Identifying successful methods for reducing long-term energy intake continues to be a challenge in obesity treatment. Basic behavioral research has found that the rate of habituation (i.e., rate of reduction in physiological and behavioral responding) to food is related to amount of food consumed, and faster habituation rates reduce food intake. The rate of habituation to food can be accelerated when variety in foods is limited, producing decreased intake. Thus, a dietary prescription that limits variety of high-energy-dense (RED) foods may boost ability to reduce long-term energy intake, enhancing long-term weight loss. Furthermore, habituation rates to food show large individual variability. Individuals with overweight habituate slower to food than individuals with a healthy weight, and slower habituation rates predict greater increases in child standardized body mass index. Thus, slower habituation rates to food may be a behavioral phenotype for increased risk of suboptimal weight outcomes. Obesity interventions that accelerate habituation to food may then be more beneficial for those with this behavioral phenotype. We have been conducting a line of translational research that applies habituation theory to obesity treatment, involving: 1) studies systematically testing basic concepts to better inform intervention development; 2) ?proof-of-concept? testing; and 3) efficacy trials. The long-term goal is to develop a dietary prescription that harnesses habituation as a mechanism for reducing long-term energy intake. We have piloted a limited variety prescription (limited variety of RED foods) within a 6-month family-based behavioral obesity treatment (FBT) for children. Twenty-four families, with a child > 85th percentile body mass index (BMI) and aged 8 to 12 years, were randomized to FBT or to FBT that included a limited dietary variety prescription (FBT+Variety). At 6-months children in FBT+Variety had a significantly greater reduction in percent overweight than those in FBT (?15.4% vs.? 8.9%). Research is needed to examine if limiting variety improves long-term weight loss, if this improvement is due to enhanced habituation, and explore if there is a behavioral phenotype that more greatly benefits from this dietary approach. We plan to implement a novel limited food variety prescription within a 24-month FBT to examine its effect on 24-month BMI. One hundred fifty-six children aged 8 to 12 years at > 85th percentile BMI will be randomized to one of two, 24- month interventions compared in our 6-month pilot study: FBT or FBT+Variety. Child and adult caregiver assessments will occur at 0, 6, 12, 18, and 24 months on anthropometrics, dietary intake, and habituation. We will determine: 1) the influence of FBT+Variety on long-term weight loss; and 2) the influence of FBT+Variety on long-term habituation and if habituation rate mediates differences in dietary intake and BMI between conditions. We will explore if the behavioral phenotype can be used to identify who benefits most from the limited variety prescription to better individualize treatment (?precision medicine?).

Public Health Relevance

Basic behavioral research on factors that influence eating provides novel obesity treatment targets to enhance long-term diet and weight outcomes. One such behavioral mechanism is rate of habituation of physiological (i.e., salivation) and psychological (i.e., motivation to eat) responding to food, which is accelerated with limited food variety. This project will test a limited variety dietary prescription delivered to children within a family- based behavioral childhood obesity intervention to determine if limiting variety improves weight loss through accelerating habituation, if this approach can improve long-term weight loss, and if there is a behavioral phenotype that more greatly benefits from this dietary approach.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK121360-03
Application #
10104491
Study Section
Clinical and Integrative Diabetes and Obesity Study Section (CIDO)
Program Officer
Osganian, Voula
Project Start
2019-03-01
Project End
2024-02-28
Budget Start
2021-03-01
Budget End
2022-02-28
Support Year
3
Fiscal Year
2021
Total Cost
Indirect Cost
Name
University of Tennessee Knoxville
Department
Nutrition
Type
Sch Allied Health Professions
DUNS #
003387891
City
Knoxville
State
TN
Country
United States
Zip Code
37996