Cargando…
Longitudinal functional changes with clinically significant radiographic progression in idiopathic pulmonary fibrosis: are we following the right parameters?
BACKGROUND: Progression of the disease in idiopathic pulmonary fibrosis (IPF) is difficult to predict, due to its variable and heterogenous course. The relationship between radiographic progression and functional decline in IPF is unclear. We sought to confirm that a simple HRCT fibrosis visual scor...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7238541/ https://www.ncbi.nlm.nih.gov/pubmed/32429952 http://dx.doi.org/10.1186/s12931-020-01371-7 |
_version_ | 1783536551771242496 |
---|---|
author | Taha, Nada D’Amato, Dejanira Hosein, Karishma Ranalli, Tiziana Sergiacomi, Gianluigi Zompatori, Maurizio Mura, Marco |
author_facet | Taha, Nada D’Amato, Dejanira Hosein, Karishma Ranalli, Tiziana Sergiacomi, Gianluigi Zompatori, Maurizio Mura, Marco |
author_sort | Taha, Nada |
collection | PubMed |
description | BACKGROUND: Progression of the disease in idiopathic pulmonary fibrosis (IPF) is difficult to predict, due to its variable and heterogenous course. The relationship between radiographic progression and functional decline in IPF is unclear. We sought to confirm that a simple HRCT fibrosis visual score is a reliable predictor of mortality in IPF, when longitudinally followed; and to ascertain which pulmonary functional variables best reflect clinically significant radiographic progression. METHODS: One-hundred-twenty-three consecutive patients with IPF from 2 centers were followed for an average of 3 years. Longitudinal changes of HRCT fibrosis scores, forced vital capacity (FVC), total lung capacity and diffusing lung capacity for carbon monoxide were considered. HRCTs were scored by 2 chest radiologists. The primary outcome was lung transplant (LTx)-free survival after the follow-up HRCT. RESULTS: During the follow-up period, 43 deaths and 11 LTx occurred. On average, the HRCT fibrosis score increased significantly, and a longitudinal increase > 7% predicted LTx-free survival significantly, with good specificity, but limited sensitivity. The correlation between radiographic and functional progression was moderately significant. HRCT progression and FVC decline predicted LTx-free survival independently and significantly, with better sensitivity, but worse specificity for a ≥ 5% decline of FVC. However, the area under the curve towards LTx-survival were only 0.61 and 0.62, respectively. CONCLUSIONS: The HRCT fibrosis visual score is a reliable and responsive tool to detect clinically meaningful disease progression. Although no individual pulmonary function test closely reflects radiographic progression, a longitudinal FVC decline improves sensitivity in the detection of clinically significant disease progression. However, the accuracy of these methods remains limited, and better prognostication models need to be found. |
format | Online Article Text |
id | pubmed-7238541 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-72385412020-05-27 Longitudinal functional changes with clinically significant radiographic progression in idiopathic pulmonary fibrosis: are we following the right parameters? Taha, Nada D’Amato, Dejanira Hosein, Karishma Ranalli, Tiziana Sergiacomi, Gianluigi Zompatori, Maurizio Mura, Marco Respir Res Research BACKGROUND: Progression of the disease in idiopathic pulmonary fibrosis (IPF) is difficult to predict, due to its variable and heterogenous course. The relationship between radiographic progression and functional decline in IPF is unclear. We sought to confirm that a simple HRCT fibrosis visual score is a reliable predictor of mortality in IPF, when longitudinally followed; and to ascertain which pulmonary functional variables best reflect clinically significant radiographic progression. METHODS: One-hundred-twenty-three consecutive patients with IPF from 2 centers were followed for an average of 3 years. Longitudinal changes of HRCT fibrosis scores, forced vital capacity (FVC), total lung capacity and diffusing lung capacity for carbon monoxide were considered. HRCTs were scored by 2 chest radiologists. The primary outcome was lung transplant (LTx)-free survival after the follow-up HRCT. RESULTS: During the follow-up period, 43 deaths and 11 LTx occurred. On average, the HRCT fibrosis score increased significantly, and a longitudinal increase > 7% predicted LTx-free survival significantly, with good specificity, but limited sensitivity. The correlation between radiographic and functional progression was moderately significant. HRCT progression and FVC decline predicted LTx-free survival independently and significantly, with better sensitivity, but worse specificity for a ≥ 5% decline of FVC. However, the area under the curve towards LTx-survival were only 0.61 and 0.62, respectively. CONCLUSIONS: The HRCT fibrosis visual score is a reliable and responsive tool to detect clinically meaningful disease progression. Although no individual pulmonary function test closely reflects radiographic progression, a longitudinal FVC decline improves sensitivity in the detection of clinically significant disease progression. However, the accuracy of these methods remains limited, and better prognostication models need to be found. BioMed Central 2020-05-19 2020 /pmc/articles/PMC7238541/ /pubmed/32429952 http://dx.doi.org/10.1186/s12931-020-01371-7 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Taha, Nada D’Amato, Dejanira Hosein, Karishma Ranalli, Tiziana Sergiacomi, Gianluigi Zompatori, Maurizio Mura, Marco Longitudinal functional changes with clinically significant radiographic progression in idiopathic pulmonary fibrosis: are we following the right parameters? |
title | Longitudinal functional changes with clinically significant radiographic progression in idiopathic pulmonary fibrosis: are we following the right parameters? |
title_full | Longitudinal functional changes with clinically significant radiographic progression in idiopathic pulmonary fibrosis: are we following the right parameters? |
title_fullStr | Longitudinal functional changes with clinically significant radiographic progression in idiopathic pulmonary fibrosis: are we following the right parameters? |
title_full_unstemmed | Longitudinal functional changes with clinically significant radiographic progression in idiopathic pulmonary fibrosis: are we following the right parameters? |
title_short | Longitudinal functional changes with clinically significant radiographic progression in idiopathic pulmonary fibrosis: are we following the right parameters? |
title_sort | longitudinal functional changes with clinically significant radiographic progression in idiopathic pulmonary fibrosis: are we following the right parameters? |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7238541/ https://www.ncbi.nlm.nih.gov/pubmed/32429952 http://dx.doi.org/10.1186/s12931-020-01371-7 |
work_keys_str_mv | AT tahanada longitudinalfunctionalchangeswithclinicallysignificantradiographicprogressioninidiopathicpulmonaryfibrosisarewefollowingtherightparameters AT damatodejanira longitudinalfunctionalchangeswithclinicallysignificantradiographicprogressioninidiopathicpulmonaryfibrosisarewefollowingtherightparameters AT hoseinkarishma longitudinalfunctionalchangeswithclinicallysignificantradiographicprogressioninidiopathicpulmonaryfibrosisarewefollowingtherightparameters AT ranallitiziana longitudinalfunctionalchangeswithclinicallysignificantradiographicprogressioninidiopathicpulmonaryfibrosisarewefollowingtherightparameters AT sergiacomigianluigi longitudinalfunctionalchangeswithclinicallysignificantradiographicprogressioninidiopathicpulmonaryfibrosisarewefollowingtherightparameters AT zompatorimaurizio longitudinalfunctionalchangeswithclinicallysignificantradiographicprogressioninidiopathicpulmonaryfibrosisarewefollowingtherightparameters AT muramarco longitudinalfunctionalchangeswithclinicallysignificantradiographicprogressioninidiopathicpulmonaryfibrosisarewefollowingtherightparameters |