An uncoupling protein 3 gene polymorphism associated with a lower risk of developing Type II diabetes and with atherogenic lipid profile in a French cohort

被引:80
作者
Meirhaeghe, A
Amouyel, P
Helbecque, N
Cottel, D
Otabe, S
Froguel, P
Vasseur, F
机构
[1] CHRU, Serv Epidemiol & Sante Publ, INSERM U508, Inst Pasteur,Dept Epidemiol & Publ Hlth, F-59019 Lille, France
[2] CHRU, CNRS UPRES A 8090, Inst Biol Lille, F-59019 Lille, France
关键词
uncoupling protein (UCP); polymorphism; Type II diabetes; obesity;
D O I
10.1007/s001250051549
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims/hypothesis. The UCP2-UCP3 gene region has been previously associated with obesity and diabetes. In a large representative cohort of Northern France (MONICA project), we studied the effect of a recently reported CIT polymorphism located in the 5' sequences of the UCP3 gene on anthropometric measurements and Lipid profile. We also examined the association of this polymorphism with obesity and Type II (non-insulin-dependent) diabetes mellitus. Methods. The -55 C/T polymorphism of the UCP3 gene has been genotyped in 1155 subjects from the MONICA project. Association studies were done with diabetes, obesity and related phenotypes. Results were ascertained in a second cohort of well-characterized Type II diabetic and control subjects. Results. The variant T allele was associated with a decreased risk of developing Type II diabetes. Frequencies of the T allele were 13.3 % compared with 22 %, p = 0.04, in the diabetic and control groups, respectively. This observation was confirmed in the second cohort of French Type II diabetic (n = 171) and control (n = 124) subjects: 17.8 % compared with 25 %, p = 0.03. Moreover, subjects bearing the TT genotype had higher plasma total cholesterol and LDL-cholesterol concentrations (p = 0.0006 and p = 0.001, respectively) than subjects bearing wild or heterozygous genotypes. Conclusion/interpretation. The UCP3 -55 C/T polymorphism was associated with a higher atherogenic profile and modified the risk for the development of Type II diabetes.
引用
收藏
页码:1424 / 1428
页数:5
相关论文
共 46 条
[41]   Effects of obesity and stable weight reduction on UCP2 and UCP3 gene expression in humans [J].
Vidal-Puig, A ;
Rosenbaum, M ;
Considine, RC ;
Leibel, RL ;
Dohm, GL ;
Lowell, BB .
OBESITY RESEARCH, 1999, 7 (02) :133-140
[42]   UCP3: An uncoupling protein homologue expressed preferentially and abundantly in skeletal muscle and brown adipose tissue [J].
VidalPuig, A ;
Solanes, G ;
Grujic, D ;
Flier, JS ;
Lowell, BB .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 235 (01) :79-82
[43]   Association between uncoupling protein polymorphisms (UCP2-UCP3) and energy metabolism obesity in Pima Indians [J].
Walder, K ;
Norman, RA ;
Hanson, RL ;
Schrauwen, P ;
Neverova, M ;
Jenkinson, CP ;
Easlick, J ;
Warden, CH ;
Pecqueur, C ;
Raimbault, S ;
Ricquier, D ;
Harper, M ;
Silver, K ;
Shuldiner, AR ;
Solanes, G ;
Lowell, BB ;
Chung, WK ;
Leibel, RL ;
Pratley, R ;
Ravussin, E .
HUMAN MOLECULAR GENETICS, 1998, 7 (09) :1431-1435
[44]   IDENTIFICATION OF 4 CHROMOSOMAL LOCI DETERMINING OBESITY IN A MULTIFACTORIAL MOUSE MODEL [J].
WARDEN, CH ;
FISLER, JS ;
SHOEMAKER, SM ;
WEN, PZ ;
SVENSON, KL ;
PACE, MJ ;
LUSIS, AJ .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (04) :1545-1552
[45]   Elevated free fatty acids induce uncoupling protein 3 expression in muscle - A potential explanation for the effect of fasting [J].
Weigle, DS ;
Selfridge, LE ;
Schwartz, MW ;
Seeley, RJ ;
Cummings, DE ;
Havel, PJ ;
Kuijper, JL ;
BeltrandelRio, H .
DIABETES, 1998, 47 (02) :298-302
[46]   Addition of low-dose rosiglitazone to sulphonylurea therapy improves glycaemic control in Type 2 diabetic patients [J].
Wolffenbuttel, BHR ;
Gomis, R ;
Squatrito, S ;
Jones, NP ;
Patwardhan, RN .
DIABETIC MEDICINE, 2000, 17 (01) :40-47