饮食失调的遗传风险因素。

Anke Hinney, Susann Friedel, Helmut Remschmidt, Johannes Hebebrand
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引用次数: 54

摘要

饮食失调如神经性厌食症和神经性贪食症涉及复杂的相互作用机制。正式的遗传研究表明,这些疾病有很大的遗传影响。饮食失调的动物模型很少。候选基因研究最初集中在血清素能和其他中枢神经递质系统以及参与体重调节的基因上。大多数研究,包括荟萃分析,都得出了否定的结果;只有一个积极的发现被独立地重复了。最近,基于有两个或更多个体患有饮食失调(神经性厌食症或神经性贪食症)的家庭的系统全基因组扫描揭示了染色体1、3和4(神经性厌食症)和10p(神经性贪食症)上的初始连锁区域。其中一个区域的精细定位导致了与神经性厌食症相关的基因的鉴定。目前对饮食失调患者的治疗还不能依赖于分子遗传学研究的结果。
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Genetic risk factors in eating disorders.

Eating disorders such as anorexia nervosa and bulimia nervosa involve complex and interacting mechanisms. Formal genetic studies suggest that there is a substantial genetic influence for these disorders. Animal models of eating disorders are scarce. Candidate gene studies have initially focused on the serotonergic and other central neurotransmitter systems and on genes involved in body weight regulation. Most of the studies, including meta-analysis, have yielded negative results; only a single positive finding has been replicated independently. Recently, systematic genome-wide scans based on families with two or more individuals with an eating disorder (anorexia nervosa or bulimia nervosa) revealed initial linkage regions on chromosomes 1, 3, and 4 (anorexia nervosa) and 10p (bulimia nervosa). Fine mapping of one of these regions led to the identification of genes where an association with anorexia nervosa was detected. Currently treatment of patients with eating disorders can not rely on results of molecular genetic studies.

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