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The Its Not JUST Idiopathic pulmonary fibrosis Study (INJUSTIS): description of the protocol for a multicentre prospective observational cohort study identifying biomarkers of progressive fibrotic lung disease

INTRODUCTION: The Its Not JUST Idiopathic pulmonary fibrosis Study (INJUSTIS) is a multicentre, prospective, observational cohort study. The aims of this study are to identify genetic, serum and other biomarkers that may identify specific molecular mechanisms, reflecting disease endotypes that are s...

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Autores principales: Khan, Fasihul, Stewart, Iain, Howard, Lucy, McKeever, Tricia M, Jones, Steve, Hearson, Glenn, Braybrooke, Rebecca, Edwards, Colin, Jenkins, Gisli, Saini, Gauri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6561382/
https://www.ncbi.nlm.nih.gov/pubmed/31258922
http://dx.doi.org/10.1136/bmjresp-2019-000439
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author Khan, Fasihul
Stewart, Iain
Howard, Lucy
McKeever, Tricia M
Jones, Steve
Hearson, Glenn
Braybrooke, Rebecca
Edwards, Colin
Jenkins, Gisli
Saini, Gauri
author_facet Khan, Fasihul
Stewart, Iain
Howard, Lucy
McKeever, Tricia M
Jones, Steve
Hearson, Glenn
Braybrooke, Rebecca
Edwards, Colin
Jenkins, Gisli
Saini, Gauri
author_sort Khan, Fasihul
collection PubMed
description INTRODUCTION: The Its Not JUST Idiopathic pulmonary fibrosis Study (INJUSTIS) is a multicentre, prospective, observational cohort study. The aims of this study are to identify genetic, serum and other biomarkers that may identify specific molecular mechanisms, reflecting disease endotypes that are shared among patients with progressive pulmonary fibrosis regardless of aetiology. Furthermore, it is anticipated that these biomarkers will help predict fibrotic activity that may identify patterns of disease behaviour with greater accuracy than current clinical phenotyping. METHODS AND ANALYSIS: 200 participants with the multidisciplinary team confirmed fibrotic lung disease (50 each of rheumatoid-interstitial lung disease (ILD), asbestosis, chronic hypersensitivity pneumonitis and unclassifiable ILD) and 50 idiopathic pulmonary fibrosis participants, recruited as positive controls, will be followed up for 2 years. Participants will have blood samples, lung function tests, quality of life questionnaires and a subgroup will be offered bronchoscopy. Participants will also be given the option of undertaking blinded home handheld spirometry for the first 3 months of the study. The primary end point will be identification of a biomarker that predicts disease progression, defined as 10% relative change in forced vital capacity (FVC) or death at 12 months. ETHICS AND DISSEMINATION: The trial has received ethical approval from the National Research Ethics Committee Nottingham (18/EM/0139). All participants must provide written informed consent. The trial will be overseen by the INJUSTIS steering group that will include a patient representative, and an independent chairperson. The results from this study will be submitted for publication in peer-reviewed journals and disseminated at regional and national conferences. TRIAL REGISTRATION NUMBER: NCT03670576.
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spelling pubmed-65613822019-06-28 The Its Not JUST Idiopathic pulmonary fibrosis Study (INJUSTIS): description of the protocol for a multicentre prospective observational cohort study identifying biomarkers of progressive fibrotic lung disease Khan, Fasihul Stewart, Iain Howard, Lucy McKeever, Tricia M Jones, Steve Hearson, Glenn Braybrooke, Rebecca Edwards, Colin Jenkins, Gisli Saini, Gauri BMJ Open Respir Res Biomarkers of Disease INTRODUCTION: The Its Not JUST Idiopathic pulmonary fibrosis Study (INJUSTIS) is a multicentre, prospective, observational cohort study. The aims of this study are to identify genetic, serum and other biomarkers that may identify specific molecular mechanisms, reflecting disease endotypes that are shared among patients with progressive pulmonary fibrosis regardless of aetiology. Furthermore, it is anticipated that these biomarkers will help predict fibrotic activity that may identify patterns of disease behaviour with greater accuracy than current clinical phenotyping. METHODS AND ANALYSIS: 200 participants with the multidisciplinary team confirmed fibrotic lung disease (50 each of rheumatoid-interstitial lung disease (ILD), asbestosis, chronic hypersensitivity pneumonitis and unclassifiable ILD) and 50 idiopathic pulmonary fibrosis participants, recruited as positive controls, will be followed up for 2 years. Participants will have blood samples, lung function tests, quality of life questionnaires and a subgroup will be offered bronchoscopy. Participants will also be given the option of undertaking blinded home handheld spirometry for the first 3 months of the study. The primary end point will be identification of a biomarker that predicts disease progression, defined as 10% relative change in forced vital capacity (FVC) or death at 12 months. ETHICS AND DISSEMINATION: The trial has received ethical approval from the National Research Ethics Committee Nottingham (18/EM/0139). All participants must provide written informed consent. The trial will be overseen by the INJUSTIS steering group that will include a patient representative, and an independent chairperson. The results from this study will be submitted for publication in peer-reviewed journals and disseminated at regional and national conferences. TRIAL REGISTRATION NUMBER: NCT03670576. BMJ Publishing Group 2019-06-04 /pmc/articles/PMC6561382/ /pubmed/31258922 http://dx.doi.org/10.1136/bmjresp-2019-000439 Text en © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and indication of whether changes were made. See: https://creativecommons.org/licenses/by/4.0/.
spellingShingle Biomarkers of Disease
Khan, Fasihul
Stewart, Iain
Howard, Lucy
McKeever, Tricia M
Jones, Steve
Hearson, Glenn
Braybrooke, Rebecca
Edwards, Colin
Jenkins, Gisli
Saini, Gauri
The Its Not JUST Idiopathic pulmonary fibrosis Study (INJUSTIS): description of the protocol for a multicentre prospective observational cohort study identifying biomarkers of progressive fibrotic lung disease
title The Its Not JUST Idiopathic pulmonary fibrosis Study (INJUSTIS): description of the protocol for a multicentre prospective observational cohort study identifying biomarkers of progressive fibrotic lung disease
title_full The Its Not JUST Idiopathic pulmonary fibrosis Study (INJUSTIS): description of the protocol for a multicentre prospective observational cohort study identifying biomarkers of progressive fibrotic lung disease
title_fullStr The Its Not JUST Idiopathic pulmonary fibrosis Study (INJUSTIS): description of the protocol for a multicentre prospective observational cohort study identifying biomarkers of progressive fibrotic lung disease
title_full_unstemmed The Its Not JUST Idiopathic pulmonary fibrosis Study (INJUSTIS): description of the protocol for a multicentre prospective observational cohort study identifying biomarkers of progressive fibrotic lung disease
title_short The Its Not JUST Idiopathic pulmonary fibrosis Study (INJUSTIS): description of the protocol for a multicentre prospective observational cohort study identifying biomarkers of progressive fibrotic lung disease
title_sort its not just idiopathic pulmonary fibrosis study (injustis): description of the protocol for a multicentre prospective observational cohort study identifying biomarkers of progressive fibrotic lung disease
topic Biomarkers of Disease
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6561382/
https://www.ncbi.nlm.nih.gov/pubmed/31258922
http://dx.doi.org/10.1136/bmjresp-2019-000439
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