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

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

Authors

  • N.P. Barlo
  • C.H.M. van Moorsel
  • H.J.T. Ruven, et al.

Keywords:

idiopathic pulmonary fibrosis, interstitial lung disease, surfactant protein, biomarker, prognosis

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.

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Published

01-12-2009

Issue

Section

Original Articles: Laboratory Research

How to Cite

1.
Barlo N, van Moorsel C, Ruven, et al. H. Surfactant protein-D predicts survival in patients with idiopathic pulmonary fibrosis. Sarcoidosis Vasc Diffuse Lung Dis [Internet]. 2009 Dec. 1 [cited 2025 Aug. 21];26(2):155-61. Available from: https://mail.mattioli1885journals.com/index.php/sarcoidosis/article/view/2602