首页> 外文期刊>Schizophrenia research >Impact of cross-disorder polygenic risk on frontal brain activation with specific effect of schizophrenia risk
【24h】

Impact of cross-disorder polygenic risk on frontal brain activation with specific effect of schizophrenia risk

机译:跨疾病多基因风险对额叶大脑激活的影响,并具有精神分裂症风险的特定作用

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Evidence suggests that there is shared genetic aetiology across the major psychiatric disorders conferred by additive effects of many common variants. Measuring their joint effects on brain function may identify common neural risk mechanisms. We investigated the effects of a cross-disorder polygenic risk score (PGRS), based on additive effects of genetic susceptibility to the five major psychiatric disorders, on brain activation during performance of a language-based executive task. We examined this relationship in healthy individuals with (n = 82) and without (n = 57) a family history of bipolar disorder to determine whether this effect was additive or interactive dependent on the presence of family history. We demonstrate a significant interaction for polygenic loading x group in left lateral frontal cortex (BA9, BA6). Further examination indicated that this was driven by a significant positive correlation in those without a family history (i.e. healthy unrelated volunteers), with no significant relationships in the familial group. We then examined the effect of the individual diagnoses contributing to the PGRS to determine evidence of disorder-specificity. We found a significant association with the schizophrenia polygenic score only, with no other significant relationships. These findings indicate differences in left lateral frontal brain activation in association with increased cross-disorder PGRS in individuals without a family history of psychiatric illness. Lack of effects in the familial group may reflect epistatic effects, shared environmental influences or effects not captured by the PGRS. The specific relationship with loading for schizophrenia is notably consistent with frontal cortical inefficiency as a circumscribed phenotype of psychotic disorders. (C) 2014 Elsevier B.V. All rights reserved.
机译:有证据表明,由于许多常见变异的累加效应,在主要的精神疾病中存在着共同的遗传病因。测量它们对大脑功能的联合影响可能会确定常见的神经风险机制。我们基于对五种主要精神疾病的遗传易感性的加和效应,研究了跨疾病多基因风险评分(PGRS)对基于语言的执行任务执行过程中大脑激活的影响。我们在有(n = 82)和没有(n = 57)躁郁症家族病史的健康个体中检查了这种关系,以确定这种作用是累加还是互动取决于家族史的存在。我们证明在左侧额叶皮层(BA9,BA6)的多基因负荷x组的重大相互作用。进一步的检查表明,这是由没有家族史的人(即健康的无亲属志愿者)之间存在显着正相关驱动的,而在家族组中则没有显着关系。然后,我们检查了有助于PGRS的个体诊断的效果,以确定疾病特异性的证据。我们发现仅与精神分裂症多基因评分存在显着关联,而没有其他显着关系。这些发现表明,在没有精神病家族史的个体中,左额额叶脑部激活与交叉性PGRS升高相关。家族性疾病缺乏影响可能反映出上位性影响,共同的环境影响或PGRS未捕获的影响。与精神分裂症负荷的具体关系特别与额叶皮质无能为精神病障碍的明确表型相一致。 (C)2014 Elsevier B.V.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号