AI Article Synopsis

  • The STAT4 gene has been linked to various autoimmune diseases, and specifically, the T allele of the rs7574865 SNP has been associated with inflammatory bowel disease (IBD) in a Spanish population.
  • A study involving 498 Crohn's disease (CD) patients, 402 ulcerative colitis (UC) patients, and 1296 healthy controls aimed to further investigate this association through genotyping.
  • While the case-control study found no significant association between the STAT4 SNP and CD or UC, a meta-analysis indicated that the T allele is significantly linked to UC susceptibility, suggesting it may be a genetic risk factor for UC in this population.

Article Abstract

Recently, the signal transducer and activator of transcription 4 (STAT4) gene has been associated with multiple autoimmune diseases. Interestingly, a recent work showed that the T allele of the rs7574865 STAT4 SNP was associated with inflammatory bowel disease (IBD) in a Spanish population. The aim of the present study was to reevaluate the role of the STAT4 rs7574865 polymorphism on IBD. The present case-control study included 498 Crohn's disease (CD) patients, 402 ulcerative colitis (UC) patients, and 1296 healthy matched controls. Genotyping was performed using a PCR system with a pre-developed TaqMan allelic discrimination assay for the rs7574865 STAT4 SNP. Moreover, a meta-analysis was performed with the previous work in a Spanish population and the current study, including a final sample size of 1574 IBD patients (820 with CD and 754 with UC) and 2012 healthy controls. No evidence of association was found for the current case-control study (CD: p = 0.23, OR = 0.9, 95% CI = 0.75-1.1; UC: p = 0.17, OR = 1.14, 95% CI = 0.95-1.38). However, the meta-analysis showed that the STAT4 rs7574865 T allele was significantly associated with susceptibility to UC (p = 0.012 pooled; OR = 1.20, 95% CI = 1.04-1.39) but not CD (p = 0.71 pooled; OR = 0.93, 95% CI = 0.65-1.34). Our data suggest that the rs7574865 STAT4 SNP is a genetic susceptibility variant for UC but not CD in the Spanish population.

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http://dx.doi.org/10.1016/j.humimm.2010.02.005DOI Listing

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