Dopamine Release to Food Reward in Bulimia Nervosa

NCT ID: NCT03471806

Last Updated: 2018-03-21

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 40 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2018-02-16
• Study Completion Date: 2020-05-31

Brief Summary

This study will assess the role of dopamine responses to food reward in Bulimia Nervosa patients, by performing simultaneous Positron Emission Tomography (PET) and Magnetic Resonance (MR) scanning. The dopamine response will be measured before and after treatment, and will be compared to healthy controls.

Detailed Description

Bulimia nervosa is a psychiatric eating disorder characterized by recurrent episodes of binge eating, followed by inappropriate compensatory behaviour. It is associated with a high disease burden and high rates of medical and psychiatric comorbidities. Only 50% of patients achieve long-term remission, indicating the need for a better understanding of the pathophysiology which can guide the development of new treatment options.

There are strong indications for an involvement of the brain's dopaminergic reward system in Bulimia Nervosa, such as the presence of elevated craving for rewarding food and poorer impulse control. However, there is no clear evidence on the exact involvement of the reward system nor direct evidence of abnormal dopamine responses to food reward. Therefore, the current study will assess dopamine release and related brain activity to food reward in Bulimia Nervosa patients, by performing simultaneous Positron Emission Tomography (PET) and Magnetic Resonance (MR) scanning. Specifically, the investigators will compare dopamine release in Bulimia Nervosa patients to healthy controls, and assess the effect of successful treatment on the food reward response. To this end, 20 Bulimia Nervosa patients will participate in one PET-MR scan before the start of inpatient treatment and in a second PET-MR scan at the end of inpatient treatment. Additionally, PET-MR scans will be obtained from a group of 20 healthy control participants.

All scan session will measure dopamine release to a combination of anticipatory (viewing high-calorie food images) and consummatory (drinking sips of chocolate milkshake) food reward and will be conducted in a fasted state. The scan sessions will consist of four blocks with a duration of 45 minutes each and 15 minute breaks in between. The first three blocks represent the 'control condition' and the fourth block the 'food reward condition'. During both sessions, blood samples will be collected at several time points to assess levels of metabolic hormones and their relation to food-induced dopamine release.

This study aims to improve our understanding of the disease process underlying Bulimia Nervosa and to enable the identification of new and specific treatment targets at multiple levels of the gut-brain axis, including the dopamine system in the brain but also metabolic hormones and the interactions between both. Additionally, the results may have the potential to guide the optimisation of behavioural treatment approaches with a stronger focus on aberrant reward system responses.

Conditions

Bulimia Nervosa; Food Reward

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: NONE

Study Groups

Bulimia Nervosa patients

Bulimia Nervosa patient group: Assessment of dopamine release to food reward at baseline (before treatment) and to food reward after treatment.

Group Type: EXPERIMENTAL

Food reward at baseline

Intervention Type: BEHAVIORAL

Exposure to a combination of anticipatory (viewing high-calorie food images) and consummatory food reward (drinking sips of chocolate milkshake), at baseline.

Food reward after treatment

Intervention Type: BEHAVIORAL

Exposure to a combination of anticipatory (viewing high-calorie food images) and consummatory food reward (drinking sips of chocolate milkshake), at the end of inpatient treatment.

Healthy controls

Healthy control group: Assessment of dopamine release to food reward at baseline, for comparison with Bulimia Nervosa patients.

Group Type: EXPERIMENTAL

Food reward at baseline

Intervention Type: BEHAVIORAL

Exposure to a combination of anticipatory (viewing high-calorie food images) and consummatory food reward (drinking sips of chocolate milkshake), at baseline.

Interventions

Food reward at baseline

Exposure to a combination of anticipatory (viewing high-calorie food images) and consummatory food reward (drinking sips of chocolate milkshake), at baseline.

Intervention Type: BEHAVIORAL

Food reward after treatment

Exposure to a combination of anticipatory (viewing high-calorie food images) and consummatory food reward (drinking sips of chocolate milkshake), at the end of inpatient treatment.

Intervention Type: BEHAVIORAL

Eligibility Criteria

Inclusion Criteria

• Diagnosed with Bulimia Nervosa based on DSM-5 criteria;
• Admission for inpatient treatment;
• Female (on hormonal contraception);
• Dutch-speaking;
• Right-handed;
• Body Mass Index (BMI) of 18.5 - 25 kg/m².

• Healthy females (on hormonal contraception);
• Dutch-speaking;
• Right-handed;
• Stable body weight with BMI of 18.5 - 25 kg/m².

Exclusion Criteria

• Medical, neurological or other psychiatric disorders;
• Use of psychotropic medication in past 6 months;
• Use of cannabis or other drugs of abuse in past 12 months;
• Lactose-intolerance or food allergies;
• Vegetarian diet;
• Smoking;
• Consumption of more than 7 alcoholic units per week;
• Exposure to a significant amount of ionizing radiation in past 12 months;
• Claustrophobia;
• Contra-indications for Magnetic Resonance Imaging;
• Pregnancy.

Healthy control participants:

• Any psychiatric disorders;
• Emotional or restraint eating behaviour.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 50 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: Yes

Sponsors

Universitaire Ziekenhuizen KU Leuven

OTHER

Sponsor Role: lead

Responsible Party

Lukas Van Oudenhove

Associate Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Lukas Van Oudenhove, Prof. dr.

Role: PRINCIPAL_INVESTIGATOR

Universitaire Ziekenhuizen KU Leuven

Locations

Universitaire ziekenhuizen Leuven

Leuven, , Belgium

Countries

Belgium

Other Identifiers

S60362-BN

Identifier Type: -

Identifier Source: org_study_id