Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
School of Psychology, Curtin University, Perth, Western Australia, Australia.
Nat Genet. 2019 Aug;51(8):1207-1214. doi: 10.1038/s41588-019-0439-2. Epub 2019 Jul 15.
Characterized primarily by a low body-mass index, anorexia nervosa is a complex and serious illness, affecting 0.9-4% of women and 0.3% of men, with twin-based heritability estimates of 50-60%. Mortality rates are higher than those in other psychiatric disorders, and outcomes are unacceptably poor. Here we combine data from the Anorexia Nervosa Genetics Initiative (ANGI) and the Eating Disorders Working Group of the Psychiatric Genomics Consortium (PGC-ED) and conduct a genome-wide association study of 16,992 cases of anorexia nervosa and 55,525 controls, identifying eight significant loci. The genetic architecture of anorexia nervosa mirrors its clinical presentation, showing significant genetic correlations with psychiatric disorders, physical activity, and metabolic (including glycemic), lipid and anthropometric traits, independent of the effects of common variants associated with body-mass index. These results further encourage a reconceptualization of anorexia nervosa as a metabo-psychiatric disorder. Elucidating the metabolic component is a critical direction for future research, and paying attention to both psychiatric and metabolic components may be key to improving outcomes.
神经性厌食症的主要特征是低体重指数,它是一种复杂且严重的疾病,影响 0.9-4%的女性和 0.3%的男性,基于双胞胎的遗传率估计值为 50-60%。死亡率高于其他精神障碍,且预后极差。在这里,我们结合神经性厌食症遗传学倡议 (ANGI) 和精神疾病基因组学联盟(PGC-ED)进食障碍工作组的数据,对 16992 例神经性厌食症病例和 55525 名对照进行全基因组关联研究,确定了 8 个显著的位点。神经性厌食症的遗传结构反映了其临床表现,与精神障碍、身体活动以及代谢(包括血糖)、脂质和人体测量特征具有显著的遗传相关性,不受与体重指数相关的常见变异的影响。这些结果进一步鼓励将神经性厌食症重新概念化为一种代谢性精神障碍。阐明代谢成分是未来研究的一个关键方向,关注精神和代谢成分可能是改善预后的关键。