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Journal of Clinical Endocrinology & Metabolism, doi:10.1210/jc.2008-0472
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The Journal of Clinical Endocrinology & Metabolism Vol. 93, No. 9 3640-3643
Copyright © 2008 by The Endocrine Society


BRIEF REPORT

Obesity Associated Genetic Variation in FTO Is Associated with Diminished Satiety

Jane Wardle, Susan Carnell, Claire M. A. Haworth, I. Sadaf Farooqi, Stephen O'Rahilly and Robert Plomin

Health Behaviour Research Centre (J.W., S.C.), Department of Epidemiology and Public Health, University College London, London WC1E 6BT, United Kingdom; Social, Genetic, and Developmental Psychiatry Centre (C.M.A.H., R.P.), Institute of Psychiatry, King’s College London, London SE5 8AF, United Kingdom; and University of Cambridge Metabolic Research Laboratories (I.S.F., S.O.), Institute of Metabolic Science, Addenbrooke’s Hospital, Cambridge CB2 2QQ, United Kingdom

Address all correspondence and requests for reprints to: Jane Wardle, Health Behavior Research Centre, University College London, Gower Street, London WC1E 6BT, United Kingdom. E-mail: j.wardle{at}ucl.ac.uk.

Context: Polymorphisms within the FTO gene have consistently been associated with obesity across multiple populations. However, to date, it is not known whether the association between genetic variation in FTO and obesity is mediated through effects on energy intake or energy expenditure.

Objective: Our objective was to examine the association between alleles of FTO known to increase obesity risk and measures of habitual appetitive behavior.

Methods: The intronic FTO single nucleotide polymorphism (rs9939609) was genotyped in 3337 United Kingdom children in whom measures of habitual appetitive behavior had been assessed using two scales (Satiety Responsiveness and Enjoyment of Food) from the Child Eating Behaviour Questionnaire, a psychometric tool that has been validated against objective measures of food intake. Associations of FTO genotype with indices of adiposity and appetite were assessed by ANOVA.

Results: As expected, the A allele was associated with increased adiposity in this cohort and in an independent case-control replication study of United Kingdom children of similar age. AA homozygotes had significantly reduced Satiety Responsiveness scores (P = 0.008, ANOVA). Mediation analysis indicated that the association of the AA genotype with increased adiposity was explained in part through effects on Satiety Responsiveness.

Conclusions: We have used a unique dataset to examine the relationship between a validated measure of children’s habitual appetitive behavior and FTO obesity risk genotype and conclude that the commonest known risk allele for obesity is likely to exert at least some of its effects by influencing appetite.







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Copyright © 2008 by The Endocrine Society