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Updated: Dec 22, 2025

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Salivary Gland Dysfunction, Protein Glycooxidation and Nitrosative Stress in Children with Chronic Kidney Disease
Mateusz Maciejczyk1, Julita Szulimowska2, Katarzyna Taranta-Janusz3
1Department of Hygiene, Epidemiology and Ergonomics, Medical University of Bialystok, 2c Mickiewicza Street, 15-233 Bialystok, Poland.
Insights
Children with chronic kidney disease (CKD) experience salivary gland dysfunction, leading to increased oxidative and nitrosative stress in saliva. This dysfunction worsens with CKD progression.
Area of Science:
- Biochemistry
- Nephrology
- Oral Medicine
Background:
- Chronic kidney disease (CKD) can affect salivary gland function.
- Oxidative stress markers are increasingly recognized in various systemic diseases.
Purpose of the Study:
- To investigate protein glycooxidation, lipid oxidative damage, and nitrosative stress in the saliva of children with CKD.
- To compare these markers in children with normal salivary secretion versus hyposalivation (reduced saliva flow).
Main Methods:
- Analysis of non-stimulated (NWS) and stimulated whole saliva (SWS) in children with CKD (stages 1-5) and healthy controls.
- Subgrouping CKD patients based on salivary flow rate (normal vs. hyposalivation).
- Measurement of salivary amylase activity, total protein, glycooxidation products, lipid peroxidation markers, and nitrosative stress markers.
Main Results:
- Hyposalivation was prevalent in advanced CKD (stage 4-5).
- CKD children with hyposalivation showed significantly lower salivary amylase and total protein.
- Elevated levels of protein glycooxidation, lipid oxidation, and nitrosative stress markers were found in the saliva and plasma of CKD children with hyposalivation.
- Salivary oxidation markers correlated negatively with salivary flow rate, amylase activity, and protein content but did not reflect plasma levels.
Conclusions:
- Children with CKD exhibit salivary gland dysfunction.
- Salivary oxidative and nitrosative stress increases with CKD severity and impaired salivary function.
- Salivary gland dysfunction is a significant complication in pediatric CKD.
Abstract:
This study is the first to evaluate protein glycooxidation products, lipid oxidative damage and nitrosative stress in non-stimulated (NWS) and stimulated whole saliva (SWS) of children with chronic kidney disease (CKD) divided into two subgroups: normal salivary secretion (n = 18) and hyposalivation (NWS flow < 0.2 mL min-1; n = 12). Hyposalivation was observed in all patients with severe renal failure (4-5 stage CKD), while saliva secretion > 0.2 mL/min in children with mild-moderate CKD (1-3 stage) and controls. Salivary amylase activity and total protein content were significantly lower in CKD children with hyposalivation compared to CKD patients with normal saliva secretion and control group. The fluorescence of protein glycooxidation products (kynurenine, N-formylkynurenine, advanced glycation end products), the content of oxidative damage to lipids (4-hydroxynonneal, 8-isoprostanes) and nitrosative stress (peroxynitrite, nitrotyrosine) were significantly higher in NWS, SWS, and plasma of CKD children with hyposalivation compared to patients with normal salivary secretion and healthy controls. In CKD group, salivary oxidation products correlated negatively with salivary flow rate, -amylase activity and total protein content; however, salivary oxidation products do not reflect their plasma level. In conclusion, children with CKD suffer from salivary gland dysfunction. Oxidation of salivary proteins and lipids increases with CKD progression and deterioration of salivary gland function.
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