Published online May 21, 2015. doi: 10.3748/wjg.v21.i19.6052
Peer-review started: October 27, 2014
First decision: November 18, 2014
Revised: December 20, 2014
Accepted: February 12, 2015
Article in press: February 13, 2015
Published online: May 21, 2015
Processing time: 210 Days and 18.1 Hours
AIM: To evaluate the relationships between CD24 gene polymorphisms and the risk of inflammatory bowel disease (IBD), including ulcerative colitis (UC) and Crohn’s disease (CD).
METHODS: The PubMed, Web of Science and Cochrane Library databases were searched (up to May 30, 2014). The search terms “CD24”, “inflammatory bowel disease”, “Crohn’s disease”, “Ulcerative colitis”, “IBD”, “CD” or “UC”; and “polymorphism”, “mutation” or “variant” were used. Association studies were limited to the English language, but no limitations in terms of race, ethnicity or geographic area were employed. Stata SE12 software was used to calculate the pooled odds ratios (ORs) with 95% confidence intervals (CIs). P < 0.05 was considered statistically significant. The information was independently extracted from each eligible study by two investigators. Two common polymorphisms, C170T (rs8734) and TG1527del (rs3838646), in the CD24 gene were assessed.
RESULTS: A total of three case-control studies including 2342 IBD patients and 1965 healthy controls were involved in this meta-analysis. The patients and controls were from Caucasian cohorts. The three articles included in this meta-analysis all conformed to Hardy-Weinberg equilibrium. This meta-analysis revealed that there were no significant associations between the two CD24 polymorphisms and the risk for IBD (all P > 0.05). However, in a disease subgroup analysis, we found that the CD24 C170T polymorphism was associated with an increased risk of UC in a dominant model (OR = 1.79, 95%CI: 1.15-2.77, P = 0.009) and an additive model (OR = 1.87, 95%CI: 1.19-2.93, P = 0.007), but this relationship was not present for CD. The CD24 TG1570del polymorphism was significantly associated with CD in the additive model (OR = 1.24, 95%CI: 1.01-1.52, P = 0.037).
CONCLUSION: Our findings provide evidence that the CD24 C170T polymorphism might contribute to the susceptibility to UC, and the CD24 TG1527del polymorphism might be associated with the risk of CD.
Core tip: CD24 is a significant immune regulatory mediator of inflammatory bowel disease (IBD). Some recent studies have demonstrated that CD24 gene polymorphisms are associated with the susceptibility to IBD, but the findings of other studies are contradictory. The present study sought to provide a more precise estimate of this potential association. A meta-analysis of Caucasian cohorts found that the CD24 C170T polymorphism was associated with the susceptibility to UC and that the CD24 TG1527del polymorphism was associated with CD.