Wardle Jane, Carnell Susan, Haworth Claire M A, Farooqi I Sadaf, O'Rahilly Stephen, Plomin Robert
Health Behavior Research Centre, University College London, Gower Street, London WC1E 6BT, United Kingdom.
J Clin Endocrinol Metab. 2008 Sep;93(9):3640-3. doi: 10.1210/jc.2008-0472. Epub 2008 Jun 26.
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.
Our objective was to examine the association between alleles of FTO known to increase obesity risk and measures of habitual appetitive behavior.
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.
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.
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.
FTO基因内的多态性在多个人群中一直与肥胖相关。然而,迄今为止,尚不清楚FTO基因变异与肥胖之间的关联是否通过对能量摄入或能量消耗的影响来介导。
我们的目的是研究已知会增加肥胖风险的FTO等位基因与习惯性食欲行为指标之间的关联。
对3337名英国儿童的FTO内含子单核苷酸多态性(rs9939609)进行基因分型,这些儿童使用儿童饮食行为问卷中的两个量表(饱腹感反应和食物享受度)对习惯性食欲行为进行了评估,该问卷是一种经过验证的与食物摄入量客观测量相对照的心理测量工具。通过方差分析评估FTO基因型与肥胖和食欲指标之间的关联。
正如预期的那样,在该队列以及一项针对年龄相仿的英国儿童的独立病例对照重复研究中,A等位基因与肥胖增加有关。AA纯合子的饱腹感反应得分显著降低(P = 0.008,方差分析)。中介分析表明,AA基因型与肥胖增加之间的关联部分是通过对饱腹感反应的影响来解释的。
我们使用了一个独特的数据集来研究儿童习惯性食欲行为的有效测量指标与FTO肥胖风险基因型之间的关系,并得出结论,肥胖最常见的已知风险等位基因可能至少部分通过影响食欲发挥作用。