Genomic scan for maximal oxygen uptake and its response to training in the HERITAGE Family Study

被引:127
作者
Bouchard, C
Rankinen, T
Chagnon, YC
Rice, T
Pérusse, L
Gagnon, J
Borecki, I
An, P
Leon, AS
Skinner, JS
Wilmore, JH
Province, M
Rao, DC
机构
[1] Louisiana State Univ, Pennington Biomed Res Ctr, Baton Rouge, LA 70808 USA
[2] Univ Laval, Phys Act Sci Lab, St Foy, PQ G1K 7P4, Canada
[3] Washington Univ, Sch Med, Div Biostat, St Louis, MO 63110 USA
[4] Washington Univ, Sch Med, Dept Genet & Psychiat, St Louis, MO 63110 USA
[5] Univ Minnesota, Sch Kinesiol & Leisure Studies, Minneapolis, MN 55455 USA
[6] Indiana Univ, Dept Kinesiol, Bloomington, IN 47405 USA
[7] Texas A&M Univ, Dept Hlth & Kinesiol, College Stn, TX 77843 USA
关键词
genetic markers; quantitative trait locus; linkage; candidate genes;
D O I
10.1152/jappl.2000.88.2.551
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
This study aimed to identify human genomic regions that are linked to maximal oxygen uptake (V(over dot)O(2)max) in sedentary individuals or to the responsiveness of V(over dot)O-2max to a standardized endurance training program. The results of a genomic scan based on 289 polymorphic markers covering all 22 pairs of autosomes performed on the Caucasian families of the HERITAGE Family Study are presented. The mean spacing of the markers was 11 cM, and a total of 99 families and 415 pairs of siblings were available for the study. V(over dot)O-2max in the sedentary state was adjusted for the effects of age, sex, body mass, fat mass, and fat-free mass, whereas the V(over dot)O-2max response was adjusted for age and baseline level of the phenotype. Two analytic strategies were used: a single-point linkage procedure using all available pairs of siblings (SIBPAL) and a multipoint variance components approach using all the family data (SEGPATH). Results indicate that linkages at P values of 0.01 and better are observed with markers on 4q, 8q, 11p, and 14q for V(over dot)O-2max before training and with markers on Ip, 2p, 4q, 6p, and 11p for the change in V(over dot)O-2max,, in response to a 20-wk standardized endurance training program. These chromosomal regions harbor many genes that may qualify as candidate genes for these quantitative traits. They should be investigated in this and other cohorts.
引用
收藏
页码:551 / 559
页数:9
相关论文
共 34 条
[1]  
[Anonymous], 1974, GENETIC ANTHR STUDIE
[2]  
BOUCHARD C, 1995, MED SCI SPORT EXER, V27, P721
[3]   Familial aggregation of VO2max response to exercise training:: results from the HERITAGE Family Study [J].
Bouchard, C ;
An, P ;
Rice, T ;
Skinner, JS ;
Wilmore, JH ;
Gagnon, J ;
Pérusse, L ;
Leon, AS ;
Rao, DC .
JOURNAL OF APPLIED PHYSIOLOGY, 1999, 87 (03) :1003-1008
[4]   Familial resemblance for VO2max in the sedentary state:: the HERITAGE Family Study [J].
Bouchard, C ;
Daw, EW ;
Rice, T ;
Pérusse, L ;
Gagnon, J ;
Province, MA ;
Leon, AS ;
Rao, DC ;
Skinner, JS ;
Wilmore, JH .
MEDICINE AND SCIENCE IN SPORTS AND EXERCISE, 1998, 30 (02) :252-258
[5]  
Bouchard C, 1992, Exerc Sport Sci Rev, V20, P27
[6]  
BOUCHARD C, 1986, MED SCI SPORT EXER, V18, P639
[7]  
BOUCHARD C, IN PRESS ENDURANCE S
[8]   ANTIBODY-RESPONSE TO A SYNTHETIC PEPTIDE COVERING A LAV-1/HTLV-IIIB NEUTRALIZATION EPITOPE AND DISEASE PROGRESSION [J].
BOUCHER, CAB ;
DEWOLF, F ;
HOUWELING, JTM ;
BAKKER, M ;
DEKKER, J ;
ROOS, MTL ;
COUTINHO, RA ;
VANDERNOORDAA, J ;
GOUDSMIT, J .
AIDS, 1989, 3 (02) :71-76
[9]   Red blood cell genetic variation in Olympic endurance athletes [J].
Chagnon, Y. C. ;
Allard, C. ;
Bouchard, C. .
JOURNAL OF SPORTS SCIENCES, 1984, 2 (02) :121-129
[10]  
CHAGNON YC, 1998, 500 LICOR