Performance of Radiomics Features in the Quantification of Idiopathic Pulmonary Fibrosis from HRCT

Background: Our study assesses the diagnostic value of different features extracted from high resolution computed tomography (HRCT) images of patients with idiopathic pulmonary fibrosis. These features are investigated over a range of HRCT lung volume measurements (in Hounsfield Units) for which no...

Full description

Bibliographic Details
Main Authors: Alessandro Stefano, Mauro Gioè, Giorgio Russo, Stefano Palmucci, Sebastiano Emanuele Torrisi, Samuel Bignardi, Antonio Basile, Albert Comelli, Viviana Benfante, Gianluca Sambataro, Daniele Falsaperla, Alfredo Gaetano Torcitto, Massimo Attanasio, Anthony Yezzi, Carlo Vancheri
Format: Article
Language:English
Published: MDPI AG 2020-05-01
Series:Diagnostics
Subjects:
Online Access:https://www.mdpi.com/2075-4418/10/5/306
_version_ 1797567924904394752
author Alessandro Stefano
Mauro Gioè
Giorgio Russo
Stefano Palmucci
Sebastiano Emanuele Torrisi
Samuel Bignardi
Antonio Basile
Albert Comelli
Viviana Benfante
Gianluca Sambataro
Daniele Falsaperla
Alfredo Gaetano Torcitto
Massimo Attanasio
Anthony Yezzi
Carlo Vancheri
author_facet Alessandro Stefano
Mauro Gioè
Giorgio Russo
Stefano Palmucci
Sebastiano Emanuele Torrisi
Samuel Bignardi
Antonio Basile
Albert Comelli
Viviana Benfante
Gianluca Sambataro
Daniele Falsaperla
Alfredo Gaetano Torcitto
Massimo Attanasio
Anthony Yezzi
Carlo Vancheri
author_sort Alessandro Stefano
collection DOAJ
description Background: Our study assesses the diagnostic value of different features extracted from high resolution computed tomography (HRCT) images of patients with idiopathic pulmonary fibrosis. These features are investigated over a range of HRCT lung volume measurements (in Hounsfield Units) for which no prior study has yet been published. In particular, we provide a comparison of their diagnostic value at different Hounsfield Unit (HU) thresholds, including corresponding pulmonary functional tests. Methods: We consider thirty-two patients retrospectively for whom both HRCT examinations and spirometry tests were available. First, we analyse the HRCT histogram to extract quantitative lung fibrosis features. Next, we evaluate the relationship between pulmonary function and the HRCT features at selected HU thresholds, namely −200 HU, 0 HU, and +200 HU. We model the relationship using a Poisson approximation to identify the measure with the highest log-likelihood. Results: Our Poisson models reveal no difference at the −200 and 0 HU thresholds. However, inferential conclusions change at the +200 HU threshold. Among the HRCT features considered, the percentage of normally attenuated lung at −200 HU shows the most significant diagnostic utility. Conclusions: The percentage of normally attenuated lung can be used together with qualitative HRCT assessment and pulmonary function tests to enhance the idiopathic pulmonary fibrosis (IPF) diagnostic process.
first_indexed 2024-03-10T19:49:04Z
format Article
id doaj.art-e5855092623b4a6c9d68b737623bf572
institution Directory Open Access Journal
issn 2075-4418
language English
last_indexed 2024-03-10T19:49:04Z
publishDate 2020-05-01
publisher MDPI AG
record_format Article
series Diagnostics
spelling doaj.art-e5855092623b4a6c9d68b737623bf5722023-11-20T00:35:56ZengMDPI AGDiagnostics2075-44182020-05-0110530610.3390/diagnostics10050306Performance of Radiomics Features in the Quantification of Idiopathic Pulmonary Fibrosis from HRCTAlessandro Stefano0Mauro Gioè1Giorgio Russo2Stefano Palmucci3Sebastiano Emanuele Torrisi4Samuel Bignardi5Antonio Basile6Albert Comelli7Viviana Benfante8Gianluca Sambataro9Daniele Falsaperla10Alfredo Gaetano Torcitto11Massimo Attanasio12Anthony Yezzi13Carlo Vancheri14Institute of Molecular Bioimaging and Physiology, National Research Council (IBFM-CNR), 90015 Cefalù, ItalyDepartment of Economics, Business, and Statistics (DSEAS), University of Palermo, 90133 Palermo, ItalyInstitute of Molecular Bioimaging and Physiology, National Research Council (IBFM-CNR), 90015 Cefalù, ItalyDepartment of Medical Surgical Sciences and Advanced Technologies, Radiology Unit I, University Hospital “Policlinico-Vittorio Emanuele”, 95123 Catania, ItalyRegional Referral Centre for Rare Lung Diseases, A.O.U. Policlinico-Vittorio Emanuele, University of Catania, 95123 Catania, ItalyLaboratory of Computational Computer Vision (LCCV), School of Electrical and Computer Engineering, Georgia Institute of Technology, Atlanta, GA 30332, USADepartment of Medical Surgical Sciences and Advanced Technologies, Radiology Unit I, University Hospital “Policlinico-Vittorio Emanuele”, 95123 Catania, ItalyInstitute of Molecular Bioimaging and Physiology, National Research Council (IBFM-CNR), 90015 Cefalù, ItalyInstitute of Molecular Bioimaging and Physiology, National Research Council (IBFM-CNR), 90015 Cefalù, ItalyDepartment of Medical Surgical Sciences and Advanced Technologies, Radiology Unit I, University Hospital “Policlinico-Vittorio Emanuele”, 95123 Catania, ItalyDepartment of Medical Surgical Sciences and Advanced Technologies, Radiology Unit I, University Hospital “Policlinico-Vittorio Emanuele”, 95123 Catania, ItalyDepartment of Medical Surgical Sciences and Advanced Technologies, Radiology Unit I, University Hospital “Policlinico-Vittorio Emanuele”, 95123 Catania, ItalyDepartment of Economics, Business, and Statistics (DSEAS), University of Palermo, 90133 Palermo, ItalyLaboratory of Computational Computer Vision (LCCV), School of Electrical and Computer Engineering, Georgia Institute of Technology, Atlanta, GA 30332, USARegional Referral Centre for Rare Lung Diseases, A.O.U. Policlinico-Vittorio Emanuele, University of Catania, 95123 Catania, ItalyBackground: Our study assesses the diagnostic value of different features extracted from high resolution computed tomography (HRCT) images of patients with idiopathic pulmonary fibrosis. These features are investigated over a range of HRCT lung volume measurements (in Hounsfield Units) for which no prior study has yet been published. In particular, we provide a comparison of their diagnostic value at different Hounsfield Unit (HU) thresholds, including corresponding pulmonary functional tests. Methods: We consider thirty-two patients retrospectively for whom both HRCT examinations and spirometry tests were available. First, we analyse the HRCT histogram to extract quantitative lung fibrosis features. Next, we evaluate the relationship between pulmonary function and the HRCT features at selected HU thresholds, namely −200 HU, 0 HU, and +200 HU. We model the relationship using a Poisson approximation to identify the measure with the highest log-likelihood. Results: Our Poisson models reveal no difference at the −200 and 0 HU thresholds. However, inferential conclusions change at the +200 HU threshold. Among the HRCT features considered, the percentage of normally attenuated lung at −200 HU shows the most significant diagnostic utility. Conclusions: The percentage of normally attenuated lung can be used together with qualitative HRCT assessment and pulmonary function tests to enhance the idiopathic pulmonary fibrosis (IPF) diagnostic process.https://www.mdpi.com/2075-4418/10/5/306idiopathic pulmonary fibrosishigh resolution computed tomographyradiomics
spellingShingle Alessandro Stefano
Mauro Gioè
Giorgio Russo
Stefano Palmucci
Sebastiano Emanuele Torrisi
Samuel Bignardi
Antonio Basile
Albert Comelli
Viviana Benfante
Gianluca Sambataro
Daniele Falsaperla
Alfredo Gaetano Torcitto
Massimo Attanasio
Anthony Yezzi
Carlo Vancheri
Performance of Radiomics Features in the Quantification of Idiopathic Pulmonary Fibrosis from HRCT
Diagnostics
idiopathic pulmonary fibrosis
high resolution computed tomography
radiomics
title Performance of Radiomics Features in the Quantification of Idiopathic Pulmonary Fibrosis from HRCT
title_full Performance of Radiomics Features in the Quantification of Idiopathic Pulmonary Fibrosis from HRCT
title_fullStr Performance of Radiomics Features in the Quantification of Idiopathic Pulmonary Fibrosis from HRCT
title_full_unstemmed Performance of Radiomics Features in the Quantification of Idiopathic Pulmonary Fibrosis from HRCT
title_short Performance of Radiomics Features in the Quantification of Idiopathic Pulmonary Fibrosis from HRCT
title_sort performance of radiomics features in the quantification of idiopathic pulmonary fibrosis from hrct
topic idiopathic pulmonary fibrosis
high resolution computed tomography
radiomics
url https://www.mdpi.com/2075-4418/10/5/306
work_keys_str_mv AT alessandrostefano performanceofradiomicsfeaturesinthequantificationofidiopathicpulmonaryfibrosisfromhrct
AT maurogioe performanceofradiomicsfeaturesinthequantificationofidiopathicpulmonaryfibrosisfromhrct
AT giorgiorusso performanceofradiomicsfeaturesinthequantificationofidiopathicpulmonaryfibrosisfromhrct
AT stefanopalmucci performanceofradiomicsfeaturesinthequantificationofidiopathicpulmonaryfibrosisfromhrct
AT sebastianoemanueletorrisi performanceofradiomicsfeaturesinthequantificationofidiopathicpulmonaryfibrosisfromhrct
AT samuelbignardi performanceofradiomicsfeaturesinthequantificationofidiopathicpulmonaryfibrosisfromhrct
AT antoniobasile performanceofradiomicsfeaturesinthequantificationofidiopathicpulmonaryfibrosisfromhrct
AT albertcomelli performanceofradiomicsfeaturesinthequantificationofidiopathicpulmonaryfibrosisfromhrct
AT vivianabenfante performanceofradiomicsfeaturesinthequantificationofidiopathicpulmonaryfibrosisfromhrct
AT gianlucasambataro performanceofradiomicsfeaturesinthequantificationofidiopathicpulmonaryfibrosisfromhrct
AT danielefalsaperla performanceofradiomicsfeaturesinthequantificationofidiopathicpulmonaryfibrosisfromhrct
AT alfredogaetanotorcitto performanceofradiomicsfeaturesinthequantificationofidiopathicpulmonaryfibrosisfromhrct
AT massimoattanasio performanceofradiomicsfeaturesinthequantificationofidiopathicpulmonaryfibrosisfromhrct
AT anthonyyezzi performanceofradiomicsfeaturesinthequantificationofidiopathicpulmonaryfibrosisfromhrct
AT carlovancheri performanceofradiomicsfeaturesinthequantificationofidiopathicpulmonaryfibrosisfromhrct