Cargando…

Quantification of dual-energy CT-derived functional parameters as potential imaging markers for progression of idiopathic pulmonary fibrosis

OBJECTIVES: The individual course of disease in idiopathic pulmonary fibrosis (IPF) is highly variable. Assessment of disease activity and prospective estimation of disease progression might have the potential to improve therapy management and indicate the onset of treatment at an earlier stage. The...

Descripción completa

Detalles Bibliográficos
Autores principales: Scharm, Sarah C., Vogel-Claussen, Jens, Schaefer-Prokop, Cornelia, Dettmer, Sabine, Knudsen, Lars, Jonigk, Danny, Fuge, Jan, Apel, Rosa-Marie, Welte, Tobias, Wacker, Frank, Prasse, Antje, Shin, Hoen-oh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8379131/
https://www.ncbi.nlm.nih.gov/pubmed/33725189
http://dx.doi.org/10.1007/s00330-021-07798-w
_version_ 1783740947192872960
author Scharm, Sarah C.
Vogel-Claussen, Jens
Schaefer-Prokop, Cornelia
Dettmer, Sabine
Knudsen, Lars
Jonigk, Danny
Fuge, Jan
Apel, Rosa-Marie
Welte, Tobias
Wacker, Frank
Prasse, Antje
Shin, Hoen-oh
author_facet Scharm, Sarah C.
Vogel-Claussen, Jens
Schaefer-Prokop, Cornelia
Dettmer, Sabine
Knudsen, Lars
Jonigk, Danny
Fuge, Jan
Apel, Rosa-Marie
Welte, Tobias
Wacker, Frank
Prasse, Antje
Shin, Hoen-oh
author_sort Scharm, Sarah C.
collection PubMed
description OBJECTIVES: The individual course of disease in idiopathic pulmonary fibrosis (IPF) is highly variable. Assessment of disease activity and prospective estimation of disease progression might have the potential to improve therapy management and indicate the onset of treatment at an earlier stage. The aim of this study was to evaluate whether regional ventilation, lung perfusion, and late enhancement can serve as early imaging markers for disease progression in patients with IPF. METHODS: In this retrospective study, contrast-enhanced dual-energy CT scans of 32 patients in inspiration and delayed expiration were performed at two time points with a mean interval of 15.4 months. The pulmonary blood volume (PBV) images obtained in the arterial and delayed perfusion phase served as a surrogate for arterial lung perfusion and parenchymal late enhancement. The virtual non-contrast (VNC) images in inspiration and expiration were non-linearly registered to provide regional ventilation images. Image-derived parameters were correlated with longitudinal changes of lung function (FVC%, DLCO%), mean lung density in CT, and CT-derived lung volume. RESULTS: Regional ventilation and late enhancement at baseline preceded future change in lung volume (R - 0.474, p 0.006/R - 0.422, p 0.016, respectively) and mean lung density (R - 0.469, p 0.007/R - 0.402, p 0.022, respectively). Regional ventilation also correlated with a future change in FVC% (R - 0.398, p 0.024). CONCLUSION: CT-derived functional parameters of regional ventilation and parenchymal late enhancement are potential early imaging markers for idiopathic pulmonary fibrosis progression. KEY POINTS: • Functional CT parameters at baseline (regional ventilation and late enhancement) correlate with future structural changes of the lung as measured with loss of lung volume and increase in lung density in serial CT scans of patients with idiopathic pulmonary fibrosis. • Functional CT parameter measurements in high-attenuation areas (- 600 to - 250 HU) are significantly different from normal-attenuation areas (- 950 to - 600 HU) of the lung. • Mean regional ventilation in functional CT correlates with a future change in forced vital capacity (FVC) in pulmonary function tests.
format Online
Article
Text
id pubmed-8379131
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Springer Berlin Heidelberg
record_format MEDLINE/PubMed
spelling pubmed-83791312021-09-02 Quantification of dual-energy CT-derived functional parameters as potential imaging markers for progression of idiopathic pulmonary fibrosis Scharm, Sarah C. Vogel-Claussen, Jens Schaefer-Prokop, Cornelia Dettmer, Sabine Knudsen, Lars Jonigk, Danny Fuge, Jan Apel, Rosa-Marie Welte, Tobias Wacker, Frank Prasse, Antje Shin, Hoen-oh Eur Radiol Computed Tomography OBJECTIVES: The individual course of disease in idiopathic pulmonary fibrosis (IPF) is highly variable. Assessment of disease activity and prospective estimation of disease progression might have the potential to improve therapy management and indicate the onset of treatment at an earlier stage. The aim of this study was to evaluate whether regional ventilation, lung perfusion, and late enhancement can serve as early imaging markers for disease progression in patients with IPF. METHODS: In this retrospective study, contrast-enhanced dual-energy CT scans of 32 patients in inspiration and delayed expiration were performed at two time points with a mean interval of 15.4 months. The pulmonary blood volume (PBV) images obtained in the arterial and delayed perfusion phase served as a surrogate for arterial lung perfusion and parenchymal late enhancement. The virtual non-contrast (VNC) images in inspiration and expiration were non-linearly registered to provide regional ventilation images. Image-derived parameters were correlated with longitudinal changes of lung function (FVC%, DLCO%), mean lung density in CT, and CT-derived lung volume. RESULTS: Regional ventilation and late enhancement at baseline preceded future change in lung volume (R - 0.474, p 0.006/R - 0.422, p 0.016, respectively) and mean lung density (R - 0.469, p 0.007/R - 0.402, p 0.022, respectively). Regional ventilation also correlated with a future change in FVC% (R - 0.398, p 0.024). CONCLUSION: CT-derived functional parameters of regional ventilation and parenchymal late enhancement are potential early imaging markers for idiopathic pulmonary fibrosis progression. KEY POINTS: • Functional CT parameters at baseline (regional ventilation and late enhancement) correlate with future structural changes of the lung as measured with loss of lung volume and increase in lung density in serial CT scans of patients with idiopathic pulmonary fibrosis. • Functional CT parameter measurements in high-attenuation areas (- 600 to - 250 HU) are significantly different from normal-attenuation areas (- 950 to - 600 HU) of the lung. • Mean regional ventilation in functional CT correlates with a future change in forced vital capacity (FVC) in pulmonary function tests. Springer Berlin Heidelberg 2021-03-16 2021 /pmc/articles/PMC8379131/ /pubmed/33725189 http://dx.doi.org/10.1007/s00330-021-07798-w Text en © The Author(s) 2021, corrected publication 2021 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 Computed Tomography
Scharm, Sarah C.
Vogel-Claussen, Jens
Schaefer-Prokop, Cornelia
Dettmer, Sabine
Knudsen, Lars
Jonigk, Danny
Fuge, Jan
Apel, Rosa-Marie
Welte, Tobias
Wacker, Frank
Prasse, Antje
Shin, Hoen-oh
Quantification of dual-energy CT-derived functional parameters as potential imaging markers for progression of idiopathic pulmonary fibrosis
title Quantification of dual-energy CT-derived functional parameters as potential imaging markers for progression of idiopathic pulmonary fibrosis
title_full Quantification of dual-energy CT-derived functional parameters as potential imaging markers for progression of idiopathic pulmonary fibrosis
title_fullStr Quantification of dual-energy CT-derived functional parameters as potential imaging markers for progression of idiopathic pulmonary fibrosis
title_full_unstemmed Quantification of dual-energy CT-derived functional parameters as potential imaging markers for progression of idiopathic pulmonary fibrosis
title_short Quantification of dual-energy CT-derived functional parameters as potential imaging markers for progression of idiopathic pulmonary fibrosis
title_sort quantification of dual-energy ct-derived functional parameters as potential imaging markers for progression of idiopathic pulmonary fibrosis
topic Computed Tomography
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8379131/
https://www.ncbi.nlm.nih.gov/pubmed/33725189
http://dx.doi.org/10.1007/s00330-021-07798-w
work_keys_str_mv AT scharmsarahc quantificationofdualenergyctderivedfunctionalparametersaspotentialimagingmarkersforprogressionofidiopathicpulmonaryfibrosis
AT vogelclaussenjens quantificationofdualenergyctderivedfunctionalparametersaspotentialimagingmarkersforprogressionofidiopathicpulmonaryfibrosis
AT schaeferprokopcornelia quantificationofdualenergyctderivedfunctionalparametersaspotentialimagingmarkersforprogressionofidiopathicpulmonaryfibrosis
AT dettmersabine quantificationofdualenergyctderivedfunctionalparametersaspotentialimagingmarkersforprogressionofidiopathicpulmonaryfibrosis
AT knudsenlars quantificationofdualenergyctderivedfunctionalparametersaspotentialimagingmarkersforprogressionofidiopathicpulmonaryfibrosis
AT jonigkdanny quantificationofdualenergyctderivedfunctionalparametersaspotentialimagingmarkersforprogressionofidiopathicpulmonaryfibrosis
AT fugejan quantificationofdualenergyctderivedfunctionalparametersaspotentialimagingmarkersforprogressionofidiopathicpulmonaryfibrosis
AT apelrosamarie quantificationofdualenergyctderivedfunctionalparametersaspotentialimagingmarkersforprogressionofidiopathicpulmonaryfibrosis
AT weltetobias quantificationofdualenergyctderivedfunctionalparametersaspotentialimagingmarkersforprogressionofidiopathicpulmonaryfibrosis
AT wackerfrank quantificationofdualenergyctderivedfunctionalparametersaspotentialimagingmarkersforprogressionofidiopathicpulmonaryfibrosis
AT prasseantje quantificationofdualenergyctderivedfunctionalparametersaspotentialimagingmarkersforprogressionofidiopathicpulmonaryfibrosis
AT shinhoenoh quantificationofdualenergyctderivedfunctionalparametersaspotentialimagingmarkersforprogressionofidiopathicpulmonaryfibrosis