Recent advances in postmortem pathology and neurochemistry in schizophrenia
Current Opinion in Psychiatry, ISSN: 0951-7367, Vol: 22, Issue: 2, Page: 154-160
2009
- 44Citations
- 44Captures
- 1Mentions
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations44
- Citation Indexes44
- 44
- CrossRef41
- Captures44
- Readers44
- 44
- Mentions1
- References1
- Wikipedia1
Review Description
Purpose of review This is a review examining recent data from the study of the postmortem central nervous system (CNS) of patients with schizophrenia. Recent findings Studies on the human CNS transcriptome suggest changes in pro-inflammatory pathways and myelination in schizophrenia, whereas changes in the proteome suggest that pathways involved in energy and metabolism may be particularly stressed. There appear to be complex changes in the expression of proposed candidate genes for schizophrenia such as NRG1, DISC1, RGS4 and DTNB1, and there are continued reports of alterations in central gamma-aminobutyric acidergic, dopaminergic, glutamatergic and cholinergic pathways in patients with the disorder. Data on epigenetic mechanisms and transcriptome regulation suggest that at least some changes in gene expression may be due to changes in levels of gene promoter methylation or microRNAs in the CNS of patients with schizophrenia. Summary Postmortem CNS studies have begun to unravel changes in the epigenetic regulation of gene expression that may be central to how gene-environment interactions contribute to the onset of schizophrenia. In addition, a recent study indicates that it is possible to use biomarkers to segregate the syndrome of schizophrenia into more biologically homogeneous populations, which should decrease the biological complexity observed within that group within the schizophrenia syndrome. © 2009 Wolters Kluwer Health|Lippincott Williams & Wilkins.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=62349095315&origin=inward; http://dx.doi.org/10.1097/yco.0b013e328323d52e; http://www.ncbi.nlm.nih.gov/pubmed/19553869; http://journals.lww.com/00001504-200903000-00006; http://content.wkhealth.com/linkback/openurl?sid=WKPTLP:landingpage&an=00001504-200903000-00006; https://dx.doi.org/10.1097/yco.0b013e328323d52e; https://insights.ovid.com/crossref?an=00001504-200903000-00006
Ovid Technologies (Wolters Kluwer Health)
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