Author/Authors :
Farshad, Shohreh Alborzi Clinical Microbiology Research Center , Rasouli, Manoochehr Alborzi Clinical Microbiology Research Center , Japoni, Aziz Alborzi Clinical Microbiology Research Center , Alborzi, Abdolvahab Alborzi Clinical Microbiology Research Center , Jamshidzadeh, Akram Nemazee Hospital - Shiraz University of Medical Sciences - Shiraz , Hosseinkhani, Ayda Nemazee Hospital - Shiraz University of Medical Sciences - Shiraz , Taghavi, Alireza Gastroenterohepatology Research Center - Nemazee Hospital - Shiraz University of Medical Sciences - Shiraz , Kazemi Asl, Hossein Gastroenterohepatology Research Center - Nemazee Hospital - Shiraz University of Medical Sciences - Shiraz , Ranjbar, Reza Molecular Biology Research Center - Baqiyatallah University of Medical Sciences - Tehran
Abstract :
Background: Previous studies imply that IL-1 and IL-8 gene variations may play a crucial
role in the genetic predisposition to different gastric disorders upon H. pylori infection.
Objective: The aim of this study was to determine the potential association between
the prevalence of certain polymorphic sites and the risk of gastric disorders in
Iranian population. Methods: One hundred and forty three unrelated individuals with
different gastric disorders and 374 normal individuals with no gastric disorders and with
a negative serology test for H. pylori (control group) were studied for the association
between IL-1β (+3953 C/T) and IL-8 (-251 A/T) gene polymorphisms and H. pylorimediated
gastritis and gastric ulcer. An analysis of genotype frequency for these genes
was performed using RFLP-PCR. Results: Based on the data obtained from culture and
pathologic findings, the patients were classified into three subpopulations: H pylori+
non-ulcerative gastritis+, H. pylori+ ulcerative gastritis+ and H. pylori- non-ulcerative
gastritis+. A significantly higher frequency of TT genotype (p=0.02) in IL-1β +3953 in
H. pylori+ ulcerative gastritis+ was revealed compared to the control group. There were
no significant differences among other subpopulations. No significant differences in allele
and genotype frequencies of IL-8 (-251A/T) were found among the patients. Conclusion:
The data suggest that TT genotype in IL-1β +3953 may be a major contributing
genetic risk factor for H. pylori induced gastric ulcer. Moreover, the role of other
bacterial and host response factors, such as bacterial adherence peptides, host chemokines,
and genes involved in gastric acid secretion, must be further investigated in different
ethnic populations.
Keywords :
Polymorphism , IL-8 , IL-1β , Helicobacter pylori , Gastric Diseases