Brief Articles
Copyright ©2009 The WJG Press and Baishideng. All rights reserved.
World J Gastroenterol. Aug 14, 2009; 15(30): 3776-3782
Published online Aug 14, 2009. doi: 10.3748/wjg.15.3776
IL-10 and TNF-α promoter haplotypes are associated with childhood Crohn’s disease location
Rocio Sanchez, Emile Levy, Florin Costea, Daniel Sinnett
Rocio Sanchez, Florin Costea, Research Center, Sainte-Justine University health center, Montreal H3T 1C5, Canada
Emile Levy, Research Center, Sainte-Justine University health center, Department of Nutrition, University of Montreal, Montreal H3T 1C5, Canada
Daniel Sinnett, Research Center, Sainte-Justine University health center, Department of Pediatrics, University of Montreal, Montreal H3T 1C5, Canada
Author contributions: Levy E and Sinnett D designed research; Sanchez R performed experiments; Costea F contributed new analytic tools; Sanchez R and Sinnett D analyzed data; Sanchez R, Levy E and Sinnett D wrote the manuscript.
Correspondence to: Dr. Daniel Sinnett, Research Center, Sainte-Justine University health center, Department of Pediatrics, University of Montreal, 3175 Ste. Catherine Road, Montreal H3T 1C5, Canada. daniel.sinnett@umontreal.ca
Telephone: +1-514-3454931
Fax: +1- 514-3454731
Received: February 19, 2009
Revised: June 19, 2009
Accepted: June 26, 2009
Published online: August 14, 2009
Abstract

AIM: To determine the distribution and frequencies of the genotypes and haplotypes of the genes encoding for the glucocorticoid receptor (GR), the tumor necrosis factor (TNF)-α and the interleukin (IL)-10 in childhood Crohn’s disease (CD) and to assess the impact of the corresponding DNA variants on clinical and disease phenotypes.

METHODS: Ten variants in GR, TNF-α and IL-10 were genotyped in 113 childhood CD cases and 95 healthy subjects, both of French-Canadian origin.

RESULTS: For the GR polymorphisms (R23K and N363S) and IL-10 variants in the 5’flanking region (-1082 G > A, -819 T > C and -592 A > C), no difference was observed in allele and genotype frequencies between CD patients and controls. At the haplotype level, we found three IL-10 haplotypes previously described in Caucasians (GCC, ACC and ATA) and three novel haplotypes only present in IBD patients. When we analyzed the haplotype distribution with the anatomical location of the disease, the GCC haplotype was associated with the colonic and the ACC haplotype with the terminal ileum location, respectively. The genotyping of five polymorphisms in the promoter region of the TNF-α gene (-1031 T > C, -863 A > C, -857 T > C, -308 A > G and -238 A > G) revealed a significant overrepresentation of homozygous -1031 CC among CD patients (OR = 9.9) and an association with the colonic location. For TNF-α, eleven haplotypes were inferred, including two frequent ones, TCCGG and CACGG, which were significantly observed more frequently in controls and cases, respectively.

CONCLUSION: This is one of the first studies investigating the association between haplotype structure and disease location in a CD pediatric cohort. Our results will help to increase our understanding of the genetic determinants of childhood CD.

Keywords: Haplotype; Polymorphism; Crohn’s disease; Glucocorticoid receptor; Interleukin-10; Tumor necrosis factor-α