Frontiers in Nutrition (Sep 2024)

Genetic associations with neural reward responsivity to food cues in children

  • Dabin Yeum,
  • Timothy J. Renier,
  • Delaina D. Carlson,
  • Grace A. Ballarino,
  • Reina K. Lansigan,
  • Meghan L. Meyer,
  • Ruth J. F. Loos,
  • Ruth J. F. Loos,
  • Jennifer A. Emond,
  • Jennifer A. Emond,
  • Travis D. Masterson,
  • Diane Gilbert-Diamond,
  • Diane Gilbert-Diamond,
  • Diane Gilbert-Diamond

DOI
https://doi.org/10.3389/fnut.2024.1387514
Journal volume & issue
Vol. 11

Abstract

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ObjectiveTo test associations of candidate obesity-related single nucleotide polymorphisms (SNPs) and obesity polygenic risk scores (PRS) with neural reward reactivity to food cues.MethodsAfter consuming a pre-load meal, 9–12-year-old children completed a functional magnetic resonance imaging (fMRI) paradigm with exposure to food and non-food commercials. Genetic exposures included FTO rs9939609, MC4R rs571312, and a pediatric-specific obesity PRS. A targeted region-of-interest (ROI) analysis for 7 bilateral reward regions and a whole-brain analysis were conducted. Independent associations between each genetic factor and reward responsivity to food cues in each ROI were evaluated using linear models.ResultsAnalyses included 151 children (M = 10.9 years). Each FTO rs9939609 obesity risk allele was related to a higher food-cue-related response in the right lateral hypothalamus after controlling for covariates including the current BMI Z-score (p < 0.01), however, the association did not remain significant after applying the multiple testing correction. MC4R rs571312 and the PRS were not related to heightened food-cue-related reward responsivity in any examined regions. The whole-brain analysis did not identify additional regions of food-cue-related response related to the examined genetic factors.ConclusionChildren genetically at risk for obesity, as indicated by the FTO genotype, may be predisposed to higher food-cue-related reward responsivity in the lateral hypothalamus in the sated state, which, in turn, could contribute to overconsumption.Clinical trial registrationhttps://clinicaltrials.gov/study/NCT03766191, identifier NCT03766191.

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