# Plasma, Urinary, and Salivary Total Redox Status in Critically Ill Patients with Brain Injury and Secondary Organ Failure

**Authors:** Ewa Rynkiewicz-Szczepanska, Urszula Kosciuczuk, Katarzyna Anikiej, Anna Zalewska, Małgorzata Żendzian-Piotrowska, Mateusz Maciejczyk

PMC · DOI: 10.3390/antiox15020185 · Antioxidants · 2026-02-02

## TL;DR

This study examines redox biomarkers in critically ill patients with brain injury and finds differences compared to healthy individuals, but not between survivors and non-survivors.

## Contribution

The study provides new insights into redox status in different biofluids of neurocritically ill patients and their correlation with organ function.

## Key findings

- Plasma FRAP was higher in patients, while salivary and urinary FRAP were lower compared to controls.
- Salivary and urinary TAC were lower in patients, and plasma TOS was higher.
- Plasma FRAP showed a significant effect on survival with moderate sensitivity and specificity.

## Abstract

Little is known about the clinical utility of blood, salivary, and urinary redox biomarkers in critically ill patients with brain injury and secondary organ failure. The aim of the study was to explore total antioxidant and oxidant status in neurocritically ill patients using ferric reducing antioxidant power (FRAP), total antioxidant capacity (TAC), and total oxidant status (TOS) in plasma, saliva, and urine from the study (n = 45) and the healthy control group (n = 49). We analyzed the relationship between well-known biomarkers of organ function and redox status in different biofluids. Plasma FRAP was significantly higher (p < 0.05), but salivary and urinary FRAP were statistically lower in the study group (p < 0.05, p < 0.001) compared with controls. The salivary and urinary TAC were statistically lower (p < 0.05, p < 0.001), while plasma TOS was significantly higher (p < 0.05) in the study group compared with the control group. Circulating redox status did not differ between survivors and non-survivors. Significant associations were observed in non-survivors: salivary TAC correlated with urea and creatinine; salivary FRAP with creatinine, troponin, and CRP; urinary TAC with troponin and PaO2/FiO2 ratio, as well as plasma FRAP with PaO2/FiO2 ratio. The plasma FRAP had a significant effect on survival (AUC = 0.687, p = 0.02), with 69% sensitivity and 83% specificity. Crucial differences in redox status in blood, saliva, and urine were observed between neurocritically ill patients and healthy controls; however, none of the biomarkers differed between survivors and non-survivors. Oxidative and antioxidant status correlated with organ function in non-survivors.

## Linked entities

- **Diseases:** brain injury (MONDO:0043510)

## Full-text entities

- **Genes:** CALCA (calcitonin related polypeptide alpha) [NCBI Gene 796] {aka CALC1, CGRP, CGRP-I, CGRP-alpha, CGRP1, CT}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** hemorrhagic stroke (MESH:D000083302), acute central nervous system disorders (MESH:D002493), ALI (MESH:D055371), TBI (MESH:D000070642), diabetes (MESH:D003920), renal failure (MESH:D051437), mitochondrial dysfunction (MESH:D028361), Critically Ill (MESH:D016638), hematoma (MESH:D006406), inflammation (MESH:D007249), condition (MESH:D020763), neuropsychiatric diseases (MESH:D004194), injury to (MESH:D014947), hemolysis (MESH:D006461), autoimmunological disorders (MESH:D009358), status epilepticus (MESH:D013226), metabolic disorders (MESH:D008659), neurological (MESH:D009461), arterial hypotension (MESH:D007022), carcinogenesis (MESH:D063646), ruptured brain aneurysm (MESH:D017542), acute secondary kidney injury (MESH:D058186), obesity (MESH:D009765), Secondary Organ Failure (MESH:D009102), arrhythmias (MESH:D001145), intraventricular hemorrhage (MESH:D000074042), respiratory failure (MESH:D012131), Brain edema (MESH:D001929), intracranial hemorrhage (MESH:D020300), ischemic stroke (MESH:D002544), subarachnoid hemorrhage (MESH:D013345), brain damage (MESH:D001925), death (MESH:D003643), neurological injury (MESH:D020196), brain herniation (MESH:D001927), Brain Injury (MESH:D001930), skull fractures (MESH:D012887), chronic diseases (MESH:D002908), sepsis (MESH:D018805), Coma (MESH:D003128), APACHE II (MESH:D000071069), septic shock (MESH:D012772), heart disease (MESH:D006331), allergies (MESH:D004342), thromboembolism (MESH:D013923), organ damage (MESH:D000092124), heart failure (MESH:D006333)
- **Chemicals:** MDA (MESH:D015104), uric acid (MESH:D014527), EDTA (MESH:D004492), bilirubin (MESH:D001663), lactate (MESH:D019344), oxygen (MESH:D010100), midazolam (MESH:D008874), thiopental (MESH:D013874), 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid (MESH:C010643), glycemia (MESH:D001786), xylenol orange (MESH:C016833), glutamate (MESH:D018698), 4-hydroxy-2-nonenal (MESH:C027576), vitamin C (MESH:D001205), isoprostanes (MESH:D028421), propofol (MESH:D015742), iron (MESH:D007501), fentanyl (MESH:D005283), malondialdehyde (MESH:D008315), arginine (MESH:D001120), Magnesium Sulfate (MESH:D008278), urea (MESH:D014508), deoxyguanosine (MESH:D003849), thiol (MESH:D013438), dexmedetomidine (MESH:D020927), catecholamine (MESH:D002395), caffeine (MESH:D002110), benzodiazepines (MESH:D001569), unsaturated fatty acids (MESH:D005231), H2O2 (MESH:D006861), Cernevit (-), ROS (MESH:D017382), lactates (MESH:D007773), creatinine (MESH:D003404), alcohol (MESH:D000438), 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (MESH:C002502), Lipid (MESH:D008055), polyphenols (MESH:D059808)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12938279/full.md

## References

62 references — full list in the complete paper: https://tomesphere.com/paper/PMC12938279/full.md

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Source: https://tomesphere.com/paper/PMC12938279