Journal article
Machine learning models predict long COVID outcomes based on baseline clinical and immunologic factors
Communications medicine, v 6(1), 1
2026
PMID: 41484172
Featured in Collection : UN Sustainable Development Goals @ Drexel
Abstract
Background
The post-acute sequelae of SARS-CoV-2 (PASC), also known as long COVID, remain a significant health issue that is incompletely understood. Predicting which acutely infected individuals will develop long COVID is challenging due to the absence of established biomarkers, clear disease mechanisms, or well-defined sub-phenotypes. Machine learning (ML) models may address this gap by leveraging clinical data to enhance diagnostic precision.
Methods
Clinical data, including antibody titers and viral load measurements collected at the time of hospital admission, are used to predict the likelihood of acute COVID-19 progressing to long COVID. Machine learning models are trained and evaluated for predictive performance. Feature importance analysis is performed to identify the most influential predictors.
Results
The machine learning models achieve median AUROC values ranging from 0.64 to 0.66 and AUPRC values between 0.51 and 0.54, demonstrating predictive capabilities. Low antibody titers and high viral loads at hospital admission emerge as the strongest predictors of long COVID outcomes. Comorbidities—such as chronic respiratory, cardiac, and neurologic diseases—and female sex are also identified as significant risk factors.
Conclusions
Machine learning models identify patients at risk for developing long COVID based on baseline clinical characteristics. These models guide early interventions, improve patient outcomes, and mitigate the long-term public health impacts of SARS-CoV-2.
Plain language summary
Long COVID, or post-acute sequelae of SARS-CoV-2, is a prolonged health condition that can occur after acute COVID-19 infection. However, the ability to predict who will develop long COVID remains limited due to the absence of clear tests or biomarkers. We looked at patients’ medical information, including the amount of virus in their body at hospital admission, and how strong their immune response was. Using computer programs that can find hidden patterns in large sets of data, we discovered that people with a weaker immune response, higher amounts of virus, certain long term health problems and women are more likely to develop long COVID. This study highlights that computer-based tools could help doctors identify high-risk patients early and provide care that may prevent long-term complications.
Jayavelu, Samaha et al., apply machine learning models on hospital admission data, including antibody titers and viral load, to identify patients at high risk for Long COVID. Low antibody levels, high viral loads, chronic diseases, and female sex are key predictors, supporting early, targeted interventions.
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Details
- Title
- Machine learning models predict long COVID outcomes based on baseline clinical and immunologic factors
- Creators
- Naresh Doni Jayavelu - University of WashingtonHady Samaha - Emory UniversitySonia Tandon Wimalasena - Emory UniversityAnnmarie Hoch - The Coordinating CenterJeremy P. Gygi - Yale UniversityGisela Gabernet - Yale UniversityAl Ozonoff - The Coordinating CenterShanshan Liu - The Coordinating CenterCarly E. Milliren - The Coordinating CenterOfer Levy - Boston Children's HospitalLindsey R. Baden - Brigham and Women's HospitalEsther Melamed - The University of Texas at AustinLauren I. R. Ehrlich - The University of Texas at AustinGrace A. McComsey - Case Western Reserve UniversityRafick P. Sekaly - University Hospitals of ClevelandCharles B. Cairns - Drexel UniversityElias K. Haddad - Drexel UniversityJoanna Schaenman - University of California, Los AngelesAlbert C. Shaw - Yale UniversityDavid A. Hafler - Yale UniversityRuth R. Montgomery - Yale UniversityDavid B. Corry - Baylor College of MedicineFarrah Kheradmand - Baylor College of MedicineMark A. Atkinson - University of FloridaScott C. Brakenridge - University of FloridaNelson I. Agudelo Higuit - OU HealthJordan P. Metcalf - University of Oklahoma Health Sciences CenterCatherine L. Hough - Oregon Health & Science UniversityWilliam B. Messer - Oregon Health & Science UniversityBali Pulendran - Stanford UniversityKari C. Nadeau - Stanford UniversityMark M. Davis - Palo Alto UniversityLinda N. Gen - Palo Alto UniversityAna Fernandez Sesma - Icahn School of Medicine at Mount SinaiViviana Simon - Icahn School of Medicine at Mount SinaiFlorian Krammer - Icahn School of Medicine at Mount SinaiMonica Kraft - University of ArizonaChris Bime - University of ArizonaCarolyn S. Calfee - University of California, San FranciscoDavid J. Erle - University of California, San FranciscoCharles R. Langelier - University of California, San FranciscoLeying Guan - Yale School of MedicineHolden T. Maecker - Stanford University School of MedicineBjoern Peters - La Jolla Institute for ImmunologySteven H. Kleinstein - Yale School of MedicineElaine F. Reed - University of California, Los AngelesAlison D. Augustine - National Institute of Allergy and Infectious DiseasesJoann Diray-Arce - Clinical and Data Coordinating Center (CDCC) Precision Vaccines Program, Boston Children’s HospitalPatrice M. Becker - National Institute of Allergy and Infectious DiseasesNadine Rouphael - Emory and Henry CollegeMatthew C. Altman - University of Washington
- Publication Details
- Communications medicine, v 6(1), 1
- Publisher
- Nature Publishing Group
- Number of pages
- 10
- Grant note
- National Institute of Allergy and Infectious Diseases (NIAID), a part of the U.S. National Institutes of Health(NIH): R01AI104870, R01AI132774, R01AI135803, R01AI145835, U19AI057229, U19AI062629, U19AI077439, U19AI089992, U19AI090023, U19AI118608, U19AI118610, U19AI125357, U19AI128910, U19AI128913, U54AI142766, U24AI52179 NIH: P51 OD011132, S10 OD026799
This study is being supported by grants R01AI104870, R01AI132774, R01AI135803, R01AI145835, U19AI057229, U19AI062629, U19AI077439, U19AI089992,U19AI090023, U19AI118608, U19AI118610, U19AI125357, U19AI128910, U19AI128913, U54AI142766, U19AI089992, U24AI52179 from the National Institute of Allergy and Infectious Diseases (NIAID), a part of the U.S. National Institutes of Health(NIH), and P51 OD011132, S10 OD026799 from NIH.
- Resource Type
- Journal article
- Language
- English
- Academic Unit
- College of Medicine; Infectious Diseases (and HIV Medicine); Emergency Medicine
- Web of Science ID
- WOS:001652493100001
- Scopus ID
- 2-s2.0-105031548760
- Other Identifier
- 991022148194204721
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- Collaboration types
- Industry collaboration
- Domestic collaboration
- International collaboration
- Web of Science research areas
- Medicine, Research & Experimental