A Unique Patient Stratification Method Combined with a Machine Learning Approach Identifies Novel Genetic Susceptibility and Protective Factors for Severe COVID-19 in a Hungarian Population

Intensive research has shown that severe COVID-19 outcomes are influenced by antiviral pathways and immune responses, both shaped by genetic predisposition. In this study, we aimed to identify genetic variants associated with disease severity in a cohort of Hungarian patients. We applied a novel stratification method based on age, disease severity, and clinical background to classify patients by susceptibility to severe COVID-19. Whole-exome sequencing (WES) was performed on 168 individuals, and gene mutation loads were assessed. Using a Random Forest machine learning approach, we identified variants of 877 genes that distinguished between severe and non-severe cases. We further categorized these genes as either susceptibility or protective factors. Gene-set enrichment analysis highlighted the most affected biological pathways. Our findings support the development of personalized diagnostic tools to assess the risk of severe COVID-19 and guide targeted treatment strategies. Our findings further extend the results of previous studies, providing novel insights into the genetic determinants of COVID-19 severity.

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Publication Details

Journal
International Journal of Molecular Sciences
Published
2026-03-03
DOI
https://doi.org/10.3390/ijms27052358
Primary Topic
COVID-19 Clinical Research Studies
Type
article
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article

A Unique Patient Stratification Method Combined with a Machine Learning Approach Identifies Novel Genetic Susceptibility and Protective Factors for Severe COVID-19 in a Hungarian Population

Ferenc Somogyvári, Attila Gyenesei, Alexandra Neller, Zoltán Péterfi et al.
International Journal of Molecular Sciences
COVID-19 Clinical Research Studies
article

A Unique Patient Stratification Method Combined with a Machine Learning Approach Identifies Novel Genetic Susceptibility and Protective Factors for Severe COVID-19 in a Hungarian Population

Ferenc Somogyvári, Attila Gyenesei, Alexandra Neller, Zoltán Péterfi, K. Gombos, Péter Urbán, József Kun, Barbara Anna Bokor, Nikoletta Nagy, Mátyás Bukva, Valéria Endrész, Márta Széll, Balázs Bende, Gábor L. Kovács, Ádám Visnyovszky, Zsófia Blazovich, Margit Pál, Szilvia Kovácsné Levang, Bence Gálik
article en

Abstract

Intensive research has shown that severe COVID-19 outcomes are influenced by antiviral pathways and immune responses, both shaped by genetic predisposition. In this study, we aimed to identify genetic variants associated with disease severity in a cohort of Hungarian patients. We applied a novel stratification method based on age, disease severity, and clinical background to classify patients by susceptibility to severe COVID-19. Whole-exome sequencing (WES) was performed on 168 individuals, and gene mutation loads were assessed. Using a Random Forest machine learning approach, we identified variants of 877 genes that distinguished between severe and non-severe cases. We further categorized these genes as either susceptibility or protective factors. Gene-set enrichment analysis highlighted the most affected biological pathways. Our findings support the development of personalized diagnostic tools to assess the risk of severe COVID-19 and guide targeted treatment strategies. Our findings further extend the results of previous studies, providing novel insights into the genetic determinants of COVID-19 severity.

International Journal of Molecular SciencesVol. 27(5)
University of Szeged (HU), HUN-REN Szegedi Biológiai Kutatóközpont (HU), University of Pecs (HU)
Openalex Percentile: Top 37%
COVID-19 Clinical Research Studies
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