Relation of Consummatory and Anticipatory Food Reward to Obesity

Sponsor
Oregon Research Institute (Other)
Overall Status
Completed
CT.gov ID
NCT01807572
Collaborator
National Institutes of Health (NIH) (NIH)
162
1
73
2.2

Study Details

Study Description

Brief Summary

Obesity is associated with increased risk for mortality, atherosclerotic cerebrovascular disease, coronary heart disease, colorectal cancer, hyperlipidemia, hypertension, gallbladder disease, and diabetes mellitus, resulting in over 111,000 deaths annually in the United States ). In the US, 65% of adults are overweight or obese. Unfortunately, the treatment of choice for obesity (behavioral weight loss treatment) only results in a 10% reduction in body weight on average and most patients regain this weight within a few years. Further, most obesity prevention programs do not reduce risk for future weight gain. The limited success of treatment and prevention interventions may be due to an incomplete understanding of the processes that increase risk for obesity. Recent data suggest that obese adults show abnormalities in reward from food intake and anticipated food intake relative to lean adults, but the precise nature of these abnormalities is unclear and it has not been established whether these abnormalities predate obesity onset or are a consequence. It is vital to elucidate risk factors for obesity onset to advance understanding of etiological processes and determine the content of prevention and treatment programs.

The goals of this study are to (1) determine whether adolescents at high-risk for obesity, by virtue of having two obese parents, show abnormalities in reward from food intake (consummatory food reward) and anticipated reward from food intake (anticipatory food reward) compared to adolescents who are at low-risk for obesity, (2) determine whether abnormalities in consummatory and anticipatory food reward increase risk for weight gain and obesity onset, (3) examine moderators that may amplify the relations of consummatory and anticipatory food reward to unhealthy weight gain, and (4) examine changes in consummatory and anticipatory food reward in those participants who show obesity onset relative to those not showing obesity onset. Each of these goals is described in more detail below.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    162 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Relation of Consummatory and Anticipatory Food Reward to Obesity
    Study Start Date :
    Jun 1, 2009
    Actual Primary Completion Date :
    May 1, 2015
    Actual Study Completion Date :
    Jul 1, 2015

    Arms and Interventions

    Arm Intervention/Treatment
    obesity risk status

    Lean adolescents at high-risk for obesity, by virtue of parental obesity, and lean adolescents at low-risk for obesity, by virtue of lean parents.

    Outcome Measures

    Primary Outcome Measures

    1. Test whether high-risk youth show abnormalities in consummatory and anticipatory food reward relative to low-risk youth [up to 3 years]

      Using fMRI to test whether high-risk youth for obesity show differential neural responses in the striatum, and oral somatosensory and gustatory related brain regions when anticipating and during intake of a palatable food, relative to youth at low risk for obesity.

    Secondary Outcome Measures

    1. Test the hypothesis that individuals showing abnormalities in anticipatory and consummatory food reward are at increased risk for future weight gain and obesity onset over a 3-year follow-up [up to 3 years]

      Determine whether those showing hyper-brain activation during anticipation and intake of a palatable food (via fMRI) gain more body weight over a three year period.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    14 Years to 16 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • We will require that adolescents have age- and sex- adjusted standardized body mass index (BMI) scores between the 25th and 75th percentile at baseline for inclusion.

    • Low risk youth: Lean parents will have a BMI between 18 and 25.

    • High risk youth: Obese parents will have a BMI value of greater than 30.

    Exclusion Criteria:
    • Students who report contraindicators of fMRI (e.g., metal implants, braces, or pregnancy).

    • Current major psychiatric disorders (including substance use disorders, conduct disorder, oppositional defiant disorder, ADHD, major depression, bipolar disorder, panic disorder, agoraphobia, or generalized anxiety disorder)

    • Current use of analgesics and other psychoactive drugs (e.g., cocaine)

    • Serious medical complications (e.g., diabetes)

    • Relevant food allergies

    • Current smoking

    • Current weight loss dieting

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Oregon Research Institute Eugene Oregon United States 97403

    Sponsors and Collaborators

    • Oregon Research Institute
    • National Institutes of Health (NIH)

    Investigators

    • Principal Investigator: Eric Stice, PhD, Oregon Research Institute

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Oregon Research Institute
    ClinicalTrials.gov Identifier:
    NCT01807572
    Other Study ID Numbers:
    • DK080760-01
    First Posted:
    Mar 8, 2013
    Last Update Posted:
    Oct 1, 2015
    Last Verified:
    Sep 1, 2015
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 1, 2015