Cargando…

Association of Fucosyltransferase 2 Gene Polymorphisms with Inflammatory Bowel Disease in Patients from Southeast China

Aims. Fucosyltransferase 2 (FUT2) gene potentially affects the constituent of intestinal microbiota, which play a crucial role in the pathogenesis of inflammatory bowel disease (IBD). This study investigated the association of FUT2 gene polymorphisms with IBD in southeast China. Methods. We collecte...

Descripción completa

Detalles Bibliográficos
Autores principales: Wu, Hao, Sun, Liang, Lin, Dao-po, Shao, Xiao-xiao, Xia, Sheng-long, Lv, Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5266819/
https://www.ncbi.nlm.nih.gov/pubmed/28167958
http://dx.doi.org/10.1155/2017/4148651
_version_ 1782500520784560128
author Wu, Hao
Sun, Liang
Lin, Dao-po
Shao, Xiao-xiao
Xia, Sheng-long
Lv, Ming
author_facet Wu, Hao
Sun, Liang
Lin, Dao-po
Shao, Xiao-xiao
Xia, Sheng-long
Lv, Ming
author_sort Wu, Hao
collection PubMed
description Aims. Fucosyltransferase 2 (FUT2) gene potentially affects the constituent of intestinal microbiota, which play a crucial role in the pathogenesis of inflammatory bowel disease (IBD). This study investigated the association of FUT2 gene polymorphisms with IBD in southeast China. Methods. We collected 671 IBD patients and 502 healthy controls. FUT2 gene polymorphisms (C357T, A385T, and G428A) were determined by SNaPshot. Frequencies of the FUT2 genotypes, alleles, and haplotype between groups were compared by χ(2) test. Results. The allele and genotype frequencies of FUT2 did not differ between ulcerative colitis patients and controls (all P > 0.05). However, mutant allele and genotype of FUT2 (A385T) were significantly increased in Crohn's disease (CD) patients (P = 0.024, OR = 1.271, and 95% CI = 1.031–1.565; P < 0.001, OR = 1.927, and 95% CI = 1.353–2.747, resp.). The same conclusion was drawn from FUT2 (G428A) (P = 0.023, OR = 3.324, and 95% CI = 1.108–9.968; P = 0.044, OR = 1.116–10.137, and 95% CI = 1.116–10.137, resp.). The haplotype TT formed with “C357T and A385T” was more prevalent in CD patients than in controls (P = 0.020, OR = 1.277, and 95% CI = 1.036–1.573). Besides, frequencies of mutant allele and genotype of FUT2 (A385T) were significantly lower in patients with ileocolonic CD than in those with colonic CD (P = 0.001 and 0.002, resp.) and ileal CD (P = 0.007 and 0.004, resp.). Conclusions. FUT2 gene polymorphisms and haplotypes were associated with the susceptibility to CD but not UC.
format Online
Article
Text
id pubmed-5266819
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Hindawi Publishing Corporation
record_format MEDLINE/PubMed
spelling pubmed-52668192017-02-06 Association of Fucosyltransferase 2 Gene Polymorphisms with Inflammatory Bowel Disease in Patients from Southeast China Wu, Hao Sun, Liang Lin, Dao-po Shao, Xiao-xiao Xia, Sheng-long Lv, Ming Gastroenterol Res Pract Research Article Aims. Fucosyltransferase 2 (FUT2) gene potentially affects the constituent of intestinal microbiota, which play a crucial role in the pathogenesis of inflammatory bowel disease (IBD). This study investigated the association of FUT2 gene polymorphisms with IBD in southeast China. Methods. We collected 671 IBD patients and 502 healthy controls. FUT2 gene polymorphisms (C357T, A385T, and G428A) were determined by SNaPshot. Frequencies of the FUT2 genotypes, alleles, and haplotype between groups were compared by χ(2) test. Results. The allele and genotype frequencies of FUT2 did not differ between ulcerative colitis patients and controls (all P > 0.05). However, mutant allele and genotype of FUT2 (A385T) were significantly increased in Crohn's disease (CD) patients (P = 0.024, OR = 1.271, and 95% CI = 1.031–1.565; P < 0.001, OR = 1.927, and 95% CI = 1.353–2.747, resp.). The same conclusion was drawn from FUT2 (G428A) (P = 0.023, OR = 3.324, and 95% CI = 1.108–9.968; P = 0.044, OR = 1.116–10.137, and 95% CI = 1.116–10.137, resp.). The haplotype TT formed with “C357T and A385T” was more prevalent in CD patients than in controls (P = 0.020, OR = 1.277, and 95% CI = 1.036–1.573). Besides, frequencies of mutant allele and genotype of FUT2 (A385T) were significantly lower in patients with ileocolonic CD than in those with colonic CD (P = 0.001 and 0.002, resp.) and ileal CD (P = 0.007 and 0.004, resp.). Conclusions. FUT2 gene polymorphisms and haplotypes were associated with the susceptibility to CD but not UC. Hindawi Publishing Corporation 2017 2017-01-12 /pmc/articles/PMC5266819/ /pubmed/28167958 http://dx.doi.org/10.1155/2017/4148651 Text en Copyright © 2017 Hao Wu et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Wu, Hao
Sun, Liang
Lin, Dao-po
Shao, Xiao-xiao
Xia, Sheng-long
Lv, Ming
Association of Fucosyltransferase 2 Gene Polymorphisms with Inflammatory Bowel Disease in Patients from Southeast China
title Association of Fucosyltransferase 2 Gene Polymorphisms with Inflammatory Bowel Disease in Patients from Southeast China
title_full Association of Fucosyltransferase 2 Gene Polymorphisms with Inflammatory Bowel Disease in Patients from Southeast China
title_fullStr Association of Fucosyltransferase 2 Gene Polymorphisms with Inflammatory Bowel Disease in Patients from Southeast China
title_full_unstemmed Association of Fucosyltransferase 2 Gene Polymorphisms with Inflammatory Bowel Disease in Patients from Southeast China
title_short Association of Fucosyltransferase 2 Gene Polymorphisms with Inflammatory Bowel Disease in Patients from Southeast China
title_sort association of fucosyltransferase 2 gene polymorphisms with inflammatory bowel disease in patients from southeast china
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5266819/
https://www.ncbi.nlm.nih.gov/pubmed/28167958
http://dx.doi.org/10.1155/2017/4148651
work_keys_str_mv AT wuhao associationoffucosyltransferase2genepolymorphismswithinflammatoryboweldiseaseinpatientsfromsoutheastchina
AT sunliang associationoffucosyltransferase2genepolymorphismswithinflammatoryboweldiseaseinpatientsfromsoutheastchina
AT lindaopo associationoffucosyltransferase2genepolymorphismswithinflammatoryboweldiseaseinpatientsfromsoutheastchina
AT shaoxiaoxiao associationoffucosyltransferase2genepolymorphismswithinflammatoryboweldiseaseinpatientsfromsoutheastchina
AT xiashenglong associationoffucosyltransferase2genepolymorphismswithinflammatoryboweldiseaseinpatientsfromsoutheastchina
AT lvming associationoffucosyltransferase2genepolymorphismswithinflammatoryboweldiseaseinpatientsfromsoutheastchina