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Updated: May 18, 2026

Glutamine Flux Imaging Using Genetically Encoded Sensors
Published on: July 31, 2014
Glutamine randomized studies in early life: the unsolved riddle of experimental and clinical studies
Efrossini Briassouli1, George Briassoulis
1First Department of Propaedeutic Medicine, National and Kapodistrian University of Athens, Athens, Greece.
Insights
Glutamine supplementation in infants and children shows no effect on mortality. While safe, routine use is not recommended due to lack of proven benefits in critical illness. Further research is needed.
Area of Science:
- Pediatric critical care
- Nutritional science
- Immunology
Background:
- Glutamine's role in early life and critical illness is debated.
- Experimental studies suggest potential benefits, but clinical evidence is inconsistent.
Purpose of the Study:
- To review randomized studies on glutamine supplementation in neonates, infants, and children.
- To assess glutamine's impact on mortality, inflammatory response, organ function, and infection.
Main Methods:
- Systematic review of randomized controlled trials.
- Inclusion of studies involving pups, premature infants, and critically ill children.
Main Results:
- No randomized studies demonstrated a significant effect of glutamine on mortality.
- Some studies indicated minor effects on inflammatory markers and organ function, with a trend towards improved infection control.
- Glutamine was found to be safe in the studied populations.
Conclusions:
- Current evidence does not support the routine use of glutamine supplementation in premature infants or critically ill children.
- Further large-scale, stratified trials are necessary to identify specific subgroups that may benefit from glutamine and to explore its interaction with stress response pathways.
Abstract:
Glutamine may have benefits during immaturity or critical illness in early life but its effects on outcome end hardpoints are controversial. Our aim was to review randomized studies on glutamine supplementation in pups, infants, and children examining whether glutamine affects outcome. Experimental work has proposed various mechanisms of glutamine action but none of the randomized studies in early life showed any effect on mortality and only a few showed some effect on inflammatory response, organ function, and a trend for infection control. Although apparently safe in animal models (pups), premature infants, and critically ill children, glutamine supplementation does not reduce mortality or late onset sepsis, and its routine use cannot be recommended in these sensitive populations. Large prospectively stratified trials are needed to better define the crucial interrelations of "glutamine-heat shock proteins-stress response" in critical illness and to identify the specific subgroups of premature neonates and critically ill infants or children who may have a greater need for glutamine and who may eventually benefit from its supplementation. The methodological problems noted in the reviewed randomized experimental and clinical trials should be seriously considered in any future well-designed large blinded randomized controlled trial involving glutamine supplementation in critical illness.

