Does transcranial direct current stimulation of the primary motor cortex improve implicit motor sequence learning in Parkinson's disease?

Author:

Firouzi Mahyar123ORCID,Baetens Kris13,Swinnen Eva23,Baeken Chris1345,Van Overwalle Frank13,Deroost Natacha13

Affiliation:

1. Brain, Body and Cognition Research Group, Faculty of Psychology and Educational Sciences Vrije Universiteit Brussel Elsene Belgium

2. Rehabilitation Research Group, Department of Physiotherapy, Human Physiology and Anatomy Vrije Universiteit Brussel Jette Belgium

3. Center for Neurosciences (C4N) Vrije Universiteit Brussel Elsene Belgium

4. Department of Psychiatry and Medical Psychology Ghent University, University Hospital Ghent (UZ Ghent) Ghent Belgium

5. Department of Psychiatry, Vrije Universiteit Brussel (VUB), Faculty of Medicine and Pharmacy University Hospital Brussel (UZ Brussel) Brussels Belgium

Abstract

AbstractImplicit motor sequence learning (IMSL) is a cognitive function that is known to be associated with impaired motor function in Parkinson's disease (PD). We previously reported positive effects of transcranial direct current stimulation (tDCS) over the primary motor cortex (M1) on IMSL in 11 individuals with PD with mild cognitive impairments (MCI), with the largest effects occurring during reacquisition. In the present study, we included 35 individuals with PD, with (n = 15) and without MCI (n = 20), and 35 age‐ and sex‐matched controls without PD, with (n = 13) and without MCI (n = 22). We used mixed‐effects models to analyze anodal M1 tDCS effects on acquisition (during tDCS), short‐term (five minutes post‐tDCS) and long‐term reacquisition (one‐week post‐tDCS) of general and sequence‐specific learning skills, as measured by the serial reaction time task. At long‐term reacquisition, anodal tDCS resulted in smaller general learning effects compared to sham, only in the PD group, p = .018, possibly due to floor effects. Anodal tDCS facilitated the acquisition of sequence‐specific learning (M = 54.26 ms) compared to sham (M = 38.98 ms), p = .003, regardless of group (PD/controls). Further analyses revealed that this positive effect was the largest in the PD‐MCI group (anodal: M = 69.07 ms; sham: M = 24.33 ms), p < .001. Although the observed effect did not exceed the stimulation period, this single‐session tDCS study confirms the potential of tDCS to enhance IMSL, with the largest effects observed in patients with lower cognitive status. These findings add to the body of evidence that anodal tDCS can beneficially modulate the abnormal basal ganglia network activity that occurs in PD.

Funder

Vrije Universiteit Brussel

Fonds Wetenschappelijk Onderzoek

Publisher

Wiley

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