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Submitted on October 19, 2001
From the Division of Biostatistics (T.R., Y.H., M.A.P., D.C.R.) and Departments of Genetics and Psychiatry (D.C.R.), Washington University School of Medicine, St Louis, Mo; Physical Activity Sciences Laboratory (J.-P.D., L.P.), Lipid Research Center (J.-P.D., J.B.), and Molecular Endocrinology Laboratory (J.G.), Laval University, Québec, Canada; School of Kinesiology and Leisure Studies (A.S.L.), University of Minnesota, Minneapolis; Department of Kinesiology (J.S.S.), Indiana University, Bloomington, Ind; Department of Health and Kinesiology (J.H.W.), Texas A&M University, College Station, Tex; and Pennington Biomedical Research Center (C.B.), Baton Rouge, La. * To whom correspondence should be addressed. E-mail: treva{at}wubios.wustl.edu.
BackgroundFasting levels of plasma lipids and lipoproteins are reported to improve with regular exercise training. However, little is known on whether the training responses are influenced by heritable factors. Methods and ResultsThe lipid profile was assessed in 115 black (224 individuals) and 99 white families (469 individuals), who participated in the HERITAGE Family Study, while in a sedentary state (baseline visit) and after exercise training for 20 weeks (post visit). Variables included total cholesterol, triglyceride, low-density lipoprotein cholesterol (LDL-C), apolipoprotein B (ApoB), high-density lipoprotein cholesterol (HDL-C), apolipoprotein A-I, and HDL-C subfractions 2 (HDL2-C) and 3 (HDL3-C). Familial correlations for the training responses ( ConclusionsHeritable factors in part determine lipid profile responses to regular exercise. Maximal heritabilities were similar across ethnic groups and variables, except for
Revised on February 13, 2002
Accepted on February 14, 2002
Familial Aggregation of Blood Lipid Response to
Exercise Training in the Health, Risk Factors, Exercise Training, and
Genetics (HERITAGE) Family Study
Treva Rice PhD*,
=post-baseline) were significant for most variables, and the percent variance accounted for by familial factors (ie, maximal heritabilities) ranged from 25% to 38%. Exceptions were for higher heritabilities near 60% for
ApoB in blacks and
HDL2-C in whites and a lower estimate of zero for
LDL-C in blacks.
LDL-C,
ApoB, and
HDL2-C. Molecular studies to identify the markers and genes associated with these influences are currently underway.
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