Department of Psychiatry, University of North Carolina, Chapel Hill, North Carolina 27599, USA.
Annu Rev Clin Psychol. 2013;9:589-620. doi: 10.1146/annurev-clinpsy-050212-185546.
Over the past decade, considerable advances have been made in understanding genetic influences on eating pathology. Eating disorders aggregate in families, and twin studies reveal that additive genetic factors account for approximately 40% to 60% of liability to anorexia nervosa (AN), bulimia nervosa (BN), and binge eating disorder (BED). Molecular genetics studies have been undertaken to identify alterations in deoxyribonucleic acid sequence and/or gene expression that may be involved in the pathogenesis of disordered eating behaviors, symptoms, and related disorders and to uncover potential genetic variants that may contribute to variability of treatment response. This article provides an in-depth review of the scientific literature on the genetics of AN, BN, and BED including extant studies, emerging hypotheses, future directions, and clinical implications.
在过去的十年中,人们对遗传因素对进食障碍的影响有了更深入的了解。进食障碍在家族中聚集,双胞胎研究表明,加性遗传因素约占神经性厌食症(AN)、神经性贪食症(BN)和暴食障碍(BED)易感性的 40%至 60%。人们进行了分子遗传学研究,以确定脱氧核糖核酸序列和/或基因表达的改变,这些改变可能与异常进食行为、症状和相关障碍的发病机制有关,并揭示可能导致治疗反应变异性的潜在遗传变异。本文深入综述了 AN、BN 和 BED 的遗传学研究文献,包括现有研究、新兴假说、未来方向和临床意义。