Effects of Macronutrient Diet on Brain Activity

NCT ID: NCT02300857

Last Updated: 2019-06-06

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 72 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2014-11-30
• Study Completion Date: 2017-04-30

Brief Summary

This study will evaluate the effect of macronutrient diets on brain activity in homeostatic and mesolimbic reward regions.

Detailed Description

A question critical to the field of obesity is "what causes overweight and obese individuals to overeat?" One common explanation holds that weight gain at the population-level is caused by increases in the widespread availability of highly palatable foods. An alternative explanation is that the biological effects of the modern diet produce effects in the central nervous system and periphery that augment homeostatic and hedonic hunger. Reducing glycemic load preferentially maintains total energy expenditure during weight-loss maintenance (Ebbeling et al., 2012), and this group of investigators previously showed that in the late postprandial period, a nutrient-controlled high glycemic load vs. low glycemic load meal increases resting regional cerebral blood flow in the nucleus accumbens (Lennerz et al., 2013), part of the mesoaccumbal reward circuitry implicated in craving and addiction. However, the effects of macronutrient composition on blood flow to and activity in homeostatic and reward-related brain regions cannot be fully ascertained from studies of acute ingestion of a single macronutrient, because these do not generalize to mixed-nutrient meals consumed as part of typical American diets. Further, retrospective designs that rely on participant report of frequency of recent macronutrient ingestion and prospective designs with limited duration of diet prescription cannot address the critical question of the long-term, cumulative effects of dietary composition on brain function. Therefore, the investigators propose an approach to identifying brain responses to randomized, mixed-meal diets of varying macronutrient composition during long-term weight-loss maintenance on these diets, using arterial spin labeling (ASL) for regional cerebral blood flow (rCBF) and blood-oxygen-level-dependent (BOLD)-based functional connectivity.

To explore these outcomes, the investigators will partner with the ongoing Framingham State Food Study (NCT02068885): Following weight loss on a standard diet, 150 overweight or obese adults (aged 18 to 65 years) will be randomized to one of three weight-loss maintenance diets varying in carbohydrate to fat ratios for 20 weeks. Investigators will invite subjects already enrolled in the Framingham State Food Study to participate with a goal of enrolling 75 subjects (aiming to be equally divided per diet group following randomization to assigned test diet in the parent study). Participants will complete 1 morning visit to the MRI imaging center at Brigham and Women's Hospital approximately 14-20 weeks into the weight maintenance test diet phase. During the visit, they will undergo a fasting baseline brain imaging session, consume their assigned diet breakfast meal, and undergo a late postprandial brain imaging session. Participants will additionally provide frequent ratings of their food cravings, mood, and anxiety level throughout the visit. The main outcomes will be resting blood flow to the nucleus accumbens and connected striatal regions in the late postprandial period, with additional secondary and other outcomes including blood flow to the hypothalamus and connectivity between the hypothalamus during the late postprandial period.

Conditions

Obesity

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: SINGLE

Study Groups

Low carbohydrate diet

Group Type: ACTIVE_COMPARATOR

Low carbohydrate diet

Intervention Type: BEHAVIORAL

Feeding study. Composition (by proportion of calories): 20% carbohydrate, 60% fat, 20% protein

Moderate carbohydrate diet

Group Type: ACTIVE_COMPARATOR

Moderate carbohydrate diet

Intervention Type: BEHAVIORAL

Feeding study. Composition (by proportion of calories): 40% carbohydrate, 40% fat, 20% protein

High carbohydrate diet

Group Type: ACTIVE_COMPARATOR

High carbohydrate diet

Intervention Type: BEHAVIORAL

Feeding study. Composition (by proportion of calories): 60% carbohydrate, 20% fat, 20% protein

Interventions

Low carbohydrate diet

Feeding study. Composition (by proportion of calories): 20% carbohydrate, 60% fat, 20% protein

Intervention Type: BEHAVIORAL

Moderate carbohydrate diet

Feeding study. Composition (by proportion of calories): 40% carbohydrate, 40% fat, 20% protein

Intervention Type: BEHAVIORAL

High carbohydrate diet

Feeding study. Composition (by proportion of calories): 60% carbohydrate, 20% fat, 20% protein

Intervention Type: BEHAVIORAL

Eligibility Criteria

Inclusion Criteria

• Aged 18 to 55 years
• BMI ≥ 23 kg/m2
• BMI < 45 kg/m2 and weight ≤ 300 lbs (136 kg)
• Medical clearance from a primary care provider
• Student or employee at Framingham State University throughout enrollment in the study
• Community-based participants from the greater Framingham and Assabet Valley communities
• Willing and able to eat and drink only the foods and beverages on the study menus
• Willing to eat in the dining hall
• Willing to abstain from consuming alcohol during participation

• Body circumference of <64 in
• Willingness to undergo 2, 30-minute MRI scans

Exclusion Criteria

• Change in body weight exceeding ±10% during prior year
• Recent adherence to a special diet
• Recent adherence to a vigorous physical activity regimen (e.g., participation in a varsity sport)
• Chronic use of any medication or dietary supplement that could affect study outcomes
• Current smoking (1 cigarette in the last week)
• Heavy baseline alcohol consumption or history of binge drinking
• Physician diagnosis of a major medical/psychiatric illness or eating disorder
• Abnormal blood glucose, TSH, CBC, BUN, Creatinine
• ALT greater than 150% of the normal upper limit
• Plans for a vacation during the study that would preclude adherence to prescribed diet
• Additional exclusions for female participants: Irregular menstrual cycles; any change in birth control medication during the 3 months prior to enrollment; pregnancy or lactation during the 12 months prior to enrollment

• Previous bariatric surgery
• Other contraindications to MRI scanning (severe claustrophobia/extensive orthopedic hardware/pacemaker, cerebral aneurysm clip)

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 55 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Boston Children's Hospital

OTHER

Sponsor Role: collaborator

Nutrition Science Initiative

OTHER

Sponsor Role: collaborator

New Balance Foundation

OTHER

Sponsor Role: collaborator

Boston Medical Center

OTHER

Sponsor Role: collaborator

Framingham State University

OTHER

Sponsor Role: collaborator

Brigham and Women's Hospital

OTHER

Sponsor Role: lead

Responsible Party

Laura M. Holsen

Assistant Professor of Psychiatry

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Laura M. Holsen, Ph.D.

Role: PRINCIPAL_INVESTIGATOR

Brigham and Women's Hospital

References

Lennerz BS, Alsop DC, Holsen LM, Stern E, Rojas R, Ebbeling CB, Goldstein JM, Ludwig DS. Effects of dietary glycemic index on brain regions related to reward and craving in men. Am J Clin Nutr. 2013 Sep;98(3):641-7. doi: 10.3945/ajcn.113.064113. Epub 2013 Jun 26.

Reference Type: BACKGROUND

PMID: 23803881 (View on PubMed)

Holsen LM, Hoge WS, Lennerz BS, Cerit H, Hye T, Moondra P, Goldstein JM, Ebbeling CB, Ludwig DS. Diets Varying in Carbohydrate Content Differentially Alter Brain Activity in Homeostatic and Reward Regions in Adults. J Nutr. 2021 Aug 7;151(8):2465-2476. doi: 10.1093/jn/nxab090.

Reference Type: DERIVED

PMID: 33852013 (View on PubMed)

Related Links

http://clinicaltrials.gov/show/NCT02068885

Link to the Framingham State Food Study (parent study)

Other Identifiers

2014P001880

Identifier Type: -

Identifier Source: org_study_id