The main objective is to study the effect of polyphenol supplementation on hepatic steatosis as measured by hepatic ultrasound, hepatic magnetic resonance imaging and on intima-media thickness and vascular elastography in obese adolescents known for hepatic steatosis as diagnosed by liver biopsy
1. Evaluate the feasibility of a larger, open-label, randomized, controlled trial on the effects of polyphenol supplementation: Recruitment, compliance to polyphenol supplementation and the visit roadmaps Duration of the radiological exams and participants' satisfaction and point of view on the experience. Test the relevance of using a food diary. Test the effectiveness of the data collection procedure during the visits. Explore the obstacles encountered while performing the radiological exams and the rate of adverse events (AE). Calculate the sample size of the future randomized clinical study 2. Effects of polyphenols IMT and vascular elastography. Anthropometric measurements, insulin resistance, inflammation, lipid/lipoprotein profile, gut microbiome and liver function 3. Evaluated different imaging modality for steatosis Different imaging modalities will be compared between children
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
60
Measurement of effect of polyphenol supplementation vs placebo on hepatic steatosis and vascular elastography and intima media thickness
CHU Sainte-Justine
Montreal, Quebec, Canada
RECRUITINGRecruitment
Rate of recruitment
Time frame: Through study completion an average of 1 year
Retention:
The percentage of adolescents who agree to participate in the study and the retention
Time frame: Through study completion an average of 1 year
Compliance with polyphenol supplementation
Percentage of compliance
Time frame: Through study completion an average of 1 year
Effectiveness of the data collection procedure during the visits
Percentage of completed visits
Time frame: Through study completion an average of 1 year
Adverse event
Percentage of adverse events
Time frame: Through study completion an average of 1 year
Satisfaction of the participants and their point of view on the experience
Percentage of satisfaction of participants enrolled
Time frame: Through study completion an average of 1 year
Sample size calculation for a randomized controlled study
A sample size for a future randomized controlled study will be calculated from the estimates obtained during this pilot study.
Time frame: Through study completion an average of 1 year
Change in hepatic steatosis MR
mDixonQuant in percentage
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Time frame: At recruitment, after 60 days, and after 120 days
Change in hepatic steatosis B-mode US
US liver echogenicity normal or increased
Time frame: At recruitment, after 60 days, and after 120 days
Change in intima media thickness (vascular compliance)
Measurement of carotid artery intima media thickness in mm
Time frame: At recruitment, after 60 days, and after 120 days
Metabolic syndrome
Insulin resistance evaluated by HOMA-IR mg\\dl
Time frame: At recruitment, after 60 days, and after 120 days
Cholesterol
Triglyceride index (no unit)
Time frame: At recruitment, after 60 days, and after 120 days
Anthropometric measure
Body mass index
Time frame: At recruitment, after 60 days, and after 120 days
Inflammatory marker 1
CRP
Time frame: At recruitment, after 60 days, and after 120 days
Inflammatory marker 2
TNF alpha
Time frame: At recruitment, after 60 days, and after 120 days
Inflammatory marker 3
IL-6
Time frame: At recruitment, after 60 days, and after 120 days
Lipid markers 1
Triglycerides
Time frame: At recruitment, after 60 days, and after 120 days
Lipid markers 2
LDL
Time frame: At recruitment, after 60 days, and after 120 days
Lipid markers 3
HDL
Time frame: At recruitment, after 60 days, and after 120 days
Lipid markers 4
Apo AI
Time frame: At recruitment, after 60 days, and after 120 days
Lipid markers 5
Apo B-100
Time frame: At recruitment, after 60 days, and after 120 days
Lipid markers 6
Adiponectin, leptin
Time frame: At recruitment, after 60 days, and after 120 days
Liver function test
ALT
Time frame: At recruitment, after 60 days, and after 120 days
Stool test
Gut microbiome composition
Time frame: At recruitment, after 60 days, and after 120 days