Association study of MICA-TM polymorphism with inflammatory bowel disease in the South Tunisian population

• Published in: Genetic testing and molecular biomarkers Vol. 17; no. 8; p. 615
• Main Authors: Kamoun, Arwa, Bouzid, Dorra, Mahfoudh, Nadia, Amouri, Ali, Gaddour, Lilia, Hakim, Faiza, Tahri, Nabil, Masmoudi, Hatem, Makni, Hafedh
• Format: Journal Article
• Language: English
• Published: United States 01-08-2013
• Subjects: Adult; Alleles; Female; Histocompatibility Antigens Class I - genetics; Humans; Inflammatory Bowel Diseases - genetics; Male; Middle Aged; Polymorphism, Genetic; Protein Structure, Tertiary; Tunisia; Tunisia
• ISSN: 1945-0257
• DOI: 10.1089/gtmb.2012.0423

Crohn's disease (CD) and ulcerative colitis (UC) are chronic inflammatory disorders of the gastro-intestinal tract with unknown etiology. Both environmental and genetic factors are involved in the pathogenesis of these inflammatory bowel diseases (IBD).
The purpose of the present study was to determine the association between the polymorphism of the transmembrane region of MICA (MICA-TM), and the genetic susceptibility in Tunisian patients with IBD.
A total of 102 Tunisian patients (66 with UC, 36 with CD) and 123 healthy controls were enrolled in our study. MICA-TM was genotyped by a semiautomatic fluorescent-labelled PCR method, amplicons were analysed on an ABI Prism 310 genotyper. Comparisons of allele frequencies between patients and controls, and between patients' subgroups were performed using SPSS 13.0.
No MICA allele was significantly increased in both groups of IBD compared to controls. The MICA-A5.1 allele was significantly decreased in CD patients (p=0.006, pc=0.03). In UC, MICA-A6 was associated with the presence of extraintestinal manifestations (p=0.04, pc=0.2), whereas MICA-A5 was associated with late age of onset (p=0.04). In CD, MICA-A6 was significantly increased in active disease patients when compared to moderately active or inactive disease (p=0.03, pc=0.15).
Some clinical features of CD and UC may be influenced by specific MICA-TM alleles. In our South Tunisian population, MICA plays a disease modifying role, rather than being an important gene in the susceptibility for developing IBD.