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. 2004 Feb;59(2):156–158. doi: 10.1136/thorax.2003.006718

Nitric oxide synthase 1 as a potential modifier gene of decline in lung function in patients with cystic fibrosis

J Texereau 1, S Marullo 1, D Hubert 1, J Coste 1, D Dusser 1, J Dall'Ava-Santucci 1, A Dinh-Xuan 1
PMCID: PMC1746921  PMID: 14760158

Abstract

Methods: Dinucleotide GT repeat polymorphism was studied in the 5' untranslated region of the NOS1 gene, immediately upstream from the transcription initiation site, in 59 patients with CF and 59 healthy controls.

Results: Nineteen alleles of the NOS1 gene were identified according to the number of GT repeats (from 18 to 36) in the 5 untranslated region. Exhaled NO levels were significantly correlated with the number of GT repeats. Patients with CF who had the NOS1 genotype associated with high NO production had a slower decline in lung function during the 5 year follow up period. There was no confounding effect of age, chronic bacterial colonisation of the airway, or CFTR genotype.

Conclusions: These data suggest a possible link between the NOS1 gene locus and the rate of decline in lung function in patients with CF.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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