<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Moore SR</submitter><funding>FIC NIH HHS</funding><pagination>393-400</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8576339</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>71(3)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>Determine the minimum dosage of alanyl-glutamine (Ala-Gln) required to improve gut integrity and growth in children at risk of environmental enteropathy (EE).&lt;h4>Methods&lt;/h4>This was a double-blinded randomized placebo-controlled dose-response trial. We enrolled 140 children residing in a low-income community in Fortaleza, Brazil. Participants were 2 to 60 months old and had weight-for-age (WAZ), height-for-age (HAZ), or weight-for-height (WHZ) z-scores less than -1. We randomized children to 10 days of nutritional supplementation: Ala-Gln at 3 g/day, Ala-Gln at 6 g/day, Ala-Gln at 12 g/day, or an isonitrogenous dose of glycine (Gly) placebo at 12.5 g/day. Our primary outcome was urinary lactulose-mannitol excretion testing. Secondary outcomes were anthropometry, fecal markers of inflammation, urine metabolic profiles, and malabsorption (spot fecal energy).&lt;h4>Results&lt;/h4>Of 140 children, 103 completed 120 days of follow-up (24% dropout). In the group receiving the highest dose of Ala-Gln, we detected a modest improvement in urinary lactulose excretion from 0.19% on day 1 to 0.17% on day 10 (P = 0.05). We observed significant but transient improvements in WHZ at day 10 in 2 Ala-Gln groups, and in WHZ and WAZ in all Ala-Gln groups at day 30. We detected no effects on fecal inflammatory markers, diarrheal morbidity, or urine metabolic profiles; but did observe modest reductions in fecal energy and fecal lactoferrin in participants receiving Ala-Gln.&lt;h4>Conclusions&lt;/h4>Intermediate dose Ala-Gln promotes short-term improvement in gut integrity and ponderal growth in children at risk of EE. Lower doses produced improvements in ponderal growth in the absence of enhanced gut integrity.</pubmed_abstract><journal>Journal of pediatric gastroenterology and nutrition</journal><pubmed_title>Intervention and Mechanisms of Alanyl-glutamine for Inflammation, Nutrition, and Enteropathy: A Randomized Controlled Trial.</pubmed_title><pmcid>PMC8576339</pmcid><funding_grant_id>K02 TW008767</funding_grant_id><pubmed_authors>Mayneris-Perxachs J</pubmed_authors><pubmed_authors>Guedes MM</pubmed_authors><pubmed_authors>Swann J</pubmed_authors><pubmed_authors>Soares AM</pubmed_authors><pubmed_authors>Quetz JS</pubmed_authors><pubmed_authors>Lanzarini Lopes GML</pubmed_authors><pubmed_authors>Filho JQ</pubmed_authors><pubmed_authors>Lima AAM</pubmed_authors><pubmed_authors>Moore SR</pubmed_authors><pubmed_authors>Ramprasad C</pubmed_authors><pubmed_authors>Havt A</pubmed_authors><pubmed_authors>Quinn LA</pubmed_authors><pubmed_authors>Junior FS</pubmed_authors><pubmed_authors>Perry M</pubmed_authors><pubmed_authors>Guerrant RL</pubmed_authors><pubmed_authors>Maier EA</pubmed_authors><pubmed_authors>Lima NL</pubmed_authors></additional><is_claimable>false</is_claimable><name>Intervention and Mechanisms of Alanyl-glutamine for Inflammation, Nutrition, and Enteropathy: A Randomized Controlled Trial.</name><description>&lt;h4>Objective&lt;/h4>Determine the minimum dosage of alanyl-glutamine (Ala-Gln) required to improve gut integrity and growth in children at risk of environmental enteropathy (EE).&lt;h4>Methods&lt;/h4>This was a double-blinded randomized placebo-controlled dose-response trial. We enrolled 140 children residing in a low-income community in Fortaleza, Brazil. Participants were 2 to 60 months old and had weight-for-age (WAZ), height-for-age (HAZ), or weight-for-height (WHZ) z-scores less than -1. We randomized children to 10 days of nutritional supplementation: Ala-Gln at 3 g/day, Ala-Gln at 6 g/day, Ala-Gln at 12 g/day, or an isonitrogenous dose of glycine (Gly) placebo at 12.5 g/day. Our primary outcome was urinary lactulose-mannitol excretion testing. Secondary outcomes were anthropometry, fecal markers of inflammation, urine metabolic profiles, and malabsorption (spot fecal energy).&lt;h4>Results&lt;/h4>Of 140 children, 103 completed 120 days of follow-up (24% dropout). In the group receiving the highest dose of Ala-Gln, we detected a modest improvement in urinary lactulose excretion from 0.19% on day 1 to 0.17% on day 10 (P = 0.05). We observed significant but transient improvements in WHZ at day 10 in 2 Ala-Gln groups, and in WHZ and WAZ in all Ala-Gln groups at day 30. We detected no effects on fecal inflammatory markers, diarrheal morbidity, or urine metabolic profiles; but did observe modest reductions in fecal energy and fecal lactoferrin in participants receiving Ala-Gln.&lt;h4>Conclusions&lt;/h4>Intermediate dose Ala-Gln promotes short-term improvement in gut integrity and ponderal growth in children at risk of EE. Lower doses produced improvements in ponderal growth in the absence of enhanced gut integrity.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Sep</publication><modification>2024-11-14T16:41:38.239Z</modification><creation>2022-02-11T12:41:53.077Z</creation></dates><accession>S-EPMC8576339</accession><cross_references><pubmed>32826717</pubmed><doi>10.1097/MPG.0000000000002834</doi></cross_references></HashMap>