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Increased regional ventilation as early imaging marker for future disease progression of interstitial lung disease: a feasibility study

OBJECTIVES: Idiopathic pulmonary fibrosis (IPF) is a disease with a poor prognosis and a highly variable course. Pathologically increased ventilation—accessible by functional CT—is discussed as a potential predecessor of lung fibrosis. The purpose of this feasibility study was to investigate whether...

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Autores principales: Scharm, Sarah C., Schaefer-Prokop, Cornelia, Willmann, Moritz, Vogel-Claussen, Jens, Knudsen, Lars, Jonigk, Danny, Fuge, Jan, Welte, Tobias, Wacker, Frank, Prasse, Antje, Shin, Hoen-oh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9381456/
https://www.ncbi.nlm.nih.gov/pubmed/35357537
http://dx.doi.org/10.1007/s00330-022-08702-w
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author Scharm, Sarah C.
Schaefer-Prokop, Cornelia
Willmann, Moritz
Vogel-Claussen, Jens
Knudsen, Lars
Jonigk, Danny
Fuge, Jan
Welte, Tobias
Wacker, Frank
Prasse, Antje
Shin, Hoen-oh
author_facet Scharm, Sarah C.
Schaefer-Prokop, Cornelia
Willmann, Moritz
Vogel-Claussen, Jens
Knudsen, Lars
Jonigk, Danny
Fuge, Jan
Welte, Tobias
Wacker, Frank
Prasse, Antje
Shin, Hoen-oh
author_sort Scharm, Sarah C.
collection PubMed
description OBJECTIVES: Idiopathic pulmonary fibrosis (IPF) is a disease with a poor prognosis and a highly variable course. Pathologically increased ventilation—accessible by functional CT—is discussed as a potential predecessor of lung fibrosis. The purpose of this feasibility study was to investigate whether increased regional ventilation at baseline CT and morphological changes in the follow-up CT suggestive for fibrosis indeed occur in spatial correspondence. METHODS: In this retrospective study, CT scans were performed at two time points between September 2016 and November 2020. Baseline ventilation was divided into four categories ranging from low, normal to moderately, and severely increased (C1–C4). Correlation between baseline ventilation and volume and density change at follow-up was investigated in corresponding voxels. The significance of the difference of density and volume change per ventilation category was assessed using paired t-tests with a significance level of p ≤ 0.05. The analysis was performed separately for normal (NAA) and high attenuation areas (HAA). RESULTS: The study group consisted of 41 patients (73 ± 10 years, 36 men). In both NAA and HAA, significant increases of density and loss of volume were seen in areas of severely increased ventilation (C4) at baseline compared to areas of normal ventilation (C2, p < 0.001). In HAA, morphological changes were more heterogeneous compared to NAA. CONCLUSION: Functional CT assessing the extent and distribution of lung parenchyma with pathologically increased ventilation may serve as an imaging marker to prospectively identify lung parenchyma at risk for developing fibrosis. KEY POINTS: • Voxelwise correlation of serial CT scans suggests spatial correspondence between increased ventilation at baseline and structural changes at follow-up. • Regional assessment of pathologically increased ventilation at baseline has the potential to prospectively identify tissue at risk for developing fibrosis. • Presence and extent of pathologically increased ventilation may serve as an early imaging marker of disease activity.
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spelling pubmed-93814562022-08-18 Increased regional ventilation as early imaging marker for future disease progression of interstitial lung disease: a feasibility study Scharm, Sarah C. Schaefer-Prokop, Cornelia Willmann, Moritz Vogel-Claussen, Jens Knudsen, Lars Jonigk, Danny Fuge, Jan Welte, Tobias Wacker, Frank Prasse, Antje Shin, Hoen-oh Eur Radiol Chest OBJECTIVES: Idiopathic pulmonary fibrosis (IPF) is a disease with a poor prognosis and a highly variable course. Pathologically increased ventilation—accessible by functional CT—is discussed as a potential predecessor of lung fibrosis. The purpose of this feasibility study was to investigate whether increased regional ventilation at baseline CT and morphological changes in the follow-up CT suggestive for fibrosis indeed occur in spatial correspondence. METHODS: In this retrospective study, CT scans were performed at two time points between September 2016 and November 2020. Baseline ventilation was divided into four categories ranging from low, normal to moderately, and severely increased (C1–C4). Correlation between baseline ventilation and volume and density change at follow-up was investigated in corresponding voxels. The significance of the difference of density and volume change per ventilation category was assessed using paired t-tests with a significance level of p ≤ 0.05. The analysis was performed separately for normal (NAA) and high attenuation areas (HAA). RESULTS: The study group consisted of 41 patients (73 ± 10 years, 36 men). In both NAA and HAA, significant increases of density and loss of volume were seen in areas of severely increased ventilation (C4) at baseline compared to areas of normal ventilation (C2, p < 0.001). In HAA, morphological changes were more heterogeneous compared to NAA. CONCLUSION: Functional CT assessing the extent and distribution of lung parenchyma with pathologically increased ventilation may serve as an imaging marker to prospectively identify lung parenchyma at risk for developing fibrosis. KEY POINTS: • Voxelwise correlation of serial CT scans suggests spatial correspondence between increased ventilation at baseline and structural changes at follow-up. • Regional assessment of pathologically increased ventilation at baseline has the potential to prospectively identify tissue at risk for developing fibrosis. • Presence and extent of pathologically increased ventilation may serve as an early imaging marker of disease activity. Springer Berlin Heidelberg 2022-03-31 2022 /pmc/articles/PMC9381456/ /pubmed/35357537 http://dx.doi.org/10.1007/s00330-022-08702-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Chest
Scharm, Sarah C.
Schaefer-Prokop, Cornelia
Willmann, Moritz
Vogel-Claussen, Jens
Knudsen, Lars
Jonigk, Danny
Fuge, Jan
Welte, Tobias
Wacker, Frank
Prasse, Antje
Shin, Hoen-oh
Increased regional ventilation as early imaging marker for future disease progression of interstitial lung disease: a feasibility study
title Increased regional ventilation as early imaging marker for future disease progression of interstitial lung disease: a feasibility study
title_full Increased regional ventilation as early imaging marker for future disease progression of interstitial lung disease: a feasibility study
title_fullStr Increased regional ventilation as early imaging marker for future disease progression of interstitial lung disease: a feasibility study
title_full_unstemmed Increased regional ventilation as early imaging marker for future disease progression of interstitial lung disease: a feasibility study
title_short Increased regional ventilation as early imaging marker for future disease progression of interstitial lung disease: a feasibility study
title_sort increased regional ventilation as early imaging marker for future disease progression of interstitial lung disease: a feasibility study
topic Chest
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9381456/
https://www.ncbi.nlm.nih.gov/pubmed/35357537
http://dx.doi.org/10.1007/s00330-022-08702-w
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