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Circulating prostasin is an independent marker of mortality risk in patients with idiopathic pulmonary fibrosis.

Publication ,  Journal Article
Todd, JL; Page, C; Wu, P; Belperio, JA; Maher, TM; Palmer, SM; Leonard, TB; Hesslinger, C; Neely, ML; Schlange, T
Published in: ERJ Open Res
May 2025

BACKGROUND: Prostasin is expressed in the lung epithelium where it regulates fluid and electrolyte balance via sodium channel proteolysis. We investigated whether circulating prostasin levels are associated with the presence and severity of idiopathic pulmonary fibrosis (IPF) and whether prostasin levels, or changes in them, are associated with mortality. METHODS: Patients with IPF came from the IPF-PRO Registry. Controls without lung disease had a similar age/sex distribution. Prostasin was quantified in plasma taken at enrolment and, in the IPF cohort, ∼6 months post-enrolment, by immunoassay. Linear regression was used to compare prostasin levels at enrolment in patients with IPF versus controls and, in the IPF cohort, determine associations between prostasin level and lung function. Multivariable Cox proportional hazards models determined associations between prostasin level at enrolment and change in prostasin level over 6 months and respiratory death. RESULTS: Prostasin level at enrolment was higher in patients with IPF (n=624) versus controls (n=100) (fold-difference 1.75; p<0.001). In the IPF cohort, the difference in disease severity per 1 standard deviation (sd) difference in prostasin was -3.85 for forced vital capacity % predicted and -4.24 for diffusing capacity of the lung for carbon monoxide % predicted (both p<0.001). The adjusted hazard ratio (HR) for respiratory death per 1 sd difference in prostasin at enrolment was 1.20 (95% CI 1.04-1.40, p=0.014, n=624). The adjusted HR for subsequent respiratory death per 1 sd difference in change in prostasin over 6 months was 1.33 (95% CI 1.01-1.74, p=0.041, n=290). CONCLUSIONS: Circulating prostasin is an independent marker of mortality risk in patients with IPF.

Duke Scholars

Published In

ERJ Open Res

DOI

ISSN

2312-0541

Publication Date

May 2025

Volume

11

Issue

3

Location

England

Related Subject Headings

  • 3211 Oncology and carcinogenesis
  • 3201 Cardiovascular medicine and haematology
 

Citation

APA
Chicago
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MLA
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Todd, J. L., Page, C., Wu, P., Belperio, J. A., Maher, T. M., Palmer, S. M., … Schlange, T. (2025). Circulating prostasin is an independent marker of mortality risk in patients with idiopathic pulmonary fibrosis. ERJ Open Res, 11(3). https://doi.org/10.1183/23120541.00738-2024
Todd, Jamie L., Courtney Page, Peitao Wu, John A. Belperio, Toby M. Maher, Scott M. Palmer, Thomas B. Leonard, Christian Hesslinger, Megan L. Neely, and Thomas Schlange. “Circulating prostasin is an independent marker of mortality risk in patients with idiopathic pulmonary fibrosis.ERJ Open Res 11, no. 3 (May 2025). https://doi.org/10.1183/23120541.00738-2024.
Todd JL, Page C, Wu P, Belperio JA, Maher TM, Palmer SM, et al. Circulating prostasin is an independent marker of mortality risk in patients with idiopathic pulmonary fibrosis. ERJ Open Res. 2025 May;11(3).
Todd, Jamie L., et al. “Circulating prostasin is an independent marker of mortality risk in patients with idiopathic pulmonary fibrosis.ERJ Open Res, vol. 11, no. 3, May 2025. Pubmed, doi:10.1183/23120541.00738-2024.
Todd JL, Page C, Wu P, Belperio JA, Maher TM, Palmer SM, Leonard TB, Hesslinger C, Neely ML, Schlange T. Circulating prostasin is an independent marker of mortality risk in patients with idiopathic pulmonary fibrosis. ERJ Open Res. 2025 May;11(3).

Published In

ERJ Open Res

DOI

ISSN

2312-0541

Publication Date

May 2025

Volume

11

Issue

3

Location

England

Related Subject Headings

  • 3211 Oncology and carcinogenesis
  • 3201 Cardiovascular medicine and haematology