首页> 美国卫生研究院文献>Translational Psychiatry >Markers of inflammation and stress distinguish subsets of individuals with schizophrenia and bipolar disorder
【2h】

Markers of inflammation and stress distinguish subsets of individuals with schizophrenia and bipolar disorder

机译:炎症和压力标志物区分患有精神分裂症和双相情感障碍的个体的子集

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Schizophrenia and bipolar disorder share a number of common features, both symptomatically and biologically. Abnormalities in the neuroimmune and the stress-signaling pathways have been previously identified in brains of individuals with both diseases. However, the possible relationship between abnormalities in stress and neuroimmune signaling within the cortex of people with psychotic illness has not been defined. To test the hypothesis that combined alterations in brain stress responsiveness and neuroimmune/inflammatory status are characteristic of some individuals suffering from major mental illness, we examined gene expression in the Stanley Array Cohort of 35 controls, 35 individuals with schizophrenia and 34 individuals with bipolar disorder. We used levels of 8 inflammatory-related transcripts, of which SERPINA3 was significantly elevated in individuals with schizophrenia (F(2,88)=4.137, P<0.05), and 12 glucocorticoid receptor signaling (stress) pathway transcripts previously examined, to identify two clusters of individuals: a high inflammation/stress group (n=32) and a low (n=68) inflammation/stress group. The high inflammation/stress group has a significantly greater number of individuals with schizophrenia (n=15), and a trend toward having more bipolar disorder individuals (n=11), when compared with controls (n=6). Using these subgroups, we tested which microarray-assessed transcriptional changes may be associated with high inflammatory/stress groups using ingenuity analysis and found that an extended network of gene expression changes involving immune, growth factors, inhibitory signaling and cell death factors also distinguished these groups. Our work demonstrates that some of the heterogeneity in schizophrenia and bipolar disorder may be partially explained by inflammation/stress interactions, and that this biological subtype cuts across Diagnostic and Statistical Manual of Mental Disorders (DSM)-defined categories.
机译:精神分裂症和躁郁症在症状和生物学上都有许多共同的特征。先前已经在两种疾病患者的大脑中发现了神经免疫和应激信号通路的异常。但是,尚未确定精神异常患者皮层内压力异常与神经免疫信号之间的可能关系。为了检验这一假设,即某些重大精神疾病患者的特征在于脑应激反应性和神经免疫/炎症状态的综合改变,我们在Stanley Array队列的35位对照,35位精神分裂症患者和34位双相情感障碍患者中检测了基因表达。我们使用了8种与炎症相关的转录本水平,其中SERPINA3在患有精神分裂症的患者中显着升高(F(2,88)= 4.137,P <0.05),以及先前检查过的12种糖皮质激素受体信号转导(应激)途径转录本,以鉴定两群人:高炎症/压力组(n = 32)和低炎症(n = 68)组。与对照组(n = 6)相比,高炎症/应激组的精神分裂症患者人数明显增加(n = 15),并且患有双相情感障碍的个体趋向于更多(n = 11)。使用这些亚组,我们使用独创性分析测试了哪些微阵列评估的转录变化可能与高发炎/应激组相关,并发现涉及免疫,生长因子,抑制性信号传导和细胞死亡因子的扩展的基因表达变化网络也区分了这些组。我们的工作表明,精神分裂症和双相情感障碍的某些异质性可以通过炎症/压力相互作用部分解释,并且这种生物学亚型贯穿《精神障碍诊断和统计手册》(DSM)定义的类别。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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