A-243A→G polymorphism upstream of the gene encoding GAD65 associates with lower levels of body mass index and glycaemia in a population-based sample of 5857 middle-aged White subjects

被引:7
作者
Boesgaard, T. W.
Castella, S. I.
Andersen, G.
Albrechtsen, A.
Sparso, T.
Borch-Johnsen, K.
Jorgensen, T.
Hansen, T.
Pedersen, O.
机构
[1] Steno Diabet Ctr, DK-2820 Gentofte, Denmark
[2] Glostrup Univ Hosp, Res Ctr Prevent & Hlth, Glostrup, Denmark
[3] Univ Aarhus, Fac Hlth Sci, DK-8000 Aarhus C, Denmark
关键词
association study; body mass index; GAD2; genetics; glucose;
D O I
10.1111/j.1464-5491.2007.02110.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims The glutamate decarboxylase gene (GAD2) encodes GAD65, an enzyme catalysing the production of the gamma-aminobutyric acid (GABA) which interacts with neuropeptide Y to stimulate food intake. It has been suggested that in pancreatic islets, GABA serves as a functional regulator of pancreatic hormone release. Conflicting results have been reported concerning the potential impact of GAD2 variation on estimates of energy metabolism. The aim of this study was to elucidate potential associations between the GAD2-243A -> G polymorphism and levels of body mass index (BMI) and estimates of glycaemia. Methods Using high-throughput chip-based matrix-assisted laser desorption/ionization time-of-flight mass spectrometry, the GAD2-243A -> G (rs2236418) polymorphism was genotyped in a population-based sample (Inter99) of 5857 middle-aged, unrelated Danish White subjects. Results The G-allele was associated with modestly lower BMI (P = 0.01). In a case-control study of obesity, the G-allele frequency in 2582 participants with BMI < 25 kg/m(2) was 19.5% (18.4-20.6) compared with 17.1% (15.5-18.8) in 968 participants having BMI >= 30 kg/m(2) (P = 0.03), odds ratio 0.9 (0.7-1.0). Of the 5857 subjects, GG carriers had lower fasting plasma glucose levels (mmol/l) [AA (n = 3859) 5.6 +/- 0.8; AG (n = 1792) 5.5 +/- 0.8; GG (n = 206) 5.5 +/- 0.8, P = 0.008] and lower 30-min oral glucose tolerance test (OGTT)-related plasma glucose levels (AA 8.7 +/- 1.9; AG 8.6 +/- 1.9; GG 8.6 +/- 2.0, P = 0.04), adjusted for sex, age and BMI. Analysing subjects who were both normoglycaemic and glucose tolerant (n = 4431) GG carriers still had lower fasting plasma glucose concentrations: AA (n = 2895) 5.3 +/- 0.4; AG (n = 1383) 5.3 +/- 0.4; GG (n = 153) 5.2 +/- 0.4 (P = 9.10(-5)). Conclusion The present study suggests that the GAD2-243A -> G polymorphism in a population of middle-aged White people associates with a modest reduction in BMI and fasting and OGTT-related plasma glucose levels.
引用
收藏
页码:702 / 706
页数:5
相关论文
共 29 条
[11]   A genome-wide scan for human obesity genes reveals a major susceptibility locus on chromosome 10 [J].
Hager, J ;
Dina, C ;
Francke, S ;
Dubois, S ;
Houari, M ;
Vatin, V ;
Vaillant, E ;
Lorentz, N ;
Basdevant, A ;
Clement, K ;
Guy-Grand, B ;
Froguel, P .
NATURE GENETICS, 1998, 20 (03) :304-308
[12]   Independent confirmation of a major locus for obesity on chromosome 10 [J].
Hinney, A ;
Ziegler, A ;
Oeffner, F ;
Wedewardt, C ;
Vogel, M ;
Wulftange, H ;
Geller, F ;
Stübing, K ;
Siegfried, W ;
Goldschmidt, HP ;
Remschmidt, H ;
Hebebrand, J .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2000, 85 (08) :2962-2965
[13]   Genome-wide scan of obesity in the old order Amish [J].
Hsueh, WC ;
Mitchell, BD ;
Schneider, JL ;
St Jean, PL ;
Pollin, TI ;
Ehm, MG ;
Wagner, MJ ;
Burns, DK ;
Sakul, H ;
Bell, CJ ;
Shuldiner, AR .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2001, 86 (03) :1199-1205
[14]   Lack of association of glutamate decarboxylase 2 gene polymorphisms with severe obesity in Utah [J].
Hunt, Steven C. ;
Xin, Yuanpei ;
Wu, Lily L. ;
Hopkins, Paul N. ;
Adams, Ted D. .
OBESITY, 2006, 14 (04) :650-655
[15]  
Jorgensen Torben, 2003, Eur J Cardiovasc Prev Rehabil, V10, P377
[16]   CLONING AND PRIMARY STRUCTURE OF A HUMAN ISLET ISOFORM OF GLUTAMIC-ACID DECARBOXYLASE FROM CHROMOSOME-10 [J].
KARLSEN, AE ;
HAGOPIAN, WA ;
GRUBIN, CE ;
DUBE, S ;
DISTECHE, CM ;
ADLER, DA ;
BARMEIER, H ;
MATHEWES, S ;
GRANT, FJ ;
FOSTER, D ;
LERNMARK, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (19) :8337-8341
[17]   DIFFERENTIAL EXPRESSION OF GAD(65) AND GAD(67) IN HUMAN, RAT, AND MOUSE PANCREATIC-ISLETS [J].
KIM, J ;
RICHTER, W ;
AANSTOOT, HJ ;
SHI, YG ;
FU, Q ;
RAJOTTE, R ;
WARNOCK, G ;
BAEKKESKOV, S .
DIABETES, 1993, 42 (12) :1799-1808
[18]   Genome-wide linkage analysis assessing parent-of-origin effects in the inheritance of type 2 diabetes and BMI in Pima Indians [J].
Lindsay, RS ;
Kobes, S ;
Knowler, WC ;
Bennett, PH ;
Hanson, RL .
DIABETES, 2001, 50 (12) :2850-2857
[19]   A locus affecting obesity in human chromosome region 10p12 [J].
Price, RA ;
Li, WD ;
Bernstein, A ;
Crystal, A ;
Golding, EM ;
Weisberg, SJ ;
Zuckerman, WA .
DIABETOLOGIA, 2001, 44 (03) :363-366
[20]   Interactions between neuropeptide Y and γ-aminobutyric acid in stimulation of feeding:: A morphological and pharmacological analysis [J].
Pu, SY ;
Jain, MR ;
Horvath, TL ;
Diano, S ;
Kalra, PS ;
Kalra, SP .
ENDOCRINOLOGY, 1999, 140 (02) :933-940