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基因多态性作为神经性厌食症的一个风险因素。

Genetic polymorphisms as a risk factor for anorexia nervosa.

作者信息

Sulek S, Lacinová Z, Dolinková M, Haluzik M

机构信息

Department of Paediatrics and Adolescent Medicine, Charles University in Prague, First Faculty of Medicine and General Teaching Hospital, Prague, Czech Republic.

出版信息

Prague Med Rep. 2007;108(3):215-25.

Abstract

Anorexia nervosa (AN) is an eating disorder affecting mostly young people which could lead to serious complications and consequences. There are ethnical and gender differences in the incidence and prevalence of AN, but the influence of urbanization has not yet been proved. The relationship of genetic background to the risk of AN is still being investigated. In this review we summarize current knowledge about the relationship between AN and polymorphism of substances known to be regulating eating behaviour or metabolic pathways e.g. serotonin, ghrelin, catechol-O-methyl transferase, neuropeptide Y, brain-derived neurotrophic factor and adipokines.

摘要

神经性厌食症(AN)是一种主要影响年轻人的饮食失调症,可能导致严重的并发症和后果。AN的发病率和患病率存在种族和性别差异,但城市化的影响尚未得到证实。遗传背景与AN风险之间的关系仍在研究中。在本综述中,我们总结了目前关于AN与已知调节饮食行为或代谢途径的物质(如血清素、胃饥饿素、儿茶酚-O-甲基转移酶、神经肽Y、脑源性神经营养因子和脂肪因子)多态性之间关系的知识。

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