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Volume 101, Issue 5, Pages 944-950 (May 2007)


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Cytokine gene polymorphisms and high-resolution-computed tomography score in idiopathic pulmonary fibrosis

Martina VasakovaaCorresponding Author Informationemail address, Ilja Strizb, Juraj Dutkac, Antonij Slavcevb, Sarka Jandovad, Libor Kolesarb, Jan Sulce

Received 10 April 2006; accepted 10 September 2006. published online 25 October 2006.

Summary 

Introduction

Idiopathic pulmonary fibrosis (IPF) is a serious disease with unknown cause and the influence of cytokine gene polymorphisms is presumed in the etiology and pathogenesis of the disease. We used high-resolution computed tomography (HRCT) as a marker of disease stage and progression and compared the alveolar and interstitial score with IL-1, IL-4, IL-12, IL-1RA and IL-4RA cytokine gene polymorphisms.

Subjects and methods

The IPF patients were all Caucasians from the Czech Republic and consisted of 20 females and 10 males, with a mean age of 65 years, range 36–85. The HRCT results were evaluated by an experienced viewer using the interstitial and alveolar score scales, which were based on the IPF HRCT description system from Gay SE, Kazerooni EA, Tows GB, Lynch JP, Gross BH, Cascade PN, et al. [Idiopathic pulmonary fibrosis. Predicting response to therapy and survival. Am J Respir Crit Care Med 1998;157:1063–72]. We evaluated the polymorphisms of cytokine genes utilizing a PCR with sequence-specific primers method.

Results

The HRCT alveolar score was more pronounced in IL-4 RA (+1902) AG heterozygotes. The HRCT interstitial score was less severe in the IL-12 (−1188) AA homozygotes. According to progression of the HRCT interstitial score, the CC homozygosity at IL-1 RA (mspa 111100), the AA homozygosity at IL-4 RA (+1902) and CC homozygosity at IL-4(+33) positions were more frequent in patients with stable disease compared to those with progressive disease.

Conclusions

We assume from our data that the polymorphisms of IL-4, IL-4RA, IL-1RA and IL-12 genes (genes of cytokines with regulatory activity) might influence the phenotype of IPF as shown by measurable changes in HRCT investigations.

a Department of Respiratory Diseases, 1st Medical School, Charles University, University Thomayer Hospital, Videnska 800, 140 59 Prague 4, Czech Republic

b Department of Immunology, Institute for Clinical and Experimental Medicine, Videnska 1958/9, 140 59, Prague, Czech Republic

c Radiologic Department, University Thomayer Hospital, Videnska 800, 140 59 Prague 4, Czech Republic

d Department of Anthropology, Charles University, Vinicna 8, 120 00 Prague 2, Czech Republic

e Cardiocenter, University Hospital Motol, V Úvalu 54, 150 06 Prague 5, Czech Republic

Corresponding Author InformationCorresponding author. Tel.: +420261083728; fax: +420241951417.

PII: S0954-6111(06)00453-7

doi:10.1016/j.rmed.2006.09.013


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