Association testing of novel type 2 diabetes risk alleles in the JAZF1, CDC123/CAMK1D, TSPAN8, THADA, ADAMTS9, and NOTCH2 loci with insulin release, insulin sensitivity, and obesity in a population-based sample of 4,516 glucose-tolerant middle-aged Danes

被引:121
作者
Grarup, Niels [1 ]
Andersen, Gitte [1 ]
Krarup, Nikolaj T. [1 ]
Albrechtsen, Anders [2 ]
Schmitz, Ole [3 ,4 ]
Jorgensen, Torben [5 ]
Borch-Johnsen, Knut [1 ,5 ,6 ]
Hansen, Torben [1 ]
Pedersen, Oluf [1 ,6 ]
机构
[1] Steno Diabet Ctr, Copenhagen, Denmark
[2] Univ Copenhagen, Dept Biostat, Copenhagen, Denmark
[3] Aarhus Univ Hosp, Dept Endocrinol & Diabet, DK-8000 Aarhus, Denmark
[4] Univ Aarhus, Dept Clin Pharmacol, Aarhus, Denmark
[5] Glostrup Univ Hosp, Res Ctr Prevent & Hlth, Glostrup, Denmark
[6] Univ Aarhus, Fac Hlth Sci, Aarhus, Denmark
基金
英国医学研究理事会;
关键词
D O I
10.2337/db08-0436
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE-We evaluated the impact on diabetes-related intermediary traits of common novel type 2 diabetes-associated variants in the JAZF1 (rs864745), CDC123/CAMK1D (rs12779790), TSPAN8 (rs7961581), THADA (rs7578597), AD AMTS9 (rs4607103), and NOTCH2 (rs10923931) loci, which were recently identified by meta-analysis of genome-wide association data. RESEARCH DESIGN AND METHODS-We genotyped the six variants in 4,516 middle-aged glucose-tolerant individuals of the population-based Inter99 cohort who were all characterized by an oral glucose tolerance test (OGTT). RESULTS-Homozygous carriers of the minor diabetes risk G-allele of the CDC123/CAMK1D rs12779790 showed an 18% decrease in insulinogenic index (95% CI 10-27%; P = 4 x 10(-5)) an 18% decrease in corrected insulin response (CIR) (8.1-29%; P = 4 x 10(-4)), and a 13% decrease in the ratio of area under the serum-insulin and plasma-glucose curves during an OGTT (AUC-insulin/AUC-glucose) (5.8-20%; P = 4 x 10(-4)). Carriers of the diabetes-associated T-allele of JAZF1 rs864745 had an allele-dependent 3% decrease in BIGTT-AIR (0.9-4.3%; P = 0.003). Furthermore, the diabetes-associated C-allele of TSPAN8 rs7961581 associated with decreased levels of CIR (4.5% [0.5-8.4]; P = 0.03), of AUC-insulin/AUC-glucose ratio (3.9% [1.2-6.7]; P = 0.005), and of the insulinogenic index (5.2% [1.9-8.6]; P = 0.002). No association with traits of insulin release or insulin action was observed for the THADA, ADAMTS9, or NOTCH2 variants. CONCLUSIONS-If replicated, our data suggest that type 2 diabetes at-risk alleles in the JAZF1, CDC123/CAMK1D, and TSPAN8 loci associate with various OGTT-based surrogate measures of insulin release, emphasizing the contribution of abnormal pancreatic beta-cell function in the pathogenesis of type 2 diabetes.
引用
收藏
页码:2534 / 2540
页数:7
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