Pinheiro Andrea Poyastro, Root Tammy, Bulik Cynthia M
Department of Psychiatry, University of North Carolina at Chapel Hill.
Int J Child Adolesc health. 2009;2(2):153-164.
Anorexia nervosa is a perplexing illness with the highest mortality rate of any psychiatric disease. In this paper, we review the genetic research on anorexia nervosa (AN). Family studies have demonstrated that anorexia nervosa is familial, and twin studies have indicated that additive genetic factors contribute to the familial aggregation. Molecular genetic research, including genomewide linkage and case control association studies, have not been successful in identifying DNA variants that are unequivocally involved in the etiology of AN. We provide a critical appraisal of these studies and discuss methodological issues that may be implicated in conflicting results. Furthermore, we discuss issues relevant to genetic research such as the importance of phenotypic refinement, the use of endophenotypes, and the implications for nosology and genetic analysis. Finally, the future of genetic research for AN is discussed in terms of genomewide association studies (GWAS) and the need for establishing large samples.
神经性厌食症是一种令人困惑的疾病,在所有精神疾病中死亡率最高。在本文中,我们回顾了神经性厌食症(AN)的遗传学研究。家族研究表明神经性厌食症具有家族性,而双胞胎研究表明加性遗传因素导致了家族聚集。分子遗传学研究,包括全基因组连锁和病例对照关联研究,尚未成功识别出明确参与AN病因的DNA变异。我们对这些研究进行了批判性评估,并讨论了可能与相互矛盾的结果相关的方法学问题。此外,我们还讨论了与遗传学研究相关的问题,如表型细化的重要性、内表型的使用以及对疾病分类学和遗传分析的影响。最后,从全基因组关联研究(GWAS)以及建立大样本的必要性方面讨论了AN遗传学研究的未来。