Validation of a method to assess emphysema severity by spirometry in the COPDGene study

Abstract Background Standard spirometry cannot identify the predominant mechanism underlying airflow obstruction in COPD, namely emphysema or airway disease. We aimed at validating a previously developed methodology to detect emphysema by mathematical analysis of the maximal expiratory flow-volume (...

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Main Authors: Mariaelena Occhipinti, Matteo Paoletti, James D. Crapo, Barry J. Make, David A. Lynch, Vito Brusasco, Federico Lavorini, Edwin K. Silverman, Elizabeth A. Regan, Massimo Pistolesi
Format: Article
Language:English
Published: BMC 2020-05-01
Series:Respiratory Research
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12931-020-01366-4
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author Mariaelena Occhipinti
Matteo Paoletti
James D. Crapo
Barry J. Make
David A. Lynch
Vito Brusasco
Federico Lavorini
Edwin K. Silverman
Elizabeth A. Regan
Massimo Pistolesi
author_facet Mariaelena Occhipinti
Matteo Paoletti
James D. Crapo
Barry J. Make
David A. Lynch
Vito Brusasco
Federico Lavorini
Edwin K. Silverman
Elizabeth A. Regan
Massimo Pistolesi
author_sort Mariaelena Occhipinti
collection DOAJ
description Abstract Background Standard spirometry cannot identify the predominant mechanism underlying airflow obstruction in COPD, namely emphysema or airway disease. We aimed at validating a previously developed methodology to detect emphysema by mathematical analysis of the maximal expiratory flow-volume (MEFV) curve in standard spirometry. Methods From the COPDGene population we selected those 5930 subjects with MEFV curve and inspiratory-expiratory CT obtained on the same day. The MEFV curve descending limb was fit real-time using forced vital capacity (FVC), peak expiratory flow, and forced expiratory flows at 25, 50 and 75% of FVC to derive an emphysema severity index (ESI), expressed as a continuous positive numeric parameter ranging from 0 to 10. According to inspiratory CT percent lung attenuation area below − 950 HU we defined three emphysema severity subgroups (%LAA-950insp < 6, 6–14, ≥14). By co-registration of inspiratory-expiratory CT we quantified persistent (%pLDA) and functional (%fLDA) low-density areas as CT metrics of emphysema and airway disease, respectively. Results ESI differentiated CT emphysema severity subgroups increasing in parallel with GOLD stages (p < .001), but with high variability within each stage. ESI had significantly higher correlations (p < .001) with emphysema than with airway disease CT metrics, explaining 67% of %pLDA variability. Conversely, standard spirometric variables (FEV1, FEV1/FVC) had significantly lower correlations than ESI with emphysema CT metrics and did not differentiate between emphysema and airways CT metrics. Conclusions ESI adds to standard spirometry the power to discriminate whether emphysema is the predominant mechanism of airway obstruction. ESI methodology has been validated in the large multiethnic population of smokers of the COPDGene study and therefore it could be applied for clinical and research purposes in the general population of smokers, using a readily available online website.
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spelling doaj.art-b36312dcc08848f0a108c6237565acf82022-12-21T18:53:02ZengBMCRespiratory Research1465-993X2020-05-012111910.1186/s12931-020-01366-4Validation of a method to assess emphysema severity by spirometry in the COPDGene studyMariaelena Occhipinti0Matteo Paoletti1James D. Crapo2Barry J. Make3David A. Lynch4Vito Brusasco5Federico Lavorini6Edwin K. Silverman7Elizabeth A. Regan8Massimo Pistolesi9Section of Respiratory Medicine, Department of Experimental and Clinical Medicine, University of FlorenceSection of Respiratory Medicine, Department of Experimental and Clinical Medicine, University of FlorenceDepartment of Medicine, National Jewish HealthDepartment of Medicine, National Jewish HealthDepartment of Radiology, National Jewish HealthDepartment of Experimental Medicine, University of GenoaSection of Respiratory Medicine, Department of Experimental and Clinical Medicine, University of FlorenceDepartment of Medicine, Harvard Medical School, Brigham and Women’s Hospital, Channing Division of Network MedicineDepartment of Medicine, National Jewish HealthSection of Respiratory Medicine, Department of Experimental and Clinical Medicine, University of FlorenceAbstract Background Standard spirometry cannot identify the predominant mechanism underlying airflow obstruction in COPD, namely emphysema or airway disease. We aimed at validating a previously developed methodology to detect emphysema by mathematical analysis of the maximal expiratory flow-volume (MEFV) curve in standard spirometry. Methods From the COPDGene population we selected those 5930 subjects with MEFV curve and inspiratory-expiratory CT obtained on the same day. The MEFV curve descending limb was fit real-time using forced vital capacity (FVC), peak expiratory flow, and forced expiratory flows at 25, 50 and 75% of FVC to derive an emphysema severity index (ESI), expressed as a continuous positive numeric parameter ranging from 0 to 10. According to inspiratory CT percent lung attenuation area below − 950 HU we defined three emphysema severity subgroups (%LAA-950insp < 6, 6–14, ≥14). By co-registration of inspiratory-expiratory CT we quantified persistent (%pLDA) and functional (%fLDA) low-density areas as CT metrics of emphysema and airway disease, respectively. Results ESI differentiated CT emphysema severity subgroups increasing in parallel with GOLD stages (p < .001), but with high variability within each stage. ESI had significantly higher correlations (p < .001) with emphysema than with airway disease CT metrics, explaining 67% of %pLDA variability. Conversely, standard spirometric variables (FEV1, FEV1/FVC) had significantly lower correlations than ESI with emphysema CT metrics and did not differentiate between emphysema and airways CT metrics. Conclusions ESI adds to standard spirometry the power to discriminate whether emphysema is the predominant mechanism of airway obstruction. ESI methodology has been validated in the large multiethnic population of smokers of the COPDGene study and therefore it could be applied for clinical and research purposes in the general population of smokers, using a readily available online website.http://link.springer.com/article/10.1186/s12931-020-01366-4SpirometryEmphysemaAirway obstructionComputed tomographyVital capacity
spellingShingle Mariaelena Occhipinti
Matteo Paoletti
James D. Crapo
Barry J. Make
David A. Lynch
Vito Brusasco
Federico Lavorini
Edwin K. Silverman
Elizabeth A. Regan
Massimo Pistolesi
Validation of a method to assess emphysema severity by spirometry in the COPDGene study
Respiratory Research
Spirometry
Emphysema
Airway obstruction
Computed tomography
Vital capacity
title Validation of a method to assess emphysema severity by spirometry in the COPDGene study
title_full Validation of a method to assess emphysema severity by spirometry in the COPDGene study
title_fullStr Validation of a method to assess emphysema severity by spirometry in the COPDGene study
title_full_unstemmed Validation of a method to assess emphysema severity by spirometry in the COPDGene study
title_short Validation of a method to assess emphysema severity by spirometry in the COPDGene study
title_sort validation of a method to assess emphysema severity by spirometry in the copdgene study
topic Spirometry
Emphysema
Airway obstruction
Computed tomography
Vital capacity
url http://link.springer.com/article/10.1186/s12931-020-01366-4
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