Evidence map›Paper›PMID 41770321›Full record

SynthesisJournal of neural transmission (Vienna, Austria : 1996)2026

Tremor in multiple system atrophy: a systematic literature review.

Maria Schneller, Frank Jagusch, Bianca Calio, Lukas Gattermeyer-Kell, Daniela Kern, Melanie Suette, Igor Kuchin, Petra Katschnig-Winter, Mariella Kögl, Uwe Siebert and 4 more

Abstract readSystematic Review
In one paragraph

Synthesis in Journal of neural transmission (Vienna, Austria : 1996), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Maria SchnellerDepartment of Neurology, Medical University of Graz, Graz, Austria.ORCID http://orcid.org/0009-0000-8388-5518
Frank JaguschDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Bianca CalioDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Lukas Gattermeyer-KellDepartment of Neurology, Medical University of Graz, Graz, Austria.
Daniela KernDepartment of Neurology, Medical University of Graz, Graz, Austria.
Melanie SuetteDepartment of Neurology, Medical University of Graz, Graz, Austria.
Igor KuchinInstitute of Public Health, Medical Decision Making and Health Technology Assessment, Department of Public Health, Health Services Research and Health Technology Assessment, UMIT TIROL - University for Health Sciences and Technology, Hall in Tirol, Austria.
Petra Katschnig-WinterDepartment of Neurology, Medical University of Graz, Graz, Austria.
Mariella KöglDepartment of Neurology, Medical University of Graz, Graz, Austria.
Uwe SiebertInstitute of Public Health, Medical Decision Making and Health Technology Assessment, Department of Public Health, Health Services Research and Health Technology Assessment, UMIT TIROL - University for Health Sciences and Technology, Hall in Tirol, Austria.
Florian KrismerDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Beate JahnInstitute of Public Health, Medical Decision Making and Health Technology Assessment, Department of Public Health, Health Services Research and Health Technology Assessment, UMIT TIROL - University for Health Sciences and Technology, Hall in Tirol, Austria.
Alessandra FanciulliDepartment of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Petra SchwingenschuhDepartment of Neurology, Medical University of Graz, Graz, Austria. petra.schwingenschuh@medunigraz.at.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Up to 80% of patients with multiple system atrophy (MSA) exhibit tremor or tremor-like phenomena, yet the clinical features of these manifestations remain insufficiently characterized. Clearer phenotypic delineation may support differential diagnosis from other tremor-associated disorders, particularly Parkinson's disease (PD). We aimed to determine characteristics and prevalence of tremor, distribution across MSA phenotypes and body regions, and its treatment responsiveness. We systematically searched PUBMED for articles reporting tremor in MSA, following PRISMA guidelines. Eligible studies were screened, with data reviewed by two reviewers and risk of bias assessed using JBI critical appraisal tools. Of 127 records, 25 studies met inclusion criteria, comprising 963 MSA patients. Tremor types and prevalence differed by phenotype. In MSA-P, rest tremor occurred in 26.5-38.1% and action tremor in 60.3-81.8%. In MSA-C, rest tremor occurred in 11-22.5%, action tremor in 44.9-97.5%. Among action tremor, a 3-Hz pseudo-orthostatic tremor occurred more often in MSA-C (76.3-97.5%) than MSA-P (24.1-38.3%). Polyminimyoclonus was present in 16.5% of MSA-P and 10.5% of MSA-C. Neurophysiologically, MSA-C typically showed ~ 3-Hz pseudo-orthostatic tremor, whereas MSA-P presented a 7-8-Hz postural tremor and 5-6-Hz rest tremor. Levodopa improved tremor in 11.8-92% of cases, with benefit more often in MSA-P and in action tremor. Preliminary reports suggest potential benefit of clonazepam and botulinum toxin, while a pilot high intensity focused ultrasound therapy showed no improvement. This first systematic review demonstrates that tremor in MSA is common and phenotypically diverse. Rest tremor is generally less frequent than action tremor and a 3-Hz pseudo-orthostatic tremor is characteristic of MSA-C.

Indexed as

Multiple System AtrophyTremorHumansMultiple system atrophyParkinson’s diseaseTremor

Identifiers

PMID41770321
PMCPMC13428687

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.