Brain, Obesity, Dopamine and You Study

NCT01094756 | Completed

• 1 other identifier: 75-01
• Study Type: interventional
• Target: 82
• Locations: 1 country
• Sites: 1

Brief Summary

Central dopamine is thought to play a significant role in obesity. In support of this idea, animal studies and one human positron emission tomography (PET) study have found reduced postsynaptic D2-like receptor availability in the striatum in obesity, with lower D2 receptor availability associated with higher weight. In addition, reward sensitivity and hedonic responses, known to be related to dopamine function, have also been implicated in obesity and obesity-related eating behavior. These reports have led to the concept that dopaminergic abnormalities (e.g. reduced D2-like receptors) influence reward sensitivity, leading to altered eating behaviors and eventually obesity. However, there are several critical limitations of the human D2 receptor studies that limit the strength of their conclusions and thus the interpretations and speculations embedded in literature that relies on this work. First, estimates of D2-like receptors in humans have been confounded by potential differences in endogenous dopamine release since the PET ligand (raclopride) used is known to be displaceable from receptors by endogenous dopamine. Second, failure to rigorously screen obese individuals for diabetes confounds conclusions, since diabetes has been independently associated with dopaminergic abnormalities such as reduced D2-like receptors and muted dopamine release in diabetic rats. Finally, no human studies have addressed whether reduced D2-like receptor levels are a risk factor for obesity, a consequence of engaging in obesity-related behaviors or being obese or all of the above.

Conditions

Obesity

Keywords

Obesity

Outcome Measures

Primary Outcomes (1)

• To determine the status of postsynaptic D2-like receptor binding in humans with obesity.

  To test this hypothesis, we will measure D2-like receptor binding with PET and a specific, non-competitive D2-like receptor ligand NMB in obese and lean individuals.

  1 year for each participant

Secondary Outcomes (1)

• To determine the relationship between D2-like receptor binding, reward sensitivity and hedonic response to sweet tastes.

  1 year per participant

Study Arms (2)

Obese group - Group 1

ACTIVE COMPARATOR

If you have a BMI between 33kg - 45kg and weight under 350 lbs you could be in group 1.

Dietary Supplement: meal replacements, psychotherapy, dietary education

Lean group - Group 2

NO INTERVENTION

If you have a BMI between 18.5 kg - 24.9 kg you could be in group 2.

Interventions

meal replacements, psychotherapy, dietary education DIETARY_SUPPLEMENT

After the screening and scan days are completed, obese subjects will begin a lifestyle intervention program that includes dietary (low-calorie diet) and behavioral education topics. Treatment will be provided in individual weekly sessions. Each hour-long session will be led by a behavioral counselor or registered dietitian in the Weight Management Center at Washington University. The behavioral program will use cognitive-behavioral techniques to foster adherence to diet prescriptions and to build a supportive environment for the participant. The program will emphasize strategies of self-monitoring and goal-setting, and will include problem-solving, overcoming high-risk situations for unhealthy eating, relapse prevention, and strategies for long-term weight maintenance. Handouts will be provided for study subjects to allow them to record the setting and reaching of dietary goals, as well as summarize the key points of the educational content.

Obese group - Group 1

Eligibility Criteria

• Age: 18 Years - 40 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• obese adults (BMI 33 kg - 45 kg.)
• lean adults (BMI 18.5 kg - 24.9 kg.)

You may not qualify if:

• Subjects who are:
• smokers,
• pregnant or lactating, postmenopausal,
• have diabetes or impaired oral glucose tolerance (fasting blood glucose level of \< 100 mg/dl and a 2 hour post-glucose challenge plasma glucose level of \< 140mg/dl, per ADA criteria; ADA 2004),
• significant organ system dysfunction, anemia (Hb \<10 g/dl),
• take medications that could influence the study results, any history of dopamine agonist or antagonist treatment (e.g. neuroleptics or metoclopramide),
• parkinsonism on exam,
• borderline or lower IQ (\<80 full scaled score), or
• Lean subjects will be excluded for being obese in the past (based on maximum BMI not related to pregnancy).

Sponsors & Collaborators

• Washington University School of Medicine: lead
• National Institutes of Health (NIH): collaborator

Study Sites (1)

Washington University Medical School

St Louis, Missouri, 63110, United States

Location

MeSH Terms

Conditions

Obesity

Interventions

Psychotherapy; Nutrition Assessment

Condition Hierarchy (Ancestors)

Overweight; Overnutrition; Nutrition Disorders; Nutritional and Metabolic Diseases; Body Weight; Signs and Symptoms; Pathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Behavioral Disciplines and Activities; Data Collection; Epidemiologic Methods; Investigative Techniques; Health Care Evaluation Mechanisms; Quality of Health Care; Health Care Quality, Access, and Evaluation; Epidemiologic Measurements; Public Health; Environment and Public Health

Study Officials

• Tamara Hershey, Ph.D.

  Washington University School of Medicine

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NON RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: March 17, 2010
• First Posted: March 29, 2010
• Study Start: July 1, 2010
• Primary Completion: June 1, 2015
• Study Completion: October 1, 2016
• Last Updated: November 2, 2016

Record last verified: 2016-10

Locations

US (1)