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进食障碍的遗传学。

Genetics of eating disorders.

机构信息

Department of Child and Adolescent Psychiatry and Psychotherapy, University of Duisburg-Essen, Virchowstrasse 171, 45147, Essen, Germany,

出版信息

Curr Psychiatry Rep. 2013 Dec;15(12):423. doi: 10.1007/s11920-013-0423-y.

Abstract

Disordered eating behavior is the core symptom of the complex disorders anorexia nervosa and bulimia nervosa. Twin and family studies derive high heritability estimates. Hence, substantial genetic influences on the etiology can be assumed for both. Initially, candidate gene studies pertaining to the monoaminergic neurotransmitter systems and to body weight regulation comprised the core of the genetic analyses. Unfortunately, confirmed, solid findings substantiated in meta-analyses are rare, so that eventually none of these associations is unequivocal. Thus, systematic, genome-wide approaches emerged to identify genes with no a priori evidence for their involvement in eating disorders. Genome-wide association studies have hinted to formerly unknown genetic regions. However, significant genome-wide findings have not yet been reported.

摘要

饮食失调行为是复杂障碍神经性厌食症和神经性贪食症的核心症状。双胞胎和家庭研究得出了很高的遗传估计值。因此,可以假设这两种疾病的病因都有很大的遗传影响。最初,与单胺能神经递质系统和体重调节相关的候选基因研究构成了遗传分析的核心。不幸的是,经荟萃分析证实的可靠发现很少,因此这些关联都没有明确的证据。因此,出现了系统的、全基因组的方法来识别那些以前没有证据表明它们与饮食失调有关的基因。全基因组关联研究暗示了以前未知的遗传区域。然而,目前还没有报告显著的全基因组发现。

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