Evidence map›Paper›PMID 37936960›Full record

ArticleDigital health

Detecting the most critical clinical variables of COVID-19 breakthrough infection in vaccinated persons using machine learning.

Olawande Daramola, Tatenda Duncan Kavu, Maritha J Kotze, Oiva Kamati, Zaakiyah Emjedi, Boniface Kabaso, Thomas Moser, Karl Stroetmann, Isaac Fwemba, Fisayo Daramola and 4 more

Open access · goldAbstract read
In one paragraph

Article in Digital health. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 46% of its field
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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
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

14 authors at 5 institutions in 3 countries.

Olawande DaramolaDepartment of Information Technology, Faculty of Informatics and Design, Cape Peninsula University of Technology, Cape Town, South Africa.ORCID https://orcid.org/0000-0001-6340-078X
Tatenda Duncan KavuDepartment of Information Technology, Faculty of Informatics and Design, Cape Peninsula University of Technology, Cape Town, South Africa.ORCID https://orcid.org/0000-0002-9479-1143
Maritha J KotzeDivision of Chemical Pathology, Department of Pathology, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.
Oiva KamatiApplied Microbial and Health Biotechnology Institute (AMHBI), Cape Peninsula University of Technology, Cape Town, South Africa.
Zaakiyah EmjediApplied Microbial and Health Biotechnology Institute (AMHBI), Cape Peninsula University of Technology, Cape Town, South Africa.
Boniface KabasoDepartment of Information Technology, Faculty of Informatics and Design, Cape Peninsula University of Technology, Cape Town, South Africa.
Thomas MoserSt. Pölten University of Applied Sciences, St. Pölten, Austria.ORCID https://orcid.org/0000-0002-9220-649X
Karl StroetmannSchool of Health Information Science, University of Victoria, Victoria, BC, Canada.ORCID https://orcid.org/0000-0002-5388-5952
Isaac FwembaDivision of Epidemiology and Biostatistics, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.
Fisayo DaramolaDivision of Epidemiology and Biostatistics, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.
Martha NyirendaDivision of Epidemiology and Biostatistics, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.
Susan J van RensburgDivision of Chemical Pathology, Department of Pathology, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.
Peter S NyasuluDivision of Epidemiology and Biostatistics, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.
Jeanine L MarnewickApplied Microbial and Health Biotechnology Institute (AMHBI), Cape Peninsula University of Technology, Cape Town, South Africa.
Cape Peninsula University of Technology · ZAStellenbosch University · ZANational Health Laboratory Service · ZAUniversity of Applied Sciences St Pölten · ATUniversity of Victoria · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: COVID-19 vaccines offer different levels of immune protection but do not provide 100% protection. Vaccinated persons with pre-existing comorbidities may be at an increased risk of SARS-CoV-2 breakthrough infection or reinfection. The aim of this study is to identify the critical variables associated with a higher probability of SARS-CoV-2 breakthrough infection using machine learning. Methods: A dataset comprising symptoms and feedback from 257 persons, of whom 203 were vaccinated and 54 unvaccinated, was used for the investigation. Three machine learning algorithms - Deep Multilayer Perceptron (Deep MLP), XGBoost, and Logistic Regression - were trained with the original (imbalanced) dataset and the balanced dataset created by using the Random Oversampling Technique (ROT), and the Synthetic Minority Oversampling Technique (SMOTE). We compared the performance of the classification algorithms when the features highly correlated with breakthrough infection were used and when all features in the dataset were used. Result: The results show that when highly correlated features were considered as predictors, with Random Oversampling to address data imbalance, the XGBoost classifier has the best performance (F1 = 0.96; accuracy = 0.96; AUC = 0.98; G-Mean = 0.98; MCC = 0.88). The Deep MLP had the second best performance (F1 = 0.94; accuracy = 0.94; AUC = 0.92; G-Mean = 0.70; MCC = 0.42), while Logistic Regression had less accurate performance (F1 = 0.89; accuracy = 0.88; AUC = 0.89; G-Mean = 0.89; MCC = 0.68). We also used Shapley Additive Explanations (SHAP) to investigate the interpretability of the models. We found that Conclusion: These results, evident from our unique data source derived from apparently healthy volunteers with cardiovascular risk factors, follow the expected pattern of positive or negative correlations previously reported in the literature. This information strengthens the body of knowledge currently applied in public health guidelines and may also be used by medical practitioners in the future to reduce the risk of SARS-CoV-2 breakthrough infection.

Indexed as

breakthrough infectionCOVID-19deep multilayer perceptronExplainable AIJ&J vaccinelogistic regressionMachine learningPfizer vaccinevaccinationXGBoost

Identifiers

PMID37936960
PMCPMC10627023
OpenAlexW4388428531

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 OpenQuestion graph.