Tanofsky-Kraff Marian, Han Joan C, Anandalingam Kavitha, Shomaker Lauren B, Columbo Kelli M, Wolkoff Laura E, Kozlosky Merel, Elliott Camden, Ranzenhofer Lisa M, Roza Caroline A, Yanovski Susan Z, Yanovski Jack A
Unit on Growth and Obesity, Program on Developmental Endocrinology and Genetics, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Department of Health and Human Services, Bethesda, MD.
Am J Clin Nutr. 2009 Dec;90(6):1483-8. doi: 10.3945/ajcn.2009.28439. Epub 2009 Oct 14.
Children with rs9939609 FTO variant alleles (homozygous = AA and heterozygous = AT) are predisposed to greater adiposity than are those with 2 wild-type alleles (TT).
Because FTO is highly expressed in hypothalamic regions that are important for appetite, FTO genotype may affect energy balance by influencing eating behavior. Loss of control (LOC) eating, a behavior commonly reported by overweight youth, predicts excessive weight gain in children. However, the relation between FTO genotype and LOC eating has not been previously examined.
Two-hundred eighty-nine youth aged 6-19 y were genotyped for rs9939609, underwent body-composition measurements, and were interviewed to determine the presence or absence of LOC eating. A subset (n = 190) participated in a lunch buffet test meal designed to model an LOC eating episode. Subjects with AA and AT genotypes were grouped together for comparison with wild-type TT subjects.
Subjects with at least one A allele (67.7%) had significantly greater body mass indexes, body mass index z scores (P < 0.01), and fat mass (P < 0.05). Of the AA/AT subjects, 34.7% reported LOC compared with 18.2% of the TT subjects (P = 0.002). Although total energy intake at the test meal did not differ significantly by genotype (P = 0.61), AA/AT subjects consumed a greater percentage of energy from fat than did the TT subjects (P < 0.01).
Children and adolescents with 1 or 2 FTO rs9939609 obesity-risk alleles report more frequent LOC eating episodes and select foods higher in fat at a buffet meal. Both LOC eating and more frequent selection of energy-dense, palatable foods may be mechanisms through which variant FTO alleles lead to excess body weight.
携带rs9939609 FTO变异等位基因(纯合子=AA,杂合子=AT)的儿童比携带两个野生型等位基因(TT)的儿童更容易肥胖。
由于FTO在下丘脑对食欲起重要作用的区域高度表达,FTO基因型可能通过影响饮食行为来影响能量平衡。失控(LOC)饮食是超重青少年常见的一种行为,可预测儿童体重过度增加。然而,FTO基因型与LOC饮食之间的关系此前尚未得到研究。
对289名6-19岁的青少年进行rs9939609基因分型,进行身体成分测量,并通过访谈确定是否存在LOC饮食。一个子集(n = 190)参与了旨在模拟LOC饮食事件的午餐自助餐测试餐。将AA和AT基因型的受试者归为一组,与野生型TT受试者进行比较。
至少携带一个A等位基因的受试者(67.7%)的体重指数、体重指数z评分(P < 0.01)和脂肪量(P < 0.05)显著更高。在AA/AT受试者中,34.7%报告有LOC饮食,而TT受试者中这一比例为18.2%(P = 0.002)。尽管测试餐时的总能量摄入在基因型之间没有显著差异(P = 0.61),但AA/AT受试者从脂肪中摄入的能量百分比高于TT受试者(P < 0.01)。
携带1个或2个FTO rs9939609肥胖风险等位基因的儿童和青少年报告的LOC饮食事件更频繁,并且在自助餐时选择脂肪含量更高的食物。LOC饮食以及更频繁地选择能量密集、美味的食物可能是变异的FTO等位基因导致体重超标体重的机制。