动脉粥样硬化的脂蛋白表型。