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The Role of Mannan-Binding Lectin (MBL) Gene Polymorphism in Ulcerative Colitis
Series studies suggest that enteropathogenic microorganisms play a substantial role in the clinical initiation and relapses of ulcerative colitis (UC). Mannan-binding lectin (MBL) is an important constituent of the innate immune system, and deficiency of MBL has been reported to increase the overall...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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the Society for Free Radical Research Japan
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2212342/ https://www.ncbi.nlm.nih.gov/pubmed/18231631 http://dx.doi.org/10.3164/jcbn.2008009 |
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author | Wang, Fang-Yu Arisawa, Tomiyasu Tahara, Tomomitsu Nagasaka, Mitsuo Fujita, Hiroshi Hirata, Ichiro Nakano, Hiroshi |
author_facet | Wang, Fang-Yu Arisawa, Tomiyasu Tahara, Tomomitsu Nagasaka, Mitsuo Fujita, Hiroshi Hirata, Ichiro Nakano, Hiroshi |
author_sort | Wang, Fang-Yu |
collection | PubMed |
description | Series studies suggest that enteropathogenic microorganisms play a substantial role in the clinical initiation and relapses of ulcerative colitis (UC). Mannan-binding lectin (MBL) is an important constituent of the innate immune system, and deficiency of MBL has been reported to increase the overall susceptibility of an individual to infectious disease. This study was aimed to investigate the associations between polymorphisms of the MBL gene and UC. Recruited in this study were 108 Japanese patients with UC and 144 healthy control subjects. Polymorphism at codon 54 of exon 1 of the MBL gene was investigated by polymerase chain reaction based restriction fragment length polymorphism. In general, no significant difference in MBL polymorphism was found between UC patients and health controls. However, the frequency of A carriers was significantly higher in the relapsing cases than controls (Odds ration = 2.19, 95%CI, 1.10–4.34; p = 0.023), and similar tendency was also found in A/A genotype. In conclusion, the polymorphism at codon 54 of exon 1 of the MBL gene associated with the susceptibility to the relapsing phenotype of ulcerative colitis. It suggests that codon 54 A variants of MBL gene may have an increased risk for the flare-ups of UC. |
format | Text |
id | pubmed-2212342 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | the Society for Free Radical Research Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-22123422008-01-29 The Role of Mannan-Binding Lectin (MBL) Gene Polymorphism in Ulcerative Colitis Wang, Fang-Yu Arisawa, Tomiyasu Tahara, Tomomitsu Nagasaka, Mitsuo Fujita, Hiroshi Hirata, Ichiro Nakano, Hiroshi J Clin Biochem Nutr Original Article Series studies suggest that enteropathogenic microorganisms play a substantial role in the clinical initiation and relapses of ulcerative colitis (UC). Mannan-binding lectin (MBL) is an important constituent of the innate immune system, and deficiency of MBL has been reported to increase the overall susceptibility of an individual to infectious disease. This study was aimed to investigate the associations between polymorphisms of the MBL gene and UC. Recruited in this study were 108 Japanese patients with UC and 144 healthy control subjects. Polymorphism at codon 54 of exon 1 of the MBL gene was investigated by polymerase chain reaction based restriction fragment length polymorphism. In general, no significant difference in MBL polymorphism was found between UC patients and health controls. However, the frequency of A carriers was significantly higher in the relapsing cases than controls (Odds ration = 2.19, 95%CI, 1.10–4.34; p = 0.023), and similar tendency was also found in A/A genotype. In conclusion, the polymorphism at codon 54 of exon 1 of the MBL gene associated with the susceptibility to the relapsing phenotype of ulcerative colitis. It suggests that codon 54 A variants of MBL gene may have an increased risk for the flare-ups of UC. the Society for Free Radical Research Japan 2008-01 2007-12-28 /pmc/articles/PMC2212342/ /pubmed/18231631 http://dx.doi.org/10.3164/jcbn.2008009 Text en Copyright © 2008 JCBN This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Wang, Fang-Yu Arisawa, Tomiyasu Tahara, Tomomitsu Nagasaka, Mitsuo Fujita, Hiroshi Hirata, Ichiro Nakano, Hiroshi The Role of Mannan-Binding Lectin (MBL) Gene Polymorphism in Ulcerative Colitis |
title | The Role of Mannan-Binding Lectin (MBL) Gene Polymorphism in Ulcerative Colitis |
title_full | The Role of Mannan-Binding Lectin (MBL) Gene Polymorphism in Ulcerative Colitis |
title_fullStr | The Role of Mannan-Binding Lectin (MBL) Gene Polymorphism in Ulcerative Colitis |
title_full_unstemmed | The Role of Mannan-Binding Lectin (MBL) Gene Polymorphism in Ulcerative Colitis |
title_short | The Role of Mannan-Binding Lectin (MBL) Gene Polymorphism in Ulcerative Colitis |
title_sort | role of mannan-binding lectin (mbl) gene polymorphism in ulcerative colitis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2212342/ https://www.ncbi.nlm.nih.gov/pubmed/18231631 http://dx.doi.org/10.3164/jcbn.2008009 |
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