پديد آورندگان :
Talnizifar Bahak نويسنده , Bagheri-Lankarani Kamran نويسنده , Naeemi Siroos نويسنده , Rismankar-Zadeh Maryam نويسنده , Taghavi Alireza نويسنده , Ghaderi Abbas نويسنده
چكيده لاتين :
Transforming growth factor-beta is a regulatory protein that plays a key role
in inflammatory, fibrotic, and immunological events in the intestinal mucosa. Recently,
attention has been focused on the role of transforming growth factor-beta in the
etiopathogenesis of inflammatory bowel disease. Enhanced expression of transforming
growth factor-beta mRNA in the lamina propria and a disordered expression pattern of
transforming growth factor-beta1 receptors I and II in epithelial cells have been documented
in the colonic mucosa of patients with ulcerative colitis and Crohnיs disease. Based on
these associations, we report in this study, the restriction fragment length polymorphismpolymerase
chain reaction and allele frequencies of the transforming growth factor-beta
gene polymorphisms in a population of Iranian patients with ulcerative colitis and healthy
controls. We analyzed whether these two polymorphisms are related with the disease
characteristics.
Methods: One hundred fifty-seven (75 males and 82 females) unrelated patients with
ulcerative colitis attending the Departments of Gastroenterology, Nemazi and Faghihi
Hospitals, affiliated to Shiraz University of Medical Sciences, Shiraz, Iran were enrolled into
this study. Ninety-four age- and sex-matched healthy volunteers with no history of chronic
bloody diarrhea and abdominal pain (41 males and 53 females) served as the control group.
The change at position -509 (CIT) of the transforming growth factor-beta1 gene was studied
using restriction יfragment length polymorphism-polymerase chain reaction in this study.
Results: The mean age of patients was 36.4 (range: 23 - 51) years. The genotype at position
-509 (CIT) in 58 (370/0) patients with ulcerative colitis, and 39 (41.5%) normal subjects, were
homozygous as CC. In addition, 65 (41.5%) patients and 44 (47%) normal individuals were
heterozygous as CT. Thirty-four (21.5%) of 157 patients, and 11 (11.5%) of 94 normal individuals,
were homozygous as TT.
There was no statistically significant difference between patients and normal female individuals
in respect to genotype distribution and allele frequency at the said position (P = 0.138).
Conclusion: No association could be found between transforming growth factor-beta1 -509
(CIT) promoter gene polymorphism and patients with ulcerative colitis.