Children's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario, Canada.
University of Ottawa, Ottawa, Ontario, Canada; Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Nutrition. 2019 May;61:208-212. doi: 10.1016/j.nut.2018.11.006. Epub 2018 Nov 22.
The genetics of binge-eating disorder (BED) is an emerging topic and one candidate pathway, namely the fat mass and obesity-associated (FTO) gene, may be implicated because of its role in food reward sensitivity and self-regulation of eating. The aims of this study were to examine the independent effects of variants of FTO on binge frequency in women with and without BED and to examine the moderating role of interpersonal attachment in this association.
Secondary data analysis was conducted on a cross-sectional comparison of three groups of women in a trial of group treatment for BED: BED with obesity (n = 73), BED without obesity (n = 55), and normal weight without BED (n = 50). Women were genotyped for five of the most common FTO single-nucleotide polymorphisms, rs9939609, rs8050136, rs3751812, rs1421085, and rs1121980, which have been related to body mass index and energy intake. Binge frequency (Eating Disorder Examination), body composition (bioelectric impedance), and attachment (Attachment Style Questionnaire) were assessed.
There were no significant between-group differences for frequencies of FTO alleles, nor were there any significant anthropometric associations. The FTO × attachment interaction was significant whereby, relative to a low-risk FTO genotype, individuals with a high-risk genotype for the SNP rs1421085 and high-avoidant attachment had higher mean binge frequency than those with high genetic risk but low-avoidant attachment (β = -7.96; t = -2.07; P = 0.042).
FTO genotypes associated with risk for obesity and loss of control of eating, specifically rs1421085, may interact with insecure attachment in a way that may exacerbate binge eating among women with BED.
暴食障碍(BED)的遗传学是一个新兴的研究课题,一种候选途径,即脂肪量和肥胖相关(FTO)基因,可能与其在食物奖励敏感性和进食自我调节中的作用有关而受到牵连。本研究的目的是检验 FTO 变体对有或无 BED 的女性 binge 频率的独立影响,并检验人际依恋在这种关联中的调节作用。
对 BED 团体治疗试验中三组女性的横断面比较进行二次数据分析:肥胖 BED 组(n=73)、非肥胖 BED 组(n=55)和正常体重无 BED 组(n=50)。女性对五个最常见的 FTO 单核苷酸多态性(rs9939609、rs8050136、rs3751812、rs1421085 和 rs1121980)进行基因分型,这些多态性与体重指数和能量摄入有关。评估 binge 频率(饮食失调检查)、身体成分(生物电阻抗)和依恋(依恋风格问卷)。
FTO 等位基因的组间差异无统计学意义,也没有任何显著的人体测量关联。FTO×依恋的相互作用具有统计学意义,即与低风险 FTO 基因型相比,SNP rs1421085 高风险基因型和高回避依恋的个体比高遗传风险但低回避依恋的个体有更高的平均 binge 频率(β=-7.96;t=-2.07;P=0.042)。
与肥胖和失控性进食风险相关的 FTO 基因型,特别是 rs1421085,可能与不安全依恋相互作用,从而加剧 BED 女性的 binge 进食。