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Published on: June 24, 2025
Urinary PGE2 metabolite levels in hospitalised infants with infections compared to age-matched controls
Johan Hamrin1,2, Monica Perez-Manzo1, Helena Idborg3,4
1Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.
Insights
Urinary tetranor-prostaglandin E2 metabolite levels are established for healthy infants. Elevated levels indicate lower respiratory and gastrointestinal infections in hospitalized infants.
Area of Science:
- Biochemistry
- Pediatrics
- Infectious Diseases
Background:
- Prostaglandin E2 (PGE2) plays a role in inflammation and immune responses.
- Urinary metabolites of PGE2 can serve as biomarkers for physiological and pathological states.
- Understanding PGE2 metabolite levels in infants is crucial for diagnosing and managing infections.
Purpose of the Study:
- To establish normal ranges of urinary tetranor-prostaglandin E2 metabolite in healthy infants.
- To investigate the association between urinary tetranor-prostaglandin E2 metabolite levels and infections in hospitalized infants.
Main Methods:
- A prospective cross-sectional study involving 81 healthy infants and 142 hospitalized infants.
- Measurement of urinary tetranor-prostaglandin E2 metabolite using liquid chromatography tandem mass spectrometry.
- Comparison of metabolite levels between healthy and infected infants, and correlation with clinical factors.
Main Results:
- Urinary tetranor-prostaglandin E2 metabolite levels decreased with age in healthy infants.
- Elevated metabolite levels were observed in infants with lower respiratory tract and gastrointestinal infections.
- Infants with upper respiratory tract infections showed similar levels to controls; acetaminophen treatment lowered levels.
Conclusions:
- This study provides reference values for urinary tetranor-prostaglandin E2 metabolite in infants.
- Elevated levels are indicative of lower respiratory and gastrointestinal infections in hospitalized infants.
- Tetranor-prostaglandin E2 metabolite may serve as a potential biomarker for specific infant infections.
Aim:
To determine the urinary tetranor-prostaglandin E2 metabolite in healthy infants and in hospitalised infants with upper and lower respiratory tract as well as gastrointestinal infections.
Methods:
A prospective cross-sectional study to determine baseline concentrations of urinary tetranor-prostaglandin E2 metabolite was conducted in 81 healthy infants aged one week to one year and in 142 hospitalised infants with infections. Prostaglandin metabolite levels were measured by liquid chromatography tandem mass spectrometry.
Results:
In healthy infants, urinary prostaglandin E2 metabolite levels decreased with age and did not differ between girls and boys. Infections of the lower respiratory (n = 78) and gastrointestinal tract (n = 12) correlated with increased levels of the prostaglandin E2 metabolite. In contrast, infants hospitalised with upper respiratory tract infections (n = 23) exhibited similar levels as healthy, age-matched controls. Lower prostaglandin E2 levels were found after treatment with acetaminophen in hospitalised children. Prostaglandin E2 metabolite levels did not correlate with length of hospitalisation or need for respiratory support.
Conclusion:
This study first provides normal levels of urinary prostaglandin E2 metabolite in infants and secondly demonstrates elevated levels in hospitalised children with lower respiratory tract and gastrointestinal infections.
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