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Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes

Authors :
Andrew Paterson
Neeraj Kumar
Luis Castaño
Jinny Willis
Valdis Pirags
David Altshuler
Farren Briggs
Neil Walker
Ondrej Cinek
Helen Schuilenburg
Francisco Javier Ampudia Blasco
Claire Vandiedonck
Mark A. Hall
Ana M Wägner
Xiaoying Li
Flemming Pociot
Didac Mauricio
Vaidotas Urbanavicius
Jennifer Couper
Adam Kretowski
Deborah Smyth
Professor David Dunger
Federico Vázquez
Ian Nicholson
Ellen Schofield
John Todd
Angela Simpson
Ingrid Kockum
Mikael Knip
Tadej Battelino
Thomas Brodnicki
Patrick Concannon
Jesús Argente
Johnny Ludvigsson
Peter Colman
Gurvinder Kaur
Vincent Plagnol
Oliver Burren
Rohana Abdul Ghani
Marta Hernández
William McLaren
Alessandro Doria
Raquel Corripio
Stephen Rich
Daniel Metzger
Jesper Johannesen
Steven Willi
Cécile JULIER
Vallo Tillmann
Bart Van der Auwera
Pathology/molecular and cellular medicine
Diabetes Pathology & Therapy
Source :
Nature genetics
Publication Year :
2009
Publisher :
Springer Science and Business Media LLC, 2009.

Abstract

Type 1 diabetes (T1D) is a common autoimmune disorder that arises from the action of multiple genetic and environmental risk factors. We report the findings of a new genome-wide association study of T1D, combined in a meta-analysis with two previously published studies. The total sample set included 7,514 cases and 9,045 reference samples. Forty-one distinct genomic locations provided evidence for association to T1D in the meta-analysis (P < 10-6). After excluding previously reported associations, 27 regions were further tested in an independent set of 4,267 cases, 4,463 controls and 2,319 affected sib-pair (ASP) families. Of these, 18 regions were replicated (P < 0.01; overall P < 5 × 10-8) and four additional regions provided nominal evidence of replication (P < 0.05). The many new candidate genes suggested by these results include IL10, IL19, IL20, GLIS3, CD69 and IL27.

Details

ISSN :
15461718 and 10614036
Volume :
41
Database :
OpenAIRE
Journal :
Nature Genetics
Accession number :
edsair.doi.dedup.....0e5da1ea4d48512559cd190de2484139