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Published on: July 28, 2022
Protective effect of parenteral glutamine supplementation on hepatic function in very low birth weight infants
Ying Wang1, Ye-Xuan Tao, Wei Cai
1Clinical Nutrition Center, Xin Hua Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200092, PR China.
Insights
Parenteral glutamine supplementation improved liver function in very low birth weight (VLBW) infants receiving parenteral nutrition. This suggests glutamine offers a hepato-protective effect for vulnerable newborns.
Area of Science:
- Neonatal Medicine
- Pediatric Gastroenterology
- Nutritional Science
Background:
- Hepatic dysfunction is a common complication of parenteral nutrition (PN), particularly in very low birth weight (VLBW) infants due to their physiological immaturity.
- Animal studies indicate that glutamine supplementation may mitigate TPN-associated liver injury.
Purpose of the Study:
- To evaluate the efficacy of parenteral glutamine supplementation in enhancing hepatic tolerance in VLBW infants.
- To determine if glutamine administration can reduce liver injury markers in this vulnerable population.
Main Methods:
- A double-blind, randomized, controlled clinical trial was conducted with 30 VLBW infants.
- Infants were randomized to receive either standard PN or PN supplemented with glutamine.
- Primary endpoints included hepatic function markers and mortality; secondary endpoints assessed nutritional and clinical outcomes.
Main Results:
- The glutamine-supplemented group showed significantly decreased serum levels of aspartate aminotransferase (AST) and total bilirubin (Tbi) post-PN (P < 0.05).
- No mortality was observed in the study.
- Withdrawal rates were similar between groups, with no statistically significant difference.
Conclusions:
- Parenteral glutamine supplementation demonstrates a hepato-protective effect in VLBW infants.
- Glutamine administration appears to improve hepatic tolerance during PN in this population.
Background & Aims:
Hepatic dysfunction is one of the most frequent complications of parenteral nutrition. Very low birth weight (VLBW) infants are more sensitive to liver injury due to physiological immaturity. Our studies in animals showed that glutamine supplementation could attenuate TPN-associated liver injury. The aim of study was to investigate whether parenteral glutamine supplementation can improve hepatic tolerance in VLBW infants.
Methods:
We performed a double-blind, randomized, and controlled clinical study to investigate whether parenteral glutamine supplementation can improve hepatic tolerance in VLBW infants. Thirty VLBW infants at two children's centers were randomly assigned to either a control group or a glutamine-supplemented group. The primary endpoints were hepatic function and mortality. The secondary endpoints were the time to achieve full enteral nutrition, episodes of gastric residuals, duration of parenteral nutrition, weight and head circumference gain, length of hospitalization, and days on ventilator.
Results:
The serum levels of aspartate aminotransferase (AST) and total bilirubin (Tbi) were decreased after PN in the glutamine-supplemented group (P < 0.05). No deaths occurred in this study. Four infants assigned to the control group and two infants in the glutamine-supplemented group were withdrawn from the study, according to intention to treat: relative risk [RR]: 1.182; 95% confidence interval [CI]: 0.937-1.490.
Conclusions:
Parenteral glutamine supplementation can improve hepatic tolerance in very low birth weight infant, suggesting a hepato-protective effect.
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