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IL18 and IL18R1 polymorphisms, lung CT and fibrosis: a longitudinal study in coal miners

¹ INSERM, U780, and ² University of Paris-Sud 11, Faculty of Medicine, IFR69, Villejuif, France, ³ Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD, and ⁴ Laboratory of Respiratory Biology, National Institute of Environmental Health Sciences, Research Triangle Park, NC, USA.

CORRESPONDENCE: R. Nadif, INSERM, Recherche en Epidémiologie et Biostatistique U780, 16 Avenue Paul Vaillant Couturier, 94807 Villejuif cédex, France. Fax: 33 145595169. E-mail: nadif{at}vjf.inserm.fr

Keywords: Computed tomography, epidemiology, genetics, IL18, IL18R1

Received: March 3, 2006
Accepted August 21, 2006

It has been suggested that interleukin (IL)-18 plays a role in the development of inflammatory and fibrosing lung diseases.

Associations of polymorphisms in the genes coding for IL-18 (IL18 /G-656T, C-607A, G-137C, T113G, C127T) and its receptor (IL18R1 /C-69T) with coal workers' pneumoconiosis (CWP) were studied in 200 miners who were examined in 1990, 1994 and 1999. Coal-dust exposure was assessed according to job history and ambient measures. The main health outcome was lung computed tomography (CT) score in 1990. Internal coherence was assessed by studying CT score in 1994, 4-yr change in CT score and CWP incidence and prevalence.

CT score in 1990 was a good predictor of radiographic grade in 1999 and, therefore, an appropriate subclinical quantitative trait. The IL18 -137C allele was associated with lower CT score in 1990 and 1994 (1.24 versus 1.69 and 1.57 versus 2.46, respectively), slower progression of CT score between 1990 and 1994 and lower pneumoconiosis prevalence in 1999 relative to the G allele (0.33 versus 0.77 and 8.2 versus 19.6%, respectively). Smoking- or dust-adjustment, and stratification on IL18R1 genotype and adjustment for haplotype effects did not change the conclusions.

In conclusion, the results of the present study suggest a role for IL18 in reducing the development of this fibrosing lung disease.

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