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Genotypes 677TT and 677CT+1298AC of methylenetetrahydrofolate reductase are associated with the severity of ulcerative colitis in central China
  1. M Chen1,
  2. B Xia1,
  3. R M Rodriguez-Gueant2,
  4. M Bigard2,
  5. J-L Gueant2
  1. 1Department of Internal Medicine and Geriatrics, Zhongnan Hospital and Research Centre of Digestive Diseases, Wuhan University Medical School, Wuhan, RP China
  2. 2INSERM-0014 and Department of Hepato-Gastroenterology, Medical Faculty and University Hospital Centre, University of Nancy, Nancy, France
  1. Correspondence to:
    Dr J-L Gueant
    INSERM-0014 and Department of Hepato-Gastroenterology, Medical Faculty and University Hospital Centre, University of Nancy, Nancy, France; jl.gueantchu-nancy.fr

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Increased blood levels of homocysteine have been found to be associated with inflammatory bowel diseased (IBD) in several studies.1,2 The main genetic determinant associated with elevated plasma levels of homocysteine (t-Hcys) is the MTHFR 677C→ T gene polymorphism of methylenetetrahydrofolate reductase, a critical enzyme involved in the remethylation pathway of homocysteine.3 An association of the MTHFR 677T allele with IBD has been reported in Northern Europe1,4 but not in three other series from Italy and France.5–7 Double heterozygosity MTHFR 677CT+1298AC also produces reduced enzyme activity and increased t-Hcys, but its association with IBD has never been studied. Similarly, the association of IBD with transcobalamin (TCN1 776CG), a genetic determinant that influences transcobalamin levels and t-Hcys, …

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  • Conflict of interest: None declared.