Genetics
CETP -629A allele linked to larger LDL particle size in 377 healthy middle-aged men (Atherosclerosis 2003)
Original title: Influence of common variants in the CETP, LPL, HL and APO E genes on LDL heterogeneity in healthy, middle-aged men
In 377 healthy middle-aged men, common variants in CETP (-629C/A), lipoprotein lipase (S447X), hepatic lipase (-480C/T), and apoE (e2/e3/e4) genes were tested against LDL particle size distribution, measured by high-resolution gradient gel electrophoresis across four LDL subfractions. The CETP -629A and LPL 447X alleles were each associated with moderately increased LDL peak particle size, in contrast to the apoE e4 allele, which was associated with markedly smaller LDL peak particle size and higher small, dense LDL. An interaction between HL-480C/T and apoE genotypes significantly increased small, dense LDL concentration in HL-480T carriers. These polymorphisms thus had diverse, function-consistent effects on LDL heterogeneity, further shaped by gene-gene and gene-environment interactions.
Original abstract
Low density lipoprotein (LDL) particle size is a genetically influenced trait associated with coronary heart disease (CHD). This study investigates the effects of genetic variation in plasma factors with important roles in lipoprotein metabolism on LDL heterogeneity. Common variants in the cholesteryl ester transfer protein (CETP-629C/A), lipoprotein lipase (LPL S447X), hepatic lipase (HL-480C/T) and apolipoprotein E (apoE e2/e3/e4) genes were studied in relation to LDL particle size distribution in 377 healthy, middle-aged men. A high-resolution polyacrylamide gradient gel electrophoresis technique was used to measure plasma concentrations of four LDL subfractions. The CETP-629A and LPL 447X alleles were associated with moderately increased LDL peak particle size. In contrast, the apoE e4 allele was associated with a marked reduction in LDL peak particle size and an increased relative proportion and plasma concentration of small, dense LDL. An interaction between the HL-480C/T and apo E polymorphisms contributed significantly to increased plasma concentration of small, dense LDL (LDL-III) in HL-480T carriers. In summary, the investigated polymorphisms were associated with diverse effects on the LDL particle size distribution, consistent with respect to protein function and proposed association with CHD risk. The observed associations were further modulated by gene-gene and gene-environment interactions.
Summary written by cetpinhibition.org from the published abstract; figures as published. Page updated 19 August 2026. Methods.