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Research Article Free access | 10.1172/JCI117603
Center for Human Nutrition, University of Texas Southwestern Medical Center, Dallas 75235-9052.
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Center for Human Nutrition, University of Texas Southwestern Medical Center, Dallas 75235-9052.
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Center for Human Nutrition, University of Texas Southwestern Medical Center, Dallas 75235-9052.
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Center for Human Nutrition, University of Texas Southwestern Medical Center, Dallas 75235-9052.
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Center for Human Nutrition, University of Texas Southwestern Medical Center, Dallas 75235-9052.
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Published December 1, 1994 - More info
Genetic factors have been shown to play an important role in determining interindividual variation in plasma HDL-C levels, but the specific genetic determinants of HDL cholesterol (HDL-C) levels have not been elucidated. In this study, the effects of variation in the genomic regions encoding hepatic lipase, apolipoprotein AI/CIII/AIV, and the cholesteryl ester transfer protein on plasma HDL-C levels were examined in 73 normotriglyceridemic, Caucasian nuclear families. Genetic factors accounted for 56.5 +/- 13% of the interindividual variation in plasma HDL-C levels. For each candidate gene, adjusted plasma HDL-C levels of sibling pairs who shared zero, one, or two parental alleles identical-by-descent were compared using sibling-pair linkage analysis. Allelic variation in the genes encoding hepatic lipase and apolipoprotein AI/CIII/AIV accounted for 25 and 22%, respectively, of the total interindividual variation in plasma HDL-C levels. In contrast, none of the variation in plasma HDL-C levels could be accounted for by allelic variation in the cholesteryl ester transfer protein. These findings indicate that a major fraction of the genetically determined variation in plasma HDL-C levels is conferred by allelic variation at the hepatic lipase and the apolipoprotein AI/CIII/AIV gene loci.