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Urinary and serum oxysterols in children: developmental pattern and potential biomarker for pediatric liver disease
Yugo Takaki1, Tatsuki Mizuochi2, Hajime Takei3
1Department of Pediatrics and Child Health, Kurume University School of Medicine, Kurume, Fukuoka, Japan.
Insights
Oxysterol levels change during childhood development. Elevated urinary and serum oxysterols, especially 24(S)-hydroxycholesterol, indicate potential biomarkers for pediatric liver disease.
Area of Science:
- Biochemistry
- Pediatric Medicine
- Analytical Chemistry
Background:
- Oxysterols, cholesterol oxidation products, are implicated in various physiological processes.
- Limited data exists on oxysterol levels in healthy children and those with liver disease.
- Understanding developmental changes in oxysterols is crucial for pediatric health assessment.
Purpose of the Study:
- To investigate developmental changes in urinary and serum oxysterols throughout childhood.
- To evaluate the potential of oxysterols as biomarkers for pediatric liver disease.
- To compare oxysterol profiles in healthy children versus children with liver disease.
Main Methods:
- Quantification of seven specific oxysterols (4β-, 20(S)-, 22(S)-, 22(R)-, 24(S)-, 25-, and 27-hydroxycholesterol) using liquid chromatography/electrospray ionization-tandem mass spectrometry (LC/ESI-MS/MS).
- Analysis of urine and serum samples from healthy neonates, infants, preschoolers, school-age children, and adults.
- Comparison of oxysterol levels between healthy children and a cohort of children diagnosed with liver disease.
Main Results:
- Urinary total oxysterols were highest in neonates and decreased significantly with age.
- Serum total oxysterols were lowest in neonates and increased significantly with age.
- Children with liver disease exhibited significantly elevated urinary and serum total oxysterols, particularly 24(S)-hydroxycholesterol, compared to healthy controls.
Conclusions:
- Oxysterol levels undergo significant developmental changes from infancy through childhood.
- Oxysterols, especially 24(S)-hydroxycholesterol, show promise as non-invasive biomarkers for detecting pediatric liver disease.
- This study provides the first report on developmental oxysterol changes and their potential as biomarkers in pediatric liver disease.
Abstract:
Few reports describe oxysterols in healthy children or in children with liver disease. We aimed to determine whether developmental changes in urinary and serum oxysterols occur during childhood, and to assess whether oxysterols might be biomarkers for pediatric liver disease. Healthy children enrolled as subjects (36 and 35 for urine and serum analysis, respectively) included neonates, infants, preschoolers, and school-age children, studied along with 14 healthy adults and 8 children with liver disease. We quantitated 7 oxysterols including 4β-, 20(S)-, 22(S)-, 22(R)-, 24(S)-, 25-, and 27-hydroxycholesterol using liquid chromatography/electrospray ionization-tandem mass spectrometry. Urinary total oxysterols were significantly greater in neonates than in infants (P < 0.05), preschoolers (P < 0.001), school-age children (P < 0.001), or adults (P < 0.001), declining with age. Serum total oxysterols in neonates were significantly lower than in infants (P < 0.05), preschoolers (P < 0.001), school-age children (P < 0.05), or adults (P < 0.01). Compared with healthy children, total oxysterols and 24(S)-hydroxycholesterol in liver disease were significantly increased in both urine (P < 0.001 and P < 0.001, respectively) and serum (P < 0.001 and P < 0.05, respectively). Oxysterols in liver disease, particularly 24(S)-hydroxycholesterol, were greater in urine than serum. Oxysterols change developmentally and might serve as a biomarker for pediatric liver disease. To our knowledge, this is the first such report.
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