
Transforming growth factor β1polymorphism and serum levels in Egyptian patients with interstitial lung diseases
Author(s) -
Rania Azmy,
Rana Helmy El Helbawy,
Ashraf Dawood,
Sami El Dahdaouh
Publication year - 2017
Publication title -
egyptian journal of chest diseases and tuberculosis/egyptian journal of chest diseases and tuberculosis
Language(s) - English
Resource type - Journals
eISSN - 2090-9950
pISSN - 0422-7638
DOI - 10.1016/j.ejcdt.2015.12.001
Subject(s) - medicine , genotype , interstitial lung disease , pathogenesis , bronchoalveolar lavage , allele , genotyping , gastroenterology , transforming growth factor , pathology , immunology , lung , gene , genetics , biology
Background: Interstitial lung diseases (ILD) are a heterogeneous group of diffuse parenchymal disorders characterized by different grades of fibrosis and inflammation. A number of proinflammatory and profibrotic extracellular mediators have been implicated in the pathogenesis of ILD. Transforming growth factor beta 1(TGF-β1) is one of these mediators.Objective: The study aimed to investigate the association between two common polymorphisms in the gene encoding TGF-β1 and the risk for the development of ILD and whether those polymorphisms affect the serum level of TGF-β1 or have a relation with disease prognosis.Subjects and methods: The study included 90 subjects who were classified into: 56 patients suffering from ILD and 34 healthy subjects served as controls. Pulmonary function tests, arterial blood gases, serum levels of TGF-β1 were determined for all subjects. Genotyping for codon 10 and codon 25 polymorphisms by PCR-RFLP analysis was performed to be correlated with the serum and bronchoalveolar lavage (BAL) levels of TGF β1 and disease prognosis.Results: The allele frequencies of both polymorphisms showed no significant differences between patients and controls. However the CC genotype of codon 10 polymorphism showed significant correlation with higher levels of serum and BAL TGF-β1 and worse prognosis of the disease.Conclusion: It could be concluded that there is no significant association between codon 10 and codon 25 polymorphisms of TGF-β1 and the risk for development of ILD while there was an association between the genetic variants of codon 10 polymorphism, the serum and BAL levels of TGF-β1 and the prognosis of the disease