AUTHOR=Yeum Dabin , Renier Timothy J. , Carlson Delaina D. , Ballarino Grace A. , Lansigan Reina K. , Meyer Meghan L. , Loos Ruth J. F. , Emond Jennifer A. , Masterson Travis D. , Gilbert-Diamond Diane
TITLE=Genetic associations with neural reward responsivity to food cues in children
JOURNAL=Frontiers in Nutrition
VOLUME=11
YEAR=2024
URL=https://www.frontiersin.org/journals/nutrition/articles/10.3389/fnut.2024.1387514
DOI=10.3389/fnut.2024.1387514
ISSN=2296-861X
ABSTRACT=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.