fMRI and Ghlrein in Obesity and Binge Eating Disorder

Not Applicable

Completed

• Conditions: Obesity; Binge Eating Disorder

• Registration Number: NCT02038712
• Lead Sponsor: New York Obesity and Nutrition Research Center

Brief Summary

Binge Eating Disorder (BED) may be associated with he development of obesity. However, the pathogenesis of BED is currently unclear, thus making the development of treatment and prevention strategies for BED difficult. Differences in the mechanisms regulating food intake may go some way to reveal potential mechanisms for BED.The purpose of this study is to investigate the responses of key gut-derived hormones that are associated with the regulation of food intake and functional brain activity to food cues using fMRI in BED patients and weight matched controls.

Detailed Description

Participants will attend the laboratory on two separate occasions following an overnight fast. Following baseline measures they will be provided wither with a 600mL (600kcal) liquid meal (Fed condition) or a volume matched amount of plain water (Fasted condition) to consume within 15 min in a randomized crossover design. Blood samples will be collected for during the subsequent 120min to measure the glucose, insulin and gut hormone responses, and subjective appetite ratings will be collected. 1500mg of acetaminophen will be added to each of the test drinks so that the appearance in the blood can be used as a proxy measure of gastric emptying. Participants will then undergo a 45min brain scan to assess the responses to visual and auditory food cues.

Study Timeline

• Study Start: 2006-06
• Primary Completion: 2008-12
• Study Completion: 2013-09
• Status Verified: 2014-01
• Study First Submitted: 2014-01-10
• Study First Submitted QC: 2014-01-14
• Last Update Submitted: 2014-01-14
• Study First Posted: 2014-01-16
• Last Update Posted: 2014-01-16

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 93

Inclusion Criteria

• Age 18-65 years
• BMI 30-50 kg/m2
• Weight stable (<5% change in body weight during past 3 months)
• Right handed

Exclusion Criteria

• Smokers
• Regular use of medications
• Current or intended participation in a weight-loss program (diet or exercise)
• Females who are pregnant or lactating

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Primary Outcome Measures

Name	Time	Method
fMRI responses to food cues	45 min	Blood oxygen dependent signal (BOLD) response in exposure to auditory and visual food cues will be measured during a fMRI scan and the difference between responses in the fed condition compared with those in the fasted condition.

Secondary Outcome Measures

Name	Time	Method
Subjective appetite ratings	120 min	Subjective ratings of appetite will be collected using a visual analogue scale (VAS) at -15, 0, 10, 30, 60, 90, 120 min following the liquid test meal
Gut hormone responses	120 min	Blood samples will be collected at -15, 0, 10, 30, 60, 90, 120 min following the ingestion of the liquid test meal and analyzed to determine the gut hormone responses.