Yale New Haven Hospital
New Haven, Connecticut, 06510, United States
Location status: Recruiting
Location contact
Ermena Refugjati
CONTACT
Nicola Santoro, MD, PhD
PRINCIPAL_INVESTIGATOR
NCT Number: NCT04634643
The main aim of the study is to discover the mechanisms underlying the pathophysiology of NAFLD in obese youth.
Interested in participating?
Request Info12 year–18 year
All sexes
Observational
New Haven, Connecticut, 06510, United States
Location status: Recruiting
Ermena Refugjati
CONTACT
Nicola Santoro, MD, PhD
PRINCIPAL_INVESTIGATOR
Nonalcoholic fatty liver disease (NAFLD) is the most common hepatic disease in pediatrics, affecting about 30% of obese youth. The term NAFLD defines a wide spectrum of disease severity ranging from simple intrahepatic fat accumulation without liver injury (steatosis) to nonalcoholic steatohepatitis (NASH), fibrosis and cirrhosis.
A 20-year retrospective study has shown that subjects who develop NAFLD during their youth have about 13 times higher mortality rate for end-stage liver disease than healthy subjects of similar age and gender. NAFLD is highly prevalent among Hispanic youth, while non-Hispanic Black (NHB) youth are protected against intrahepatic fat accumulation even in the presence of severe obesity and insulin resistance. Understanding the pathophysiology underlying these differences could shed new light on the mechanisms leading to NAFLD in obese youth.
Preliminary data suggest that Hispanic and NHB obese youth might have a different ability to metabolize carbohydrates (CHO) through glycolysis, with Hispanics showing higher glycolysis than NHB. Therefore, Hispanics might experience a higher rated tricyclic acid cycle (TCA) and hepatic de novo lipogenesis (DNL).
In the present study, the investigators aim to address the following questions:
To address these aims, the investigators plan to recruit 30 Hispanics and 30 NHB obese youth and to measure glycolysis by using a new method to assess lactate kinetics and to determine the TCA cycle and DNL by using 13C-Propionate and D2O.
The investigators will also assess glycolysis and intrahepatic fat content in a group of 200Hispanic obese youth without fatty liver at baseline every 12 months for two years to determine whether higher glycolytic rates precede intrahepatic fat accumulation. To assess whether metabolic changes in glycolysis are driven by higher but not-pathologic glucose levels, the investigators will measure glucose changes over ten days every six months by using a continuous glucose monitoring system. If successful, these studies will provide novel insight into the pathogenesis of pediatric NAFLD and will open new avenues to test novel therapeutic approaches.
Study was paused in 2022 and reopened recruitment in November 2023.
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Patients will be followed up to assess the effect of the usual diet and physical activity on development of NAFLD
Time frame: 60 months
lactate synthesis will be measured during an oral glucose tolerance test by measuring lactate. Synthetic rates will be measured by using a mathematical model.
Contact information is provided by the study sponsor or research team.
Yale University
Other
Pathophysiologic Mechanisms Leading to Intrahepatic Fat Accumulation in Obese Youth
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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