Large-scale studies of the HphI insulin gene variable-number-of-tandem-repeats polymorphism in relation to Type 2 diabetes mellitus and insulin release

被引:41
作者
Hansen, SK
Gjesing, AP
Rasmussen, SK
Glümer, C
Urhammer, SA
Andersen, G
Rose, CS
Drivsholm, T
Torekov, SK
Jensen, DP
Ekstrom, CT
Borch-Johnsen, K
Jorgensen, T
McCarthy, MI
Hansen, T
Pedersen, O
机构
[1] Steno Diabet Ctr, DK-2820 Gentofte, Denmark
[2] Hagedorn Res Inst, DK-2820 Gentofte, Denmark
[3] Glostrup Univ Hosp, Res Ctr Prevent & Hlth, Glostrup, Denmark
[4] Univ Aarhus, Fac Hlth Sci, Aarhus, Denmark
[5] Univ Oxford, Oxfoed Ctr Diabet Endocrinol & Metab, Oxford, England
关键词
altered birthweight; HphI insulin gene variable-number-of-tandem-repeats (INS-VNTR); polymorphism; insulin release; Type; 2; diabetes;
D O I
10.1007/s00125-004-1418-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims/hypothesis. The class III allele of the variable-number-of-tandem-repeats polymorphism located 5' of the insulin gene (INS-VNTR) has been associated with Type 2 diabetes and altered birthweight. It has also been suggested, although inconsistently, that the class III allele plays a role in glucose-induced insulin response among NGT individuals. Methods. We investigated the impact of the class III allele on Type 2 diabetes susceptibility in a case-control study involving 1462 Type 2 diabetic patients and 4931 NGT subjects. We also examined the potential impact of the class III allele in genotype-quantitative trait studies in three Danish study populations containing (i) 358 young healthy subjects; (ii) 4444 middle-aged NGT subjects, 490 subjects with IFG and 678 subjects with IGT; and (iii) 221 NGT subjects, of whom one parent had Type 2 diabetes. Results. There was no difference in frequency of the class III allele or in genotype distribution between the 1462 Type 2 diabetic patients and the 4931 NGT subjects. Among the 358 young subjects the class III/III carriers had significantly reduced post-IVGTT acute serum insulin and C-peptide responses (p=0.04 and 0.03 respectively). However, among the 4444 middle-aged subjects we failed to demonstrate any association between the class III allele and post-OGTT serum insulin and C-peptide levels. Conclusions/interpretation. The class III allele of the INS-VNTR does not confer susceptibility to Type 2 diabetes or consistent alterations in glucose-induced insulin release in the examined populations, which consisted of Danish Caucasians.
引用
收藏
页码:1079 / 1087
页数:9
相关论文
共 37 条
[1]   INS VNTR allelic variation and dynamic insulin secretion in healthy adult non-diabetic Caucasian subjects [J].
Ahmed, S ;
Bennett, ST ;
Huxtable, SJ ;
Todd, JA ;
Matthews, DR ;
Gough, SCL .
DIABETIC MEDICINE, 1999, 16 (11) :910-917
[2]   The common PPARγ Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes [J].
Altshuler, D ;
Hirschhorn, JN ;
Klannemark, M ;
Lindgren, CM ;
Vohl, MC ;
Nemesh, J ;
Lane, CR ;
Schaffner, SF ;
Bolk, S ;
Brewer, C ;
Tuomi, T ;
Gaudet, D ;
Hudson, TJ ;
Daly, M ;
Groop, L ;
Lander, ES .
NATURE GENETICS, 2000, 26 (01) :76-80
[3]   Insulin gene VNTR genotype is associated with insulin sensitivity and secretion in infancy [J].
Bazaes, RA ;
Petry, CJ ;
Ong, KK ;
Avila, A ;
Dunger, DB ;
Mericq, MV .
CLINICAL ENDOCRINOLOGY, 2003, 59 (05) :599-603
[4]   SUSCEPTIBILITY TO HUMAN TYPE-1 DIABETES AT IDDM2 IS DETERMINED BY TANDEM REPEAT VARIATION AT THE INSULIN GENE MINISATELLITE LOCUS [J].
BENNETT, ST ;
LUCASSEN, AM ;
GOUGH, SCL ;
POWELL, EE ;
UNDLIEN, DE ;
PRITCHARD, LE ;
MERRIMAN, ME ;
KAWAGUCHI, Y ;
DRONSFIELD, MJ ;
POCIOT, F ;
NERUP, J ;
BOUZEKRI, N ;
CAMBONTHOMSEN, A ;
RONNINGEN, KS ;
BARNETT, AH ;
BAIN, SC ;
TODD, JA .
NATURE GENETICS, 1995, 9 (03) :284-292
[5]   Human type 1 diabetes and the insulin gene: Principles of mapping polygenes [J].
Bennett, ST ;
Todd, JA .
ANNUAL REVIEW OF GENETICS, 1996, 30 :343-370
[6]  
Borch-Johnsen K, 1999, LANCET, V354, P617
[7]   High-throughput development and characterization of a genomewide collection of gene-based single nucleotide polymorphism markers by chip-based matrix-assisted laser desorption/ionization time-of-flight mass spectrometry [J].
Buetow, KH ;
Edmonson, M ;
MacDonald, R ;
Clifford, R ;
Yip, P ;
Kelley, J ;
Little, DP ;
Strausberg, R ;
Koester, H ;
Cantor, CR ;
Braun, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (02) :581-584
[8]   Insulin sensitivity index, acute insulin response, and glucose effectiveness in a population-based sample of 380 young healthy Caucasians - Analysis of the impact of gender, body fat, physical fitness, and life-style factors [J].
Clausen, JO ;
BorchJohnsen, K ;
Ibsen, H ;
Bergman, RN ;
Hougaard, P ;
Winther, K ;
Pedersen, O .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 98 (05) :1195-1209
[9]   POLYMORPHISM AT THE 5' END FLANKING REGION OF THE INSULIN GENE IS ASSOCIATED WITH REDUCED INSULIN-SECRETION IN HEALTHY-INDIVIDUALS [J].
COCOZZA, S ;
RICCARDI, G ;
MONTICELLI, A ;
CAPALDO, B ;
GENOVESE, S ;
KROGH, V ;
CELENTANO, E ;
FARINARO, E ;
VARRONE, S ;
AVVEDIMENTO, VE .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 1988, 18 (06) :582-586
[10]   TISSUE-SPECIFIC AND DEVELOPMENTAL STAGE-SPECIFIC IMPRINTING OF THE MOUSE PROINSULIN GENE, INS2 [J].
DELTOUR, L ;
MONTAGUTELLI, X ;
GUENET, JL ;
JAMI, J ;
PALDI, A .
DEVELOPMENTAL BIOLOGY, 1995, 168 (02) :686-688