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HLA-DRB1 alleles influence clinical phenotypes in Japanese patients with ulcerative colitis
Y Matsumura1, Y Kinouchi, E Nomura
1Division of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, Japan. matmat@white.plala.or.jp
Insights
Human leukocyte antigen (HLA) associations with ulcerative colitis (UC) in Japanese patients reveal HLA-DRB1*09 links to later diagnosis and HLA-DRB1*08 to extended disease, impacting UC phenotypes.
Area of Science:
- Immunogenetics
- Gastroenterology
Background:
- The human leukocyte antigen (HLA) region is linked to inflammatory bowel disease susceptibility.
- HLA-DRB1 influences ulcerative colitis (UC) clinical phenotypes in Caucasians.
- Previous studies identified HLA-DRB1*1502 association with UC in Japanese individuals.
Purpose of the Study:
- To investigate the association between HLA-DRB1 alleles and clinical phenotypes in Japanese patients with UC.
- To determine if specific HLA-DRB1 alleles correlate with disease extent, age at diagnosis, or treatment needs in Japanese UC patients.
Main Methods:
- Genotyping of HLA-DRB1 alleles in 353 Japanese UC patients.
- Classification of patients based on sex, age at diagnosis, disease extent, and treatment requirements.
- Statistical analysis to compare allele frequencies across different clinical subgroups.
Main Results:
- HLA-DRB1*08 allele frequency was significantly higher in patients with extensive UC compared to proctitis (OR=2.20, Pc=0.043).
- HLA-DRB1*09 allele frequency was significantly higher in patients diagnosed at age 40 or older versus before 40 (OR=2.31, Pc=0.022).
- No significant associations were found for other subgroups or alleles.
Conclusions:
- HLA-DRB1*09 is associated with later age at diagnosis in Japanese UC patients.
- HLA-DRB1*08 is associated with greater disease extent in Japanese UC patients.
- HLA-DRB1 alleles contribute to both UC susceptibility and clinical phenotype variation in the Japanese population.
Abstract:
The human leukocyte antigen (HLA) region has been implicated in the disease susceptibility of inflammatory bowel disease by several linkage and association studies. In Caucasians, HLA-DRB1 has been reported to determine the clinical phenotypes of ulcerative colitis (UC). Others and we previously reported that HLA-DRB1*1502 was strongly associated with UC in the Japanese population. However, the contribution of HLA-DRB1 to the clinical phenotypes in Japanese UC has not been elucidated yet. The aim of this study was to determine whether HLA-DRB1 alleles were associated with the clinical phenotypes in Japanese patients with UC. A total of 353 patients with UC were recruited. Patients were classified into subgroups by sex, age at diagnosis, disease extent, need for steroid therapy or need for surgical treatment. The allele frequency of HLA-DRB1*08 was significantly higher in patients whose disease extended beyond the rectum (left-sided and extensive UC) than in those with proctitis [odds ratio (OR)=2.20, Pc=0.043). The allele frequency of HLA-DRB1*09 was significantly higher in patients with UC diagnosed at the age of 40 years or older than in those with UC diagnosed before the age of 40 years (OR=2.31, Pc=0.022). Besides these positive associations, no significant differences were found in the allele frequencies between the other subgroups. We conclude that HLA-DRB1*09 is associated with the age at diagnosis and HLA-DRB1*08 is associated with the disease extent of UC in Japanese. These results indicate that HLA-DRB1 is not only associated with the overall UC susceptibility but also associated with the clinical phenotypes in Japanese.
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