Absence of association between the multidrug resistance (MDR1) gene and inflammatory bowel disease

• Published in: Scandinavian journal of gastroenterology 2006-10, Vol.41 (10), p.1174-1182
• Main Authors: Oostenbrug, Liekele E., Dijkstra, Gerard, Nolte, Ilja M., Van Dullemen, Hendrik M., Oosterom, Elvira, Faber, Klaas N., De Jong, Dirk J., Van Der Linde, Klaas, Te Meerman, Gerard J., Van Der Steege, Gerrit, Kleibeuker, Jan H., Jansen, Peter L. M.
• Format: Article
• Language: English
• Subjects: Adult; ATP-Binding Cassette, Sub-Family B, Member 1 - genetics; Biological and medical sciences; CARD15; Colitis, Ulcerative - genetics; Crohn Disease - genetics; Crohn's disease; Drug Resistance, Multiple - genetics; Female; Gastroenterology. Liver. Pancreas. Abdomen; genetic predisposition; Genotype; haplotype sharing statistic; Humans; Inflammatory Bowel Diseases - genetics; Male; MDR1; Medical sciences; Microsatellite Repeats; NOD2; Other diseases. Semiology; Phenotype; Polymorphism, Single Nucleotide; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus; ulcerative colitis
• ISSN: 0036-5521; 1502-7708
• DOI: 10.1080/00365520600575746

Objective. The multidrug resistance (MDR1) gene encodes for P-glycoprotein, a drug efflux pump. Mice deficient for the MDR1a gene spontaneously develop colitis. In humans, a polymorphism in exon 26 (C3435T) is associated with reduced expression levels and function of MDR1. Currently there are controversial data on the association between MDR1 and inflammatory bowel disease (IBD). The purpose of this study was to examine the involvement of this gene in IBD in a large population of Dutch patients with IBD and family-based controls. Material and methods. A total of 781 IBD cases and 315 controls were investigated. CD phenotypes were determined according to the Vienna Classification. Individuals were genotyped for six single nucleotide polymorphisms (SNPs) close to and in the MDR1 locus. This included the C3435T variant and six microsatellite markers close to and in the MDR1 locus. Single locus association analysis, haplotype association analysis and haplotype sharing statistic (HSS) were used to search for differences between patients and controls. Results. No association was observed for any of the SNPs with IBD as a group, or for ulcerative colitis, Crohn's disease and Crohn's disease phenotypes, either by single locus or haplotype association analysis or by HSS. Conclusions. No association was observed between the MDR1 gene and IBD. This suggests that it is unlikely that MDR1 plays a role in IBD susceptibility.