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Reduced fractional anisotropy in patients with major depressive disorder and associations with vascular stiffness

Previous studies revealed several alterations of the cerebral white matter in patients with major depressive disorder. However, it is unknown if these alterations are associated with vascular changes in the brain and other body parts. We compared diffusion tensor imaging derived fractional anisotrop...

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Autores principales: Hermesdorf, Marco, Berger, Klaus, Szentkirályi, András, Schwindt, Wolfram, Dannlowski, Udo, Wersching, Heike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5279701/
https://www.ncbi.nlm.nih.gov/pubmed/28180073
http://dx.doi.org/10.1016/j.nicl.2017.01.013
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author Hermesdorf, Marco
Berger, Klaus
Szentkirályi, András
Schwindt, Wolfram
Dannlowski, Udo
Wersching, Heike
author_facet Hermesdorf, Marco
Berger, Klaus
Szentkirályi, András
Schwindt, Wolfram
Dannlowski, Udo
Wersching, Heike
author_sort Hermesdorf, Marco
collection PubMed
description Previous studies revealed several alterations of the cerebral white matter in patients with major depressive disorder. However, it is unknown if these alterations are associated with vascular changes in the brain and other body parts. We compared diffusion tensor imaging derived fractional anisotropy in a well characterized sample of middle-aged patients with major depressive disorder (n = 290) and never-depressed controls (n = 346) by the method of tract-based spatial statistics. Subsequently, the potential role of pulse wave velocity as a mediator of depression- and age-related changes in extracted estimates of fractional anisotropy were analyzed. The results of the tract-based analysis revealed significantly reduced fractional anisotropy in the left posterior thalamic radiation associated with depression. Analyses of extracted data indicated additional reductions of fractional anisotropy bilaterally in the posterior thalamic radiation and in the left sagittal stratum. The analyses of indirect effects did not show any significant mediation of depression-related effects on fractional anisotropy via pulse wave velocity. However, age-related effects on fractional anisotropy were partially mediated by pulse wave velocity. In conclusion, major depressive disorder is associated with detrimental effects on cerebral white matter microstructure properties which are independent of vascular changes, as measured by pulse wave velocity. However, a portion of age-related detrimental effects on white matter is explained by vascular changes. Longitudinal studies are required for investigating changes in white matter and vascular parameters over time and their association with incident depression.
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spelling pubmed-52797012017-02-08 Reduced fractional anisotropy in patients with major depressive disorder and associations with vascular stiffness Hermesdorf, Marco Berger, Klaus Szentkirályi, András Schwindt, Wolfram Dannlowski, Udo Wersching, Heike Neuroimage Clin Regular Article Previous studies revealed several alterations of the cerebral white matter in patients with major depressive disorder. However, it is unknown if these alterations are associated with vascular changes in the brain and other body parts. We compared diffusion tensor imaging derived fractional anisotropy in a well characterized sample of middle-aged patients with major depressive disorder (n = 290) and never-depressed controls (n = 346) by the method of tract-based spatial statistics. Subsequently, the potential role of pulse wave velocity as a mediator of depression- and age-related changes in extracted estimates of fractional anisotropy were analyzed. The results of the tract-based analysis revealed significantly reduced fractional anisotropy in the left posterior thalamic radiation associated with depression. Analyses of extracted data indicated additional reductions of fractional anisotropy bilaterally in the posterior thalamic radiation and in the left sagittal stratum. The analyses of indirect effects did not show any significant mediation of depression-related effects on fractional anisotropy via pulse wave velocity. However, age-related effects on fractional anisotropy were partially mediated by pulse wave velocity. In conclusion, major depressive disorder is associated with detrimental effects on cerebral white matter microstructure properties which are independent of vascular changes, as measured by pulse wave velocity. However, a portion of age-related detrimental effects on white matter is explained by vascular changes. Longitudinal studies are required for investigating changes in white matter and vascular parameters over time and their association with incident depression. Elsevier 2017-01-16 /pmc/articles/PMC5279701/ /pubmed/28180073 http://dx.doi.org/10.1016/j.nicl.2017.01.013 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Regular Article
Hermesdorf, Marco
Berger, Klaus
Szentkirályi, András
Schwindt, Wolfram
Dannlowski, Udo
Wersching, Heike
Reduced fractional anisotropy in patients with major depressive disorder and associations with vascular stiffness
title Reduced fractional anisotropy in patients with major depressive disorder and associations with vascular stiffness
title_full Reduced fractional anisotropy in patients with major depressive disorder and associations with vascular stiffness
title_fullStr Reduced fractional anisotropy in patients with major depressive disorder and associations with vascular stiffness
title_full_unstemmed Reduced fractional anisotropy in patients with major depressive disorder and associations with vascular stiffness
title_short Reduced fractional anisotropy in patients with major depressive disorder and associations with vascular stiffness
title_sort reduced fractional anisotropy in patients with major depressive disorder and associations with vascular stiffness
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5279701/
https://www.ncbi.nlm.nih.gov/pubmed/28180073
http://dx.doi.org/10.1016/j.nicl.2017.01.013
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