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Neural Functioning of Feeding Centers in Obese Youth

Neural Functioning of Feeding Centers in Obese Youth

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01808846
Enrollment
51
Registered
2013-03-11
Start date
2010-07-31
Completion date
2017-02-28
Last updated
2017-04-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Insulin Resistance, Obesity

Keywords

Obesity, Insulin Resistance, functional magnetic resonance imaging, glucose, fructose, hypothalamus, neuronal circuits, feeding behavior

Brief summary

To explore whether obese adolescents with insulin resistance and relative low leptin levels exhibit functional alterations of the neuronal circuits involved in the regulation of energy metabolism and food seeking behaviors. We here propose to test the hypothesis that the reward circuitry is dysregulated in obese adolescents and is related to the degree of insulin resistance and hyperinsulinemia.

Detailed description

Functional Magnetic Resonance Imaging (fMRI) provides a non-invasive method to assess the functional pathways affected by nutrient ingestion and therefore can help answer important questions regarding potential differences in the response of brain regions involved in feeding.

Interventions

None listed

Sponsors

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
CollaboratorNIH
Yale University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
12 Years to 17 Years
Healthy volunteers
Yes

Inclusion criteria

* Obese adolescents * Good general health, * taking no medication on a chronic basis * Age 12 to 17 yrs, * in puberty (girls and boys: Tanner stage II - IV) Obese Insulin Resistant Adolescents * (BMI\> 95th) * (WBISI\<1.2 plus a low adiponectin \<6 ug/dl and * high triglyceride levels \>130mg/dl) Obese Insulin Sensitive Adolescents * (BMI\>95th) * (WBISI \>3) plus high adiponectin \>8 ug/ml and * triglyceride levels \> 80 mg/dl Girls who begin menstruating must have a negative pregnancy test during the study Eligibility criteria for healthy non-obese children and adolescents: * Brother or sister with obesity * Age 12 to 17 years * Normal fasting glucose and lipids in the child, and * normal OGTT * No use of any medication known to affect glucose, lipid metabolism and inflammation * No endocrinopathies * No use of any antipsychotic medication * BMI \>25th to \<75th ( Center for Disease Control (CDC) BMI Charts) * Minimum weight of 90lbs (CDC Growth Charts)

Exclusion criteria

* Baseline creatinine \>1.0 mg * Pregnancy * Presence of endocrinopathies (e.g. Cushing syndrome) * Cardiac or pulmonary or other significant chronic illness * Adolescents with psychiatric disorder or with substance abuse determined via self-report. * Use of anorexic agents No metal implants

Design outcomes

Primary

MeasureTime frameDescription
measure of cerebral blood flow response to glucose ingestionBaseline and 2 year follow upfmri on 3T to measure blood flow response after ingestion of glucose drink

Secondary

MeasureTime frameDescription
measure of cerebral blood flow response to fructose ingestionBaseline and 2 year follow upfmri on 3T to measure blood flow response after ingestion of fructose drink

Other

MeasureTime frameDescription
measure of BOLD signal brain reactivity to food cuesBaseline and 2 year follow upfmri on 3T to measure blood flow response to visually presented food cues

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026