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Updated: Aug 6, 2026

Isolation of Neonatal Extrahepatic Cholangiocytes
Published on: June 5, 2014
Urinary monohydroxy bile acids in young infants with obstructive jaundice
Insights
Young infants lack lithocholic acid but excrete 3 beta-hydroxy-5-cholenoic acid, a finding significant for diagnosing obstructive jaundice in infants and adults. This bile acid
Area of Science:
- Biochemistry
- Pediatric Gastroenterology
- Metabolic Disorders
Background:
- Bile acids are crucial for digestion and metabolism.
- Monohydroxy bile acids play a role in liver function and disease.
- Understanding bile acid profiles in infants is vital for diagnosing pediatric liver conditions.
Purpose of the Study:
- To quantitatively determine urinary monohydroxy bile acids in young infants.
- To compare bile acid profiles in infants with and without obstructive jaundice.
- To investigate the presence and levels of specific monohydroxy bile acids, such as 3 beta-hydroxy-5-cholenoic acid, in different age groups and conditions.
Main Methods:
- Urine samples were fractionated using an aluminum oxide column.
- Quantitative determination of urinary monohydroxy bile acids was performed.
- Bile acid levels were measured in young infants, older children, and adults with obstructive jaundice.
Main Results:
- Lithocholic acid was absent in all young infant samples.
- 3 beta-hydroxy-5-cholenoic acid was detected in all young infants.
- Infants with biliary atresia and neonatal hepatitis showed elevated 3 beta-hydroxy-5-cholenoic acid excretion compared to total bile acids.
- Older children and adults with obstructive jaundice exhibited higher excretion rates of 3 beta-hydroxy-5-cholenoic acid.
- Excretion of 3 beta-hydroxy-5-cholenoic acid correlated with chenodeoxycholic acid in infants and with both chenodeoxycholic acid and cholic acid in older individuals.
Conclusions:
- The absence of lithocholic acid and presence of 3 beta-hydroxy-5-cholenoic acid are characteristic of young infants.
- Urinary 3 beta-hydroxy-5-cholenoic acid levels may serve as a biomarker for obstructive jaundice in pediatric populations.
- The correlation between 3 beta-hydroxy-5-cholenoic acid and other bile acids provides insights into metabolic pathways in liver disease.
Abstract:
Using an aluminum oxide column, we fractionated and quantitatively determined urinary monohydroxy bile acids in young infants. For comparison purposes, monohydroxy bile acids were also measured in urine from older children and adults with obstructive jaundice. Lithocholic acid was not found in any specimens of the young infants examined, while 3 beta-hydroxy-5-cholenoic acid was detected in all. In the biliary atresia group, 3 beta-hydroxy-5-cholenoic acid excreted was 0.45+/-0.28 mumol per day (n=7), and in the neonatal hepatitis group, 0.48+/-0.44 mumol per day (n=9). The mean rate of 3 beta-hydroxy-5-cholenoic acid to total urinary bile acids in the biliary atresia group was 2.1%, and 1.3% in the neonatal hepatitis group. In the older children and adults with obstructive jaundice (n=6), 3 beta-hydroxy-5-cholenoic acid was excreted at a mean rate of 3.9% of total urinary bile acids, ranging from 0.63 to 14.81 mol per day. The excretion rate of 3 beta-hydroxy-5-cholenoic acid was related to that of chenodeoxycholic acid (p less than 0.05) in infants, while it was related to that of both chenodeoxycholic acid (p less than 0.01) and cholic acid (p less than 0.05) in older children and adults.
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