Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/92168
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dc.contributorDepartment of Rehabilitation Sciencesen_US
dc.creatorKan, RLDen_US
dc.creatorXu, GXJen_US
dc.creatorShu, KTen_US
dc.creatorLai, FHYen_US
dc.creatorKranz, Gen_US
dc.creatorKranz, GSen_US
dc.date.accessioned2022-02-17T05:53:27Z-
dc.date.available2022-02-17T05:53:27Z-
dc.identifier.issn2040-6223en_US
dc.identifier.urihttp://hdl.handle.net/10397/92168-
dc.language.isoenen_US
dc.publisherSage Publicationsen_US
dc.rights© The Author(s), 2022.en_US
dc.rightsThis article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).en_US
dc.rightsKan, R. L., Xu, G. X., Shu, K. T., Lai, F. H., Kranz, G., & Kranz, G. S. (2022). Effects of non-invasive brain stimulation in multiple sclerosis: systematic review and meta-analysis. Therapeutic Advances in Chronic Disease, 13, 20406223211069198 is available at https://doi.org/10.1177/20406223211069198en_US
dc.subjectMultiple sclerosisen_US
dc.subjectRepetitive transcranial magneticen_US
dc.subjectTranscranial direct current stimulationen_US
dc.subjectFatigueen_US
dc.subjectMeta-analysisen_US
dc.titleEffects of non-invasive brain stimulation in multiple sclerosis : systematic review and meta-analysisen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage1en_US
dc.identifier.epage21en_US
dc.identifier.volume13en_US
dc.identifier.doi10.1177/20406223211069198en_US
dcterms.abstractObjective: The objective of this meta-analysis was to summarize evidence on the therapeutic effects of non-invasive brain stimulation (NIBS) on core symptoms of multiple sclerosis (MS). Specifically, findings from studies deploying transcranial direct current stimulation (tDCS) and repetitive transcranial magnetic stimulation (rTMS) protocols were summarized in this review.en_US
dcterms.abstractMethods: We systematically searched articles published in four databases, until 31 May 2021, which compared the effects of active tDCS or rTMS with sham intervention in MS patients. We used a random-effects model for this meta-analysis. Meta-regression and subgroup meta-analysis were used to examine the effects of stimulation dose and different stimulation protocols, respectively.en_US
dcterms.abstractResults: Twenty-five randomized controlled trials (RCTs) were included in this review, consisting of 19 tDCS and 6 rTMS studies. tDCS led to a significant and immediate reduction of fatigue with a large effect size (Hedges’s g = −0.870, 95% confidence intervals (CI) = [−1.225 to −0.458], number needed to treat (NNT) = 2). Particularly, a subgroup analysis showed that applying tDCS over the left DLPFC and bilateral S1 led to fatigue reductions compared to sham stimulation. Furthermore, tDCS had favorable effects on fatigue in MS patients with low physical disability but not those with high physical disability, and additionally improved cognitive function. Finally, whereas rTMS was observed to reduce muscle spasticity, these NIBS protocols showed no further effect on MS-associated pain and mood symptoms.en_US
dcterms.abstractConclusion: tDCS in MS alleviates fatigue and improves cognitive function whereas rTMS reduces muscle spasticity. More high-quality studies are needed to substantiate the therapeutic effects of different NIBS protocols in MS.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationTherapeutic advances in chronic disease, 1 Jan. 2022, v. 13, p. 1-23en_US
dcterms.isPartOfTherapeutic advances in chronic diseaseen_US
dcterms.issued2022-01-01-
dc.identifier.pmid35126965-
dc.identifier.eissn2040-6231en_US
dc.description.validate202202 bcvcen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumbera1168-n02-
dc.identifier.SubFormID44050-
dc.description.fundingSourceRGCen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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