Evidence map›Paper›PMID 42344108›Full record

ArticleJAMIA open2026

Comparing risk factors in severe COVID-19 using machine learning and non-machine learning methods: analysis from 2 international randomized controlled trials.

Christian Møller Jensen, Ramtin Zargari Marandi, Kasper Sommerlund Moestrup, Ahmad Mourad, Alfredo J Mena Lora, Brad T Sherman, David M Vock, Jacqueline A Nordwall, Joanne M Carson, Nathan Peiffer-Smadja and 11 more

Abstract read
In one paragraph

Article in JAMIA open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors.

Christian Møller JensenCHIP, Centre of Excellence for Health, Immunity, and Infections, Rigshospitalet, University of Copenhagen, Copenhagen Ø, 2100, Denmark.ORCID https://orcid.org/0000-0002-0873-4127
Ramtin Zargari MarandiCHIP, Centre of Excellence for Health, Immunity, and Infections, Rigshospitalet, University of Copenhagen, Copenhagen Ø, 2100, Denmark.ORCID https://orcid.org/0000-0001-9233-1656
Kasper Sommerlund MoestrupCHIP, Centre of Excellence for Health, Immunity, and Infections, Rigshospitalet, University of Copenhagen, Copenhagen Ø, 2100, Denmark.ORCID https://orcid.org/0000-0003-3736-6156
Ahmad MouradDivision of Infectious Diseases, Department of Medicine, Duke University School of Medicine, Durham, NC 27710, United States.ORCID https://orcid.org/0000-0002-3149-597X
Alfredo J Mena LoraUniversity of Illinois Chicago, Chicago, IL 60607, United States.ORCID https://orcid.org/0000-0002-8337-757X
Brad T ShermanFrederick National Laboratory for Cancer Research, Frederick, MD 21701, United States.ORCID https://orcid.org/0000-0001-5815-7359
David M VockDivision of Biostatistics & Health Data Science, University of Minnesota, Minneapolis, MN 55414, United States.ORCID https://orcid.org/0000-0002-5459-9579
Jacqueline A NordwallDivision of Biostatistics & Health Data Science, University of Minnesota, Minneapolis, MN 55414, United States.ORCID https://orcid.org/0009-0005-6339-1701
Joanne M CarsonKirby Institute, University of New South Wales, Sydney, NSW 2052, Australia.ORCID https://orcid.org/0000-0001-8043-0200
Nathan Peiffer-SmadjaUniversité Paris Cité et Université Sorbonne Paris Nord, Inserm, IAME, Paris, 75018, France.ORCID https://orcid.org/0000-0003-1166-1958
Neil R AggarwalDivision of Pulmonary, Allergy, and Critical Care Medicine, University of Colorado School of Medicine, Aurora, CO 80045, United States.ORCID https://orcid.org/0000-0002-0922-8824
Nicole E NaimanDepartment of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390, United States.ORCID https://orcid.org/0000-0002-6116-555X
Samuel M BrownPulmonary/Critical Care Medicine, Intermountain Medical Center, Salt Lake City, UT 84132, United States.ORCID https://orcid.org/0000-0003-1206-6261
Thomas W BarrettVA Portland Health Care System, Portland, OR 97239, United States.ORCID https://orcid.org/0009-0002-9392-0764
Timothy HatlenHarbor-UCLA Medical Center, Torrance, CA 90502, United States.ORCID https://orcid.org/0000-0003-3755-4309
Victoria S KjærgaardCHIP, Centre of Excellence for Health, Immunity, and Infections, Rigshospitalet, University of Copenhagen, Copenhagen Ø, 2100, Denmark.ORCID https://orcid.org/0000-0002-3062-0206
Weizhong ChangFrederick National Laboratory for Cancer Research, Frederick, MD 21701, United States.ORCID https://orcid.org/0000-0002-1413-2763
Matthew R SydesMRC Clinical Trials Unit at UCL, Institute of Clinical Trials and Methodology, UCL, London WC1V 6LJ, United Kingdom.ORCID https://orcid.org/0000-0002-9323-1371
Jens LundgrenCHIP, Centre of Excellence for Health, Immunity, and Infections, Rigshospitalet, University of Copenhagen, Copenhagen Ø, 2100, Denmark.ORCID https://orcid.org/0000-0001-8901-7850
Tomas O JensenCHIP, Centre of Excellence for Health, Immunity, and Infections, Rigshospitalet, University of Copenhagen, Copenhagen Ø, 2100, Denmark.ORCID https://orcid.org/0000-0003-0398-4431
STRIVE Network and ITAC and TICO Study Groups

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: To compare differences in risk factors and 90-day mortality prediction from 2 machine learning (ML) models with a previously published non-ML model and investigate their validity in an external cohort. Materials and methods: Prospectively collected data from 2 separate randomized controlled trial (RCT) cohorts from 2020 to 2021, the Therapeutics for Inpatients with COVID-19 (TICO/ACTIV-3) Trial (derivation and internal validation cohort) and the Inpatient Treatment with Anti-Coronavirus Immunoglobulin (ITAC) Trial (external validation cohort) were used. Data were collected from 114 sites in 10 countries (TICO/ACTIV-3) and 63 sites in 11 countries (ITAC). A ML pipeline including 5 classification models, and 1 survival model was used for risk factor identification and clinical outcome prediction. Risk factors were compared between a ML-based classification model, a ML-based survival model and a previously published Cox model. Performance of the ML-based classification model was compared across TICO/ACTIV-3 and ITAC. Results: A total of 2625 (TICO/ACTIV-3) and 579 (ITAC) adults hospitalized for COVID-19 were included. Some overlap of risk factors was identified across models. Five were identified in all models, 3 only in ML models, and 4 only in the non-ML model. The ML model showed good predictive performance in TICO/ACTIV-3. Internal validation showed no overfitting. Lower model performance was observed in ITAC (-15.8%), but performance remained above chance level. Discussion: Differences in methods for risk factor identification using ML and non-ML complicates the comparison of results derived from each approach, but using multiple approaches may unveil overlooked risk factors. Conclusion: Risk factor identification may benefit from integrating both ML and non-ML methods, but external validation is necessary, even in RCTs.

Indexed as

biostatisticsmachine learningmedical informaticsrandomized controlled trialSARS-CoV-2

Identifiers

PMID42344108
PMCPMC13289610

What Socratic holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.