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Oxidative stress and anti-oxidant status in children with sepsis
Hatice Feray Arı1, Murat Arı2, Serdal Ogut3
1Department of Pediatrics, Division of Pediatric Intensive Care Unit, Faculty of Medicine, Aydin Adnan Menderes University, Aydin, 09100, Turkey. dr.hferayyavas@gmail.com.
Insights
Pediatric sepsis is linked to increased oxidants and decreased antioxidants. Thiol-disulfide levels may help diagnose sepsis in critically ill children, aiding early treatment and reducing mortality.
Area of Science:
- Biochemistry
- Pediatric Critical Care
- Oxidative Stress Research
Background:
- Sepsis poses a significant life-threatening risk in children, necessitating early recognition and treatment to reduce mortality.
- Pathogenesis of sepsis involves imbalances in oxidative and antioxidant markers, with increased oxidants and decreased antioxidants observed.
- Investigating novel biomarkers like thiol-disulfides is crucial for improving sepsis diagnosis and management in pediatric intensive care units (PICUs).
Purpose of the Study:
- To investigate and compare thiol-disulfide levels in children with and without sepsis in a pediatric intensive care unit (PICU).
- To evaluate the potential of thiol-disulfide parameters as diagnostic tools for pediatric sepsis.
Main Methods:
- A cohort study involving 64 children with sepsis and 62 controls was conducted in a PICU from October 2022 to March 2023.
- Blood samples were collected, processed, and stored, with thiol-disulfide values analyzed using the ELISA kit method.
- Key parameters measured included total oxidant status, 8-OHdG, native thiol, and thiol/disulfide ratios.
Main Results:
- Children with sepsis exhibited significantly elevated levels of total oxidant status, plasma 8-OHdG, total-native thiol, and native/total thiol percent ratio compared to controls (p < 0.05).
- Conversely, antioxidant parameters such as total antioxidant status, paraoxonase 1 activity, disulfide, and disulfide/thiol ratios were significantly lower in the sepsis group (p < 0.05).
Conclusions:
- The study confirms that critically ill children with sepsis have significantly higher oxidant parameters and lower antioxidant parameters.
- Thiol-disulfide levels demonstrate potential as a diagnostic biomarker for sepsis in critically ill children, complementing existing inflammation markers.
Background:
Sepsis is a life-threating cause in childhood ages. The recognition and treatment early are significant for decreasing mortality. Sepsis has many factors and various biomarkers function in the pathogenesis, the stress indicators oxidants increased and antioxidants decreased. The objective of our study was to investigate the levels of thiol disulfides with and without sepsis in a pediatric intensive care unit (PICU).
Materials And Methods:
A cohort study was conducted between October 2022 and March 2023 at the PICU, comprising 64 with sepsis and 62 children without sepsis. Blood samples from sepsis and the control group were collected and centrifuged. Subsequently, the samples were stored at -80 °C until the day of the experiment. Once the requisite number of patients had been enrolled, the thiol-disulfide values in the collected samples were analysed in accordance with the ELISA kit method.
Results:
The research parameters investigated, namely total oxidant status, plasma 8-OHdG, total-native thiol and native/total thiol percent ratio, were found to be considerably elevated in the sepsis group in comparison to the control (p < 0.05). Furthermore, the oxidative stress parameters investigated (total antioxidant status, paraoxonase 1 activity, disulfide, disulfide/native thiol percent ratio, disulfide/total thiol percent ratio) were found to be significantly lower in the sepsis group than in control (p < 0.05).
Conclusions:
In our study as well, we detected all antioxidant parameters are low and oxidant parameters are statistically significantly higher in sepsis. Our study posits that thiol-disulfide levels have the potential to serve as a diagnostic tool in conjunction with traditional established biomarkers of inflammation in critically ill children in the PICU who are being treated for sepsis.
Clinical Trial Registration:
Not applicable.
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