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Using machine learning to predict COVID-19 infection and severity risk among 4,510 aged adults: a UK Biobank cohort study

BACKGROUND: Many risk factors have emerged for novel 2019 coronavirus disease (COVID-19). It is relatively unknown how these factors collectively predict COVID-19 infection risk, as well as risk for a severe infection (i.e., hospitalization). METHODS: Among aged adults (69.3 ± 8.6 years) in UK Bioba...

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Detalles Bibliográficos
Autores principales: Willette, Auriel A., Willette, Sara A., Wang, Qian, Pappas, Colleen, Klinedinst, Brandon S., Le, Scott, Larsen, Brittany, Pollpeter, Amy, Li, Tianqi, Brenner, Nicole, Waterboer, Tim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7302228/
https://www.ncbi.nlm.nih.gov/pubmed/32577673
http://dx.doi.org/10.1101/2020.06.09.20127092
Descripción
Sumario:BACKGROUND: Many risk factors have emerged for novel 2019 coronavirus disease (COVID-19). It is relatively unknown how these factors collectively predict COVID-19 infection risk, as well as risk for a severe infection (i.e., hospitalization). METHODS: Among aged adults (69.3 ± 8.6 years) in UK Biobank, COVID-19 data was downloaded for 4,510 participants with 7,539 test cases. We downloaded baseline data from 10–14 years ago, including demographics, biochemistry, body mass, and other factors, as well as antibody titers for 20 common to rare infectious diseases. Permutation-based linear discriminant analysis was used to predict COVID-19 risk and hospitalization risk. Probability and threshold metrics included receiver operating characteristic curves to derive area under the curve (AUC), specificity, sensitivity, and quadratic mean. RESULTS: The “best-fit” model for predicting COVID-19 risk achieved excellent discrimination (AUC=0.969, 95% CI=0.934–1.000). Factors included age, immune markers, lipids, and serology titers to common pathogens like human cytomegalovirus. The hospitalization “best-fit” model was more modest (AUC=0.803, 95% CI=0.663–0.943) and included only serology titers. CONCLUSIONS: Accurate risk profiles can be created using standard self-report and biomedical data collected in public health and medical settings. It is also worthwhile to further investigate if prior host immunity predicts current host immunity to COVID-19.