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Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge.

Authors :
Saxena R
Hivert MF
Langenberg C
Tanaka T
Pankow JS
Vollenweider P
Lyssenko V
Bouatia-Naji N
Dupuis J
Jackson AU
Kao WH
Li M
Glazer NL
Manning AK
Luan J
Stringham HM
Prokopenko I
Johnson T
Grarup N
Boesgaard TW
Lecoeur C
Shrader P
O'Connell J
Ingelsson E
Couper DJ
Rice K
Song K
Andreasen CH
Dina C
Köttgen A
Le Bacquer O
Pattou F
Taneera J
Steinthorsdottir V
Rybin D
Ardlie K
Sampson M
Qi L
van Hoek M
Weedon MN
Aulchenko YS
Voight BF
Grallert H
Balkau B
Bergman RN
Bielinski SJ
Bonnefond A
Bonnycastle LL
Borch-Johnsen K
Böttcher Y
Brunner E
Buchanan TA
Bumpstead SJ
Cavalcanti-Proença C
Charpentier G
Chen YD
Chines PS
Collins FS
Cornelis M
J Crawford G
Delplanque J
Doney A
Egan JM
Erdos MR
Firmann M
Forouhi NG
Fox CS
Goodarzi MO
Graessler J
Hingorani A
Isomaa B
Jørgensen T
Kivimaki M
Kovacs P
Krohn K
Kumari M
Lauritzen T
Lévy-Marchal C
Mayor V
McAteer JB
Meyre D
Mitchell BD
Mohlke KL
Morken MA
Narisu N
Palmer CN
Pakyz R
Pascoe L
Payne F
Pearson D
Rathmann W
Sandbaek A
Sayer AA
Scott LJ
Sharp SJ
Sijbrands E
Singleton A
Siscovick DS
Smith NL
Sparsø T
Swift AJ
Syddall H
Thorleifsson G
Tönjes A
Tuomi T
Tuomilehto J
Valle TT
Waeber G
Walley A
Waterworth DM
Zeggini E
Zhao JH
Illig T
Wichmann HE
Wilson JF
van Duijn C
Hu FB
Morris AD
Frayling TM
Hattersley AT
Thorsteinsdottir U
Stefansson K
Nilsson P
Syvänen AC
Shuldiner AR
Walker M
Bornstein SR
Schwarz P
Williams GH
Nathan DM
Kuusisto J
Laakso M
Cooper C
Marmot M
Ferrucci L
Mooser V
Stumvoll M
Loos RJ
Altshuler D
Psaty BM
Rotter JI
Boerwinkle E
Hansen T
Pedersen O
Florez JC
McCarthy MI
Boehnke M
Barroso I
Sladek R
Froguel P
Meigs JB
Groop L
Wareham NJ
Watanabe RM
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)).

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