Salivary biomarkers may measure stress responses in critically ill children
Despoina Tzira1, Anargyroula Prezerakou1, Ioannis Papadatos1
1Pediatric Intensive Care Unit, "P. & A. Kyriakou" Children's Hospital, Athens, Greece.
Insights
Salivary stress markers like cortisol, alpha-amylase, and IgA are elevated in critically ill children. Higher levels correlate with increased risk scores and younger age, aiding early detection and intervention.
Area of Science:
- Pediatric Critical Care Medicine
- Endocrinology
- Immunology
Background:
- Salivary biomarkers offer insights into hypothalamic-pituitary-adrenal (HPA) axis activity under stress.
- Assessing stress markers in critically ill children can inform clinical management.
- Non-invasive methods are valuable for monitoring pediatric intensive care unit (PICU) patients.
Purpose of the Study:
- To correlate salivary stress markers (cortisol, alpha-amylase, IgA) with clinical severity scores in PICU children.
- To investigate the relationship between these biomarkers and factors like underlying disease, ventilation needs, and admission delay.
- To explore potential disruptions in circadian rhythms of salivary biomarkers.
Main Methods:
- Saliva samples were collected from 65 pediatric patients (2-14 years) within 24 hours of PICU admission.
- Samples were analyzed at 8 a.m., 2 p.m., and 8 p.m. to assess diurnal variations.
- Biomarkers measured included cortisol, alpha-amylase (sAA), and immunoglobulin A (IgA).
Main Results:
- Elevated median levels of cortisol, sAA, and IgA were observed in PICU patients.
- Significantly higher biomarker levels were found in children younger than 6 years and those with a Pediatric Risk Index Score of Mortality (PRISM) score ≥8.
- Disturbances in cortisol circadian rhythm were noted in high-risk patients (PRISM ≥8), while sAA rhythm remained normal.
Conclusions:
- Salivary biomarkers are sensitive, non-invasive indicators in critically ill children.
- These markers aid in early identification of high-risk patients, guiding timely interventions.
- Utilizing salivary biomarkers can enhance healthcare quality for the pediatric population.
Objective:
Measurement of salivary biomarkers can provide important information regarding hypothalamic-pituitary-adrenal axis activity both under normal conditions as well as in response to psychological or physical stress. Our aim was to correlate salivary stress markers, such as cortisol, α-amylase and immunoglobulin A, with the Pediatric Risk Index Score of Mortality, underlying disease (pathologic, trauma and postoperative), need for mechanical ventilation/sedation and time lag between onset of illness and admission in children admitted in the pediatric intensive care unit.
Methods:
We enrolled 79 pediatric intensive care unit patients (2-14 years) over a 2-year period, which satisfy the including criteria, but finally salivary biomarkers were evaluated in 65 patients. Saliva samples were collected within 24 h of admission at 8 a.m., 2 p.m. and 8 p.m. to examine potential disruption of circadian rhythm.
Results:
Overall, the salivary biomarkers were increased; specifically, median values were (a) cortisol at 8 a.m.: 50.04 nmol/L, 2 p.m.: 30.69 nmol/L and 8 p.m.: 247.12 nmol/L; (b) α-amylase: at 8 a.m.: 22.567 U/L; 2 p.m.: 22.702 U/L and 8 p.m.: 21.484 U/L and (c) IgA at 8 a.m.: 95.10 mg/dL, 2 p.m.: 88.55 mg/dL and 8 p.m.: 80.80 mg/dL. Significantly higher levels were demonstrated in children younger than 6 years and those with Pediatric Risk Index Score of Mortality ⩾8 upon admission. Disturbances in circadian rhythm were observed. Cortisol circadian rhythm disturbance was observed only in children with Pediatric Risk Index Score of Mortality score ⩾8 upon admission while maintaining normal α-amylase circadian rhythm, which was associated with less than 3 days hospitalization in pediatric intensive care unit. No daily variance in IgA was observed.
Conclusion:
Salivary biomarkers may serve, in critically ill children, as a sensitive, non-invasive method, important for the early recognition of those at high risk and guiding intervention, before clinical deterioration, promoting the quality of health care in pediatric population.
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