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Clinical Trial Summary

The goal of this study is to understand the role of brain glucose transport in individuals with obesity and the association with cerebral hypometabolism and these individuals' response to plasma glucose elevations. The main premise is that obesity leads to reduced brain glucose transport and that we can measure this reduction with magnetic resonance spectroscopy (MRS). The secondary premises are that this reduction is driven by elevated non esterified fatty acids which act to turn on specific signaling pathways that regulate brain GLUT1 levels.


Clinical Trial Description

There are 2 aims of this study. The intent of aim 1 is to measure the effect of obesity on glucose transport and metabolism in the human brain. This study aim will be conducted in non-diabetic, obese individuals and age- and HbA1c-matched normal weight individuals. A total of 15 non-diabetic - normal weight individuals and 15 obese individuals will be enrolled. The second aim randomizes 40 non-diabetic, normal weight individuals. The intent of aim 2 is to determine whether acute elevation of NEFA levels in lean, healthy individuals will alter cerebral glucose transport. Eligible participants will be randomized (1:1) to receive either intralipid or normal saline. The focus of this protocol registration is the randomized portion of the study (aim 2). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04328337
Study type Interventional
Source University of North Carolina, Chapel Hill
Contact Joseph Palmiotto
Phone 919-966-9184
Email joseph_palmiotto@med.unc.edu
Status Recruiting
Phase Phase 1/Phase 2
Start date December 8, 2020
Completion date June 1, 2025

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