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

Research output: Contribution to journalJournal articleResearchpeer-review

  • Jeffrey C Barrett
  • David G Clayton
  • Patrick Concannon
  • Beena Akolkar
  • Jason D Cooper
  • Henry A Erlich
  • Cécile Julier
  • Grant Morahan
  • Jørn Nerup
  • Concepcion Nierras
  • Vincent Plagnol
  • Pociot, Flemming
  • Helen Schuilenburg
  • Deborah J Smyth
  • Helen Stevens
  • John A Todd
  • Neil M Walker
  • Stephen S Rich
  • The Type 1 Diabetes Genetics Consortium
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 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 with T1D in the meta-analysis (P < 10(-6)). After excluding previously reported associations, we further tested 27 regions 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 x 10(-8)) and 4 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.
Original languageEnglish
JournalNature Genetics
ISSN1061-4036
DOIs
Publication statusPublished - 2009

ID: 21183814