FTO variation and early frontostriatal brain development in children

Author:

Thapaliya Gita1ORCID,Kundu Poorbita2,Jansen Elena1,Naymik Marcus A.3,Lee Richard4,Bruchhage Muriel Marisa Katharina567,D'Sa Viren6,Huentelman Matthew J.3,Lewis Candace R.38,Müller Hans‐Georg2,Deoni Sean C. L.9,Carnell Susan1,

Affiliation:

1. Division of Child and Adolescent Psychiatry, Department of Psychiatry and Behavioral Sciences Johns Hopkins University School of Medicine Baltimore Maryland USA

2. Department of Statistics University of California, Davis Davis California USA

3. Neurogenomics Division The Translational Genomics Research Institute (TGen) Phoenix Arizona USA

4. Department of Psychiatry, and Behavioral Sciences Johns Hopkins University School of Medicine Baltimore Maryland USA

5. Advanced Baby Imaging Lab Hasbro Children's Hospital, Rhode Island Hospital Providence Rhode Island USA

6. Department of Pediatrics Warren Alpert Medical School at Brown University Providence Rhode Island USA

7. Department of Psychology, Social Sciences University of Stavanger Stavanger Norway

8. School of Life Sciences Arizona State University Phoenix Arizona USA

9. Maternal, Newborn and Child Health Discovery & Tools Bill & Melinda Gates Foundation Seattle Washington USA

Abstract

AbstractObjectiveCommon obesity‐associated genetic variants at the fat mass and obesity‐associated (FTO) locus have been associated with appetitive behaviors and altered structure and function of frontostriatal brain regions. The authors aimed to investigate the influence of FTO variation on frontostriatal appetite circuits in early life.MethodsData were drawn from RESONANCE, a longitudinal study of early brain development. Growth trajectories of nucleus accumbens and frontal lobe volumes, as well as total gray matter and white matter volume, by risk allele (AA) carrier status on FTO single‐nucleotide polymorphism rs9939609 were examined in 228 children (102 female, 126 male) using magnetic resonance imaging assessments obtained from infancy through middle childhood. The authors fit functional concurrent regression models with brain volume outcomes over age as functional responses, and FTO genotype, sex, BMI z score, and maternal education were included as predictors.ResultsBootstrap pointwise 95% CI for regression coefficient functions in the functional concurrent regression models showed that the AA group versus the group with no risk allele (TT) had greater nucleus accumbens volume (adjusted for total brain volume) in the interval of 750 to 2250 days (2–6 years).ConclusionsThese findings suggest that common genetic risk for obesity is associated with differences in early development of brain reward circuitry and argue for investigating dynamic relationships among genotype, brain, behavior, and weight throughout development.

Funder

Bill and Melinda Gates Foundation

Korea National Institute of Health

National Science Foundation

Publisher

Wiley

Subject

Nutrition and Dietetics,Endocrinology,Endocrinology, Diabetes and Metabolism,Medicine (miscellaneous)

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