19880

Idiopathic Pulmonary Fibrosis and Mutation of TGF-beta Gene, Codon 10

Pourabdollah Mihan نويسنده , Bikhof Maryam نويسنده , Rakhshan Azadeh نويسنده , Mohammad-Taheri Zohreh نويسنده , Mansoori Seyed-Davood نويسنده , Mohammadi Foroozan نويسنده , Masjedi Mohammad-Reza نويسنده

23

28

6

Idiopathic pulmonary fibrosis (IPF) is associated with histological appearance of usual interstitial pneumonia. These fibrotic changes in lung interstitium are mostly attributed to cytokine production such as TGFâ which stimulate migration and differentiation of fibroblast to myofibroblasts. The polymorphism of TGFâ gene was found to be associated with development of IPF. We investigated whether TGFâ1 gene polymorphism in codon 10 is associated with interstitial pulmonary fibrosis in Iranian population. Materials and Methods: The different genotypes of TGFâ1 at (+ 870) position (in codon 10) was studied in41 cases and 83 control subjects. The allele specific PCR method was used for genotyping. Results: In the patient group, the frequency of T allele (NO: 58) was 70.7% and C allele (NO: 24) was 29.3%. The frequency of TT genotype (NO: 20) was 48.8%, followed by T/C (NO: 18) 43.9% and CC (No. 3) 7.3% while in the control group, the frequency of T allele (N:117) was approximately 70.5% and C allele (NO: 49) was 29.5%. The frequency of TT genotype in control group (NO: 41) was 49.4%, followed by T/C (NO: 35) 42.2% and C/C (NO: 7)8.4% Conclusion: In comparison with the control group, there was no association between TGFâ1 codon 10 T/C polymorphism in our cases with IPF. (Tanaffos 2009; 8(1): 23-28)

1203909