Klump Kelly L, Culbert Kristen M, O'Connor Shannon, Fowler Natasha, Burt S Alexandra
Department of Psychology, Michigan State University, East Lansing, Michigan.
Department of Psychology, University of Nevada, Las Vegas, Nevada.
Int J Eat Disord. 2017 Aug;50(8):984-989. doi: 10.1002/eat.22727. Epub 2017 May 31.
Recent data show significant phenotypic and genetic associations between ovarian hormones and binge eating in adulthood. Theories of hormonal risk focus on puberty and the possibility that hormone activation induces changes in genetic effects that then lead to differential risk for binge eating in postpuberty and adulthood. Although this theory is difficult to test in humans, an indirect test is to examine whether genetic influences on binge eating increase during the pubertal period in girls. Prior work has shown pubertal increases in genetic influences on overall disordered eating symptoms, but no study to date has examined binge eating. The present study was the first to examine these increases for binge eating.
Participants included 1,568 female twins (aged 8-25 years) from the Michigan State University Twin Registry. Binge eating and pubertal development were assessed with self-report questionnaires.
Twin moderation models showed significant linear increases in genetic effects from prepuberty (5%) to postpuberty (42%), even after controlling for the effects of age and body mass index.
Results provide critical support for increased genetic influences on binge eating during puberty. Additional studies are needed to identify hormonal mechanisms and fully test contemporary models of ovarian hormone risk.
近期数据显示,成年期卵巢激素与暴饮暴食之间存在显著的表型和遗传关联。激素风险理论聚焦于青春期,以及激素激活可能引发基因效应变化,进而导致青春期后及成年期暴饮暴食风险差异的可能性。尽管这一理论难以在人类身上进行验证,但一种间接验证方法是检验女孩青春期期间基因对暴饮暴食的影响是否增加。此前的研究表明,基因对总体饮食失调症状的影响在青春期会增加,但迄今为止尚无研究考察暴饮暴食情况。本研究首次对暴饮暴食的这种增加情况进行了考察。
研究对象包括来自密歇根州立大学双胞胎登记处的1568名女性双胞胎(年龄8 - 25岁)。通过自我报告问卷评估暴饮暴食和青春期发育情况。
双胞胎调节模型显示,即使在控制了年龄和体重指数的影响后,从青春期前(5%)到青春期后(42%),基因效应仍有显著的线性增加。
研究结果为青春期基因对暴饮暴食影响增加提供了关键支持。需要进一步研究以确定激素机制,并全面验证当代卵巢激素风险模型。