A prevalent polymorphism in the promoter of the UCP3 gene and its relationship to body mass index and long term body weight change in the Danish population

被引:47
作者
Dalgaard, LT
Sorensen, TIA
Drivsholm, T
Borch-Johnsen, K
Andersen, T
Hansen, T
Pedersen, O
机构
[1] Steno Diabet Ctr, DK-2820 Gentofte, Denmark
[2] Copenhagen Univ Hosp, Inst Prevent Med, Danish Epidemiol Sci Ctr, DK-1399 Copenhagen, Denmark
[3] Glostrup Univ Hosp, Ctr Prevent Med, DK-2600 Glostrup, Denmark
[4] Roskilde Cty Hosp, DK-4000 Roskilde, Denmark
关键词
D O I
10.1210/jc.86.3.1398
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Variability of the uncoupling protein 3 (UCP3) promoter has been associated with increased body mass index (BMI) and altered lipid profiles. Here we tested the hypothesis that variation of the UCP3 promoter is associated with either juvenile or maturity-onset obesity or body weight change over a 26-yr follow-up among Danish subjects. Mutation screening of approximately 1 kb 5' upstream of the UCP3 gene revealed one previously described -55 C->T variant. The frequency of the polymorphism was evaluated by restriction fragment length polymorphism analysis in four groups of subjects: 1) a group of 744 obese Danish men who at the draft board examinations had a body mass index (BMI) of at least 31 kg/m(2), 2) a randomly selected control group consisting of 857 draftees, 3) 258 middle-aged subjects, and 4) 409 60-yr-old subjects. The frequency of the T allele was 26.0% (95% confidence interval, 23.8-28.2%) among the obese draftees and 26.9% (24.8-29.0%) in the control group (P = 0.6). The variant was not associated with BMI at a young age or with weight gain after a 26-yr follow-up. The frequency of the T allele was 29.5% (25.6-33.4%) in the middle-aged group and 25.8% (22.8-28.8%) among the 60-yr-old subjects. The polymorphism was not associated with increased BMT or percent body fat in these 2 groups. It is concluded that this variant does not play a major role in the development of common obesity among Danish subjects.
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页码:1398 / 1402
页数:5
相关论文
共 29 条
[1]   Cloning and characterization of the 5′ flanking region of the human uncoupling protein 3 (UCP3) gene [J].
Acín, A ;
Rodriguez, M ;
Rique, H ;
Canet, E ;
Boutin, JA ;
Galizzi, JP .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 258 (02) :278-283
[2]  
Alberti KGMM, 1998, DIABETIC MED, V15, P539, DOI 10.1002/(SICI)1096-9136(199807)15:7<539::AID-DIA668>3.0.CO
[3]  
2-S
[4]   Evidence for at least two major loci influencing human fatness [J].
Borecki, IB ;
Blangero, J ;
Rice, T ;
Pérusse, L ;
Bouchard, C ;
Rao, DC .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (03) :831-838
[5]   Uncoupling protein-3 expression in skeletal muscle and free fatty acids in obesity [J].
Boss, O ;
Bobbioni-Harsch, E ;
Assimacopoulos-Jeannet, F ;
Muzzin, P ;
Munger, R ;
Giacobino, JP ;
Golay, A .
LANCET, 1998, 351 (9120) :1933-1933
[6]   Linkage between markers in the vicinity of the uncoupling protein 2 gene and resting metabolic rate in humans [J].
Bouchard, C ;
Perusse, L ;
Chagnon, YC ;
Warden, C ;
Ricquier, D .
HUMAN MOLECULAR GENETICS, 1997, 6 (11) :1887-1889
[7]   Mice overexpressing human uncoupling protein-3 in skeletal muscle are hyperphagic and lean [J].
Clapham, JC ;
Arch, JRS ;
Chapman, H ;
Haynes, A ;
Lister, C ;
Moore, GBT ;
Piercy, V ;
Carter, SA ;
Lehner, I ;
Smith, SA ;
Beeley, LJ ;
Godden, RJ ;
Herrity, N ;
Skehel, M ;
Changani, KK ;
Hockings, PD ;
Reid, DG ;
Squires, SM ;
Hatcher, J ;
Trail, B ;
Latcham, J ;
Rastan, S ;
Harper, AJ ;
Cadenas, S ;
Buckingham, JA ;
Brand, MD ;
Abuin, A .
NATURE, 2000, 406 (6794) :415-418
[8]  
Colilla S, 2000, GENET EPIDEMIOL, V18, P360, DOI 10.1002/(SICI)1098-2272(200004)18:4<360::AID-GEPI8>3.3.CO
[9]  
2-8
[10]   Linkage exclusion analysis of the chromosome 11 region containing UCP2 and UCP3 with obesity-related phenotypes in Mexican Americans [J].
Comuzzie, AG ;
Almasy, L ;
Cole, SA ;
Boss, O ;
Giacobino, JP ;
Muzzin, P ;
Stern, MP ;
MacCluer, JW ;
Blangero, J ;
Hixson, JE .
INTERNATIONAL JOURNAL OF OBESITY, 2000, 24 (08) :1065-1068