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Published on: July 28, 2022
Glutamine supplementation in preterm infants receiving parenteral nutrition leads to an early improvement in liver
Ying Wang1, Wei Cai, Ye-Xuan Tao
1Department of Clinical Nutrition, Xin Hua Hospital, Kongjiang Road 1665, Shanghai 200092, China. caiw204@yahoo.com.cn.
Insights
Parenteral glutamine supplementation may protect premature infants from liver injury caused by parenteral nutrition. This nutritional support showed early hepatoprotective effects, reducing liver enzymes within 7-14 days.
Area of Science:
- Neonatalogy
- Pediatric Gastroenterology
- Nutritional Science
Background:
- Parenteral nutrition (PN) is essential for premature infants but can lead to liver injury.
- The duration of PN correlates with the severity of hepatic dysfunction.
- Glutamine, an amino acid, plays a crucial role in intestinal and hepatic health.
Purpose of the Study:
- To investigate the hepatoprotective effects of parenteral glutamine supplementation in premature infants.
- To determine the timeline for observing these protective effects.
Main Methods:
- A double-blind, randomized, controlled clinical trial was conducted.
- Thirty premature infants received either standard PN or PN supplemented with glutamine.
- Hepatic function markers (AST, GGT, AKP) and clinical outcomes were assessed.
Main Results:
- Glutamine supplementation significantly decreased AST and GGT levels within 7-14 days.
- Alkaline phosphatase (AKP) levels did not increase in the glutamine group, unlike the control group.
- No significant differences were observed in overall PN duration, growth, or hospitalization length.
Conclusions:
- Parenteral glutamine supplementation demonstrates a hepatoprotective effect in premature infants.
- The benefits of glutamine supplementation on liver function become evident relatively quickly during PN.
- This highlights glutamine as a potential therapeutic agent to mitigate PN-induced liver injury.
Objective:
The aim of study was to confirm the protective effects of parenteral glutamine supplementation on liver injury in premature infants and determine how quickly effects became evident.
Methods:
We performed a double-blind, randomized, controlled clinical study to assess the effect of parenteral nutrition (PN) supplemented with glutamine in premature infants. Thirty infants from two children's centers, were randomly assigned to either a control group (Standard PN; n=15) or a glutamine-supplemented group (GlnPN; n=15). The primary endpoint was hepatic function. The secondary endpoints were total duration of PN, weight and head circumference gain, length of hospitalization, and days on a ventilator.
Results:
The serum level of alkaline phosphatase (AKP) after parenteral nutrition for 14 days was significantly higher (p<0.05) in the control group. But in the glutamine-supplemented group, the serum concentration of aspartate aminotransferase (AST) and gamma glutamyltransferase (GGT) significantly decreased after PN for 7 days and 14 days (p<0.05), and the level of alkaline phosphatase (AKP) showed no increase. The levels of AKP and GGT were significantly different with time by group interaction. Levels of AKP was higher in control group than glutamine-supplemented group, and GGT level was lower in glutamine-supplemented group compared with controls. There were no significant differences between the groups in terms of total duration of PN, weight gain (g/d), increase in head circumference (cm/w), length of hospitalization, and duration of mechanical ventilation.
Conclusion:
The longer the duration of parenteral nutrition, the more severe hepatic dysfunction became. Parenteral glutamine supplementation suggested a hepatoprotective effect.
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