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RecruitingNCT05430178

Metabolic Pathology of Pediatric NAFLD

Understanding the Metabolic Pathology of Pediatric Obesity and NAFLD

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
University of Oklahoma · Academic / Other
Sex
All
Age
10 Years – 20 Years
Healthy volunteers
Accepted

Summary

Nonalcoholic fatty liver disease (NAFLD) is now the most common liver disease worldwide and affects nearly 40% of obese youth and up to 10% of the general pediatric population. Some features of NAFLD are similar in children and adults, yet fibrosis and inflammation are more common in the portal zone and occur earlier in pediatric NAFLD patients than adults. This portends a rapid progression to end-stage liver disease in early adulthood. For the majority of children with NAFLD, mechanisms driving the origin and rapid progression of disease remain unknown. Thus, there is a critical, unmet need to study the specific underlying patterns of metabolic and molecular changes in the liver underlying the development and progression unique to children with NAFLD. This proposal will test the hypotheses that children with NAFLD have excess glucose and lipid produced by the liver, that those events are regulated by specific variations in the amount and location of RNAs and proteins in liver, and that the concentration of specific micro-RNAs in the blood can be used as a biomarker for NAFLD in pediatric patients.

Detailed description

This project uses a cross-sectional design with a single testing period without a formal intervention (e.g., diet, drug, exercise) or natural follow-up period. Participants with nonalcoholic fatty liver disease (NAFLD), and age-matched control groups classified as either obese (Ob control) or normal weight (NW control) will complete all metabolic and descriptive tests, including blood analyses. The NAFLD group will also have a liver biopsy as part of their standard clinical care; a portion of the biopsy will be used for the research testing. The Ob and NW control groups will not undergo liver biopsy. To provide a set of reference liver samples to compare with the NAFLD group, we will enroll a "liver control" group, consisting of age-matched patients who are scheduled to have a cholecystectomy with liver biopsy or are undergoing liver resection for tumor removal.

Conditions

Interventions

TypeNameDescription
OTHEROral sugar tolerance testMeasurement of glucose and insulin for calculation of insulin sensitivity
OTHERDe novo lipogenesis testOral consumption of deuterated water to measure incorporation of label into lipids
OTHERGluconeogenesis testOral consumption of 13C-labeled glycerol to measure incorporation into glucose

Timeline

Start date
2022-05-25
Primary completion
2026-02-01
Completion
2026-06-01
First posted
2022-06-24
Last updated
2024-03-06

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT05430178. Inclusion in this directory is not an endorsement.