High-Resolution Computed Tomography (HRCT) Reflects Disease Progression in Patients with Idiopathic Pulmonary Fibrosis (IPF): Relationship with Lung Pathology
High-Resolution Computed Tomography (HRCT) plays a central role in diagnosing Idiopathic Pulmonary Fibrosis (IPF) while its role in monitoring disease progression is not clearly defined. Given the variable clinical course of the disease, we evaluated whether HRCT abnormalities predict disease behavi...
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Format: | Article |
Language: | English |
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MDPI AG
2019-03-01
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Series: | Journal of Clinical Medicine |
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Online Access: | https://www.mdpi.com/2077-0383/8/3/399 |
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doaj-9fdea9fb42d54406a5ab57095e6711a5 |
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record_format |
Article |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Elisabetta Cocconcelli Elisabetta Balestro Davide Biondini Giulio Barbiero Roberta Polverosi Fiorella Calabrese Federica Pezzuto Donato Lacedonia Federico Rea Marco Schiavon Erica Bazzan Maria Pia Foschino Barbaro Graziella Turato Paolo Spagnolo Manuel G. Cosio Marina Saetta |
spellingShingle |
Elisabetta Cocconcelli Elisabetta Balestro Davide Biondini Giulio Barbiero Roberta Polverosi Fiorella Calabrese Federica Pezzuto Donato Lacedonia Federico Rea Marco Schiavon Erica Bazzan Maria Pia Foschino Barbaro Graziella Turato Paolo Spagnolo Manuel G. Cosio Marina Saetta High-Resolution Computed Tomography (HRCT) Reflects Disease Progression in Patients with Idiopathic Pulmonary Fibrosis (IPF): Relationship with Lung Pathology Journal of Clinical Medicine HRCT disease progression and lung pathology |
author_facet |
Elisabetta Cocconcelli Elisabetta Balestro Davide Biondini Giulio Barbiero Roberta Polverosi Fiorella Calabrese Federica Pezzuto Donato Lacedonia Federico Rea Marco Schiavon Erica Bazzan Maria Pia Foschino Barbaro Graziella Turato Paolo Spagnolo Manuel G. Cosio Marina Saetta |
author_sort |
Elisabetta Cocconcelli |
title |
High-Resolution Computed Tomography (HRCT) Reflects Disease Progression in Patients with Idiopathic Pulmonary Fibrosis (IPF): Relationship with Lung Pathology |
title_short |
High-Resolution Computed Tomography (HRCT) Reflects Disease Progression in Patients with Idiopathic Pulmonary Fibrosis (IPF): Relationship with Lung Pathology |
title_full |
High-Resolution Computed Tomography (HRCT) Reflects Disease Progression in Patients with Idiopathic Pulmonary Fibrosis (IPF): Relationship with Lung Pathology |
title_fullStr |
High-Resolution Computed Tomography (HRCT) Reflects Disease Progression in Patients with Idiopathic Pulmonary Fibrosis (IPF): Relationship with Lung Pathology |
title_full_unstemmed |
High-Resolution Computed Tomography (HRCT) Reflects Disease Progression in Patients with Idiopathic Pulmonary Fibrosis (IPF): Relationship with Lung Pathology |
title_sort |
high-resolution computed tomography (hrct) reflects disease progression in patients with idiopathic pulmonary fibrosis (ipf): relationship with lung pathology |
publisher |
MDPI AG |
series |
Journal of Clinical Medicine |
issn |
2077-0383 |
publishDate |
2019-03-01 |
description |
High-Resolution Computed Tomography (HRCT) plays a central role in diagnosing Idiopathic Pulmonary Fibrosis (IPF) while its role in monitoring disease progression is not clearly defined. Given the variable clinical course of the disease, we evaluated whether HRCT abnormalities predict disease behavior and correlate with functional decline in untreated IPF patients. Forty-nine patients (with HRCT<sub>1</sub>) were functionally categorized as rapid or slow progressors. Twenty-one had a second HRCT<sub>2</sub>. Thirteen patients underwent lung transplantation and pathology was quantified. HRCT Alveolar (AS) and Interstitial Scores (IS) were assessed and correlated with Forced Vital Capacity (FVC) decline between HRCT<sub>1</sub> and HRCT<sub>2</sub>. At baseline, AS was greater in rapids than in slows, while IS was similar in the two groups. In the 21 subjects with HRCT<sub>2</sub>, IS increased over time in both slows and rapids, while AS increased only in rapids. The IS change from HRCT<sub>1</sub> to HRCT<sub>2</sub> normalized per month correlated with FVC decline/month in the whole population, but the change in AS did not. In the 13 patients with pathology, the number of total lymphocytes was higher in rapids than in slows and correlated with AS. Quantitative estimation of HRCTs AS and IS reflects the distinct clinical and pathological behavior of slow and rapid decliners. Furthermore, AS, which reflects the immune/inflammatory infiltrate in lung tissue, could be a useful tool to differentiate rapid from slow progressors at presentation. |
topic |
HRCT disease progression and lung pathology |
url |
https://www.mdpi.com/2077-0383/8/3/399 |
work_keys_str_mv |
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doaj-9fdea9fb42d54406a5ab57095e6711a52020-11-24T22:28:17ZengMDPI AGJournal of Clinical Medicine2077-03832019-03-018339910.3390/jcm8030399jcm8030399High-Resolution Computed Tomography (HRCT) Reflects Disease Progression in Patients with Idiopathic Pulmonary Fibrosis (IPF): Relationship with Lung PathologyElisabetta Cocconcelli0Elisabetta Balestro1Davide Biondini2Giulio Barbiero3Roberta Polverosi4Fiorella Calabrese5Federica Pezzuto6Donato Lacedonia7Federico Rea8Marco Schiavon9Erica Bazzan10Maria Pia Foschino Barbaro11Graziella Turato12Paolo Spagnolo13Manuel G. Cosio14Marina Saetta15Department of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padova and Padova City Hospital, 35128 Padova, ItalyDepartment of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padova and Padova City Hospital, 35128 Padova, ItalyDepartment of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padova and Padova City Hospital, 35128 Padova, ItalyInstitute of Radiology, Department of Medicine, University of Padova, 35128 Padova, ItalyIstituto Diagnostico Antoniano - Affidea, 35100 Padova, ItalyDepartment of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padova and Padova City Hospital, 35128 Padova, ItalyDepartment of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padova and Padova City Hospital, 35128 Padova, ItalyDepartment of Medical and Surgical Sciences, University of Foggia, Policlinico “OO. Riuniti”, 71122 Foggia, ItalyDepartment of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padova and Padova City Hospital, 35128 Padova, ItalyDepartment of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padova and Padova City Hospital, 35128 Padova, ItalyDepartment of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padova and Padova City Hospital, 35128 Padova, ItalyDepartment of Medical and Surgical Sciences, University of Foggia, Policlinico “OO. Riuniti”, 71122 Foggia, ItalyDepartment of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padova and Padova City Hospital, 35128 Padova, ItalyDepartment of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padova and Padova City Hospital, 35128 Padova, ItalyDepartment of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padova and Padova City Hospital, 35128 Padova, ItalyDepartment of Cardiac, Thoracic, Vascular Sciences and Public Health, University of Padova and Padova City Hospital, 35128 Padova, ItalyHigh-Resolution Computed Tomography (HRCT) plays a central role in diagnosing Idiopathic Pulmonary Fibrosis (IPF) while its role in monitoring disease progression is not clearly defined. Given the variable clinical course of the disease, we evaluated whether HRCT abnormalities predict disease behavior and correlate with functional decline in untreated IPF patients. Forty-nine patients (with HRCT<sub>1</sub>) were functionally categorized as rapid or slow progressors. Twenty-one had a second HRCT<sub>2</sub>. Thirteen patients underwent lung transplantation and pathology was quantified. HRCT Alveolar (AS) and Interstitial Scores (IS) were assessed and correlated with Forced Vital Capacity (FVC) decline between HRCT<sub>1</sub> and HRCT<sub>2</sub>. At baseline, AS was greater in rapids than in slows, while IS was similar in the two groups. In the 21 subjects with HRCT<sub>2</sub>, IS increased over time in both slows and rapids, while AS increased only in rapids. The IS change from HRCT<sub>1</sub> to HRCT<sub>2</sub> normalized per month correlated with FVC decline/month in the whole population, but the change in AS did not. In the 13 patients with pathology, the number of total lymphocytes was higher in rapids than in slows and correlated with AS. Quantitative estimation of HRCTs AS and IS reflects the distinct clinical and pathological behavior of slow and rapid decliners. Furthermore, AS, which reflects the immune/inflammatory infiltrate in lung tissue, could be a useful tool to differentiate rapid from slow progressors at presentation.https://www.mdpi.com/2077-0383/8/3/399HRCTdisease progression and lung pathology |