| Literature DB >> 15503241 |
Keiko Yamazaki1, Masakazu Takazoe2, Torao Tanaka2, Toshiki Ichimori3, Susumu Saito4, Aritoshi Iida4, Yoshihiro Onouchi5, Akira Hata5, Yusuke Nakamura6.
Abstract
Crohn disease (CD) is an inflammatory bowel disease characterized by chronic transmural, segmental, and typically granulomatous inflammation of the gut. Recently, two novel candidate gene loci associated with CD, SLC22A4 and SLC22A5 on chromosome 5 known as IBD5 and DLG5 on chromosome 10, were identified through association analysis of Caucasian CD patients. We validated these candidate genes in Japanese patients with CD and found a weak but possible association with both SLC22A4 (P=0.028) and DLG5 (P=0.023). However, the reported genetic variants that were indicated to be causative in the Caucasian population were completely absent in or were not associated with Japanese CD patients. These findings imply significant differences in genetic background with CD susceptibility among different ethnic groups and further indicate some difficulty of population-based studies.Entities:
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Year: 2004 PMID: 15503241 DOI: 10.1007/s10038-004-0204-x
Source DB: PubMed Journal: J Hum Genet ISSN: 1434-5161 Impact factor: 3.172