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Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge.
- Source :
-
Nature genetics [Nat Genet] 2010 Feb; Vol. 42 (2), pp. 142-8. Date of Electronic Publication: 2010 Jan 17. - Publication Year :
- 2010
-
Abstract
- Glucose levels 2 h after an oral glucose challenge are a clinical measure of glucose tolerance used in the diagnosis of type 2 diabetes. We report a meta-analysis of nine genome-wide association studies (n = 15,234 nondiabetic individuals) and a follow-up of 29 independent loci (n = 6,958-30,620). We identify variants at the GIPR locus associated with 2-h glucose level (rs10423928, beta (s.e.m.) = 0.09 (0.01) mmol/l per A allele, P = 2.0 x 10(-15)). The GIPR A-allele carriers also showed decreased insulin secretion (n = 22,492; insulinogenic index, P = 1.0 x 10(-17); ratio of insulin to glucose area under the curve, P = 1.3 x 10(-16)) and diminished incretin effect (n = 804; P = 4.3 x 10(-4)). We also identified variants at ADCY5 (rs2877716, P = 4.2 x 10(-16)), VPS13C (rs17271305, P = 4.1 x 10(-8)), GCKR (rs1260326, P = 7.1 x 10(-11)) and TCF7L2 (rs7903146, P = 4.2 x 10(-10)) associated with 2-h glucose. Of the three newly implicated loci (GIPR, ADCY5 and VPS13C), only ADCY5 was found to be associated with type 2 diabetes in collaborating studies (n = 35,869 cases, 89,798 controls, OR = 1.12, 95% CI 1.09-1.15, P = 4.8 x 10(-18)).
- Subjects :
- Adenylyl Cyclases genetics
Body Mass Index
Denmark
Diabetes Mellitus, Type 2 genetics
Female
Gene Expression Profiling
Gene Expression Regulation
Genetic Loci genetics
Genome-Wide Association Study
Glucose Tolerance Test
Humans
Incretins genetics
Male
Meta-Analysis as Topic
Polymorphism, Single Nucleotide genetics
Proteins genetics
RNA, Messenger genetics
RNA, Messenger metabolism
Receptors, Gastrointestinal Hormone metabolism
Genetic Variation
Glucose metabolism
Insulin metabolism
Receptors, Gastrointestinal Hormone genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1546-1718
- Volume :
- 42
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Nature genetics
- Publication Type :
- Academic Journal
- Accession number :
- 20081857
- Full Text :
- https://doi.org/10.1038/ng.521