Abstract | OBJECTIVES: METHODS: We genotyped FUT2 (rs281377, rs1047781 and rs601338) and FUT3 (rs28362459, rs3745635 and rs3894326) in 485 UC patients and 580 healthy controls using SNaPshot. We also evaluated expression of Lewis a and b antigens in the sigmoid colon of 7 UC patients and 7 patients with benign colonic polyps. RESULTS: The frequencies of mutant allele (A) and genotype (GA+AA) in FUT3 (rs3745635) were higher in UC patients than controls (P = 0.016, 95%CI: 1.339-1.699; P = 0.038, 95%CI: 1.330-1.742, respectively). Stratified analyses revealed that the frequencies of mutant allele (G) and genotype (TG+GG) of FUT3 (rs28362459) were significantly lower in patients with extensive colitis than those with distal colitis (P<0.001, 95%CI: 0.503-0.742; P = 0.001, 95%CI: 0.567-0.786, respectively). Similar conclusions were drawn for the mutant allele (A) and genotype (GA+AA) of FUT3 (rs3745635) in patients with extensive colitis compared to those with distal colitis (P = 0.006, 95%CI: 0.553-0.845; P = 0.011, 95%CI: 0.621-0.900, respectively). Although expression of Lewis b antigen in the sigmoid colon did not differ between UC patients and controls, Lewis a antigen expression was higher in the cryptic epithelium of both inflammatory and non-inflammatory sigmoid colon of UC patients than controls (P = 0.028). CONCLUSIONS: Our findings indicated that polymorphisms in FUT3 and its intestinal expression might be associated with UC pathogenesis.
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Authors | Dingyuan Hu, Daguan Zhang, Shuzi Zheng, Maodong Guo, Xinxin Lin, Yi Jiang |
Journal | PloS one
(PLoS One)
Vol. 11
Issue 1
Pg. e0146557
( 2016)
ISSN: 1932-6203 [Electronic] United States |
PMID | 26766790
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Fucosyltransferases
- 3-galactosyl-N-acetylglucosaminide 4-alpha-L-fucosyltransferase
- galactoside 2-alpha-L-fucosyltransferase
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Topics |
- Adult
- Case-Control Studies
- China
- Colitis, Ulcerative
(genetics)
- Female
- Fucosyltransferases
(genetics, metabolism)
- Humans
- Intestinal Mucosa
(metabolism)
- Male
- Middle Aged
- Polymorphism, Single Nucleotide
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