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Idiopathic pulmonary fibrosis disease progression: a dynamic quantitative chest computed tomography follow-up analysis

BACKGROUND: To clarify whether dynamic quantification of variables derived from chest high-resolution computed tomography (HRCT) can assess the progression of idiopathic pulmonary fibrosis (IPF). METHODS: Patients with IPF who underwent serial computed tomography (CT) imaging were retrospectively en...

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Autores principales: Sun, Haishuang, Liu, Min, Kang, Han, Yang, Xiaoyan, Zhang, Peiyao, Zhang, Rongguo, Dai, Huaping, Wang, Chen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10006139/
https://www.ncbi.nlm.nih.gov/pubmed/36915349
http://dx.doi.org/10.21037/qims-22-843
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author Sun, Haishuang
Liu, Min
Kang, Han
Yang, Xiaoyan
Zhang, Peiyao
Zhang, Rongguo
Dai, Huaping
Wang, Chen
author_facet Sun, Haishuang
Liu, Min
Kang, Han
Yang, Xiaoyan
Zhang, Peiyao
Zhang, Rongguo
Dai, Huaping
Wang, Chen
author_sort Sun, Haishuang
collection PubMed
description BACKGROUND: To clarify whether dynamic quantification of variables derived from chest high-resolution computed tomography (HRCT) can assess the progression of idiopathic pulmonary fibrosis (IPF). METHODS: Patients with IPF who underwent serial computed tomography (CT) imaging were retrospectively enrolled. Several structural abnormalities seen on HRCT in IPF were segmented and quantified. Patients were divided into 2 groups according to their pulmonary function test (PFT) results: those with disease stabilization and those with disease progression, and differences between the groups were analyzed. RESULTS: There were no statistically significant differences between the 2 patient groups for the following parameters: baseline PFTs, total lesion extent, lesion extent at different sites in the lungs, and pulmonary vessel-related parameters (with P values ranging from 0.057 to 0.894). Median changes in total lung volume, total lesion volume, and total lesion ratio were significantly higher in patients with worsening disease compared with those with stable disease (P<0.001). There was a significant increase in total lesion volume of 214.73 mL [interquartile range (IQR), 68.26 to 501.46 mL] compared with 3.67 mL (IQR, −71.70 to 85.33 mL) in the disease progression group compared with the disease stability group (P=0.001). The decline in pulmonary vessel volume and number of pulmonary vessel branches was more pronounced in the group with functional worsening compared with the group with functional stability. Moreover, changes in lesion volume ratio were negatively correlated with changes in diffusing capacity of the lungs for carbon monoxide (DLco) during follow-up (R=−0.57, P<0.001), and changes in pulmonary vessel-related parameters demonstrated positive correlation with DLco (with R ranging from 0.27 to 0.53, P<0.001) and forced vital capacity (FVC) (with R ranging from 0.44 to 0.61, P<0.001). CONCLUSIONS: Changes in CT-related parameters during follow-up may have better predictive performance compared with baseline imaging parameters and PFTs for disease progression in IPF.
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spelling pubmed-100061392023-03-12 Idiopathic pulmonary fibrosis disease progression: a dynamic quantitative chest computed tomography follow-up analysis Sun, Haishuang Liu, Min Kang, Han Yang, Xiaoyan Zhang, Peiyao Zhang, Rongguo Dai, Huaping Wang, Chen Quant Imaging Med Surg Original Article BACKGROUND: To clarify whether dynamic quantification of variables derived from chest high-resolution computed tomography (HRCT) can assess the progression of idiopathic pulmonary fibrosis (IPF). METHODS: Patients with IPF who underwent serial computed tomography (CT) imaging were retrospectively enrolled. Several structural abnormalities seen on HRCT in IPF were segmented and quantified. Patients were divided into 2 groups according to their pulmonary function test (PFT) results: those with disease stabilization and those with disease progression, and differences between the groups were analyzed. RESULTS: There were no statistically significant differences between the 2 patient groups for the following parameters: baseline PFTs, total lesion extent, lesion extent at different sites in the lungs, and pulmonary vessel-related parameters (with P values ranging from 0.057 to 0.894). Median changes in total lung volume, total lesion volume, and total lesion ratio were significantly higher in patients with worsening disease compared with those with stable disease (P<0.001). There was a significant increase in total lesion volume of 214.73 mL [interquartile range (IQR), 68.26 to 501.46 mL] compared with 3.67 mL (IQR, −71.70 to 85.33 mL) in the disease progression group compared with the disease stability group (P=0.001). The decline in pulmonary vessel volume and number of pulmonary vessel branches was more pronounced in the group with functional worsening compared with the group with functional stability. Moreover, changes in lesion volume ratio were negatively correlated with changes in diffusing capacity of the lungs for carbon monoxide (DLco) during follow-up (R=−0.57, P<0.001), and changes in pulmonary vessel-related parameters demonstrated positive correlation with DLco (with R ranging from 0.27 to 0.53, P<0.001) and forced vital capacity (FVC) (with R ranging from 0.44 to 0.61, P<0.001). CONCLUSIONS: Changes in CT-related parameters during follow-up may have better predictive performance compared with baseline imaging parameters and PFTs for disease progression in IPF. AME Publishing Company 2023-01-09 2023-03-01 /pmc/articles/PMC10006139/ /pubmed/36915349 http://dx.doi.org/10.21037/qims-22-843 Text en 2023 Quantitative Imaging in Medicine and Surgery. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Sun, Haishuang
Liu, Min
Kang, Han
Yang, Xiaoyan
Zhang, Peiyao
Zhang, Rongguo
Dai, Huaping
Wang, Chen
Idiopathic pulmonary fibrosis disease progression: a dynamic quantitative chest computed tomography follow-up analysis
title Idiopathic pulmonary fibrosis disease progression: a dynamic quantitative chest computed tomography follow-up analysis
title_full Idiopathic pulmonary fibrosis disease progression: a dynamic quantitative chest computed tomography follow-up analysis
title_fullStr Idiopathic pulmonary fibrosis disease progression: a dynamic quantitative chest computed tomography follow-up analysis
title_full_unstemmed Idiopathic pulmonary fibrosis disease progression: a dynamic quantitative chest computed tomography follow-up analysis
title_short Idiopathic pulmonary fibrosis disease progression: a dynamic quantitative chest computed tomography follow-up analysis
title_sort idiopathic pulmonary fibrosis disease progression: a dynamic quantitative chest computed tomography follow-up analysis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10006139/
https://www.ncbi.nlm.nih.gov/pubmed/36915349
http://dx.doi.org/10.21037/qims-22-843
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