Author:
Rezoagli Emanuele,Xin Yi,Signori Davide,Sun Wenli,Gerard Sarah,Delucchi Kevin L.,Magliocca Aurora,Vitale Giovanni,Giacomini Matteo,Mussoni Linda,Montomoli Jonathan,Subert Matteo,Ponti Alessandra,Spadaro Savino,Poli Giancarla,Casola Francesco,Herrmann Jacob,Foti Giuseppe,Calfee Carolyn S.,Laffey John,Bellani Giacomo,Cereda Maurizio, ,Lorini Ferdinando Luca,Bonaffini Pietro,Cazzaniga Matteo,Ottaviani Irene,Tavola Mario,Borgo Asia,Ferraris Livio,Serra Filippo,Gatti Stefano,Ippolito Davide,Tamagnini Beatrice,Gatti Marino,Arlotti Massimo,Gamberini Emiliano,Cavagna Enrico,Galbiati Giuseppe,De Ponti Davide
Abstract
Abstract
Background
Automated analysis of lung computed tomography (CT) scans may help characterize subphenotypes of acute respiratory illness. We integrated lung CT features measured via deep learning with clinical and laboratory data in spontaneously breathing subjects to enhance the identification of COVID-19 subphenotypes.
Methods
This is a multicenter observational cohort study in spontaneously breathing patients with COVID-19 respiratory failure exposed to early lung CT within 7 days of admission. We explored lung CT images using deep learning approaches to quantitative and qualitative analyses; latent class analysis (LCA) by using clinical, laboratory and lung CT variables; regional differences between subphenotypes following 3D spatial trajectories.
Results
Complete datasets were available in 559 patients. LCA identified two subphenotypes (subphenotype 1 and 2). As compared with subphenotype 2 (n = 403), subphenotype 1 patients (n = 156) were older, had higher inflammatory biomarkers, and were more hypoxemic. Lungs in subphenotype 1 had a higher density gravitational gradient with a greater proportion of consolidated lungs as compared with subphenotype 2. In contrast, subphenotype 2 had a higher density submantellar–hilar gradient with a greater proportion of ground glass opacities as compared with subphenotype 1. Subphenotype 1 showed higher prevalence of comorbidities associated with endothelial dysfunction and higher 90-day mortality than subphenotype 2, even after adjustment for clinically meaningful variables.
Conclusions
Integrating lung-CT data in a LCA allowed us to identify two subphenotypes of COVID-19, with different clinical trajectories. These exploratory findings suggest a role of automated imaging characterization guided by machine learning in subphenotyping patients with respiratory failure.
Trial registration: ClinicalTrials.gov Identifier: NCT04395482. Registration date: 19/05/2020.
Funder
Università degli Studi di Milano-Bicocca
National Institutes of Health
Publisher
Springer Science and Business Media LLC