Atherogenic lipoprotein phenotype. A proposed genetic marker for coronary heart disease risk.

TLDR

A community‑based study of 301 individuals from 61 nuclear families used nondenaturing gradient gel electrophoresis of LDL subclasses to identify two distinct phenotypes, A and B. Phenotype A comprised large, buoyant LDL particles, whereas phenotype B consisted of small, dense LDL particles and was linked to a single‑gene inheritance pattern and an atherogenic lipoprotein profile characterized by elevated triglycerides, apolipoprotein B, VLDL/IDL, and reduced HDL, HDL2, and apolipoprotein A‑I.

Abstract

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.