Literature DB >> 17603484

Common variants in WFS1 confer risk of type 2 diabetes.

Manjinder S Sandhu1, Michael N Weedon, Katherine A Fawcett, Jon Wasson, Sally L Debenham, Allan Daly, Hana Lango, Timothy M Frayling, Rosalind J Neumann, Richard Sherva, Ilana Blech, Paul D Pharoah, Colin N A Palmer, Charlotte Kimber, Roger Tavendale, Andrew D Morris, Mark I McCarthy, Mark Walker, Graham Hitman, Benjamin Glaser, M Alan Permutt, Andrew T Hattersley, Nicholas J Wareham, Inês Barroso.   

Abstract

We studied genes involved in pancreatic beta cell function and survival, identifying associations between SNPs in WFS1 and diabetes risk in UK populations that we replicated in an Ashkenazi population and in additional UK studies. In a pooled analysis comprising 9,533 cases and 11,389 controls, SNPs in WFS1 were strongly associated with diabetes risk. Rare mutations in WFS1 cause Wolfram syndrome; using a gene-centric approach, we show that variation in WFS1 also predisposes to common type 2 diabetes.

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Year:  2007        PMID: 17603484      PMCID: PMC2672152          DOI: 10.1038/ng2067

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


  14 in total

1.  A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome).

Authors:  H Inoue; Y Tanizawa; J Wasson; P Behn; K Kalidas; E Bernal-Mizrachi; M Mueckler; H Marshall; H Donis-Keller; P Crock; D Rogers; M Mikuni; H Kumashiro; K Higashi; G Sobue; Y Oka; M A Permutt
Journal:  Nat Genet       Date:  1998-10       Impact factor: 38.330

2.  Chemical chaperones reduce ER stress and restore glucose homeostasis in a mouse model of type 2 diabetes.

Authors:  Umut Ozcan; Erkan Yilmaz; Lale Ozcan; Masato Furuhashi; Eric Vaillancourt; Ross O Smith; Cem Z Görgün; Gökhan S Hotamisligil
Journal:  Science       Date:  2006-08-25       Impact factor: 47.728

3.  Association studies of genetic variation in the WFS1 gene and type 2 diabetes in U.K. populations.

Authors:  Jayne A L Minton; Andrew T Hattersley; Katharine Owen; Mark I McCarthy; Mark Walker; Farida Latif; Timothy Barrett; Timothy M Frayling
Journal:  Diabetes       Date:  2002-04       Impact factor: 9.461

4.  The common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes.

Authors:  D Altshuler; J N Hirschhorn; M Klannemark; C M Lindgren; M C Vohl; J Nemesh; C R Lane; S F Schaffner; S Bolk; C Brewer; T Tuomi; D Gaudet; T J Hudson; M Daly; L Groop; E S Lander
Journal:  Nat Genet       Date:  2000-09       Impact factor: 38.330

5.  The E23K variant of Kir6.2 associates with impaired post-OGTT serum insulin response and increased risk of type 2 diabetes.

Authors:  Eva-Maria D Nielsen; Lars Hansen; Bendix Carstensen; Søren M Echwald; Thomas Drivsholm; Charlotte Glümer; Birger Thorsteinsson; Knut Borch-Johnsen; Torben Hansen; Oluf Pedersen
Journal:  Diabetes       Date:  2003-02       Impact factor: 9.461

6.  Large-scale association studies of variants in genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) confirm that the KCNJ11 E23K variant is associated with type 2 diabetes.

Authors:  Anna L Gloyn; Michael N Weedon; Katharine R Owen; Martina J Turner; Bridget A Knight; Graham Hitman; Mark Walker; Jonathan C Levy; Mike Sampson; Stephanie Halford; Mark I McCarthy; Andrew T Hattersley; Timothy M Frayling
Journal:  Diabetes       Date:  2003-02       Impact factor: 9.461

7.  Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein.

Authors:  T M Strom; K Hörtnagel; S Hofmann; F Gekeler; C Scharfe; W Rabl; K D Gerbitz; T Meitinger
Journal:  Hum Mol Genet       Date:  1998-12       Impact factor: 6.150

8.  Genetically programmed selective islet beta-cell loss in diabetic subjects with Wolfram's syndrome.

Authors:  A Karasik; C O'Hara; S Srikanta; M Swift; J S Soeldner; C R Kahn; R D Herskowitz
Journal:  Diabetes Care       Date:  1989-02       Impact factor: 19.112

9.  A common polymorphism in the upstream promoter region of the hepatocyte nuclear factor-4 alpha gene on chromosome 20q is associated with type 2 diabetes and appears to contribute to the evidence for linkage in an ashkenazi jewish population.

Authors:  Latisha D Love-Gregory; Jonathon Wasson; Jiyan Ma; Carol H Jin; Benjamin Glaser; Brian K Suarez; M Alan Permutt
Journal:  Diabetes       Date:  2004-04       Impact factor: 9.461

10.  Genetic variation near the hepatocyte nuclear factor-4 alpha gene predicts susceptibility to type 2 diabetes.

Authors:  Kaisa Silander; Karen L Mohlke; Laura J Scott; Erin C Peck; Pablo Hollstein; Andrew D Skol; Anne U Jackson; Panagiotis Deloukas; Sarah Hunt; George Stavrides; Peter S Chines; Michael R Erdos; Narisu Narisu; Karen N Conneely; Chun Li; Tasha E Fingerlin; Sharanjeet K Dhanjal; Timo T Valle; Richard N Bergman; Jaakko Tuomilehto; Richard M Watanabe; Michael Boehnke; Francis S Collins
Journal:  Diabetes       Date:  2004-04       Impact factor: 9.461

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  165 in total

1.  Gene-Lifestyle Interactions in Complex Diseases: Design and Description of the GLACIER and VIKING Studies.

Authors:  Azra Kurbasic; Alaitz Poveda; Yan Chen; Asa Agren; Elisabeth Engberg; Frank B Hu; Ingegerd Johansson; Ines Barroso; Anders Brändström; Göran Hallmans; Frida Renström; Paul W Franks
Journal:  Curr Nutr Rep       Date:  2014-12-01

Review 2.  Determining genetic risk factors for pediatric type 2 diabetes.

Authors:  Angharad R Morgan
Journal:  Curr Diab Rep       Date:  2012-02       Impact factor: 4.810

3.  Type 2 diabetes risk alleles near ADCY5, CDKAL1 and HHEX-IDE are associated with reduced birthweight.

Authors:  E A Andersson; K Pilgaard; C Pisinger; M N Harder; N Grarup; K Faerch; P Poulsen; D R Witte; T Jørgensen; A Vaag; T Hansen; O Pedersen
Journal:  Diabetologia       Date:  2010-05-20       Impact factor: 10.122

4.  Candidate gene studies reveal that the WFS1 gene joins the expanding list of novel type 2 diabetes genes.

Authors:  J Wasson; M A Permutt
Journal:  Diabetologia       Date:  2008-01-15       Impact factor: 10.122

Review 5.  Genes and type 2 diabetes mellitus.

Authors:  Leif Groop; Valeriya Lyssenko
Journal:  Curr Diab Rep       Date:  2008-06       Impact factor: 4.810

6.  Metabolic and cardiovascular traits: an abundance of recently identified common genetic variants.

Authors:  Karen L Mohlke; Michael Boehnke; Gonçalo R Abecasis
Journal:  Hum Mol Genet       Date:  2008-10-15       Impact factor: 6.150

Review 7.  Type 2 diabetes: new genes, new understanding.

Authors:  Inga Prokopenko; Mark I McCarthy; Cecilia M Lindgren
Journal:  Trends Genet       Date:  2008-10-25       Impact factor: 11.639

8.  Impact of polymorphisms in WFS1 on prediabetic phenotypes in a population-based sample of middle-aged people with normal and abnormal glucose regulation.

Authors:  T Sparsø; G Andersen; A Albrechtsen; T Jørgensen; K Borch-Johnsen; A Sandbaek; T Lauritzen; J Wasson; M A Permutt; B Glaser; S Madsbad; O Pedersen; T Hansen
Journal:  Diabetologia       Date:  2008-06-21       Impact factor: 10.122

9.  Association between polymorphisms in SLC30A8, HHEX, CDKN2A/B, IGF2BP2, FTO, WFS1, CDKAL1, KCNQ1 and type 2 diabetes in the Korean population.

Authors:  Yong-Ho Lee; Eun Seok Kang; So Hun Kim; Seung Jin Han; Chul Hoon Kim; Hyeong Jin Kim; Chul Woo Ahn; Bong Soo Cha; Moonsuk Nam; Chung Mo Nam; Hyun Chul Lee
Journal:  J Hum Genet       Date:  2008-11-11       Impact factor: 3.172

10.  The search for putative unifying genetic factors for components of the metabolic syndrome.

Authors:  M Sjögren; V Lyssenko; A Jonsson; G Berglund; P Nilsson; L Groop; M Orho-Melander
Journal:  Diabetologia       Date:  2008-10-14       Impact factor: 10.122

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