Metabolomic Biomarkers Evaluation in Pulmonary Fibrosis (FIBROMET)

University of Campania Luigi Vanvitelli

Status: Completed

Conditions: Pulmonary Fibrosis

Treatments: Diagnostic Test: Fatty acids measurement

Study type: Observational

Funder types: Other

Identifiers

NCT06974799

7721

Details and patient eligibility

About

Pulmonary fibrosis (PF) are a heterogeneous group of interstitial lung diseases who may have a progressive phenotype often associated with loss of lung function, chronic respiratory symptoms, quality of life limitation as well significant morbidity and mortality. The identification of reliable biomarkers able to help in early diagnosis and predict disease progression are crucial for improving patient life. Although many biomarkers have been proposed, there is no consensus on reliable markers for IPF. Alterations in fatty acid (FA) metabolism have drawn increasing attention in the IPF pathogenesis, but there is no consensus on the specific FA changes. Alterations in FA composition have been shown to promote pro-fibrotic traits in epithelial cells, fibroblasts, and myofibroblasts. However, while specific fatty acid (FA) alterations have been identified in the serum of IPF patients, no consensus exists on the exact changes for individual FAs

Enrollment: 59 patients

Sex: All

Ages: 40+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Confirmed IPF diagnosis based on the 2018 ATS/ERS/JRS/ALAT guidelines [PMID: 30168753] or other fibrotising ILDs within the past five years,
• Age ≥ 40 years, 3) ability to provide informed consent.

Exclusion criteria

• A current diagnosis of asthma or chronic obstructive pulmonary disease (COPD), 2) an acute PF exacerbation within the past three months.
• Use of medications who may alter metabolomic biomarkers, ex. statins.

Trial design

59 participants in 1 patient group

Pulmonary Fibrosis patients

Treatment:

Diagnostic Test: Fatty acids measurement