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Transforming Growth Factor-β1 Gene Polymorphisms Are Associated with Disease Progression in Idiopathic Pulmonary Fibrosis

Authors :
Juan Ruiz-Manzano
Josep M. Campistol
Sergio Lario
Antoni Xaubet
César Picado
Alejandra Marin-Arguedas
Julio Ancochea
Jose M. Rodriguez-Arias
Pablo Iñigo
Joaquim Mullol
Eulogio Rodriguez-Becerra
Sergi Sanz
Ferran Morell
Source :
American Journal of Respiratory and Critical Care Medicine. 168:431-435
Publication Year :
2003
Publisher :
American Thoracic Society, 2003.

Abstract

Transforming growth factor-beta1 (TGF-beta1) is a cytokine that plays a key role in the development of idiopathic pulmonary fibrosis. There have been reports on the presence of two genetic polymorphisms in the DNA sequence encoding the leader sequence of the TGF-beta1 protein, located in codons 10 and 25. The objective of this study was to investigate the association between TGF-beta1 gene polymorphisms in codons 10 and 25 and the susceptibility to idiopathic pulmonary fibrosis and the progression of the disease. Compared with healthy control subjects (n = 140), patients with idiopathic pulmonary fibrosis (n = 128) showed no significant deviations in genotype or allele frequencies. One hundred and ten patients with idiopathic pulmonary fibrosis were followed up for 30.3 +/- 25 months. The presence of a proline allele at codon 10 was independently associated with a significant increase in alveolar arterial oxygen tension difference during follow-up, after controlling for the effect of treatment (coefficient = 0.59; 95% confidence intervals, 0.23 to 0.96; p = 0.002). These findings suggest that (1) TGF-beta1 gene polymorphisms in codons 10 and 25 do not predispose to the development of idiopathic pulmonary fibrosis; and (2) TGF-beta1 gene polymorphisms may affect disease progression in patients with idiopathic pulmonary fibrosis.

Details

ISSN :
15354970 and 1073449X
Volume :
168
Database :
OpenAIRE
Journal :
American Journal of Respiratory and Critical Care Medicine
Accession number :
edsair.doi.dedup.....9509389646f4c91c384dbeb5df3ba352
Full Text :
https://doi.org/10.1164/rccm.200210-1165oc