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Schizophrenia Bulletin Advance Access originally published online on May 7, 2007
Schizophrenia Bulletin 2008 34(1):72-92; doi:10.1093/schbul/sbm034
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© The Author 2007. Published by Oxford University Press on behalf of the Maryland Psychiatric Research Center. All rights reserved. For permissions, please email: journals.permissions@oxfordjournals.org.

Disturbed Structural Connectivity in Schizophrenia—Primary Factor in Pathology or Epiphenomenon?

Andreas Konrad1,2 and Georg Winterer3
2 Department of Psychiatry, Johannes Gutenberg-University, Untere Zahlbacher Strasse 8, 55131 Mainz, Germany
3 Department of Psychiatry, Heinrich-Heine University, Duesseldorf, Germany

1 To whom correspondence should be addressed; tel: +49-6131-17-2920, fax: +49-6131-17-6690, e-mail: andreas_konrad{at}gmx.de.

Indirect evidence for disturbed structural connectivity of subcortical fiber tracts in schizophrenia has been obtained from functional neuroimaging and electrophysiologic studies. During the past few years, new structural imaging methods have become available. Diffusion tensor imaging and magnetization transfer imaging (MTI) have been used to investigate directly whether fiber tract abnormalities are indeed present in schizophrenia. To date, findings are inconsistent that may express problems related to methodological issues and sample size. Also, pathological processes detectable with these new techniques are not yet well understood. Nevertheless, with growing evidence of disturbed structural connectivity, myelination has been in the focus of postmortem investigations. Several studies have shown a significant reduction of oligodendroglial cells and ultrastructural alterations of myelin sheats in schizophrenia. There is also growing evidence for abnormal expression of myelin-related genes in schizophrenia: Neuregulin (NRG1) is important for oligodendrocyte development and function, and altered expression of erbB3, one of the NRG1 receptors, has been shown in schizophrenia patients. This is consistent with recent genetic studies suggesting that NRG1 may contribute to the genetic risk for schizophrenia. In conclusion, there is increasing evidence from multiple sides that structural connectivity might be pathologically changed in schizophrenia illness. Up to the present, however, it has not been possible to decide whether alterations of structural connectivity are intrinsically linked to the primary risk factors for schizophrenia or to secondary downstream effects (ie, degeneration of fibers secondarily caused by cortical neuronal dysfunction)—an issue that needs to be clarified by future research.

Keywords: postmortem / myelination / oligodendrocytes / neuregulin


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