RECEPTOR FOR THE ADVANCED GLYCATION END PRODUCTS (RAGE) PROMOTER GENE POLYMORPHISMS IN INFLAMMATORY BOWEL DISEASE | ||||
| Bulletin of Pharmaceutical Sciences Assiut University | ||||
| Volume 47, Issue 2, December 2024, Page 1189-1202 PDF (882.29 K) | ||||
| Document Type: Original Article | ||||
| DOI: 10.21608/bfsa.2024.316076.2255 | ||||
 View on SCiNiTO | ||||
| Authors | ||||
Noha Refaat Abdelhamid  1; Elham Abdelsamie ALi2; Dalia Tarik Kamal3; Abeer Ahmed Mokhtar3; Mohammed Ahmed Medhat 4
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| 1Clinical Pathology Department, Faculty of Medicine, Assuit University | ||||
| 2Clinical Pathology department, Faculty of Medicine, Assuit University. Assuit, Egypt | ||||
| 3Clinical Pathology Department, Faculty of Medicine, Assuit University, Assuit, Egypt | ||||
| 4Tropical Medicine and Gastroenterology, Faculty of Medicine, Assiut University | ||||
| Abstract | ||||
| Background: Inflammatory bowel disease (IBD), consisting of Crohn's disease (CD) and ulcerative colitis (UC), is a chronic immune-mediated disorder, characterised by relapsing and remitting course. As a pattern recognition receptor, RAGE has a known role in intestinal inflammatory responses via the activation of multiple intracellular signalling molecules, such as NF-κB, and mediates neutrophil migration across intestinal epithelial in inflamed intestinal lumen. Aim: We aimed to study the association between RAGE promoter gene polymorphisms (-374T>A & -429 T>C) and risk of disease development, and probable effect on clinical characteristics and management. The study was conducted on 81 control subjects and 90 IBD patients (71 UC & 19 CD), genotyping of -374T>A & -429 T>C SNPs was done using Polymerase Chain Reaction-Restriction Fragment Length Polymorphism (PCR-REFLP). Results: when CD genotypes compared with UC genotypes, the genotype AA and A allele were significantly associated with CD (P=0.014 & 0.026). No significant association between CD and -429T/C genotype, however, the genotype TC of -429T>C SNP might decrease the risk of UC disease (P=0.049, OR=0.047,CI(0.22-0.98)), in addition, patients with extra intestinal manifestations and carrying C allele (TC or CC) were more than those carrying the TT genotype (P=0.007, OR= 22.08, CI= 3.19-444.38) and also patients receiving to biological treatment were having C allele more than TT genotype (P= 0.023, OR=3.9, CI=1.21-12.95). Conclusion: These observed results suggest that RAGE may have a role in disease development and may influence the disease phenotype and further may affect the choice of medical treatment. | ||||
| Keywords | ||||
| Ulcerative Colitis; RAGE; IBD; SNP | ||||
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