Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1997 Apr 29;94(9):4532-7.
doi: 10.1073/pnas.94.9.4532.

A hepatic lipase (LIPC) allele associated with high plasma concentrations of high density lipoprotein cholesterol

Affiliations

A hepatic lipase (LIPC) allele associated with high plasma concentrations of high density lipoprotein cholesterol

R Guerra et al. Proc Natl Acad Sci U S A. .

Abstract

Genetic factors strongly influence interindividual variation in plasma high density lipoprotein cholesterol (HDL-C) levels, but the specific genetic polymorphisms that confer heritable variation in HDL-C levels have not been identified. In this study we examined the relationship between polymorphism in LIPC, the gene encoding hepatic lipase, and plasma HDL-C concentrations using a sequential approach comprising linkage analysis, DNA sequencing, and association studies. Linkage studies in 1465 American white subjects from 218 nuclear families indicated that allelic variation at, or closely linked to, the hepatic lipase gene accounts for a significant fraction ( approximately 25%) of the variation in plasma HDL-C concentrations. The hepatic lipase gene was then sequenced in selected individuals, and four novel polymorphisms were identified in the 5' flanking region of the gene. These polymorphisms were in complete linkage disequilibrium and thus identified a single novel allele. Association studies indicated that heterozygosity for the rare allele was associated with modestly increased concentrations of plasma HDL-C (41 +/- 11 vs. 37 +/- 10 mg/dl, P < 0.05) and apolipoprotein AI in men (131 +/- 23 vs. 122 +/- 21 mg/dl, P < 0.05) but not in women. Homozygosity for the rare allele was associated with markedly higher plasma HDL-C (63 +/- 3 mg/dl) and apolipoprotein AI (153 +/- 9 mg/dl) concentrations in men. The results of the association study were replicated in a second, independently ascertained sample. Taken together, the results of the linkage and association studies provide strong evidence that genetic variation in hepatic lipase activity is a major determinant of plasma HDL-C levels.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Distributions of squared sibling-pair differences of plasma HDL-C levels in siblings sharing none, one, or two hepatic lipase alleles identical-by-descent. Median values are indicated by bars within boxes; upper and lower quartiles are indicated by the tops and bottoms of the boxes, respectively; whiskers indicate the points closest to one-half of the interquartile range from the tops of the boxes.

Similar articles

Cited by

References

    1. Miller N E, Miller G J. Lancet. 1975;i:1033. - PubMed
    1. National Cholesterol Education Program. NIH Publication No. 93–3095. Bethesda, MD: National Institutes of Health; 1993.
    1. Bucher K D, Friedlander Y, Kaplan E B, Namboodiri K K, Kark J D, Eisenberg S, Stein Y, Rifkind B M. Genet Epidemiol. 1988;5:17–33. - PubMed
    1. Craig W Y, Palomaki G E, Haddow J E. Br Med J. 1996;298:784–788. - PMC - PubMed
    1. Sutherland W H, Temple W A, Nye E R, Herbison G P. Am J Clin Nutr. 1980;33:2581–2587. - PubMed

Publication types