Occurrence of Polymorphism of Tumor Necrosis Factor Alpha (TNFα-308) in
Children with Chronic Inflammatory Bowel Diseases
Čierna I., Švec P., Jančovičová K., Kovács L.
II. detská klinika LFUK a DFNsP, Bratislava prednosta prof. MUDr. L. Kovács, DrSc., MPH |
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Summary:
Background: Experimental and clinical studies support the important role of tumor necrosis
factor alpha (TNF alpha) in the pathogenesis of inflammatory bowel disease (IBD). Expression
rate of TNF alpha, which is one of the key regulators of inflammatory processes, is genetically
determined. This interindividual variability of expression might be influenced by functional
polymorphisms in the gene of TNF alpha located on chromosome 6. The -308 G/A polymorphism
belong to the most recognized polymorphisms. The promoter with the minor allele A shows a significantly
higher transcriptional activity compared to the common allele G.
Objective: The authors analyzed the frequency of the -308 G/A TNF alpha polymorphism in
a cohort of pediatric patients suffering from Crohn’s disease (CD) and the ulcerative colitis (UC).
Thus far, no study of this kind has been conducted in Slovakia and there is less data available
from pediatric populations in the world literature compared to adults, as well.
Patients and methods: The authors analyzed the polymorphism status in the position -308 of
the TNF alpha gene using a polymerase chain reaction – restriction fragment length polymorphism
(PCR-RFLP) method in 75 pediatric patients with IBD (36 UC and 39 CD) and 120 healthy
controls. They estimated the genotype (GG, GA, AA) as well as the allele frequencies (G, A). The
frequencies of genotypes were related to relapse rates of the patients.Results: In the Crohn’s disease group the authors found a significantly decreased allele frequency
of the studied polymorphism compared to healthy controls (p = 0.049). On the contrary, they
found no significant differences in allele frequencies between the UC patients and healthy controls
(p = 0.615), between UC and CD group (p = 0.191) and between healthy controls and the whole
IBD group (p = 0.11). They did not find any statistically significant differences in relapse rates
between wild type and allele carriers.
Conclusion: The authors report a significantly decreased frequency of the allele A of the TNF
alpha -308 polymorphism in pediatric patients with Crohn’s disease. They could not show any
association between the genotypes (GG, GA, AA) and relapse rates in their cohort.
Key words:
ulcerative colitis, Crohn’s disease, tumor necrosis factor alpha polymorphism TNF
alpha-308
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