Evidence map›Paper›PMID 40979489›Full record

ArticleJournal of inflammation research2025

Investigation of Antioxidant Enzymes (GST, GSH, R-GSSG) in Erythrocytes of COVID-19 Patients: A One-Month Observation.

Elżbieta Cecerska-Heryć, Natalia Serwin, Ewa Pius-Sadowska, Klaudia Głowacka, Aleksandra Polikowska, Małgorzata Goszka, Radosław Birger, Marta Budkowska, Bogusław Machaliński, Barbara Dołęgowska

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In one paragraph

Article in Journal of inflammation research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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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

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5 · Who and what money

Authors and funding

10 authors.

Elżbieta Cecerska-HeryćDepartment of Laboratory Medicine, Pomeranian Medical University of Szczecin, Szczecin, Poland.ORCID 0000-0002-7313-7193
Natalia SerwinDepartment of Laboratory Medicine, Pomeranian Medical University of Szczecin, Szczecin, Poland.
Ewa Pius-SadowskaDepartment of General Pathology, Pomeranian Medical University of Szczecin, Szczecin, Poland.
Klaudia GłowackaDepartment of Laboratory Medicine, Pomeranian Medical University of Szczecin, Szczecin, Poland.
Aleksandra PolikowskaDepartment of Laboratory Medicine, Pomeranian Medical University of Szczecin, Szczecin, Poland.
Małgorzata GoszkaDepartment of Laboratory Medicine, Pomeranian Medical University of Szczecin, Szczecin, Poland.
Radosław BirgerDepartment of Laboratory Medicine, Pomeranian Medical University of Szczecin, Szczecin, Poland.ORCID 0009-0008-6256-5695
Marta BudkowskaDepartment of Analytical Medicine Pomeranian Medical University of Szczecin, Szczecin, Poland.
Bogusław MachalińskiDepartment of General Pathology, Pomeranian Medical University of Szczecin, Szczecin, Poland.
Barbara DołęgowskaDepartment of Laboratory Medicine, Pomeranian Medical University of Szczecin, Szczecin, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Oxidative stress (OS) occurs when there is an imbalance between reactive oxygen species (ROS) production and the body's ability to neutralize them. This can lead to cellular damage and is associated with aging and various diseases. Glutathione (GSH) acts as a vital non-enzymatic antioxidant, while enzymes such as glutathione S-transferase (GST) and glutathione reductase (GR) help maintain the body's redox balance. OS from viruses, including coronavirus, can disrupt inflammation regulation and cause prolonged tissue damage. Aim: This study examines GSH levels and the activities of GST and R-GSSG in the erythrocytes of COVID-19 patients compared to those of healthy controls. Materials and Methods: The study involved 85 COVID-19 patients (42 females and 43 males), with blood samples collected at the time of disease detection and at 7, 14, and 28 days later. The control group included 85 healthy individuals. Antioxidant levels (GSH, GST, R-GSSG) were measured using spectrophotometric methods. Results: COVID-19 patients exhibited a significant decrease in GSH concentration (p < 0.001) and an increase in R-GSSG (p < 0.001) and GST (p = 0.046) activity. Lower GSH levels correlated with a higher risk of death (p = 0.008). Multivariate analysis revealed relationships between GSH and factors such as time since detection, survival rate, hospital stay, and disease severity. Conclusion: COVID-19 disrupts antioxidant enzyme balance, potentially worsening disease severity and increasing mortality risk, especially in older patients.

Indexed as

antioxidant enzymesCOVID-19GSHGSTR-GSSG oxidative stress

Identifiers

PMID40979489
PMCPMC12449866

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