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. 2011 Nov 14;2011:617597. doi: 10.1155/2011/617597

Table 3.

Glutamine supplementation in pediatric patients with gastrointestinal disease.

Reference Subjects Design Gln Control Outcomes Results
Albers et al. 2005 [131] 80 newborns and infants age ≤2 y requiring PN after major digestive tract surgery (GA ≥30 wk) Randomized double-blind Parenteral Gln; isonitrogenous isocaloric Gln (≤0.4 g/kg/d) supplemented PN started on d-2 after surgery and reached 90% of recommended AA intake of 1.5–2.5 g/kg/d (90% of Gln target dose of 0.4 g/kg/d) by d-4 until d-31, full EN, discharge or death; with tapering of PN started on or after d-6 (n = 41) Standard PN started on d-2 after surgery and reached 90% of recommended AA intake of 1.5–2.5 g/kg/d by d-4 until d-31, full EN discharge or death, with tapering of PN started on or after d-6 (n = 39) (1) Intestinal permeability (urinary lactulose/rhamnose ratio measured wk-1 through -4 after surgery, (2) nitrogen balance on d-4, -5, -6, urinary 3-MH excretion on d-5, mortality, LOS in ICU and in hospital, septic episodes, usage of antibiotics and ICU resources (1) No effect on intestinal permeability, (2) no effect on nitrogen balance, urinary 3-MH excretion, mortality, LOS in ICU or in hospital, culture-proven sepsis, usage of antibiotics or ICU resources, and no adverse effects
Duggan et al. 2004 [130] 20 neonates and infants aged <12 mo requiring PN after surgery for congenital or acquired gastrointestinal disease Randomized double-blind Enteral Gln; breastmilk or protein hydrolysate formula supplemented with enteral Gln (≤0.4 g/kg/d) until 7 consecutive d of full EN or hospital discharge (N = 9) Breastmilk or protein hydrolysate formula supplemented with enteral iso-osmolar mix of nonessential AA (≤0.4 g/kg/d) until 7 consecutive d of full EN or hospital discharge (N = 11) (1) Duration (d) on PN and d to achieve enteral feedings providing ≥80% of US-recommended dietary allowance for energy, (2) changes in macronutrient and energy absorption after supplementation, growth, and frequency of infections during trial (1) No differences in d on PN or d to achieve ≥80% energy requirements by EN, (2) no improvement in energy absorption, no differences in frequency of infections, wt gain, length gain, or changes in anthropometric measures, safe
Zhu et al. 2002 [142] 27 patients aged 9–67 y with SBS Case series Enteral/parenteral Gln; enteral and/or parenteral glycyl-Gln powder (0.6 g/kg/d) for ~1.5 ± 1.0 y or alanyl-Gln solution (0.3 g/kg/d) in combination with 3 wk rhGH and rehabilitative diet None Nutritional status and intestinal absorptive capacity after an average of 1.5 ± 1.0 y treatment Increased wt, serum total protein, albumin, hemoglobin, reduced stool frequency and stool nitrogen, increased D-xylose absorption
Weiming et al. 2004 [141] 37 patients aged 9–74 y with SBS (including 6 children aged 9–13 y) Case series Enteral Gln; oral Gln powder (0.6 g/kg/d) for 1-2 y in combination with rhGH (0.05 mg/kg/d) for 3 wk and rehabilitative diet None Efficacy in weaning off PN, intestinal absorptive capacity (D-xylose absorption, stool frequency, stool nitrogen) and plasma protein concentrations after 2-3 y of treatment Improved intestinal absorptive capacity and increased plasma protein concentrations, 57% of patients weaned off PN
Ladd et al. 2005 [140] 2 female pediatric patients aged 6 y (GA: 33 wk) and 6.5 y (GA: 26 wk) with SBS from neonatal gastrointestinal catastrophes Retrospective review of medical records Enteral Gln, SC rhGH (0.3 mg/kg/wk) and concurrent enteral Gln supplementation (30 mg/d) started at 6 y and 6.5 y, for 8 and 2.5 y, respectively None Retrospective review of supplemental nutritional requirement and serial growth parameters of height and wt over treatment period Improvement in growth (approximating target percentiles for height and wt), improved intestinal tolerance/adaptation, weaned from PN
Akobeng et al. 2000* [148] 18 children aged 6.8–15.7 y with active Crohn's disease Randomized double-blind Enteral Gln, exclusive polymeric EN with 42% of AA content as Gln for 4 wk (n = 9) Isocaloric isonitrogenous exclusive standard polymeric EN with identical essential AA and 4% of AA content as Gln for 4 wk (n = 9) Remission rates after 4 wk exclusive EN, changes in clinical and laboratory parameters of disease activity during 4 wk exclusive EN No differences in remission rates, changes in platelet count, orosomucoid level or wt, less improvement in pediatric Crohn's disease activity index
Akobeng et al. 2000* [150] 16 children aged 6.8–15.7 y with active Crohn's disease Randomized double-blind Enteral Gln, exclusive polymeric EN with 42% of AA content as Gln for 4 wk (n = 7) Isocaloric isonitrogenous exclusive standard polymeric EN with identical essential AA and 4% of AA content as Gln for 4 wk (n = 9) Intestinal permeability as assessed by lactulose/mannitol urinary excretion ratio after 4 wk exclusive EN Decreased lactulose/mannitol intestinal permeability ratio (both groups)
Akobeng et al. 2002* [151] 15 children aged 6.8–15.7 y with active Crohn's disease Randomized double-blind Enteral Gln, exclusive polymeric EN with 42% of AA content as Gln for 4 wk (n = 7) Isocaloric isonitrogenous exclusive standard polymeric EN with identical essential AA and 4% of AA content as Gln for 4 wk (n = 8) Serum IGF-1 concentrations and growth after 4 wk exclusive EN No improvement in serum IGF1 (both groups), less improvement in wt, wt for height and MUAC
Akobeng et al. 2007* [152] 15 children aged 6.8–15.7 y with active Crohn's disease Randomized double-blind Enteral Gln, polymeric EN with 42% of AA content as Gln for 4 wk (n = 7) Isocaloric isonitrogenous exclusive standard polymeric EN with identical essential AA and 4% of AA content as Gln for 4 wk (n = 8) Plasma antioxidant concentrations after 4 wk exclusive EN Increased plasma selenium concentrations (both groups), decreased concentrations of vitamin C and E (both groups), no change in vitamin A, urates, glutathione, and malondialdehyde

PN: parenteral nutrition; EN: enteral nutrition; wt: weight; GA: gestational age; AA: amino acid; 3-MH: 3-methyl-histidine; LOS: length of stay; ICU: intensive care unit; SBS: short bowel syndrome; rhGH: recombinant growth hormone; SC: subcutaneous; IGF-1: insulin-like growth factor-1; MUAC: mid upper arm circumference.

*Originating from the same cohort.