Oxidative stress index as a potent predictor of disease severity and inflammatory burden in hospitalized COVID-19 patients

• COVID-19 causes a profound redox imbalance characterized by elevated total oxidant status and depleted antioxidant status, translating to an increased oxidative index • A severity-related increase follows the COVID-19 infection in the oxidative index • The COVID-19-induced increase in the oxidative index is strongly correlated with increased inflammatory cytokines and acute-phase proteins While the acute phase of the COVID-19 pandemic has passed, understanding its pathophysiology remains critical for managing long-term sequelae and future viral threats. Oxidative stress is a proposed key driver of COVID-19 severity, but its relationship with the dynamic inflammatory cascade and its value as a standalone biomarker requires further validation. Case-control study was conducted to quantify systemic oxidative stress burden in 109 hospitalized COVID-19 patients (56 severe, 53 mild-moderate) and 112 healthy controls. Serum total oxidant status (TOS) and total antioxidant status (TAS) were measured, and the oxidative stress index (OSI) was calculated and correlated to the inflammatory mediators (IL-6, IL-8, IL-10, IP-10, CRP, SAA). COVID-19 patients exhibited a profound redox imbalance, characterized by elevated TOS and OSI, and depleted TAS compared to controls ( p < 0.05). This imbalance was exacerbated in severe disease, where TOS and OSI were significantly increased. The OSI demonstrated superior diagnostic performance for disease severity (AUC = 0.90; 95% CI: 0.86–0.95) compared to TOS (AUC = 0.89) and TAS (AUC = 0.78). Crucially, both TOS and OSI showed strong positive correlations with inflammatory cytokines and acute-phase proteins (IL-6, IL-10, IP-10, CRP, SAA; all p < 0.001). After adjusting for age, time from symptom onset, and comorbidity burden (Charlson Comorbidity Index), multivariate analysis confirmed that high OSI was independently associated with disease severity (adjusted OR: 4.8; 95% CI: 1.9–12.1). The OSI is a robust, integrative biomarker that strongly reflects COVID-19 severity and is closely linked to the hyperinflammatory state. The OSI is strongly correlated with increased inflammatory cytokines and acute-phase proteins in acute COVID-19.

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Publication Details

Journal
Infectious Medicine
Published
2026-05-01
DOI
https://doi.org/10.1016/j.imj.2026.100261
Primary Topic
COVID-19 Clinical Research Studies
Type
article
Field-Weighted Citation Impact
0.00

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article

Oxidative stress index as a potent predictor of disease severity and inflammatory burden in hospitalized COVID-19 patients

Dominic‐Luc Webb, Tewodros Haile Gebremariam, Tsegahun Manyazewal, Yidnekachew Asrat Birhan et al.
Infectious Medicine
COVID-19 Clinical Research Studies
article

Oxidative stress index as a potent predictor of disease severity and inflammatory burden in hospitalized COVID-19 patients

Dominic‐Luc Webb, Tewodros Haile Gebremariam, Tsegahun Manyazewal, Yidnekachew Asrat Birhan, Abdisa Tufa Bedada, Per Martin Hellström, Solomon Genet Gebre, Tesfaye Tolessa Dugul
article en

Abstract

• COVID-19 causes a profound redox imbalance characterized by elevated total oxidant status and depleted antioxidant status, translating to an increased oxidative index • A severity-related increase follows the COVID-19 infection in the oxidative index • The COVID-19-induced increase in the oxidative index is strongly correlated with increased inflammatory cytokines and acute-phase proteins While the acute phase of the COVID-19 pandemic has passed, understanding its pathophysiology remains critical for managing long-term sequelae and future viral threats. Oxidative stress is a proposed key driver of COVID-19 severity, but its relationship with the dynamic inflammatory cascade and its value as a standalone biomarker requires further validation. Case-control study was conducted to quantify systemic oxidative stress burden in 109 hospitalized COVID-19 patients (56 severe, 53 mild-moderate) and 112 healthy controls. Serum total oxidant status (TOS) and total antioxidant status (TAS) were measured, and the oxidative stress index (OSI) was calculated and correlated to the inflammatory mediators (IL-6, IL-8, IL-10, IP-10, CRP, SAA). COVID-19 patients exhibited a profound redox imbalance, characterized by elevated TOS and OSI, and depleted TAS compared to controls ( p < 0.05). This imbalance was exacerbated in severe disease, where TOS and OSI were significantly increased. The OSI demonstrated superior diagnostic performance for disease severity (AUC = 0.90; 95% CI: 0.86–0.95) compared to TOS (AUC = 0.89) and TAS (AUC = 0.78). Crucially, both TOS and OSI showed strong positive correlations with inflammatory cytokines and acute-phase proteins (IL-6, IL-10, IP-10, CRP, SAA; all p < 0.001). After adjusting for age, time from symptom onset, and comorbidity burden (Charlson Comorbidity Index), multivariate analysis confirmed that high OSI was independently associated with disease severity (adjusted OR: 4.8; 95% CI: 1.9–12.1). The OSI is a robust, integrative biomarker that strongly reflects COVID-19 severity and is closely linked to the hyperinflammatory state. The OSI is strongly correlated with increased inflammatory cytokines and acute-phase proteins in acute COVID-19.

Infectious Medicine
Uppsala University (SE), Uppsala University Hospital (SE), Bioanalytica (Switzerland) (CH), Africa Centres for Disease Control and Prevention (ET), Department of Medical Sciences (RU), St. Joseph University In Tanzania (TZ), Addis Ababa University (ET)
Uppsala Universitet
Good health and well-being
Openalex Percentile: Top 6%
COVID-19 Clinical Research Studies
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