The Cerebral Microvasculature in Schizophrenia: A Laser Capture Microdissection Study
2008

The Cerebral Microvasculature in Schizophrenia: A Laser Capture Microdissection Study

Sample size: 24 publication Evidence: moderate

Author Information

Author(s): Harris Laura W., Wayland Matthew, Lan Martin, Ryan Margaret, Giger Thomas, Lockstone Helen, Wuethrich Irene, Mimmack Michael, Wang Lan, Kotter Mark, Craddock Rachel, Bahn Sabine

Primary Institution: Department of Chemical Engineering and Biotechnology, University of Cambridge, Cambridge, United Kingdom

Hypothesis

This study investigates the cerebral vascular endothelium of schizophrenia patients at the level of transcriptomics.

Conclusion

The study provides preliminary evidence of molecular alterations in the cerebral microvasculature of schizophrenia patients, suggesting a hypo-inflammatory state.

Supporting Evidence

  • Previous studies indicated impaired energy supply to the brain in schizophrenia patients.
  • Altered glucose metabolism has been observed in schizophrenia.
  • Microvascular dysfunction has been suggested as a contributing factor in schizophrenia.
  • Gene expression profiling revealed downregulation of genes involved in inflammatory processes.

Takeaway

Researchers looked at brain cells from people with schizophrenia and found some differences that might show how blood flow in the brain is affected.

Methodology

Laser capture microdissection was used to isolate microvascular endothelial cells and neurons from post mortem brain tissue, followed by RNA analysis using microarray platforms.

Potential Biases

Potential biases may arise from the post mortem nature of the samples and the technical challenges of laser capture microdissection.

Limitations

The small sample size may limit the ability to detect significant gene expression changes.

Participant Demographics

12 schizophrenia patients and 12 matched controls, with additional subjects having bipolar disorder.

Statistical Information

P-Value

p<0.05

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1371/journal.pone.0003964

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