Surfactant protein-D predicts survival in patients with idiopathic pulmonary fibrosis

N. P. Barlo, C. H.M. Van Moorsel, H. J.T. Ruven, P. Zanen, J. M.M. Van Den Bosch, J. C. Grutters

Research output: Contribution to journalArticleAcademicpeer-review

63 Citations (Scopus)

Abstract

Background: Idiopathic pulmonary fibrosis is a progressive interstitial lung disease with a high mortality rate. As lung transplantation is the only therapeutic option, it is important to predict survival. Objective: This study evaluates the clinical value of surfactant protein-D as a marker of prognosis in patients with idiopathic pulmonary fibrosis. Design: Surfactant protein-D was measured in serum of 72 patients and 305 healthy controls. The optimal cut-off level to define unfavourable prognosis was determined using a ROC analysis. A Cox's proportional Hazards model was used to evaluate variables that were significant predictors of survival. Results: Serum levels of surfactant protein-D were significantly higher in patients than in controls. ROC analysis showed 460 ng/ml to be the optimal cut-off level to discriminate survivor from non-survivors after 1 year. Patients with high levels (> 460 ng/ml) had a median survival time of 13 months, compared to 67 months in the group with low levels (< 460 ng/ml). Surfactant protein-D showed to be a significant predictor of prognosis, even when corrected for age, sex, smoking, and lung function. Conclusion: The measurement of surfactant protein-D in serum of patients with idiopathic pulmonary fibrosis might be a clinically relevant tool to predict survival.

Original languageEnglish
Pages (from-to)155-161
Number of pages7
JournalSarcoidosis Vasculitis and Diffuse Lung Diseases
Volume26
Issue number2
Publication statusPublished - 2009

Keywords

  • Biomarker
  • Idiopathic pulmonary fibrosis
  • Interstitial lung disease
  • Prognosis
  • Surfactant protein

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