Skip Navigation

This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Lussier-Cacan, S.
Right arrow Articles by Sing, C. F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Lussier-Cacan, S.
Right arrow Articles by Sing, C. F.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

American Journal of Epidemiology Vol. 150, No. 11: 1229-1237
Copyright © 1999 by The Johns Hopkins University School of Hygiene and Public Health


other

Sources of Variation in Plasma Lipid and Lipoprotein Traits in a Sample Selected for Health

Suzanne Lussier-Cacan1, Marianne Xhignesse1, Anna M. Kessling2, Jean Davignon1 and Charles F. Sing3

1Hyperlipidemia and Atherosclerosis Research Group, Clinical Research Institute of Montreal, Montreal Quebec, Canada
2Department of Medical and Community Genetics (Imperial College), Kennedy Galton Centre, North West London Hospitals Trust London, England
3Department of Human Genetics, University of Michigan Ann Arbor, MI

Substantial variation in plasma lipid, lipoprotein, and apolipoprotein B levels was found in a sample of healthy white collar workers aged 23–59 years (144 women, 371 men) devoid of most clinically identifiable manifestations of cardiovascular disease or major biochemical anomalies and for whom data were gathered in Montreal, Canada, in 1987. The nature of this variability was examined for each gender by means of a stepwise linear regression analysis using indices of biologic variation and behavioral traits. In women, age, height, and weight together accounted for =10% and uric acid for another 7–10% of total cholesterol, low density lipoprotein (LDL) cholesterol, and apolipoprotein B level variation. In men, age alone accounted for 13–16% of the total variation in these traits while uric acid contributed only 3%. The additional contribution of behavioral traits was found to be at least double that associated with the indices of biologic variation for measures of very low density lipoprotein (VLDL) and high density lipoprotein (HDL) cholesterol in women and HDL cholesterol in men. After taking all of the above into account, genetic variation determined by the three common apo Ealleles explained an additional 6% of LDL cholesterol variation in women and 3.5% in men. These results emphasize the range of variability in lipid, lipoprotein, and apolipoprotein values in healthy individuals as well as important gender differences in the contribution of biologic, behavioral, and genetic factors in this variability. Am J Epidemiol 1999; 150: 1229–37.

cardiovascular diseases; health status; men; risk factors; women


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Hum Mol GenetHome page
C.C. Shoulders, E.L. Jones, and R.P. Naoumova
Genetics of familial combined hyperlipidemia and risk of coronary heart disease
Hum. Mol. Genet., April 1, 2004; 13(90001): R149 - 160.
[Abstract] [Full Text] [PDF]


Home page
Arterioscler. Thromb. Vasc. Bio.Home page
S. Lussier-Cacan, A. Bolduc, M. Xhignesse, T. Niyonsenga, and C. F. Sing
Impact of Alcohol Intake on Measures of Lipid Metabolism Depends on Context Defined by Gender, Body Mass Index, Cigarette Smoking, and Apolipoprotein E Genotype
Arterioscler. Thromb. Vasc. Biol., May 1, 2002; 22(5): 824 - 831.
[Abstract] [Full Text] [PDF]


Home page
J. Lipid Res.Home page
C. Pallaud, R. Gueguen, C. Sass, M. Grow, S. Cheng, G. Siest, and S. Visvikis
Genetic influences on lipid metabolism trait variability within the Stanislas Cohort
J. Lipid Res., November 1, 2001; 42(11): 1879 - 1890.
[Abstract] [Full Text] [PDF]


Home page
Genome ResHome page
M.R. Nelson, S.L.R. Kardia, R.E. Ferrell, and C.F. Sing
A Combinatorial Partitioning Method to Identify Multilocus Genotypic Partitions That Predict Quantitative Trait Variation
Genome Res., March 1, 2001; 11(3): 458 - 470.
[Abstract] [Full Text]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.