Dopamine substitution alters effective connectivity of cortical prefrontal, premotor, and motor regions during complex bimanual finger movements in Parkinson's disease.


Journal

NeuroImage
ISSN: 1095-9572
Titre abrégé: Neuroimage
Pays: United States
ID NLM: 9215515

Informations de publication

Date de publication:
15 04 2019
Historique:
received: 21 01 2018
revised: 23 03 2018
accepted: 12 04 2018
pubmed: 27 4 2018
medline: 28 1 2020
entrez: 27 4 2018
Statut: ppublish

Résumé

Bimanual coordination is impaired in Parkinson's disease (PD), affecting patients' quality of life. Besides dysfunction of the basal ganglia network, alterations of cortical oscillatory coupling, particularly between prefrontal and (pre-)motoric areas, are thought to underlie this impairment. Here, we studied 16 PD patients OFF and ON medication and age-matched healthy controls recording high-resolution electroencephalography (EEG) during performance of spatially coupled and uncoupled bimanual finger movements. Dynamic causal modeling (DCM) for induced responses was used to infer task-induced effective connectivity within a network comprising bilateral prefrontal cortex (PFC), lateral premotor cortex (lPM), supplementary motor area (SMA), and primary motor cortex (M1). Performing spatially coupled movements, excitatory left-hemispheric PFC to lPM coupling was significantly stronger in controls compared to unmedicated PD patients. Levodopa-induced enhancement of this connection correlated with increased movement accuracy. During performance of spatially uncoupled movements, PD patients OFF medication exhibited inhibitory connectivity from left PFC to SMA. Levodopa intake diminished these inhibitory influences and restored excitatory PFC to lPM coupling. This restoration, however, did not improve motor function. Concluding, our results indicate that lateralization of prefrontal to premotor connectivity in PD can be augmented by levodopa substitution and is of compensatory nature up to a certain extent of complexity.

Identifiants

pubmed: 29698732
pii: S1053-8119(18)30339-2
doi: 10.1016/j.neuroimage.2018.04.030
pii:
doi:

Substances chimiques

Dopamine Agents 0
Levodopa 46627O600J

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

118-132

Informations de copyright

Copyright © 2018 Elsevier Inc. All rights reserved.

Auteurs

Felix Sebastian Nettersheim (FS)

Department of Neurology, University Hospital Cologne, Cologne, Germany.

Philipp Alexander Loehrer (PA)

Department of Neurology, University Hospital Cologne, Cologne, Germany; Department of Neurology, University Hospital Giessen and Marburg, Marburg, Germany. Electronic address: philipp.loehrer@uk-gm.de.

Immo Weber (I)

Department of Neurology, University Hospital Giessen and Marburg, Marburg, Germany.

Fabienne Jung (F)

Department of Neurology, University Hospital Cologne, Cologne, Germany.

Till Anselm Dembek (TA)

Department of Neurology, University Hospital Cologne, Cologne, Germany.

Esther Annegret Pelzer (EA)

Department of Neurology, University Hospital Cologne, Cologne, Germany; Max Planck Institute for Metabolism Research, Cologne, Germany.

Haidar Salimi Dafsari (HS)

Department of Neurology, University Hospital Cologne, Cologne, Germany; National Parkinson Foundation International Centre of Excellence, King's College Hospital, London, United Kingdom.

Carlo Andreas Huber (CA)

Department of Psychiatry (UPK), University of Basel, Basel, Switzerland.

Marc Tittgemeyer (M)

Max Planck Institute for Metabolism Research, Cologne, Germany.

Lars Timmermann (L)

Department of Neurology, University Hospital Giessen and Marburg, Marburg, Germany. Electronic address: lars.timmermann@uk-gm.de.

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Classifications MeSH