Prediction models for COVID-19 disease outcomes

SARS-CoV-2 has caused over 6.9 million deaths and continues to produce lasting health consequences. COVID-19 manifests broadly from no symptoms to death. In a retrospective cross-sectional study, we developed personalized risk assessment models that predict clinical outcomes for individuals with COV...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Tang, Cynthia Y., Gao, Cheng, Prasai, Kritika, Li, Tao, Dash, Shreya, McElroy, Jane A., Hang, Jun, Wan, Xiu-Feng
Format: Dataset
Sprache:eng
Schlagworte:
Online-Zugang:Volltext bestellen
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue
container_start_page
container_title
container_volume
creator Tang, Cynthia Y.
Gao, Cheng
Prasai, Kritika
Li, Tao
Dash, Shreya
McElroy, Jane A.
Hang, Jun
Wan, Xiu-Feng
description SARS-CoV-2 has caused over 6.9 million deaths and continues to produce lasting health consequences. COVID-19 manifests broadly from no symptoms to death. In a retrospective cross-sectional study, we developed personalized risk assessment models that predict clinical outcomes for individuals with COVID-19 and inform targeted interventions. We sequenced viruses from SARS-CoV-2-positive nasopharyngeal swab samples between July 2020 and July 2022 from 4450 individuals in Missouri and retrieved associated disease courses, clinical history, and urban-rural classification. We integrated this data to develop machine learning-based predictive models to predict hospitalization, ICU admission, and long COVID. The mean age was 38.3 years (standard deviation = 21.4) with 55.2% (N = 2453) females and 44.8% (N = 1994) males (not reported, N = 4). Our analyses revealed a comprehensive set of predictors for each outcome, encompassing human, environment, and virus genome-wide genetic markers. Immunosuppression, cardiovascular disease, older age, cardiac, gastrointestinal, and constitutional symptoms, rural residence, and specific amino acid substitutions were associated with hospitalization. ICU admission was associated with acute respiratory distress syndrome, ventilation, bacterial co-infection, rural residence, and non-wild type SARS-CoV-2 variants. Finally, long COVID was associated with hospital admission, ventilation, and female sex. Overall, we developed risk assessment models that offer the capability to identify patients with COVID-19 necessitating enhanced monitoring or early interventions. Of importance, we demonstrate the value of including key elements of virus, host, and environmental factors to predict patient outcomes, serving as a valuable platform in the field of personalized medicine with the potential for adaptation to other infectious diseases. Model summary and motivation. Individuals infected with SARS-CoV-2 experience a wide spectrum of clinical manifestations ranging from no symptoms to death. Using the Virus-Human Outcomes Prediction (ViHOP) algorithm, we aim to utilize the individual’s clinical characteristics, the individual’s location, and the infecting SARS-CoV-2 virus characteristics obtained by whole genome sequencing to determine their likelihood of admission to the hospital, admission to the intensive care unit (ICU), or experiencing long COVID. This model allows clinicians to identify at-risk patients for further monitoring and/or early tr
doi_str_mv 10.6084/m9.figshare.26042178
format Dataset
fullrecord <record><control><sourceid>datacite_PQ8</sourceid><recordid>TN_cdi_datacite_primary_10_6084_m9_figshare_26042178</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_6084_m9_figshare_26042178</sourcerecordid><originalsourceid>FETCH-datacite_primary_10_6084_m9_figshare_260421783</originalsourceid><addsrcrecordid>eNpjYJAxNNAzM7Aw0c-11EvLTC_OSCxK1TMyMzAxMjS34GTQDyhKTclMLsnMz1PIzU9JzSlWSMsvUnD2D_N00TW0VEjJLE5NLE5VyC8tSc7PTS3mYWBNS8wpTuWF0twMJm6uIc4euimJJYnJmSWp8QVFmbmJRZXxhgbxIHvjcy3jYfbGw-w1JlMbAB4xP2g</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>dataset</recordtype></control><display><type>dataset</type><title>Prediction models for COVID-19 disease outcomes</title><source>DataCite</source><creator>Tang, Cynthia Y. ; Gao, Cheng ; Prasai, Kritika ; Li, Tao ; Dash, Shreya ; McElroy, Jane A. ; Hang, Jun ; Wan, Xiu-Feng</creator><creatorcontrib>Tang, Cynthia Y. ; Gao, Cheng ; Prasai, Kritika ; Li, Tao ; Dash, Shreya ; McElroy, Jane A. ; Hang, Jun ; Wan, Xiu-Feng</creatorcontrib><description>SARS-CoV-2 has caused over 6.9 million deaths and continues to produce lasting health consequences. COVID-19 manifests broadly from no symptoms to death. In a retrospective cross-sectional study, we developed personalized risk assessment models that predict clinical outcomes for individuals with COVID-19 and inform targeted interventions. We sequenced viruses from SARS-CoV-2-positive nasopharyngeal swab samples between July 2020 and July 2022 from 4450 individuals in Missouri and retrieved associated disease courses, clinical history, and urban-rural classification. We integrated this data to develop machine learning-based predictive models to predict hospitalization, ICU admission, and long COVID. The mean age was 38.3 years (standard deviation = 21.4) with 55.2% (N = 2453) females and 44.8% (N = 1994) males (not reported, N = 4). Our analyses revealed a comprehensive set of predictors for each outcome, encompassing human, environment, and virus genome-wide genetic markers. Immunosuppression, cardiovascular disease, older age, cardiac, gastrointestinal, and constitutional symptoms, rural residence, and specific amino acid substitutions were associated with hospitalization. ICU admission was associated with acute respiratory distress syndrome, ventilation, bacterial co-infection, rural residence, and non-wild type SARS-CoV-2 variants. Finally, long COVID was associated with hospital admission, ventilation, and female sex. Overall, we developed risk assessment models that offer the capability to identify patients with COVID-19 necessitating enhanced monitoring or early interventions. Of importance, we demonstrate the value of including key elements of virus, host, and environmental factors to predict patient outcomes, serving as a valuable platform in the field of personalized medicine with the potential for adaptation to other infectious diseases. Model summary and motivation. Individuals infected with SARS-CoV-2 experience a wide spectrum of clinical manifestations ranging from no symptoms to death. Using the Virus-Human Outcomes Prediction (ViHOP) algorithm, we aim to utilize the individual’s clinical characteristics, the individual’s location, and the infecting SARS-CoV-2 virus characteristics obtained by whole genome sequencing to determine their likelihood of admission to the hospital, admission to the intensive care unit (ICU), or experiencing long COVID. This model allows clinicians to identify at-risk patients for further monitoring and/or early treatment.</description><identifier>DOI: 10.6084/m9.figshare.26042178</identifier><language>eng</language><publisher>Taylor &amp; Francis</publisher><subject>Biological Sciences not elsewhere classified ; Biotechnology ; Cancer ; FOS: Health sciences ; Infectious Diseases ; Information Systems not elsewhere classified ; Mathematical Sciences not elsewhere classified ; Medicine ; Mental Health ; Virology</subject><creationdate>2024</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>776,1888</link.rule.ids><linktorsrc>$$Uhttps://commons.datacite.org/doi.org/10.6084/m9.figshare.26042178$$EView_record_in_DataCite.org$$FView_record_in_$$GDataCite.org$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>Tang, Cynthia Y.</creatorcontrib><creatorcontrib>Gao, Cheng</creatorcontrib><creatorcontrib>Prasai, Kritika</creatorcontrib><creatorcontrib>Li, Tao</creatorcontrib><creatorcontrib>Dash, Shreya</creatorcontrib><creatorcontrib>McElroy, Jane A.</creatorcontrib><creatorcontrib>Hang, Jun</creatorcontrib><creatorcontrib>Wan, Xiu-Feng</creatorcontrib><title>Prediction models for COVID-19 disease outcomes</title><description>SARS-CoV-2 has caused over 6.9 million deaths and continues to produce lasting health consequences. COVID-19 manifests broadly from no symptoms to death. In a retrospective cross-sectional study, we developed personalized risk assessment models that predict clinical outcomes for individuals with COVID-19 and inform targeted interventions. We sequenced viruses from SARS-CoV-2-positive nasopharyngeal swab samples between July 2020 and July 2022 from 4450 individuals in Missouri and retrieved associated disease courses, clinical history, and urban-rural classification. We integrated this data to develop machine learning-based predictive models to predict hospitalization, ICU admission, and long COVID. The mean age was 38.3 years (standard deviation = 21.4) with 55.2% (N = 2453) females and 44.8% (N = 1994) males (not reported, N = 4). Our analyses revealed a comprehensive set of predictors for each outcome, encompassing human, environment, and virus genome-wide genetic markers. Immunosuppression, cardiovascular disease, older age, cardiac, gastrointestinal, and constitutional symptoms, rural residence, and specific amino acid substitutions were associated with hospitalization. ICU admission was associated with acute respiratory distress syndrome, ventilation, bacterial co-infection, rural residence, and non-wild type SARS-CoV-2 variants. Finally, long COVID was associated with hospital admission, ventilation, and female sex. Overall, we developed risk assessment models that offer the capability to identify patients with COVID-19 necessitating enhanced monitoring or early interventions. Of importance, we demonstrate the value of including key elements of virus, host, and environmental factors to predict patient outcomes, serving as a valuable platform in the field of personalized medicine with the potential for adaptation to other infectious diseases. Model summary and motivation. Individuals infected with SARS-CoV-2 experience a wide spectrum of clinical manifestations ranging from no symptoms to death. Using the Virus-Human Outcomes Prediction (ViHOP) algorithm, we aim to utilize the individual’s clinical characteristics, the individual’s location, and the infecting SARS-CoV-2 virus characteristics obtained by whole genome sequencing to determine their likelihood of admission to the hospital, admission to the intensive care unit (ICU), or experiencing long COVID. This model allows clinicians to identify at-risk patients for further monitoring and/or early treatment.</description><subject>Biological Sciences not elsewhere classified</subject><subject>Biotechnology</subject><subject>Cancer</subject><subject>FOS: Health sciences</subject><subject>Infectious Diseases</subject><subject>Information Systems not elsewhere classified</subject><subject>Mathematical Sciences not elsewhere classified</subject><subject>Medicine</subject><subject>Mental Health</subject><subject>Virology</subject><fulltext>true</fulltext><rsrctype>dataset</rsrctype><creationdate>2024</creationdate><recordtype>dataset</recordtype><sourceid>PQ8</sourceid><recordid>eNpjYJAxNNAzM7Aw0c-11EvLTC_OSCxK1TMyMzAxMjS34GTQDyhKTclMLsnMz1PIzU9JzSlWSMsvUnD2D_N00TW0VEjJLE5NLE5VyC8tSc7PTS3mYWBNS8wpTuWF0twMJm6uIc4euimJJYnJmSWp8QVFmbmJRZXxhgbxIHvjcy3jYfbGw-w1JlMbAB4xP2g</recordid><startdate>20240614</startdate><enddate>20240614</enddate><creator>Tang, Cynthia Y.</creator><creator>Gao, Cheng</creator><creator>Prasai, Kritika</creator><creator>Li, Tao</creator><creator>Dash, Shreya</creator><creator>McElroy, Jane A.</creator><creator>Hang, Jun</creator><creator>Wan, Xiu-Feng</creator><general>Taylor &amp; Francis</general><scope>DYCCY</scope><scope>PQ8</scope></search><sort><creationdate>20240614</creationdate><title>Prediction models for COVID-19 disease outcomes</title><author>Tang, Cynthia Y. ; Gao, Cheng ; Prasai, Kritika ; Li, Tao ; Dash, Shreya ; McElroy, Jane A. ; Hang, Jun ; Wan, Xiu-Feng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-datacite_primary_10_6084_m9_figshare_260421783</frbrgroupid><rsrctype>datasets</rsrctype><prefilter>datasets</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Biological Sciences not elsewhere classified</topic><topic>Biotechnology</topic><topic>Cancer</topic><topic>FOS: Health sciences</topic><topic>Infectious Diseases</topic><topic>Information Systems not elsewhere classified</topic><topic>Mathematical Sciences not elsewhere classified</topic><topic>Medicine</topic><topic>Mental Health</topic><topic>Virology</topic><toplevel>online_resources</toplevel><creatorcontrib>Tang, Cynthia Y.</creatorcontrib><creatorcontrib>Gao, Cheng</creatorcontrib><creatorcontrib>Prasai, Kritika</creatorcontrib><creatorcontrib>Li, Tao</creatorcontrib><creatorcontrib>Dash, Shreya</creatorcontrib><creatorcontrib>McElroy, Jane A.</creatorcontrib><creatorcontrib>Hang, Jun</creatorcontrib><creatorcontrib>Wan, Xiu-Feng</creatorcontrib><collection>DataCite (Open Access)</collection><collection>DataCite</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Tang, Cynthia Y.</au><au>Gao, Cheng</au><au>Prasai, Kritika</au><au>Li, Tao</au><au>Dash, Shreya</au><au>McElroy, Jane A.</au><au>Hang, Jun</au><au>Wan, Xiu-Feng</au><format>book</format><genre>unknown</genre><ristype>DATA</ristype><title>Prediction models for COVID-19 disease outcomes</title><date>2024-06-14</date><risdate>2024</risdate><abstract>SARS-CoV-2 has caused over 6.9 million deaths and continues to produce lasting health consequences. COVID-19 manifests broadly from no symptoms to death. In a retrospective cross-sectional study, we developed personalized risk assessment models that predict clinical outcomes for individuals with COVID-19 and inform targeted interventions. We sequenced viruses from SARS-CoV-2-positive nasopharyngeal swab samples between July 2020 and July 2022 from 4450 individuals in Missouri and retrieved associated disease courses, clinical history, and urban-rural classification. We integrated this data to develop machine learning-based predictive models to predict hospitalization, ICU admission, and long COVID. The mean age was 38.3 years (standard deviation = 21.4) with 55.2% (N = 2453) females and 44.8% (N = 1994) males (not reported, N = 4). Our analyses revealed a comprehensive set of predictors for each outcome, encompassing human, environment, and virus genome-wide genetic markers. Immunosuppression, cardiovascular disease, older age, cardiac, gastrointestinal, and constitutional symptoms, rural residence, and specific amino acid substitutions were associated with hospitalization. ICU admission was associated with acute respiratory distress syndrome, ventilation, bacterial co-infection, rural residence, and non-wild type SARS-CoV-2 variants. Finally, long COVID was associated with hospital admission, ventilation, and female sex. Overall, we developed risk assessment models that offer the capability to identify patients with COVID-19 necessitating enhanced monitoring or early interventions. Of importance, we demonstrate the value of including key elements of virus, host, and environmental factors to predict patient outcomes, serving as a valuable platform in the field of personalized medicine with the potential for adaptation to other infectious diseases. Model summary and motivation. Individuals infected with SARS-CoV-2 experience a wide spectrum of clinical manifestations ranging from no symptoms to death. Using the Virus-Human Outcomes Prediction (ViHOP) algorithm, we aim to utilize the individual’s clinical characteristics, the individual’s location, and the infecting SARS-CoV-2 virus characteristics obtained by whole genome sequencing to determine their likelihood of admission to the hospital, admission to the intensive care unit (ICU), or experiencing long COVID. This model allows clinicians to identify at-risk patients for further monitoring and/or early treatment.</abstract><pub>Taylor &amp; Francis</pub><doi>10.6084/m9.figshare.26042178</doi><oa>free_for_read</oa></addata></record>
fulltext fulltext_linktorsrc
identifier DOI: 10.6084/m9.figshare.26042178
ispartof
issn
language eng
recordid cdi_datacite_primary_10_6084_m9_figshare_26042178
source DataCite
subjects Biological Sciences not elsewhere classified
Biotechnology
Cancer
FOS: Health sciences
Infectious Diseases
Information Systems not elsewhere classified
Mathematical Sciences not elsewhere classified
Medicine
Mental Health
Virology
title Prediction models for COVID-19 disease outcomes
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-20T20%3A17%3A56IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-datacite_PQ8&rft_val_fmt=info:ofi/fmt:kev:mtx:book&rft.genre=unknown&rft.au=Tang,%20Cynthia%20Y.&rft.date=2024-06-14&rft_id=info:doi/10.6084/m9.figshare.26042178&rft_dat=%3Cdatacite_PQ8%3E10_6084_m9_figshare_26042178%3C/datacite_PQ8%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true