Department of Child and Adolescent Psychiatry, Erasmus Medical Centre, Rotterdam, Netherlands.
Curr Top Med Chem. 2012;12(21):2393-403. doi: 10.2174/156802612805289953.
The tremendous heterogeneity in the clinical symptoms and cognitive/emotional deficits seen in patients with schizophrenia has made it challenging to determine the underlying pathogenesis of the illness. One leading hypothesis that has come to the forefront over the past several decades is that schizophrenia is caused by aberrant connectivity between brain regions. In fact, a new field of connectomics has emerged to study the effects of brain connectivity in health and illness. It is known that schizophrenia is highly heritable, although in the search for the underlying genetic factors we have only scratched the tips of the omics icebergs. One technique to help identify underlying genetic factors is the use of heritable intermediate phenotypes, or endophenotypes. Endophenotypes provide mechanisms to study the genetic underpinnings of the disorder by focusing on measureable traits that are more proximal to gene regulation and expression than are symptoms. Thus, the goal of this paper is to conduct a critical review of the evidence linking both structural and functional connectivity as an endophenotype for schizophrenia.
精神分裂症患者的临床症状和认知/情感缺陷存在巨大异质性,这使得确定该病的潜在发病机制具有挑战性。过去几十年来,一个领先的假设是,精神分裂症是由大脑区域之间的连接异常引起的。事实上,一个新的连接组学领域已经出现,用于研究大脑连接在健康和疾病中的作用。众所周知,精神分裂症具有高度遗传性,尽管在寻找潜在的遗传因素时,我们只是触及了组学冰山的一角。一种有助于识别潜在遗传因素的技术是使用可遗传的中间表型或内表型。内表型通过关注比症状更接近基因调控和表达的可测量特征,为研究疾病的遗传基础提供了机制。因此,本文的目的是对将结构和功能连接作为精神分裂症的内表型的证据进行批判性回顾。