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Genome wide analysis for mouth ulcers identifies associations at immune regulatory loci.

Tom DuddingSimown HowarthPenelope A LindJ Fah Sathirapongsasutinull nullJoyce Y TungRuth E MitchellLucia Colodro-CondeSarah E MedlandScott D GordonBenjamin ElsworthLavinia PaternosterPaul W FranksSteven J ThomasNicholas G MartinNicholas J Timpson
Published in: Nature communications (2019)
Mouth ulcers are the most common ulcerative condition and encompass several clinical diagnoses, including recurrent aphthous stomatitis (RAS). Despite previous evidence for heritability, it is not clear which specific genetic loci are implicated in RAS. In this genome-wide association study (n = 461,106) heritability is estimated at 8.2% (95% CI: 6.4%, 9.9%). This study finds 97 variants which alter the odds of developing non-specific mouth ulcers and replicate these in an independent cohort (n = 355,744) (lead variant after meta-analysis: rs76830965, near IL12A, OR 0.72 (95% CI: 0.71, 0.73); P = 4.4e-483). Additional effect estimates from three independent cohorts with more specific phenotyping and specific study characteristics support many of these findings. In silico functional analyses provide evidence for a role of T cell regulation in the aetiology of mouth ulcers. These results provide novel insight into the pathogenesis of a common, important condition.
Keyphrases
  • genome wide association study
  • genome wide
  • systematic review
  • copy number
  • genome wide analysis
  • randomized controlled trial
  • dna methylation
  • high throughput
  • genome wide association
  • meta analyses