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Altered DNA methylation within DNMT3A, AHRR, LTA/TNF loci mediates the effect of smoking on inflammatory bowel disease.

Han ZhangRahul KallaTherese HeskethJianhui ZhaoXuan ZhouAlex AdamsAlexandra NobleNicholas T VenthamJudith WellensGwo-Tzer HoMalcolm G DunlopJan Krzysztof NowakYuan DingZhan Ju LiuJack SatsangiEvropi TheodoratouXue Li
Published in: Nature communications (2024)
This work aims to investigate how smoking exerts effect on the development of inflammatory bowel disease (IBD). A prospective cohort study and a Mendelian randomization study are first conducted to evaluate the association between smoking behaviors, smoking-related DNA methylation and the risks of Crohn's disease (CD) and ulcerative colitis (UC). We then perform both genome-wide methylation analysis and co-localization analysis to validate the observed associations. Compared to never smoking, current and previous smoking habits are associated with increased CD (P = 7.09 × 10 -10 ) and UC (P < 2 × 10 -16 ) risk, respectively. DNA methylation alteration at cg17742416 [DNMT3A] is linked to both CD (P = 7.30 × 10 -8 ) and UC (P = 1.04 × 10 -4 ) risk, while cg03599224 [LTA/TNF] is associated with CD risk (P = 1.91 × 10 -6 ), and cg14647125 [AHRR] and cg23916896 [AHRR] are linked to UC risk (P = 0.001 and 0.002, respectively). Our study identifies biological mechanisms and pathways involved in the effects of smoking on the pathogenesis of IBD.
Keyphrases
  • dna methylation
  • genome wide
  • smoking cessation
  • ulcerative colitis
  • gene expression
  • rheumatoid arthritis
  • copy number
  • climate change