Intervention and Mechanisms of Alanyl-Glutamine for Inflammation, Nutrition, and Enteropathy (IMAGINE)
Primary Purpose
Malnutrition, Environmental Enteropathy, Diarrhea
Status
Completed
Phase
Phase 3
Locations
Brazil
Study Type
Interventional
Intervention
Alanyl-Glutamine
Sponsored by
About this trial
This is an interventional treatment trial for Malnutrition focused on measuring L-Alanyl-L-Glutamine, Environmental enteric dysfunction, Tropical enteropathy
Eligibility Criteria
Inclusion Criteria:
- Children who are undernourished or at risk of undernutrition, with anthropometric z-scores less than or equal to -1 for one of these parameters: height-for-age, weight-for-age, or weight-for-height.
- Children ages 2 months to 5 years old.
Exclusion Criteria:
- Children who are exclusively breastfed.
- Have participated in another intervention study in the past two years.
- Fever greater than 38.8 ° C.
- Use of antibiotics.
- Systemic disease or other serious medical condition (including, but not limited to meningitis, pneumonia, tuberculosis, and chickenpox).
- Children who are unable to ingest, retain or absorb nutritional supplements.
- Children whose families plan to move from the study area within the next 6 months.
Sites / Locations
- Universidade Federal do Ceara
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Active Comparator
Active Comparator
Active Comparator
Placebo Comparator
Arm Label
Alanyl-Glutamine 3g/d
Alanyl-Glutamine 6g/d
Alanyl-Glutamine 12g/d
Glycine 12.5g/d
Arm Description
Alanyl-Glutamine orally 3g/day for 10 days
Alanyl-Glutamine orally 6g/day for 10 days
Alanyl-Glutamine orally 12g/d for 10 days
Glycine orally 12.5 g/d for 10 days. This dose is calculated to be isonitrogenous to 12g of Alanyl-Glutamine.
Outcomes
Primary Outcome Measures
Urinary Lactulose: Mannitol Intestinal Permeability Test
Determine the dose-and time-effect of alanyl-glutamine on intestinal barrier function recovery using the intestinal permeability test, with measurement of the percentage of urinary excretion of lactulose, mannitol and ratio of lactulose:mannitol.
Secondary Outcome Measures
Fecal Lactoferrin Test
To evaluate the effect of time and dose-response of alanyl-glutamine on intestinal inflammation, as measured by qualitative or quantitative testing for fecal lactoferrin in stools of children at risk of undernutrition.
Fecal Cytokine Measurement
To evaluate the effect of alanyl-glutamine on intestinal inflammation, by measuring proinflammatory cytokines interleukin-1, interleukin-8, tumor necrosis factor-alpha (TNF), and regenerating gene 1B (REG1B) in stools of children at risk of undernutrition.
Anthropometry
To evaluate the time and dose-effect of alanyl-glutamine on short and medium-term nutritional status by evaluating changes in anthropometric measures (z scores) over time: height-for-age, weight-for-age, and weight-for-height.
Fecal Calorimetry
To evaluate the effect of time and dose-response of alanyl-glutamine on the intestinal absorption of fat, protein, and carbohydrates, by measurement of fecal energy content by bomb calorimetry.
Metabolomic Profile of Urine
To evaluate the time and dose-effect of alanyl-glutamine on metabolism in children at risk of undernutrition by means of urine metabolomic profile tests.
History of Diarrhea in the Previous Two Weeks
History of diarrhea in the previous two weeks. A day of diarrhea will be defined as 3 or more looser than normal bowel movements in a 24-hour period. Distinct episodes must be separated by at least 2 days without diarrhea. Duration of episodes will be classified as acute (< 7 days), prolonged acute (>6 and <14 days), or persistent (>13 days).
Full Information
NCT ID
NCT01832636
First Posted
April 12, 2013
Last Updated
July 28, 2016
Sponsor
Children's Hospital Medical Center, Cincinnati
Collaborators
Universidade Federal do Ceara
1. Study Identification
Unique Protocol Identification Number
NCT01832636
Brief Title
Intervention and Mechanisms of Alanyl-Glutamine for Inflammation, Nutrition, and Enteropathy
Acronym
IMAGINE
Official Title
Intervention and Mechanisms of Alanyl-Glutamine for Inflammation, Nutrition, and Enteropathy (IMAGINE)
Study Type
Interventional
2. Study Status
Record Verification Date
July 2016
Overall Recruitment Status
Completed
Study Start Date
October 2013 (undefined)
Primary Completion Date
December 2015 (Actual)
Study Completion Date
December 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Children's Hospital Medical Center, Cincinnati
Collaborators
Universidade Federal do Ceara
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Several host factors underlie the pathogenesis of the reciprocal cycle of childhood diarrhea and undernutrition in developing countries. These include intestinal inflammation, mucosal damage, and alterations in intestinal barrier function that lead to malabsorption, growth failure, and heightened susceptibility to recurrent and prolonged episodes of diarrhea. Recent studies from Northeast Brazil demonstrate the benefits of a novel alanyl-glutamine-based oral rehydration and nutrition therapy (Ala-Gln ORNT) in speeding the recovery of damaged intestinal barrier function in cell culture, animal models, patients with AIDS, and underweight children.
Oral supplementation with Alanyl-Glutamine (Ala-Gln; 24g a day for 10 days) improves short-term gut integrity and weight velocity 4 months after therapy in a group of undernourished children from Northeast Brazil. Intervention and Mechanisms of Alanyl-Glutamine for Inflammation, Nutrition, and Enteropathy (IMAGINE) is a study designed to answer the following questions: 1) What is the lowest dose of Ala-Gln that improves intestinal barrier function, intestinal inflammation, and nutritional status in children at risk of underweight, wasting, or stunting? 2) What are the mechanisms by which Ala-Gln exerts these benefits?
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Malnutrition, Environmental Enteropathy, Diarrhea
Keywords
L-Alanyl-L-Glutamine, Environmental enteric dysfunction, Tropical enteropathy
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
112 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Alanyl-Glutamine 3g/d
Arm Type
Active Comparator
Arm Description
Alanyl-Glutamine orally 3g/day for 10 days
Arm Title
Alanyl-Glutamine 6g/d
Arm Type
Active Comparator
Arm Description
Alanyl-Glutamine orally 6g/day for 10 days
Arm Title
Alanyl-Glutamine 12g/d
Arm Type
Active Comparator
Arm Description
Alanyl-Glutamine orally 12g/d for 10 days
Arm Title
Glycine 12.5g/d
Arm Type
Placebo Comparator
Arm Description
Glycine orally 12.5 g/d for 10 days. This dose is calculated to be isonitrogenous to 12g of Alanyl-Glutamine.
Intervention Type
Dietary Supplement
Intervention Name(s)
Alanyl-Glutamine
Other Intervention Name(s)
AminoStable (Ajinomoto)
Intervention Description
Alanyl-Glutamine and Glycine doses will be prepared immediately prior to administration by dissolving in formula, milk, or fruit juice. Administration of each dose will be directly observed by a study nurse or health agent.
Primary Outcome Measure Information:
Title
Urinary Lactulose: Mannitol Intestinal Permeability Test
Description
Determine the dose-and time-effect of alanyl-glutamine on intestinal barrier function recovery using the intestinal permeability test, with measurement of the percentage of urinary excretion of lactulose, mannitol and ratio of lactulose:mannitol.
Time Frame
Urine Collection on Day 1, 10-13, 30-37
Secondary Outcome Measure Information:
Title
Fecal Lactoferrin Test
Description
To evaluate the effect of time and dose-response of alanyl-glutamine on intestinal inflammation, as measured by qualitative or quantitative testing for fecal lactoferrin in stools of children at risk of undernutrition.
Time Frame
Fecal sample collected on Day 1, 10-13, 30-37
Title
Fecal Cytokine Measurement
Description
To evaluate the effect of alanyl-glutamine on intestinal inflammation, by measuring proinflammatory cytokines interleukin-1, interleukin-8, tumor necrosis factor-alpha (TNF), and regenerating gene 1B (REG1B) in stools of children at risk of undernutrition.
Time Frame
Fecal sample collected on Day 1, 10-13
Title
Anthropometry
Description
To evaluate the time and dose-effect of alanyl-glutamine on short and medium-term nutritional status by evaluating changes in anthropometric measures (z scores) over time: height-for-age, weight-for-age, and weight-for-height.
Time Frame
Measured and calculated Day 1, 10-13, 30-37, 90-104, 120-141
Title
Fecal Calorimetry
Description
To evaluate the effect of time and dose-response of alanyl-glutamine on the intestinal absorption of fat, protein, and carbohydrates, by measurement of fecal energy content by bomb calorimetry.
Time Frame
Fecal sample collected on Day 1, 10-13, 30-37
Title
Metabolomic Profile of Urine
Description
To evaluate the time and dose-effect of alanyl-glutamine on metabolism in children at risk of undernutrition by means of urine metabolomic profile tests.
Time Frame
Collected on Day 1, 10-13, 30-37
Title
History of Diarrhea in the Previous Two Weeks
Description
History of diarrhea in the previous two weeks. A day of diarrhea will be defined as 3 or more looser than normal bowel movements in a 24-hour period. Distinct episodes must be separated by at least 2 days without diarrhea. Duration of episodes will be classified as acute (< 7 days), prolonged acute (>6 and <14 days), or persistent (>13 days).
Time Frame
Day 1, 30-37, 90-104, 120-141
10. Eligibility
Sex
All
Minimum Age & Unit of Time
2 Months
Maximum Age & Unit of Time
5 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Children who are undernourished or at risk of undernutrition, with anthropometric z-scores less than or equal to -1 for one of these parameters: height-for-age, weight-for-age, or weight-for-height.
Children ages 2 months to 5 years old.
Exclusion Criteria:
Children who are exclusively breastfed.
Have participated in another intervention study in the past two years.
Fever greater than 38.8 ° C.
Use of antibiotics.
Systemic disease or other serious medical condition (including, but not limited to meningitis, pneumonia, tuberculosis, and chickenpox).
Children who are unable to ingest, retain or absorb nutritional supplements.
Children whose families plan to move from the study area within the next 6 months.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sean R Moore, MD, MS
Organizational Affiliation
Cincinnati Children´s Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Aldo Lima, MD, PhD
Organizational Affiliation
Universidade Federal do Ceara
Official's Role
Principal Investigator
Facility Information:
Facility Name
Universidade Federal do Ceara
City
Fortaleza
State/Province
Ceara
Country
Brazil
12. IPD Sharing Statement
Citations:
PubMed Identifier
17325559
Citation
Lima NL, Soares AM, Mota RM, Monteiro HS, Guerrant RL, Lima AA. Wasting and intestinal barrier function in children taking alanyl-glutamine-supplemented enteral formula. J Pediatr Gastroenterol Nutr. 2007 Mar;44(3):365-74. doi: 10.1097/MPG.0b013e31802eecdd.
Results Reference
background
PubMed Identifier
32826717
Citation
Moore SR, Quinn LA, Maier EA, Guedes MM, Quetz JS, Perry M, Ramprasad C, Lanzarini Lopes GML, Mayneris-Perxachs J, Swann J, Soares AM, Filho JQ, Junior FS, Havt A, Lima NL, Guerrant RL, Lima AAM. Intervention and Mechanisms of Alanyl-glutamine for Inflammation, Nutrition, and Enteropathy: A Randomized Controlled Trial. J Pediatr Gastroenterol Nutr. 2020 Sep;71(3):393-400. doi: 10.1097/MPG.0000000000002834.
Results Reference
derived
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Intervention and Mechanisms of Alanyl-Glutamine for Inflammation, Nutrition, and Enteropathy
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