Association of eating behaviour with clock gene polymorphism 3111 T > C in children based on nutritional status

M. Valladares*, J. P. Chaput, S. Vásquez, C. Pino, A. M. Obregón

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

3 Scopus citations

Abstract

Background: The CLOCK (circadian locomotor output cycle kaput) gene is a central regulator of circadian rhythm. The CLOCK gene has been related to energy intake and therefore to nutritional status. However, its specific associations with aspects of food behaviour in children have been scarcely investigated. Aim: To determine the association between the CLOCK gene polymorphism 3111 T > C and eating behaviours in children based on nutritional status. Methods: A cross-sectional study of the association between a CLOCK gene variant and eating behaviour in children (n = 256) was performed. Eating behaviour was evaluated by the Child Eating Behaviour Questionnaire (CEBQ). In addition, the genotype of the CLOCK 3111 T > C (TT, CC, TC) gene polymorphism and BMI were determined. Results: The obese carriers of the C allele of the polymorphism had lower scores in the dimensions “response to satiety” and “slowness to eat” (p < 0.001), both of which constitute an anti-intake dimension and are related to food satiety. Conclusions: The C allele CLOCK gene could be considered a genetic risk factor for satiety-altered eating behaviour dimensions.

Original languageEnglish
Pages (from-to)76-80
Number of pages5
JournalAnnals of Human Biology
Volume47
Issue number1
DOIs
StatePublished - 2020

Bibliographical note

Publisher Copyright:
© 2019, © 2019 Informa UK Limited, trading as Taylor & Francis Group.

ASJC Scopus subject areas

  • Epidemiology
  • Physiology
  • Aging
  • Genetics
  • Public Health, Environmental and Occupational Health

Fingerprint

Dive into the research topics of 'Association of eating behaviour with clock gene polymorphism 3111 T > C in children based on nutritional status'. Together they form a unique fingerprint.

Cite this