Klump Kelly L, Mikhail Megan E, Anaya Carolina, Keel Pamela K, Culbert Kristen M, Sisk Cheryl L, Johnson Alexander, Boker Steven, Neale Micheal C, Burt S Alexandra
Department of Psychology, Michigan State University, East Lansing, MI, USA.
Department of Psychology, Florida State University, Tallahassee, FL, USA.
Psychol Med. 2024 Dec 4;54(15):1-9. doi: 10.1017/S0033291724002770.
Past studies indicate daily increases in estrogen across the menstrual cycle protect against binge-eating (BE) phenotypes (e.g. emotional eating), whereas increases in progesterone enhance risk. Two previous studies from our laboratory suggest these associations could be due to differential genomic effects of estrogen and progesterone. However, these prior studies were unable to directly model effects of daily changes in hormones on etiologic risk, instead relying on menstrual cycle phase or mean hormone levels. The current study used newly modified twin models to examine, for the first time, the effects of daily changes in estradiol and progesterone on genetic/environmental influences on emotional eating in our archival twin sample assessed across 45 consecutive days.
Participants included 468 female twins from the Michigan State University Twin Registry. Daily emotional eating was assessed with the Dutch Eating Behavior Questionnaire, and daily saliva samples were assayed for ovarian hormone levels. Modified genotype × environment interaction models examined daily changes in genetic/environmental effects across hormone levels.
Findings revealed differential effects of daily changes in hormones on etiologic risk, with increasing genetic influences across progesterone levels, and increasing shared environmental influences at the highest estradiol levels. Results were consistent across primary analyses examining all study days and sensitivity analyses within menstrual cycle phases.
Findings are significant in being the first to identify changes in etiologic risk for BE symptoms across daily hormone levels and highlighting novel mechanisms (e.g. hormone threshold effects, regulation of conserved genes) that may contribute to the etiology of BE.
既往研究表明,整个月经周期中雌激素的每日增加可预防暴饮暴食(BE)表型(如情绪化进食),而孕激素增加则会增加风险。我们实验室之前的两项研究表明,这些关联可能是由于雌激素和孕激素的基因组效应不同所致。然而,这些先前的研究无法直接模拟激素每日变化对病因风险的影响,而是依赖月经周期阶段或平均激素水平。本研究首次使用新修改的双胞胎模型,在我们连续45天评估的存档双胞胎样本中,研究雌二醇和孕激素的每日变化对情绪化进食的遗传/环境影响。
参与者包括来自密歇根州立大学双胞胎登记处的468名女性双胞胎。使用荷兰饮食行为问卷评估每日情绪化进食情况,并检测每日唾液样本中的卵巢激素水平。修改后的基因型×环境交互模型研究了激素水平上遗传/环境效应的每日变化。
研究结果揭示了激素每日变化对病因风险的不同影响,随着孕激素水平的升高,遗传影响增加,而在最高雌二醇水平时,共同环境影响增加。在检查所有研究日的主要分析和月经周期阶段内的敏感性分析中,结果是一致的。
这些发现具有重要意义,首次确定了每日激素水平下BE症状病因风险的变化,并突出了可能导致BE病因的新机制(如激素阈值效应、保守基因的调控)。