Association of signal transducer and activator of transcription 4 genetic variants with extra-intestinal manifestations in inflammatory bowel disease

Chang Mo Moon, Jae Hee Cheon, Seung Won Kim, Dong Jik Shin, Eun Soo Kim, Eun Soon Shin, Yoon Kang, Jae Jun Park, Sung Pil Hong, Su Youn Nam, Tae Il Kim, Won Ho Kim

Research output: Contribution to journalArticlepeer-review

20 Scopus citations

Abstract

Aims: The STAT4 gene encodes a transcription factor which plays an important role in the development of inflammation of many immune-mediated diseases. We investigated the relationship between STAT4 single nucleotide polymorphisms (SNPs) and susceptibility to ulcerative colitis (UC) and Crohn's disease (CD) and disease phenotypes in the Korean population. Main methods: We performed a case-control association study in individuals with UC (N=246), CD (N=182), and healthy controls (N=229). Key findings: We genotyped 8 STAT4 SNPs (rs11889341, rs7574865, rs8179673, rs6752770, rs925847, rs10168266, rs10181656, and rs11685878) in the STAT4 gene in patients and controls. SNP rs925847 in the STAT4 gene was significantly associated with susceptibility to UC (P=0.025; OR. =0.63) in dominant genotype analysis, though none of these SNPs were associated with CD susceptibility. Moreover, a significant association was identified between SNP rs11889341 and joint involvement (P=0.040; OR. =3.79), and between SNP rs925847 and eye involvement (P=0.030; OR. =2.42) in UC patients. For CD, rs925847 genetic variant was associated with joint (P=0.029; OR. =3.93) and perianal lesions (P=0.033; OR. =2.27). Significance: Our data demonstrated that the STAT4 genetic variants could predispose an individual to IBD and its extra-intestinal ailments in Koreans, suggesting the common pathogenesis of IBD (especially, extra-intestinal manifestations) and other autoimmune diseases.

Original languageEnglish
Pages (from-to)661-667
Number of pages7
JournalLife Sciences
Volume86
Issue number17-18
DOIs
StatePublished - Apr 2010

Bibliographical note

Funding Information:
This work was supported by a grant of the 2009 Good Health R&D Project, Ministry of Health and Welfare, Republic of Korea [grant number A084943 ]. We would like to thank the blood donors for their contribution to this study.

Keywords

  • Crohn's disease
  • Inflammatory bowel disease
  • Polymorphism
  • Signal transducer and activator of transcription 4
  • Ulcerative colitis

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