The influence of food insecurity on reward neurobiology in children

Information

  • Research Project
  • 10287136
  • ApplicationId
    10287136
  • Core Project Number
    R21DA054438
  • Full Project Number
    1R21DA054438-01
  • Serial Number
    054438
  • FOA Number
    PA-20-195
  • Sub Project Id
  • Project Start Date
    9/1/2021 - 3 years ago
  • Project End Date
    8/31/2023 - a year ago
  • Program Officer Name
    FEDOTA, JOHN RAPHAEL
  • Budget Start Date
    9/1/2021 - 3 years ago
  • Budget End Date
    8/31/2022 - 2 years ago
  • Fiscal Year
    2021
  • Support Year
    01
  • Suffix
  • Award Notice Date
    8/16/2021 - 3 years ago

The influence of food insecurity on reward neurobiology in children

Project Summary Food insecurity (FI) ? i.e., the ?lack of consistent access to enough food for an active and healthy life? - is a relatively common type of adversity in the United States and one which disproportionately impacts families in rural counties (e.g., ~17% of rural families experience FI, compared to ~10% of all US families). FI is associated with an increased risk for substance use (SU) in adults and adolescence and SU risk is also generally greater for adolescents in rural areas, compared to their urban and suburban peers. While a causal link between FI and SUD liability has not been established, prior work supports the postulation that the experience of FI might increase the risk for SU via an impact on the neural substrates of reward processing. For example, of the key components of FI (i.e., acute and repeated food deprivation and associated hunger, stress, and poor nutrition), stress and poor nutrition have been shown to influence SU-relevant neurodevelopmental trajectories, while food deprivation in children impacts neural processing for food rewards. Furthermore, in adult humans and animal models, food deprivation increases reward sensitivity and risky decision-making for primary and secondary rewards and increases drug-seeking and craving via functional alterations in reward network areas in the brain (i.e., mesocorticolimbic regions). To more fully understand how food deprivation in the context of FI might influence reward processes, this developmental study will examine whether states of acute food deprivation that are sufficient to cause subjective feelings of hunger enhance sensitivity for food and non-food rewards and increase risky decision-making (Aim 1). Moreover, we will consider how associations between food deprivation and the neural substrates of reward processing are impacted by FI (Aim 2) and whether FI mediates the associations between related factors (e.g., SES) and reward processes (Aim 3) To address these aims, children (8-10 years old) from food secure (N=30) and insecure (N=30) households in rural PA will undergo a counter-balanced, repeated measures fMRI paradigm, once while food deprived (i.e., fasted) and once after a meal sufficient to satiate them (i.e., fed). We will focus on children in order to minimize the impact of aspects of adolescence that might also influence these processes and confound our results (e.g., SU, puberty). During fMRI participants will complete 2 versions of a reward task in which they will make reward-related decisions (i.e., placing a bet of varying magnitude) for food (i.e., candy) and non-food (i.e., money) rewards Data analyses will model the impacts of food deprivation (fasted/fed; Aim 1) and food security status (secure/insecure; Aim 2) on reward neurobiology. Mediation analysis will consider the relative contributions of FI vs. SES (Aim 3) and exploratory analysis will consider potential moderators of FI-related effects (i.e., stress, nutrition, chronicity of FI; Aim 4). By considering whether food deprivation in the context of FI drives functional alterations in reward processes, this exploratory R21 study will constitute a critical first step in identifying pathways by which FI drives SU-liability.

IC Name
NATIONAL INSTITUTE ON DRUG ABUSE
  • Activity
    R21
  • Administering IC
    DA
  • Application Type
    1
  • Direct Cost Amount
    150000
  • Indirect Cost Amount
    87285
  • Total Cost
    237285
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    279
  • Ed Inst. Type
    SCH ALLIED HEALTH PROFESSIONS
  • Funding ICs
    NIDA:237285\
  • Funding Mechanism
    Non-SBIR/STTR RPGs
  • Study Section
    ARM
  • Study Section Name
    Addiction Risks and Mechanisms Study Section
  • Organization Name
    PENNSYLVANIA STATE UNIVERSITY-UNIV PARK
  • Organization Department
    MISCELLANEOUS
  • Organization DUNS
    003403953
  • Organization City
    UNIVERSITY PARK
  • Organization State
    PA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    168021503
  • Organization District
    UNITED STATES