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关于神经性厌食症遗传学的当代观点。

Contemporary views on the genetics of anorexia nervosa.

作者信息

Shih Pei-an Betty, Woodside D Blake

机构信息

Department of Psychiatry, University of California, San Diego, 9500 Gilman Drive #0664, La Jolla, CA 92093-0664, USA.

Inpatient Eating Disorders Service, Toronto General Hospital, Canada; Department of Psychiatry, University of Toronto, Canada.

出版信息

Eur Neuropsychopharmacol. 2016 Apr;26(4):663-73. doi: 10.1016/j.euroneuro.2016.02.008. Epub 2016 Feb 20.

Abstract

Anorexia nervosa (AN) is a serious mental illness characterized by severe dietary restriction that leads to high rates of morbidity, chronicity, and mortality. Unfortunately, effective treatment is lacking and few options are available. High rates of familial aggregation and significant heritability suggested that the complex etiology of AN is affected by both genetic and environmental factors. In this paper, we review studies that reported common and rare genetic variation that influence susceptibility of AN through candidate gene studies, genome-wide association studies, and sequencing-based studies. We also discuss gene expression, methylation, imaging genetics, and pharmacogenetics to demonstrate that these studies have collectively advanced our knowledge of how genetic variation contributes to AN susceptibility and clinical course. Lastly, we highlight the importance of gene by environment interactions (G×E) and share our enthusiasm for the use of nutritional genomic approaches to elucidate the interaction among nutrients, metabolic intermediates, and genetic variation in AN. A deeper understanding of how nutrition alters genome stability, how genetic variation influences uptake and metabolism of nutrients, and how response to food components affects disordered eating, will lead to personalized dietary interventions and effective nutraceutical and pharmacological treatments for AN.

摘要

神经性厌食症(AN)是一种严重的精神疾病,其特征为严重的饮食限制,可导致高发病率、慢性病程及死亡率。遗憾的是,目前缺乏有效的治疗方法,且治疗选择有限。较高的家族聚集率和显著的遗传度表明,AN复杂的病因受到遗传和环境因素的共同影响。在本文中,我们回顾了通过候选基因研究、全基因组关联研究及基于测序的研究报道的影响AN易感性的常见和罕见遗传变异的相关研究。我们还讨论了基因表达、甲基化、影像遗传学和药物遗传学,以证明这些研究共同推进了我们对于遗传变异如何影响AN易感性及临床病程的认识。最后,我们强调基因与环境相互作用(G×E)的重要性,并分享我们对于运用营养基因组学方法来阐明AN中营养素、代谢中间体及遗传变异之间相互作用的热情。深入了解营养如何改变基因组稳定性、遗传变异如何影响营养素的摄取和代谢,以及对食物成分的反应如何影响饮食失调,将有助于为AN制定个性化饮食干预措施以及有效的营养补充剂和药物治疗方法。

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