Cortico-Cortical White Matter Motor Pathway Microstructure Is Related to Psychomotor Retardation in Major Depressive Disorder

Tobias Bracht*, Andrea Federspiel, Susanne Schnell, Helge Horn, Oliver Höfle, Roland Wiest, Thomas Dierks, Werner Strik, Thomas J. Müller, Sebastian Walther

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

68 Scopus citations

Abstract

Alterations of brain structure and function have been associated with psychomotor retardation in major depressive disorder (MDD). However, the association of motor behaviour and white matter integrity of motor pathways in MDD is unclear. The aim of the present study was to first investigate structural connectivity of white matter motor pathways in MDD. Second, we explore the relation of objectively measured motor activity and white matter integrity of motor pathways in MDD. Therefore, 21 patients with MDD and 21 healthy controls matched for age, gender, education and body mass index underwent diffusion tensor imaging and 24 hour actigraphy (measure of the activity level) the same day. Applying a probabilistic fibre tracking approach we extracted connection pathways between the dorsolateral prefrontal cortex (dlPFC), the rostral anterior cingulate cortex (rACC), the pre-supplementary motor area (pre-SMA), the SMA-proper, the primary motor cortex (M1), the caudate nucleus, the putamen, the pallidum and the thalamus. Patients had lower activity levels and demonstrated increased mean diffusivity (MD) in pathways linking left pre-SMA and SMA-proper, and right SMA-proper and M1. Exploratory analyses point to a positive association of activity level and mean-fractional anisotropy in the right rACC-pre-SMA connection in MDD. Only MDD patients with low activity levels had a negative linear association of activity level and mean-MD in the left dlPFC-pre-SMA connection. Our results point to structural alterations of cortico-cortical white matter motor pathways in MDD. Altered white matter organisation of rACC-pre-SMA and dlPFC-pre-SMA pathways may contribute to movement initiation in MDD.

Original languageEnglish (US)
Article numbere52238
JournalPloS one
Volume7
Issue number12
DOIs
StatePublished - Dec 20 2012

Funding

Dr. Horn has received speaker's fees from Eli-Lilly, Bristol-Myers-Squibb, Lundbeck, Boehringer-Ingelheim and Vifor. Prof. Strik received speaker's fees from/is advisory board member of Eli-Lilly, Pfizer and Lundbeck. Prof. Müller has received research support from Eli-Lilly, speaker's fees from AstraZeneca, Bristol-Myers-Squibb, Janssen-Cilag, Eli-Lilly, Pfizer, Sanofi-Aventis, Glaxo-Smith-Kline, Desitin-Pharma and Vifor. Prof. Müller is advisory board member of Eli-Lilly, Janssen-Cillag, Board Sandoz and Lundbeck; he has been a consultant to Janssen-Cilag and Glaxo-Smith-Kline. Dr. Walther received speakers fees from Sandoz and Janssen-cilag. There are no patents, products in development or marketed products to declare. This does not alter the authors' adherence to all the PLOS ONE policies on sharing data and materials, as detailed online in the guide for authors.

ASJC Scopus subject areas

  • General

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