Ben-Dor David H, Laufer Neil, Apter Alan, Frisch Amos, Weizman Abraham
Research Unit, Geha Mental Health Center, POB 102, Petah Tikva 49100, Israel.
Isr J Psychiatry Relat Sci. 2002;39(4):262-70.
Anorexia nervosa (AN) is a severe psychiatric disorder, characterized by a combination of abnormal eating behavior and weight regulation with disturbances of attitudes toward body weight and shape. Prevalence is estimated at 1/1000, but with a high prevalence of the partial syndrome and a 10% mortality rate. This article reviews the findings concerning the heritability and the contributing genes of the disorder, with a focus on candidate genes. In family studies, a higher frequency of AN and BN was found among relatives of AN probands. The heritability rate was estimated at 0.71, similar to twin studies, which estimate 0.58-0.76. The search for genes responsible for the disorder focuses on the monoaminergic and peptidergic systems that are related to appetite and weight regulation. So far, for serotonin and dopamine there are no consistent findings in association studies of AN. However, in an Israeli study, an association was found between susceptibility for AN and the COMT gene, which is involved in monoamine metabolism. Another Israeli study found a relation between AN and the gene encoding for the potassium channel (hSKCa3), which is involved in regulation of neuronal activity. In the endocrine system an unequivocal finding was described of an association to the gene encoding the receptor for beta-estrogen. In the appetite and weight regulation system an association was described between AN and a marker of the uncoupling protein-2 and -3 chromosomal region, raising the likelihood that the mutation within the gene is close to a positive marker. To conclude, although there is a strong familial component in AN, so far the search for candidate genes has not been fruitful and further large scale prospective and adoption studies are needed to confirm genetic factors. We hope that relative studies using a wide genome scan, as well as subtyping the different types of AN, will bring us closer to understanding of the heritability of AN and enable the development of improved means of prevention and treatment.
神经性厌食症(AN)是一种严重的精神障碍,其特征是异常饮食行为和体重调节与对体重和体型的态度紊乱相结合。患病率估计为千分之一,但部分综合征的患病率较高,死亡率为10%。本文综述了有关该疾病遗传力和相关基因的研究结果,重点关注候选基因。在家族研究中,AN先证者的亲属中AN和BN的发生率更高。遗传率估计为0.71,与双胞胎研究相似,后者估计为0.58 - 0.76。对导致该疾病的基因的研究集中在与食欲和体重调节相关的单胺能和肽能系统。到目前为止,在AN的关联研究中,血清素和多巴胺方面没有一致的发现。然而,在一项以色列的研究中,发现AN易感性与参与单胺代谢的COMT基因之间存在关联。另一项以色列研究发现AN与编码钾通道(hSKCa3)的基因之间存在关联,该基因参与神经元活动的调节。在内分泌系统中,明确发现了与β - 雌激素受体编码基因的关联。在食欲和体重调节系统中,描述了AN与解偶联蛋白 - 2和 - 3染色体区域的一个标记之间的关联,这增加了该基因内突变接近阳性标记的可能性。总之,尽管AN有很强的家族成分,但到目前为止,对候选基因的搜索尚未取得成果,需要进一步进行大规模的前瞻性研究和收养研究来证实遗传因素。我们希望使用全基因组扫描的相关研究以及对不同类型的AN进行亚型分类,将使我们更接近理解AN的遗传力,并能够开发出更好的预防和治疗方法。