ArticleBMC infectious diseases2026
Development and validation of a cytokine-driven predictive model for COVID-19 severity.
Article in BMC infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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Who cites it
2 citing papers in PubMed.
- Immunopathogenesis of severe pneumonia in children with emphasis on CD4+ T cells, Tim-3 and cytokine-mediated immune dysregulation.Frontiers in medicine · 2026Review
- Serum cytokine profiling reveals CXCL10 (IP-10) as a major predictor of severe COVID-19 outcomes in hospitalized patients during the first pandemic wave in Italy.Frontiers in immunology · 2026Article
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Authors and funding
7 authors.
Funding
Abstract
backgroundThis study aims to identify key factors influencing the severity of COVID-19 and to develop a predictive model for assessing disease severity.
methodsA retrospective analysis was conducted on 164 patients with COVID-19 admitted to the First Affiliated Hospital of Dali University from July 2022 to February 2024, and the integrity of electronic medical records and laboratory databases of all included patients was systematically reviewed. Based on established diagnostic criteria for COVID-19 severity, patients were categorized into two groups: mild/ordinary (94 cases) and severe/critical (70 cases). Lasso regression and multivariate logistic regression were employed to identify independent risk factors, and a predictive model was constructed using a column chart. Internal validation of the model was conducted with receiver operating characteristic (ROC) curves, 10-fold cross-validation and calibration curves. The clinical utility of the model was evaluated using decision curve analysis.
resultsUnivariate analysis revealed significant differences between the mild/ordinary and severe/critical groups in levels of IL-4, IL-6, IL-8, IL-10, IL-17, IFN-γ, WBC count, neutrophils (N), lymphocytes (L), red blood cells (RBC), hematocrit (HCT), R-CV, R-SD, CRP, PCT, DBI, AST, TP, ALB, urea, creatinine (CREA), uric acid (UA), sodium (Na), magnesium (Mg), calcium (Ca), and total cholesterol (TC) (all P < 0.05). Lasso regression identified IL-6, IL-8, IL-17, IFN-γ, N, R-CV, TP, ALB, and urea as predictive variables. Multivariate logistic regression confirmed that IL-6, IL-8, and IL-17 were independent risk factors for COVID-19 severity. The model demonstrated an area under the curve (AUC) of 0.88, with a sensitivity of 74.3% and specificity of 94.7%. The 10-fold AUCs are 0.691, 0.939, 0.657, 1.00, 0.81, 0.797, 0.75, 0.847, 0.969, and 1.00, with an average AUC of 0.856 (95% confidence interval: 0.791–0.922). The calibration curve showed strong agreement between predicted and actual values. Clinical decision curve analysis shows that the model offers optimal clinical utility, with a net benefit higher than alternative strategies when the probability threshold is between 15% and 95%.
conclusionsIL-6, IL-8, and IL-17 are identified as independent risk factors for the severity of COVID-19. The predictive model based on these factors provides a reliable tool for assessing disease severity in COVID-19 patients.
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