Association analysis of SLC22A4, SLC22A5 and DLG5 in Japanese patients with Crohn disease
- 19 October 2004
- journal article
- research article
- Published by Springer Nature in Journal of Human Genetics
- Vol. 49 (12) , 664-668
- https://doi.org/10.1007/s10038-004-0204-x
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.Keywords
This publication has 31 references indexed in Scilit:
- Haplotype structure and association to Crohn's disease of CARD15 mutations in two ethnically divergent populationsEuropean Journal of Human Genetics, 2003
- Absence of mutation in the NOD2/CARD15 gene among 483 Japanese patients with Crohn's diseaseJournal of Human Genetics, 2002
- CARD15/NOD2 Mutational Analysis and Genotype-Phenotype Correlation in 612 Patients with Inflammatory Bowel DiseaseAmerican Journal of Human Genetics, 2002
- A high-throughput SNP typing system for genome-wide association studiesJournal of Human Genetics, 2001
- Association between a Single-Nucleotide Polymorphism in the Promoter of the Human Interleukin-3 Gene and Rheumatoid Arthritis in Japanese Patients, and Maximum-Likelihood Estimation of Combinatorial Effect That Two Genetic Loci Have on Susceptibility to the DiseaseAmerican Journal of Human Genetics, 2001
- Associations of distinct variants of the intestinal mucin gene MUC3A with ulcerative colitis and Crohn's diseaseJournal of Human Genetics, 2001
- Two stage genome–wide search in inflammatory bowel disease provides evidence for susceptibility loci on chromosomes 3, 7 and 12Nature Genetics, 1996
- Mapping of a susceptibility locus for Crohn's disease on chromosome 16Nature, 1996
- Classification of Inflammatory Bowel DiseaseScandinavian Journal of Gastroenterology, 1989
- Counting methods (EM algorithm) in human pedigree analysis: Linkage and segregation analysisAnnals of Human Genetics, 1977