Targeting the Gut Microbiome for Prader-Willi Syndrome Treatment (BALPWS)
Primary Purpose
Prader-Willi Syndrome
Status
Completed
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Placebo
Probiotic
Sponsored by
About this trial
This is an interventional treatment trial for Prader-Willi Syndrome
Eligibility Criteria
Inclusion Criteria:
- Diagnosed with Prader-Willi Syndrome with genetic confirmation
- On a stable diet and medication regimen for at least the last two months before enrollment
Exclusion Criteria:
- Current enrollment in or discontinuation within the last 30 days from a clinical trial
- Presence of other medical problems that would preclude study participation
- Patients with a history of bariatric surgery
- Unsuitable for inclusion in the study in the opinion of the investigator
Sites / Locations
- Hospital Sant Joan de Deu
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Experimental
Arm Label
Placebo
Probiotic
Arm Description
Outcomes
Primary Outcome Measures
Change in percent body fat
Measured by DXA scan
Secondary Outcome Measures
Change in lipid profile (triglyceride, cholesterol)
Blood test after overnight fasting
Change in glucose metabolic parameters (glucose, insulin, HbA1c)
Blood test after overnight fasting
Change in circulating cytokine levels
Quantified in plasma samples
Change in hyperphagia
Measured by validated questionnaire (HQ-CT)
Change in thermoregulation
Measured by thermal imaging
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03548480
Brief Title
Targeting the Gut Microbiome for Prader-Willi Syndrome Treatment
Acronym
BALPWS
Official Title
Targeting the Gut Microbiome for Prader-Willi Syndrome Treatment
Study Type
Interventional
2. Study Status
Record Verification Date
March 2020
Overall Recruitment Status
Completed
Study Start Date
January 1, 2018 (Actual)
Primary Completion Date
January 31, 2019 (Actual)
Study Completion Date
January 31, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Fundació Sant Joan de Déu
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The gut microbiome has recently emerged as a major contributor to obesity, systemic inflammation, and metabolic disease. Furthermore, intestinal bacteria are crucial players in the gut-brain axis, regulating a broad range of central nervous system processes, from satiety mechanisms to anxiety and social behavior. Thus, targeting the microbiome is being actively investigated as a therapeutic strategy for a wide array of diseases, including obesity, anxiety, depression, and autism. Among all intestinal bacteria, Bifidobacterium animalis spp. lactis (BAL) has shown promise for obesity treatment in experimental animal models and human subjects, improving body composition and metabolic health, and reducing energy intake. Moreover, tryptophan metabolism, a crucial regulator of satiety mechanisms and anxiety, is a main target of BAL. Given that clinical manifestations of Prader-Willi syndrome (PWS) include hyperphagia, anxiety, altered body composition, and metabolic dysregulation, the aforementioned effects of BAL might prove highly beneficial for children with PWS. Here, the investigators will test this hypothesis by performing a randomized double-blinded placebo-controlled crossover clinical study to assess the effects of BAL supplementation on an array of clinical manifestations of PWS. Children with PWS will undergo a 3-month placebo/probiotic treatment period, a 3-month washout period, followed by a 3-month probiotic/placebo supplementation. Anthropometric, biochemical, and psychological data as well as biological samples will be obtained at the beginning of the study, and after each of the study periods, with a total of four time-points. Specifically, the investigators will determine body composition by DXA analysis; metabolic health by assessing glucose and lipid metabolic parameters as well as circulating hormonal and cytokine levels; thermoregulation by non-invasive thermal imaging; and hyperphagia and emotional and behavioral problems by applying parental-rated validated questionnaires.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prader-Willi Syndrome
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
39 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Title
Probiotic
Arm Type
Experimental
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
Intervention with a daily dose of placebo
Intervention Type
Dietary Supplement
Intervention Name(s)
Probiotic
Intervention Description
Intervention with a daily dose of probiotic
Primary Outcome Measure Information:
Title
Change in percent body fat
Description
Measured by DXA scan
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Change in lipid profile (triglyceride, cholesterol)
Description
Blood test after overnight fasting
Time Frame
3 months
Title
Change in glucose metabolic parameters (glucose, insulin, HbA1c)
Description
Blood test after overnight fasting
Time Frame
3 months
Title
Change in circulating cytokine levels
Description
Quantified in plasma samples
Time Frame
3 months
Title
Change in hyperphagia
Description
Measured by validated questionnaire (HQ-CT)
Time Frame
3 months
Title
Change in thermoregulation
Description
Measured by thermal imaging
Time Frame
3 months
Other Pre-specified Outcome Measures:
Title
Change in plasma metabolome
Description
Liquid chromatography coupled to mass spectrometry will be used to obtain a comprehensive metabolic profile of plasma samples
Time Frame
3 months
Title
Change in urine metabolome
Description
Liquid chromatography coupled to mass spectrometry will be used to obtain a comprehensive metabolic profile of urine samples
Time Frame
3 months
Title
Change in intestinal microbiome
Description
DNA isolated from fecal samples will be analyzed by sequencing.
Time Frame
3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Diagnosed with Prader-Willi Syndrome with genetic confirmation
On a stable diet and medication regimen for at least the last two months before enrollment
Exclusion Criteria:
Current enrollment in or discontinuation within the last 30 days from a clinical trial
Presence of other medical problems that would preclude study participation
Patients with a history of bariatric surgery
Unsuitable for inclusion in the study in the opinion of the investigator
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Carles Lerin, PhD
Organizational Affiliation
Fundació Sant Joan de Déu
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Sant Joan de Deu
City
Barcelona
ZIP/Postal Code
08950
Country
Spain
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
33066107
Citation
Amat-Bou M, Garcia-Ribera S, Climent E, Piquer-Garcia I, Corripio R, Sanchez-Infantes D, Villalta L, Elias M, Jimenez-Chillaron JC, Chenoll E, Ramon D, Ibanez L, Ramon-Krauel M, Lerin C. Effects of Bifidobacterium animalis Subsp. lactis (BPL1) Supplementation in Children and Adolescents with Prader-Willi Syndrome: A Randomized Crossover Trial. Nutrients. 2020 Oct 13;12(10):3123. doi: 10.3390/nu12103123.
Results Reference
derived
Learn more about this trial
Targeting the Gut Microbiome for Prader-Willi Syndrome Treatment
We'll reach out to this number within 24 hrs