| Literature DB >> 24944807 |
Tomomitsu Tahara1, Tomoyuki Shibata1, Masaaki Okubo1, Takamitsu Ishizuka1, Tomohiko Kawamura1, Hiromi Yamashita1, Masakatsu Nakamura2, Yoshihito Nakagawa1, Mitsuo Nagasaka1, Tomiyasu Arisawa2, Naoki Ohmiya1, Ichiro Hirata1.
Abstract
Previous studies have demonstrated the protective role of inducible heat-shock protein (HSP) 70 in intestinal cells. The HSP70-2 gene has a PstI site due to an A-G transition at the 1,267 position and different genotypes are associated with various levels of mRNA expression. The present study aimed to clarify the effect of the HSP70-2 polymorphism on the risk of ulcerative colitis (UC), including its clinical phenotypes. A total of 121 patients with UC and 500 healthy control (HC) subjects participated in the study. To assess the polymorphisms at the 1,267 position of the HSP70-2 gene, restriction fragment length polymorphism analysis was performed. The subjects in the study were classified by disease behavior, severity and extent of disease. Although no significant difference of the HSP70-2 genotype distribution was identified between the HC and UC groups, the BB genotype exhibited a lower risk of the steroid-dependent phenotype [odds ratio (OR), 0.12; 95% confidence interval (CI), 0.02-0.95; P=0.02]. The same genotype was also associated with a lower risk of the refractory phenotype (OR, 0.16; 95% CI, 0.04-0.73; P=0.01). There was no direct correlation between the polymorphism of the HSP70-2 gene and UC susceptibility. However, there was an association between a reduced risk of the steroid-dependent and refractory phenotypes of UC and the BB genotype.Entities:
Keywords: heat-shock protein 70-2; polymorphism; ulcerative colitis
Year: 2014 PMID: 24944807 PMCID: PMC4051472 DOI: 10.3892/br.2014.288
Source DB: PubMed Journal: Biomed Rep ISSN: 2049-9434