Identification of Endotypes of Hospitalized COVID-19 Patients
Background: Characterization of coronavirus disease 2019 (COVID-19) endotypes may help explain variable clinical presentations and response to treatments. While risk factors for COVID-19 have been described, COVID-19 endotypes have not been elucidated.Objectives: We sought to identify and describe C...
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Frontiers Media S.A.
2021
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oai:doaj.org-article:9d7a77ef5dc944e898229fffc152ff9a2021-11-11T07:01:27ZIdentification of Endotypes of Hospitalized COVID-19 Patients2296-858X10.3389/fmed.2021.770343https://doaj.org/article/9d7a77ef5dc944e898229fffc152ff9a2021-11-01T00:00:00Zhttps://www.frontiersin.org/articles/10.3389/fmed.2021.770343/fullhttps://doaj.org/toc/2296-858XBackground: Characterization of coronavirus disease 2019 (COVID-19) endotypes may help explain variable clinical presentations and response to treatments. While risk factors for COVID-19 have been described, COVID-19 endotypes have not been elucidated.Objectives: We sought to identify and describe COVID-19 endotypes of hospitalized patients.Methods: Consensus clustering (using the ensemble method) of patient age and laboratory values during admission identified endotypes. We analyzed data from 528 patients with COVID-19 who were admitted to telemetry capable beds at Columbia University Irving Medical Center and discharged between March 12 to July 15, 2020.Results: Four unique endotypes were identified and described by laboratory values, demographics, outcomes, and treatments. Endotypes 1 and 2 were comprised of low numbers of intubated patients (1 and 6%) and exhibited low mortality (1 and 6%), whereas endotypes 3 and 4 included high numbers of intubated patients (72 and 85%) with elevated mortality (21 and 43%). Endotypes 2 and 4 had the most comorbidities. Endotype 1 patients had low levels of inflammatory markers (ferritin, IL-6, CRP, LDH), low infectious markers (WBC, procalcitonin), and low degree of coagulopathy (PTT, PT), while endotype 4 had higher levels of those markers.Conclusions: Four unique endotypes of hospitalized patients with COVID-19 were identified, which segregated patients based on inflammatory markers, infectious markers, evidence of end-organ dysfunction, comorbidities, and outcomes. High comorbidities did not associate with poor outcome endotypes. Further work is needed to validate these endotypes in other cohorts and to study endotype differences to treatment responses.Benjamin L. RanardBenjamin L. RanardMurad MegjhaniMurad MegjhaniKalijah TerilliKalijah TerilliKevin DoyleJan ClaassenMichael R. PinskyGilles ClermontYoram VodovotzShadnaz AsgariSoojin ParkSoojin ParkFrontiers Media S.A.articleCOVID-19cluster analysisendotypephenotypemachine learningtreatmentMedicine (General)R5-920ENFrontiers in Medicine, Vol 8 (2021) |
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COVID-19 cluster analysis endotype phenotype machine learning treatment Medicine (General) R5-920 |
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COVID-19 cluster analysis endotype phenotype machine learning treatment Medicine (General) R5-920 Benjamin L. Ranard Benjamin L. Ranard Murad Megjhani Murad Megjhani Kalijah Terilli Kalijah Terilli Kevin Doyle Jan Claassen Michael R. Pinsky Gilles Clermont Yoram Vodovotz Shadnaz Asgari Soojin Park Soojin Park Identification of Endotypes of Hospitalized COVID-19 Patients |
description |
Background: Characterization of coronavirus disease 2019 (COVID-19) endotypes may help explain variable clinical presentations and response to treatments. While risk factors for COVID-19 have been described, COVID-19 endotypes have not been elucidated.Objectives: We sought to identify and describe COVID-19 endotypes of hospitalized patients.Methods: Consensus clustering (using the ensemble method) of patient age and laboratory values during admission identified endotypes. We analyzed data from 528 patients with COVID-19 who were admitted to telemetry capable beds at Columbia University Irving Medical Center and discharged between March 12 to July 15, 2020.Results: Four unique endotypes were identified and described by laboratory values, demographics, outcomes, and treatments. Endotypes 1 and 2 were comprised of low numbers of intubated patients (1 and 6%) and exhibited low mortality (1 and 6%), whereas endotypes 3 and 4 included high numbers of intubated patients (72 and 85%) with elevated mortality (21 and 43%). Endotypes 2 and 4 had the most comorbidities. Endotype 1 patients had low levels of inflammatory markers (ferritin, IL-6, CRP, LDH), low infectious markers (WBC, procalcitonin), and low degree of coagulopathy (PTT, PT), while endotype 4 had higher levels of those markers.Conclusions: Four unique endotypes of hospitalized patients with COVID-19 were identified, which segregated patients based on inflammatory markers, infectious markers, evidence of end-organ dysfunction, comorbidities, and outcomes. High comorbidities did not associate with poor outcome endotypes. Further work is needed to validate these endotypes in other cohorts and to study endotype differences to treatment responses. |
format |
article |
author |
Benjamin L. Ranard Benjamin L. Ranard Murad Megjhani Murad Megjhani Kalijah Terilli Kalijah Terilli Kevin Doyle Jan Claassen Michael R. Pinsky Gilles Clermont Yoram Vodovotz Shadnaz Asgari Soojin Park Soojin Park |
author_facet |
Benjamin L. Ranard Benjamin L. Ranard Murad Megjhani Murad Megjhani Kalijah Terilli Kalijah Terilli Kevin Doyle Jan Claassen Michael R. Pinsky Gilles Clermont Yoram Vodovotz Shadnaz Asgari Soojin Park Soojin Park |
author_sort |
Benjamin L. Ranard |
title |
Identification of Endotypes of Hospitalized COVID-19 Patients |
title_short |
Identification of Endotypes of Hospitalized COVID-19 Patients |
title_full |
Identification of Endotypes of Hospitalized COVID-19 Patients |
title_fullStr |
Identification of Endotypes of Hospitalized COVID-19 Patients |
title_full_unstemmed |
Identification of Endotypes of Hospitalized COVID-19 Patients |
title_sort |
identification of endotypes of hospitalized covid-19 patients |
publisher |
Frontiers Media S.A. |
publishDate |
2021 |
url |
https://doaj.org/article/9d7a77ef5dc944e898229fffc152ff9a |
work_keys_str_mv |
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