Journal article
Deep neural network analyses of spirometry for structural phenotyping of chronic obstructive pulmonary disease
JCI insight, Vol.5(13), e132781
07/09/2020
DOI: 10.1172/jci.insight.132781
PMCID: PMC7406302
PMID: 32554922
Abstract
BACKGROUNDCurrently recommended traditional spirometry outputs do not reflect the relative contributions of emphysema and airway disease to airflow obstruction. We hypothesized that machine-learning algorithms can be trained on spirometry data to identify these structural phenotypes.METHODSParticipants enrolled in a large multicenter study (COPDGene) were included. The data points from expiratory flow-volume curves were trained using a deep-learning model to predict structural phenotypes of chronic obstructive pulmonary disease (COPD) on CT, and results were compared with traditional spirometry metrics and an optimized random forest classifier. Area under the receiver operating characteristic curve (AUC) and weighted F-score were used to measure the discriminative accuracy of a fully convolutional neural network, random forest, and traditional spirometry metrics to phenotype CT as normal, emphysema-predominant (>5% emphysema), airway-predominant (Pi10 > median), and mixed phenotypes. Similar comparisons were made for the detection of functional small airway disease phenotype (>20% on parametric response mapping).RESULTSAmong 8980 individuals, the neural network was more accurate in discriminating predominant emphysema/airway phenotypes (AUC 0.80, 95%CI 0.79-0.81) compared with traditional measures of spirometry, FEV1/FVC (AUC 0.71, 95%CI 0.69-0.71), FEV1% predicted (AUC 0.70, 95%CI 0.68-0.71), and random forest classifier (AUC 0.78, 95%CI 0.77-0.79). The neural network was also more accurate in discriminating predominant emphysema/small airway phenotypes (AUC 0.91, 95%CI 0.90-0.92) compared with FEV1/FVC (AUC 0.80, 95%CI 0.78-0.82), FEV1% predicted (AUC 0.83, 95%CI 0.80-0.84), and with comparable accuracy with random forest classifier (AUC 0.90, 95%CI 0.88-0.91).CONCLUSIONSStructural phenotypes of COPD can be identified from spirometry using deep-learning and machine-learning approaches, demonstrating their potential to identify individuals for targeted therapies.TRIAL REGISTRATIONClinicalTrials.gov NCT00608764.FUNDINGThis study was supported by NIH grants K23 HL133438 and R21EB027891 and an American Thoracic Foundation 2018 Unrestricted Research Grant. The COPDGene study is supported by NIH grants NHLBI U01 HL089897 and U01 HL089856. The COPDGene study (NCT00608764) is also supported by the COPD Foundation through contributions made to an Industry Advisory Committee comprising AstraZeneca, Boehringer-Ingelheim, GlaxoSmithKline, Novartis, and Sunovion.
Details
- Title: Subtitle
- Deep neural network analyses of spirometry for structural phenotyping of chronic obstructive pulmonary disease
- Creators
- Sandeep Bodduluri - Division of Pulmonary, Allergy and Critical Care Medicine, andArie Nakhmani - Department of Electrical and Computer Engineering, University of Alabama at Birmingham, Birmingham, Alabama, USAJoseph M Reinhardt - Department of Biomedical Engineering, University of Iowa, Iowa City, Iowa, USACarla G Wilson - Department of Biostatistics and Bioinformatics, National Jewish Health, Denver, Colorado, USAMerry-Lynn McDonald - Division of Pulmonary, Allergy and Critical Care Medicine, andRamaraju Rudraraju - Division of Cardiothoracic Surgery andByron C Jaeger - Department of Biostatistics, University of Alabama at Birmingham, Birmingham, Alabama, USANirav R Bhakta - Division of Pulmonary, Critical Care, Allergy and Sleep Medicine, University California, San Francisco, San Francisco, California, USAPeter J Castaldi - Channing Division of Network Medicine, Brigham and Women's Hospital, Boston, Massachusetts, USAFrank C Sciurba - Division of Pulmonary, Allergy and Critical Care Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, USAChengcui Zhang - Department of Computer Science, University of Alabama at Birmingham, Birmingham, Alabama, USAPurushotham V Bangalore - Department of Computer Science, University of Alabama at Birmingham, Birmingham, Alabama, USASurya P Bhatt - Division of Pulmonary, Allergy and Critical Care Medicine, and
- Resource Type
- Journal article
- Publication Details
- JCI insight, Vol.5(13), e132781
- DOI
- 10.1172/jci.insight.132781
- PMID
- 32554922
- PMCID
- PMC7406302
- NLM abbreviation
- JCI Insight
- ISSN
- 2379-3708
- eISSN
- 2379-3708
- Publisher
- United States
- Grant note
- U01 HL089856 / NHLBI NIH HHS U01 HL089897 / NHLBI NIH HHS K23 HL133438 / NHLBI NIH HHS R21 EB027891 / NIBIB NIH HHS P30 DK054759 / NIDDK NIH HHS R01 HL151421 / NHLBI NIH HHS
- Language
- English
- Date published
- 07/09/2020
- Academic Unit
- Roy J. Carver Department of Biomedical Engineering; Radiology
- Record Identifier
- 9984066114302771
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