Prediction models for COVID-19 disease outcomes

被引:3
|
作者
Tang, Cynthia Y. [1 ,2 ,3 ,4 ]
Gao, Cheng [1 ,2 ,3 ,5 ]
Prasai, Kritika [1 ,2 ,3 ,5 ]
Li, Tao [6 ]
Dash, Shreya [1 ,2 ,3 ]
McElroy, Jane A. [7 ]
Hang, Jun [6 ]
Wan, Xiu-Feng [1 ,2 ,3 ,4 ,5 ,8 ]
机构
[1] Univ Missouri, Ctr Influenza & Emerging Infect Dis, Columbia, MO USA
[2] Univ Missouri, Sch Med, Mol Microbiol & Immunol, Columbia, MO USA
[3] Univ Missouri, Bond Life Sci Ctr, Columbia, MO USA
[4] Univ Missouri, Inst Data Sci & Informat, Columbia, MO USA
[5] Univ Missouri, Coll Engn, Dept Elect Engn & Comp Sci, Columbia, MO USA
[6] Walter Reed Army Inst Res, Viral Dis Branch, Silver Spring, MD USA
[7] Univ Missouri, Family & Community Med, Columbia, MO USA
[8] 1201 Rollins St, 443-444, Columbia, MO 65211 USA
基金
美国国家卫生研究院;
关键词
Long COVID; machine learning; personalized medicine; predictive model for COVID-19; COVID-19; prediction; disease outcome prediction; SARS-COV-2; REGRESSION; URBAN;
D O I
10.1080/22221751.2024.2361791
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页数:16
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