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Reduced fronto–striatal white matter integrity in schizophrenia patients and unaffected siblings: a DTI study

BACKGROUND: Schizophrenia is characterized by impairments in the fronto–striatal network. Underlying these impairments may be disruptions in anatomical pathways connecting frontal and striatal regions. However, the specifics of these disruptions remain unclear and whether these impairments are relat...

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Autores principales: de Leeuw, Max, Bohlken, Marc M, Mandl, René C W, Kahn, René S, Vink, Matthijs
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4849442/
https://www.ncbi.nlm.nih.gov/pubmed/27336028
http://dx.doi.org/10.1038/npjschz.2015.1
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author de Leeuw, Max
Bohlken, Marc M
Mandl, René C W
Kahn, René S
Vink, Matthijs
author_facet de Leeuw, Max
Bohlken, Marc M
Mandl, René C W
Kahn, René S
Vink, Matthijs
author_sort de Leeuw, Max
collection PubMed
description BACKGROUND: Schizophrenia is characterized by impairments in the fronto–striatal network. Underlying these impairments may be disruptions in anatomical pathways connecting frontal and striatal regions. However, the specifics of these disruptions remain unclear and whether these impairments are related to the genetic vulnerability of schizophrenia is not known. METHODS: Here, we investigated fronto–striatal tract connections in 24 schizophrenia patients, 30 unaffected siblings, and 58 healthy controls using diffusion tensor imaging. Mean fractional anisotropy (FA) was calculated for tracts connecting the striatum with frontal cortex regions including the dorsolateral prefrontal cortex (DLPFC), medial orbital frontal cortex, and inferior frontal gyrus. Specifically, the striatum was divided into three subregions (caudate nucleus, putamen, and nucleus accumbens) and mean FA was computed for tracts originating from these striatal subregions. RESULTS: We found no differences between patients, siblings, and controls in mean FA when taking the whole striatum as a seed region. However, subregion analyses showed reduced FA in the tract connecting the left nucleus accumbens and left DLPFC in both patients (P=0.0003) and siblings (P=0.0008) compared with controls. CONCLUSIONS: The result of reduced FA in the tract connecting the left nucleus accumbens and left DLPFC indicates a possible reduction of white matter integrity, commonly associated with schizophrenia. As both patients and unaffected siblings show reduced FA, this may represent a vulnerability factor for schizophrenia.
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spelling pubmed-48494422016-06-22 Reduced fronto–striatal white matter integrity in schizophrenia patients and unaffected siblings: a DTI study de Leeuw, Max Bohlken, Marc M Mandl, René C W Kahn, René S Vink, Matthijs NPJ Schizophr Article BACKGROUND: Schizophrenia is characterized by impairments in the fronto–striatal network. Underlying these impairments may be disruptions in anatomical pathways connecting frontal and striatal regions. However, the specifics of these disruptions remain unclear and whether these impairments are related to the genetic vulnerability of schizophrenia is not known. METHODS: Here, we investigated fronto–striatal tract connections in 24 schizophrenia patients, 30 unaffected siblings, and 58 healthy controls using diffusion tensor imaging. Mean fractional anisotropy (FA) was calculated for tracts connecting the striatum with frontal cortex regions including the dorsolateral prefrontal cortex (DLPFC), medial orbital frontal cortex, and inferior frontal gyrus. Specifically, the striatum was divided into three subregions (caudate nucleus, putamen, and nucleus accumbens) and mean FA was computed for tracts originating from these striatal subregions. RESULTS: We found no differences between patients, siblings, and controls in mean FA when taking the whole striatum as a seed region. However, subregion analyses showed reduced FA in the tract connecting the left nucleus accumbens and left DLPFC in both patients (P=0.0003) and siblings (P=0.0008) compared with controls. CONCLUSIONS: The result of reduced FA in the tract connecting the left nucleus accumbens and left DLPFC indicates a possible reduction of white matter integrity, commonly associated with schizophrenia. As both patients and unaffected siblings show reduced FA, this may represent a vulnerability factor for schizophrenia. Nature Publishing Group 2015-04-01 /pmc/articles/PMC4849442/ /pubmed/27336028 http://dx.doi.org/10.1038/npjschz.2015.1 Text en Copyright © 2015 Schizophrenia International Research Group/Nature Publishing Group http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
de Leeuw, Max
Bohlken, Marc M
Mandl, René C W
Kahn, René S
Vink, Matthijs
Reduced fronto–striatal white matter integrity in schizophrenia patients and unaffected siblings: a DTI study
title Reduced fronto–striatal white matter integrity in schizophrenia patients and unaffected siblings: a DTI study
title_full Reduced fronto–striatal white matter integrity in schizophrenia patients and unaffected siblings: a DTI study
title_fullStr Reduced fronto–striatal white matter integrity in schizophrenia patients and unaffected siblings: a DTI study
title_full_unstemmed Reduced fronto–striatal white matter integrity in schizophrenia patients and unaffected siblings: a DTI study
title_short Reduced fronto–striatal white matter integrity in schizophrenia patients and unaffected siblings: a DTI study
title_sort reduced fronto–striatal white matter integrity in schizophrenia patients and unaffected siblings: a dti study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4849442/
https://www.ncbi.nlm.nih.gov/pubmed/27336028
http://dx.doi.org/10.1038/npjschz.2015.1
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