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Vol. 59, No. 1, 2005   

Free Abstract     Article (References)     Article (PDF 120 KB)     

Original Paper

Common Genetic and Environmental Effects on Lipid Phenotypes: The HERITAGE Family Study
Mary F. Feitosaa, Treva Ricea, Tuomo Rankinenb, Laura Almasyc, Arthur S. Leond, James S. Skinnere, Jack H. Wilmoref, Claude Bouchardb, D.C. Raoa, g

aDivision of Biostatistics and
gDepartments of Genetics and Psychiatry, Washington University School of Medicine, Saint Louis, Mo.;
bPennington Biomedical Research Center, Louisiana State University System, Baton Rouge, La.;
cDepartment of Genetics, Southwest Foundation for Biomedical Research, San Antonio, Tex.;
dSchool of Kinesiology, University of Minnesota, Minneapolis, Minn.;
eDepartment of Kinesiology, Indiana University, Bloomington, Ind.;
fDepartment of Health and Kinesiology, Texas A&M University, College Station, Tex., USA

Address of Corresponding Author

Hum Hered 2005;59:34-40 (DOI: 10.1159/000084735)


 goto top of page Key Words

  • Lipids
  • Lipoproteins
  • Pleiotropic effect
  • Genetics
  • Exercise
  • Risk factors
  • Coronary heart disease

 goto top of page Abstract

Objective: Despite the well known genetic component influencing plasma lipid-lipoprotein levels and the observed correlations among these traits, little is known about pleiotropic heritable determinants among them. Our aim is to investigate pair-wise polygenic and environmental correlations among lipid-lipoprotein levels at baseline and in response to regular exercise in Whites and Blacks. Methods: Common pair-wise genetic and environmental correlations among levels of total cholesterol (TC), LDL-C, ApoB, HDL-C (also HDL2-C and HDL3-C), triglycerides (TG, HDL-TG and LDL-TG) and ApoA-1 were investigated at baseline and again after a 20-week endurance exercise program using a variance-components-decomposition. Results: With a few exceptions, all lipid phenotypes were heritable at baseline and for training responses in Blacks and Whites. Strong to high genetic and environmental correlations (0.4 < rhog < 0.7) were observed for the majority of the baseline pair-wise traits. For training responses, many of the same patterns were noted, although fewer genetic correlations were significant as compared to the baseline results. Conclusions: Results suggest that the observed phenotypic correlations among many of these traits may be due to in part to pleiotropic genes, in particular between LDL-C and ApoB and between TG and HDL-C. This shared genetic architecture should be considered in follow-up gene finding studies.

Copyright © 2005 S. Karger AG, Basel


 goto top of page Author Contacts

Mary Furlan Feitosa, PhD
Division of Biostatistics, Campus Box 8067
Washington University School of Medicine, 660 S. Euclid
St. Louis, MO 63110-1093 (USA)
Tel. +1 314 747 3792, Fax +1 314 362 2693, E-Mail maryf@wubios.wustl.edu


 goto top of page Article Information

Received: October 11, 2004
Accepted after revision: December 13, 2004
Published online: March 30, 2005
Number of Print Pages : 7
Number of Figures : 0, Number of Tables : 3, Number of References : 28

 
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