Development of a multiomics model for identification of predictive biomarkers for COVID-19 severity: a retrospective cohort study

Seul Kee Byeon, Anil K. Madugundu, Kishore Garapati, Madan Gopal Ramarajan, Mayank Saraswat, Praveen Kumar-M, Travis Hughes, Rameen Shah, Mrinal M. Patnaik, Nicholas Chia, Susan Ashrafzadeh-Kian, Joseph D. Yao, Bobbi S. Pritt, Roberto Cattaneo, Mohamed E. Salama, Roman M. Zenka, Benjamin R. Kipp, Stefan K.G. Grebe, Ravinder J. Singh, Amir A. Sadighi AkhaAlicia Algeciras-Schimnich, Surendra Dasari, Janet E. Olson, Jesse R. Walsh, A. J. Venkatakrishnan, Garrett Jenkinson, John C. O'Horo, Andrew D. Badley, Akhilesh Pandey

Research output: Contribution to journalArticlepeer-review


Background: COVID-19 is a multi-system disorder with high variability in clinical outcomes among patients who are admitted to hospital. Although some cytokines such as interleukin (IL)-6 are believed to be associated with severity, there are no early biomarkers that can reliably predict patients who are more likely to have adverse outcomes. Thus, it is crucial to discover predictive markers of serious complications. Methods: In this retrospective cohort study, we analysed samples from 455 participants with COVID-19 who had had a positive SARS-CoV-2 RT-PCR result between April 14, 2020, and Dec 1, 2020 and who had visited one of three Mayo Clinic sites in the USA (Minnesota, Arizona, or Florida) in the same period. These participants were assigned to three subgroups depending on disease severity as defined by the WHO ordinal scale of clinical improvement (outpatient, severe, or critical). Our control cohort comprised of 182 anonymised age-matched and sex-matched plasma samples that were available from the Mayo Clinic Biorepository and banked before the COVID-19 pandemic. We did a deep profiling of circulatory cytokines and other proteins, lipids, and metabolites from both cohorts. Most patient samples were collected before, or around the time of, hospital admission, representing ideal samples for predictive biomarker discovery. We used proximity extension assays to quantify cytokines and circulatory proteins and tandem mass spectrometry to measure lipids and metabolites. Biomarker discovery was done by applying an AutoGluon-tabular classifier to a multiomics dataset, producing a stacked ensemble of cutting-edge machine learning algorithms. Global proteomics and glycoproteomics on a subset of patient samples with matched pre-COVID-19 plasma samples was also done. Findings: We quantified 1463 cytokines and circulatory proteins, along with 902 lipids and 1018 metabolites. By developing a machine-learning-based prediction model, a set of 102 biomarkers, which predicted severe and clinical COVID-19 outcomes better than the traditional set of cytokines, were discovered. These predictive biomarkers included several novel cytokines and other proteins, lipids, and metabolites. For example, altered amounts of C-type lectin domain family 6 member A (CLEC6A), ether phosphatidylethanolamine (P-18:1/18:1), and 2-hydroxydecanoate, as reported here, have not previously been associated with severity in COVID-19. Patient samples with matched pre-COVID-19 plasma samples showed similar trends in muti-omics signatures along with differences in glycoproteomics profile. Interpretation: A multiomic molecular signature in the plasma of patients with COVID-19 before being admitted to hospital can be exploited to predict a more severe course of disease. Machine learning approaches can be applied to highly complex and multidimensional profiling data to reveal novel signatures of clinical use. The absence of validation in an independent cohort remains a major limitation of the study. Funding: Eric and Wendy Schmidt.

Original languageEnglish (US)
Pages (from-to)e632-e645
JournalThe Lancet Digital Health
Issue number9
StatePublished - Sep 2022

ASJC Scopus subject areas

  • Medicine (miscellaneous)
  • Health Informatics
  • Decision Sciences (miscellaneous)
  • Health Information Management


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