Neural Correlates of Reward and Symptom Expression in Anorexia Nervosa

Sponsor
University of Minnesota (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT03275545
Collaborator
(none)
79
1
53.1
1.5

Study Details

Study Description

Brief Summary

The objective of this study is to identify the patterns of brain activity in reward circuitry that promote symptoms of anorexia nervosa. This project will compare weight-restored individuals with anorexia nervosa to a non-eating disorder control group on reward brain circuitry patterns in response to typically rewarding cues (i.e., entertaining videos) and disorder-specific restrictive eating cues (i.e., low-fat food choice) using fMRI. In addition, this study will examine which neurobiological reward responses among weight-restored individuals with anorexia nervosa predict objective restrictive eating (measured by laboratory meal intake) and longitudinal risk of relapse one year later.

Condition or Disease Intervention/Treatment Phase
  • Other: No intervention

Detailed Description

Aim 1: To compare patterns of brain activity in reward circuits to typically rewarding cues and disorder-specific cues between weight-restored individuals with anorexia nervosa and non-eating disorder controls

Hypothesis 1a: Activity in reward circuitry will be elevated in response to typically rewarding cues in the non-eating disorder control group versus weight-restored anorexia nervosa group.

Hypothesis 1b: Activity in reward circuitry will be elevated in response to disorder-specific in the weight-restored anorexia nervosa group versus the non-eating disorder control group.

Aim 2: To specify the relationship between brain patterns related to reward and restrictive eating among weight-restored individuals with anorexia nervosa

Hypothesis 2a: Lower reward circuit activity in response to typically rewarding cues will predict lower test meal intake for weight-restored anorexia nervosa group versus the non-eating disorder control group.

Hypothesis 2b: Higher reward circuit activity in response to disorder-specific cues will predict lower test meal intake for the weight-restored anorexia nervosa group versus the non-eating disorder control group.

Aim 3: To identify the brain patterns in reward circuitry associated with the risk of relapse among weight-restored individuals with anorexia nervosa in the year following weight-restoration.

Hypothesis 3a: Lower reward circuit activity in response to typically rewarding cues will predict relapse in the weight-restored anorexia nervosa group.

Hypothesis 3b: Higher reward circuit activity in response to disorder-specific cues will predict relapse in the weight-restored anorexia nervosa group.

Study Design

Study Type:
Observational
Actual Enrollment :
79 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
Neural Correlates of Reward and Symptom Expression in Anorexia Nervosa
Actual Study Start Date :
Feb 28, 2018
Actual Primary Completion Date :
Jul 12, 2022
Anticipated Study Completion Date :
Aug 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Anorexia Nervosa, Weight Restored

Individuals with a recent diagnosis of anorexia nervosa (within the past 6 months), who currently have their weight in a healthy range (BMI > or = 18.5 kg/m2)

Other: No intervention
No intervention is being examined in this study

Non-eating disorder Control

Individuals without a history of an eating disorder and no current DSM-5 psychiatric diagnoses.

Other: No intervention
No intervention is being examined in this study

Outcome Measures

Primary Outcome Measures

  1. Brain activation in reward circuits [Baseline]

    Activation in regions of interest in reward brain circuitry (i.e., ventral tegmental area, nucleus accumbens) in response to typically-rewarding and disorder-specific tasks

Secondary Outcome Measures

  1. Restrictive eating [Baseline]

    Caloric consumption from a laboratory test meal

  2. Relapse [12 months]

    Relapse from anorexia nervosa, defined as: BMI < 18.5 kg/m2 and/or binge eating and/or purging > 1x/week for 3 consecutive months

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Age > 18 years old

  • Current BMI > 18.5 kg/m2

  • Ability to read and speak in English

  • Right-handed

  • Weight restored Anorexia Nervosa group: 1) DSM-5 diagnosis of AN in the past 6 months, with the exception of body image disturbance and intense fear of weight gain criteria;

  1. BMI < 18.5 kg/m2 within past 6 months
Exclusion Criteria:
  • Medical instability or current pregnancy

  • Current substance use disorder, psychosis, or bipolar-I disorder

  • Contraindication for fMRI

  • History of neurological disorder/injury (e.g., stroke; head injury with > 10 minutes loss of consciousness)

  • Food allergy that cannot be accommodated through substitutions to the laboratory test meal

  • Lacking capacity to consent

  • Non-eating disorder Control group: Current DSM-5 Axis-I diagnosis or current or past eating disorder diagnosis

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Minnesota Minneapolis Minnesota United States 55414

Sponsors and Collaborators

  • University of Minnesota

Investigators

  • Principal Investigator: Ann Haynos, PhD, University of Minnesota

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Minnesota
ClinicalTrials.gov Identifier:
NCT03275545
Other Study ID Numbers:
  • PSYCH-2017-25878
First Posted:
Sep 7, 2017
Last Update Posted:
Jul 13, 2022
Last Verified:
Jul 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 13, 2022