Level of urinary catecholamine in children with Sleep Disordered Breathing: A systematic review and meta-analysis

Esther T W Cheng1, Raymond N C Chan1, Kate C C Chan2

  • 1Faculty of Medicine, The Chinese University of Hong Kong, Hong Kong.

Sleep Medicine
|November 3, 2022
PubMed

Insights

Elevated urinary noradrenaline and adrenaline levels are linked to sleep-disordered breathing (SDB) in children. These catecholamines may serve as biomarkers for SDB and its complications, warranting further investigation.

Area of Science:

  • Pediatric Pulmonology
  • Neuroendocrinology
  • Biomarker Discovery

Background:

  • Sleep-disordered breathing (SDB) affects children, potentially impacting their health.
  • Urinary catecholamines, such as noradrenaline, adrenaline, and dopamine, are indicators of the body's stress response.
  • Understanding the relationship between SDB and catecholamine levels can provide insights into SDB pathophysiology.

Approach:

  • A systematic literature search was performed on PubMed and EMBASE for studies comparing urinary catecholamines in pediatric patients with and without SDB.
  • Nine studies involving 838 subjects were included in a quantitative meta-analysis.
  • Standardized mean differences (SMD) were calculated for urinary catecholamine levels between groups with varying SDB severity.

Key Points:

  • Urinary noradrenaline levels were significantly higher in children with SDB compared to controls.
  • Children with obstructive sleep apnea (OSA), a severe form of SDB, exhibited elevated urinary noradrenaline and adrenaline levels.
  • Urinary noradrenaline levels increased with OSA severity, being higher in moderate/severe OSA than in mild OSA.

Conclusions:

  • Urinary noradrenaline and adrenaline may serve as potential biomarkers for sympathetic nervous system overactivity in pediatric SDB.
  • These catecholamines could act as surrogate markers for identifying children at risk for SDB-related complications.
  • Further research is recommended to confirm the association and clinical utility of these biomarkers in SDB management.
Abstract

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