Serum metalloproteinase-7 as a biomarker of progressive pulmonary fibrosis

Data de publicação:

Autores da FMUP

  • Oksana Sokhatska

    Autor

  • Hélder Novais E Bastos

    Autor

  • José Luís Dias Delgado

    Autor

  • Antonio Manuel Martins De Morais

    Autor

Participantes de fora da FMUP

  • Beltr?o, M
  • Melo, N
  • Caetano Mota, P
  • Terras, A
  • Coelho, D
  • Ara?jo, M

Unidades de investigação

Abstract

<jats:sec><jats:title>Introduction</jats:title><jats:p>Progressive pulmonary fibrosis (PPF) corresponds to any fibrotic interstitial lung disease (ILD) other than idiopathic pulmonary fibrosis (IPF) that presents clinical, physiological and/or radiological evidence of disease progression similar to IPF. Matrix metalloproteinases (MMPs) have been implicated in the pathogenesis of pulmonary fibrosis and are associated with disease progression and reduced survival in IPF and other fibrotic ILDs.</jats:p></jats:sec><jats:sec><jats:title>Aim</jats:title><jats:p>This study aimed to investigate the role of the serum levels of MMP-1 and MMP-7 in patients with fibrotic non-IPF ILD as possible biomarkers of patients at risk of developing PPF.</jats:p></jats:sec><jats:sec><jats:title>Methods</jats:title><jats:p>Newly diagnosed patients with fibrotic non-IPF ILD were included in this study. Serum levels of MMP-1 and MMP-7 were quantified at baseline, and disease progression was monitored. PPF was defined according to the recent ATS/ERS/JRS/ALAT Clinical Practice Guidelines.</jats:p></jats:sec><jats:sec><jats:title>Results</jats:title><jats:p>Seventy-nine patients with fibrotic non-IPF ILDs were included and classified as having PPF or non-PPF. Significantly higher levels of MMP-7, but not MMP-1, were detected in the PPF group (p=0.01). MMP-7 was independently associated with PPF (aOR=1.263; 95% CI 1.029?1.551, p=0.026) after adjustment for sex, age and smoking history. A cut-off value of 3.53?ng?mL<jats:sup>?1</jats:sup>for serum MMP-7 levels had a sensitivity of 61% and a specificity of 74% for predicting PPF in non-IPF ILDs.</jats:p></jats:sec><jats:sec><jats:title>Conclusions</jats:title><jats:p>In patients with fibrotic non-IPF ILDs, serum MMP-7 levels were significantly greater in the subgroup of patients meeting the PPF criteria at follow-up. This can be considered and further investigated as a possible biomarker to identify fibrotic ILD patients at risk of PPF.</jats:p></jats:sec>

Dados da publicação

ISSN/ISSNe:
2312-0541, 2312-0541

ERJ Open Research  European Respiratory Society

Tipo:
Article
Páginas:
2024-

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Keywords

  • DIAGNOSIS; SARCOIDOSIS; VALIDATION; UPDATE; MMP-7

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