4.8 Article

Genome-wide expression profiling of schizophrenia using a large combined cohort

期刊

MOLECULAR PSYCHIATRY
卷 18, 期 2, 页码 215-225

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/mp.2011.172

关键词

schizophrenia; gene expression; microarray; post-mortem brain; prefrontal cortex

资金

  1. National Institutes of Health [GM076990]
  2. MIND Foundation of BC for Schizophrenia Research
  3. CIHR
  4. Michael Smith Foundation for Health Research
  5. CIHR New Investigator award
  6. Canadian Foundation for Innovation

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Numerous studies have examined gene expression profiles in post-mortem human brain samples from individuals with schizophrenia compared with healthy controls, to gain insight into the molecular mechanisms of the disease. Although some findings have been replicated across studies, there is a general lack of consensus on which genes or pathways are affected. It has been unclear if these differences are due to the underlying cohorts or methodological considerations. Here, we present the most comprehensive analysis to date of expression patterns in the prefrontal cortex of schizophrenic, compared with unaffected controls. Using data from seven independent studies, we assembled a data set of 153 affected and 153 control individuals. Remarkably, we identified expression differences in the brains of schizophrenics that are validated by up to seven laboratories using independent cohorts. Our combined analysis revealed a signature of 39 probes that are upregulated in schizophrenia and 86 that are downregulated. Some of these genes were previously identified in studies that were not included in our analysis, while others are novel to our analysis. In particular, we observe gene expression changes associated with various aspects of neuronal communication and alterations of processes affected as a consequence of changes in synaptic functioning. A gene network analysis predicted previously unidentified functional relationships among the signature genes. Our results provide evidence for a common underlying expression signature in this heterogeneous disorder. Molecular Psychiatry (2013) 18, 215-225; doi:10.1038/mp.2011.172; published online 3 January 2012

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