Cargando…

Disentangling motor planning and motor execution in unmedicated de novo Parkinson's disease patients: An fMRI study

Many studies have used functional magnetic resonance imaging to unravel the neuronal underpinnings of motor system abnormalities in Parkinson's disease, indicating functional inhibition at the level of basal ganglia-thalamo-cortical motor networks. The study aim was to extend the characterizati...

Descripción completa

Detalles Bibliográficos
Autores principales: Martin, Jason A., Zimmermann, Nadine, Scheef, Lukas, Jankowski, Jakob, Paus, Sebastian, Schild, Hans H., Klockgether, Thomas, Boecker, Henning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6438987/
https://www.ncbi.nlm.nih.gov/pubmed/30925383
http://dx.doi.org/10.1016/j.nicl.2019.101784
_version_ 1783407187775717376
author Martin, Jason A.
Zimmermann, Nadine
Scheef, Lukas
Jankowski, Jakob
Paus, Sebastian
Schild, Hans H.
Klockgether, Thomas
Boecker, Henning
author_facet Martin, Jason A.
Zimmermann, Nadine
Scheef, Lukas
Jankowski, Jakob
Paus, Sebastian
Schild, Hans H.
Klockgether, Thomas
Boecker, Henning
author_sort Martin, Jason A.
collection PubMed
description Many studies have used functional magnetic resonance imaging to unravel the neuronal underpinnings of motor system abnormalities in Parkinson's disease, indicating functional inhibition at the level of basal ganglia-thalamo-cortical motor networks. The study aim was to extend the characterization of functional motor changes in Parkinson's Disease by dissociating between two phases of action (i.e. motor planning and motor execution) during an automated unilateral finger movement sequence with the left and right hand, separately. In essence, we wished to identify neuronal dysfunction and potential neuronal compensation before (planning) and during (execution) automated sequential motor behavior in unmedicated early stage Parkinson's Disease patients. Twenty-two Parkinson's Disease patients (14 males; 53 ± 11 years; Hoehn and Yahr score 1.4 ± 0.6; UPDRS (part 3) motor score 16 ± 6) and 22 healthy controls (14 males; 49 ± 12 years) performed a pre-learnt four finger sequence (index, ring, middle and little finger, in order), either self-initiated (FREE) or externally triggered (REACT), within an 8-second time window. Findings were most pronounced during FREE with the clinically most affected side, where motor execution revealed significant underactivity of contralateral primary motor cortex, contralateral posterior putamen (sensorimotor territory), ipsilateral anterior cerebellum / cerebellar vermis, along with underactivity in supplementary motor area (based on ROI analyses only), corroborating previous findings in Parkinson's Disease. During motor planning, Parkinson's Disease patients showed a significant relative overactivity in dorsolateral prefrontal cortex (DLPFC), suggesting a compensatory overactivity. To a variable extent this relative overactivity in the DLPFC went along with a relative overactivity in the precuneus and the ipsilateral anterior cerebellum/cerebellar vermis Our study illustrates that a refined view of disturbances in motor function and compensatory processes can be gained from experimental designs that try to dissociate motor planning from motor execution, emphasizing that compensatory mechanisms are triggered in Parkinson's Disease when voluntary movements are conceptualized for action.
format Online
Article
Text
id pubmed-6438987
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-64389872019-04-11 Disentangling motor planning and motor execution in unmedicated de novo Parkinson's disease patients: An fMRI study Martin, Jason A. Zimmermann, Nadine Scheef, Lukas Jankowski, Jakob Paus, Sebastian Schild, Hans H. Klockgether, Thomas Boecker, Henning Neuroimage Clin Regular Article Many studies have used functional magnetic resonance imaging to unravel the neuronal underpinnings of motor system abnormalities in Parkinson's disease, indicating functional inhibition at the level of basal ganglia-thalamo-cortical motor networks. The study aim was to extend the characterization of functional motor changes in Parkinson's Disease by dissociating between two phases of action (i.e. motor planning and motor execution) during an automated unilateral finger movement sequence with the left and right hand, separately. In essence, we wished to identify neuronal dysfunction and potential neuronal compensation before (planning) and during (execution) automated sequential motor behavior in unmedicated early stage Parkinson's Disease patients. Twenty-two Parkinson's Disease patients (14 males; 53 ± 11 years; Hoehn and Yahr score 1.4 ± 0.6; UPDRS (part 3) motor score 16 ± 6) and 22 healthy controls (14 males; 49 ± 12 years) performed a pre-learnt four finger sequence (index, ring, middle and little finger, in order), either self-initiated (FREE) or externally triggered (REACT), within an 8-second time window. Findings were most pronounced during FREE with the clinically most affected side, where motor execution revealed significant underactivity of contralateral primary motor cortex, contralateral posterior putamen (sensorimotor territory), ipsilateral anterior cerebellum / cerebellar vermis, along with underactivity in supplementary motor area (based on ROI analyses only), corroborating previous findings in Parkinson's Disease. During motor planning, Parkinson's Disease patients showed a significant relative overactivity in dorsolateral prefrontal cortex (DLPFC), suggesting a compensatory overactivity. To a variable extent this relative overactivity in the DLPFC went along with a relative overactivity in the precuneus and the ipsilateral anterior cerebellum/cerebellar vermis Our study illustrates that a refined view of disturbances in motor function and compensatory processes can be gained from experimental designs that try to dissociate motor planning from motor execution, emphasizing that compensatory mechanisms are triggered in Parkinson's Disease when voluntary movements are conceptualized for action. Elsevier 2019-03-19 /pmc/articles/PMC6438987/ /pubmed/30925383 http://dx.doi.org/10.1016/j.nicl.2019.101784 Text en © 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Regular Article
Martin, Jason A.
Zimmermann, Nadine
Scheef, Lukas
Jankowski, Jakob
Paus, Sebastian
Schild, Hans H.
Klockgether, Thomas
Boecker, Henning
Disentangling motor planning and motor execution in unmedicated de novo Parkinson's disease patients: An fMRI study
title Disentangling motor planning and motor execution in unmedicated de novo Parkinson's disease patients: An fMRI study
title_full Disentangling motor planning and motor execution in unmedicated de novo Parkinson's disease patients: An fMRI study
title_fullStr Disentangling motor planning and motor execution in unmedicated de novo Parkinson's disease patients: An fMRI study
title_full_unstemmed Disentangling motor planning and motor execution in unmedicated de novo Parkinson's disease patients: An fMRI study
title_short Disentangling motor planning and motor execution in unmedicated de novo Parkinson's disease patients: An fMRI study
title_sort disentangling motor planning and motor execution in unmedicated de novo parkinson's disease patients: an fmri study
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6438987/
https://www.ncbi.nlm.nih.gov/pubmed/30925383
http://dx.doi.org/10.1016/j.nicl.2019.101784
work_keys_str_mv AT martinjasona disentanglingmotorplanningandmotorexecutioninunmedicateddenovoparkinsonsdiseasepatientsanfmristudy
AT zimmermannnadine disentanglingmotorplanningandmotorexecutioninunmedicateddenovoparkinsonsdiseasepatientsanfmristudy
AT scheeflukas disentanglingmotorplanningandmotorexecutioninunmedicateddenovoparkinsonsdiseasepatientsanfmristudy
AT jankowskijakob disentanglingmotorplanningandmotorexecutioninunmedicateddenovoparkinsonsdiseasepatientsanfmristudy
AT paussebastian disentanglingmotorplanningandmotorexecutioninunmedicateddenovoparkinsonsdiseasepatientsanfmristudy
AT schildhansh disentanglingmotorplanningandmotorexecutioninunmedicateddenovoparkinsonsdiseasepatientsanfmristudy
AT klockgetherthomas disentanglingmotorplanningandmotorexecutioninunmedicateddenovoparkinsonsdiseasepatientsanfmristudy
AT boeckerhenning disentanglingmotorplanningandmotorexecutioninunmedicateddenovoparkinsonsdiseasepatientsanfmristudy