Modafinil treatment modulates functional connectivity in stroke survivors with severe fatigue.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
04 07 2019
Historique:
received: 17 10 2018
accepted: 20 06 2019
entrez: 6 7 2019
pubmed: 6 7 2019
medline: 28 10 2020
Statut: epublish

Résumé

Post-stroke fatigue has a significant impact on stroke survivors' mental and physical well-being. Our recent clinical trial showed significant reduction of post-stroke fatigue with modafinil treatment, however functional connectivity changes in response to modafinil have not yet been explored in stroke survivors with post-stroke fatigue. Twenty-eight participants (multidimensional fatigue inventory-20 ≥ 60) had MRI scans at baseline, and during modafinil and placebo treatment. Resting-state functional MRI data were obtained, and independent component analysis was used to extract functional networks. Resting-state functional connectivity (rsFC) was examined between baseline, modafinil and placebo treatment using permutation testing with threshold-free cluster enhancement. Overall twenty-eight participants (mean age: 62 ± 14.3, mean baseline MFI-20: 72.3 ± 9.24) were included. During modafinil treatment, increased rsFC was observed in the right hippocampus (p = 0.004, 11 voxels) compared to placebo. This coincided with lower rsFC in the left frontoparietal (inferior parietal lobule, p = 0.023, 13 voxels), somatosensory (primary somatosensory cortex; p = 0.009, 32 voxels) and mesolimbic network (temporal pole, p = 0.016, 35 voxels). In conclusion, modafinil treatment induces significant changes in rsFC in post-stroke fatigue. This modulation of rsFC may relate to a reduction of post-stroke fatigue; however, the relationship between sensory processing, neurotransmitter expression and fatigue requires further exploration.

Identifiants

pubmed: 31273283
doi: 10.1038/s41598-019-46149-0
pii: 10.1038/s41598-019-46149-0
pmc: PMC6609702
doi:

Substances chimiques

Central Nervous System Stimulants 0
Modafinil R3UK8X3U3D

Types de publication

Clinical Trial, Phase II Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

9660

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Auteurs

Milanka M Visser (MM)

School of Medicine and Public Health, Faculty of Health and Medicine, University of Newcastle, University Drive, Callaghan, 2308, New South Wales, Australia. milanka.visser@unimelb.edu.au.

Peter Goodin (P)

Department of Neurology, Royal Melbourne Hospital, University of Melbourne, Melbourne, Australia.

Mark W Parsons (MW)

Department of Neurology, Royal Melbourne Hospital, University of Melbourne, Melbourne, Australia.
Department of Neurology, John Hunter Hospital, University of Newcastle, Newcastle, Australia.

Thomas Lillicrap (T)

Department of Neurology, John Hunter Hospital, University of Newcastle, Newcastle, Australia.

Neil J Spratt (NJ)

Department of Neurology, John Hunter Hospital, University of Newcastle, Newcastle, Australia.
School of Biomedical Sciences and Pharmacy, Faculty of Health and Medicine, University of Newcastle, Newcastle, Australia.

Christopher R Levi (CR)

Department of Neurology, John Hunter Hospital, University of Newcastle, Newcastle, Australia.

Andrew Bivard (A)

Department of Neurology, Royal Melbourne Hospital, University of Melbourne, Melbourne, Australia.
Department of Neurology, John Hunter Hospital, University of Newcastle, Newcastle, Australia.

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Classifications MeSH