Evidence map›Paper›PMID 42059110›Full record

SynthesisMovement disorders : official journal of the Movement Disorder Society2026

Speech and Deep Brain Stimulation in Parkinson's Disease, Essential Tremor, and Dystonia: A Systematic Review and Meta-analysis.

Elina Tripoliti, Takashi Tsuboi, Michael T Barbe, Mario Sousa, Julie Barkmeier-Kraemer, Hannah Jergas, Gaia Arno, Nicole Buie, Mikayla Day, Petr Krýže and 6 more

Abstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in Movement disorders : official journal of the Movement Disorder Society, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

16 authors.

Elina TripolitiDepartment of Clinical and Movement Neurosciences, UCL, Institute of Neurology and National Hospital for Neurology and Neurosurgery, UCLH NHS Trust, London, United Kingdom.
Takashi TsuboiDepartment of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Michael T BarbeDepartment of Neurology, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.
Mario SousaDepartment of Neurology, Inselspital University Hospital Bern, Bern, Switzerland.
Julie Barkmeier-KraemerDepartment of Otolaryngology-Head and Neck Surgery, University of Utah, Salt Lake City, Utah, USA.
Hannah JergasDepartment of Neurology, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.
Gaia ArnoDepartment of Otolaryngology-Head & Neck Surgery, Massachusetts Eye and Ear, Harvard Medical School, Boston, Massachusetts, USA.
Nicole BuieDepartment of Otolaryngology-Head & Neck Surgery, Massachusetts Eye and Ear, Harvard Medical School, Boston, Massachusetts, USA.
Mikayla DayDepartment of Otolaryngology-Head & Neck Surgery, Massachusetts Eye and Ear, Harvard Medical School, Boston, Massachusetts, USA.
Petr KrýžeDepartment of Circuit Theory, Faculty of Electrical Engineering, Czech Technical University in Prague, Prague, Czech Republic.
Jayson R NelsonDepartment of Neurosurgery, University of Utah, Clinical Neurosciences Center, Salt Lake City, Utah, USA.
Aaron E L WarrenDepartment of Neurosurgery, Mass General Brigham, Harvard Medical School, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0001-6534-2800
Shervin RahimpourDepartment of Neurosurgery, University of Utah, Clinical Neurosciences Center, Salt Lake City, Utah, USA.
Jan RuszDepartment of Circuit Theory, Faculty of Electrical Engineering, Czech Technical University in Prague, Prague, Czech Republic.
Paul KrackDepartment of Neurology, Inselspital University Hospital Bern, Bern, Switzerland.
Kristina SimonyanDepartment of Otolaryngology-Head & Neck Surgery, Massachusetts Eye and Ear, Harvard Medical School, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0001-7444-0437

Funding

Understanding disorder-specific neural pathophysiology in laryngeal dystonia and voice tremorP50DC019900 · NIDCD · MASSACHUSETTS EYE AND EAR INFIRMARY · PI Kristina Simonyan · 2021 to 2026
$11.9M
Physiologic Correlates of Vocal Tremor affecting those with Essential TremorR01DC016838 · NIDCD · UNIVERSITY OF UTAH · PI BARKMEIER-KRAEMER, JULIE M · 2019 to 2023
$3.0M
Czech Science Foundation 21-14216LEXCELES LX22NPO5107KAKENHI 23K24443KAKENHI 24K10489NIDCD NIH HHS P50 DC019900NIDCD NIH HHS P50DC019900NIDCD NIH HHS R01 DC016838NIH HHS P50DC019900Parkinson's Progression Biomarkers Initiative 2 16916R01DC016838 DC016838SFB1252 "Prominence in Language" 281511265SFN 32003BL 197709SGS23/170/OHK3/3T/13 170/OHK3/3T/13
6 · The paper itself

Abstract

Deep brain stimulation (DBS) effectively treats motor symptoms in movement disorders but often compromises speech through incompletely defined mechanisms. We conducted a PROSPERO-registered systematic review and meta-analysis of publications through August 2024 (CRD42024527738). Among 2726 screened records, we included 184 studies: 131 in Parkinson's disease (PD), 32 in essential tremor (ET), and 21 in dystonia, assessing perceptual, acoustic, and patient-reported speech outcomes. Meta-analyses showed that subthalamic nucleus DBS in PD resulted in poorer speech intelligibility compared with best medical treatment (effect size -0.24; 95% confidence interval: -0.46 to -0.03; P = 0.027), with state-dependent decline under active stimulation on longitudinal analysis (Unified Parkinson's Disease Rating Scale Part III item 18 monthly change: medication on +0.016, P < 0.001; medication off +0.002, P = 0.50). In ET, DBS consistently suppressed vocal tremor but increased the risk of dysarthria, particularly with bilateral stimulation. Dystonia outcomes showed greater heterogeneity. Across disorders, sustained phonation measures improved, whereas connected speech performance worsened, indicating selective vulnerability of complex motor tasks. Neuroanatomical mapping identified two nonexclusive mechanisms: current spread to corticobulbar fibers producing spastic speech features and to the cerebellothalamocortical pathway producing ataxic features. Hypokinetic and stuttering-like phenotypes also occurred but likely reflect network-level interactions rather than tract-specific spread. These tract-mediated and network-level alterations appear to interact with hemispheric lateralization, medication state, and longer-term plasticity to produce complex clinical phenotypes. We outline a clinical framework integrating systematic screening, phenotype identification, and targeted programming adjustments. Enhanced speech assessment, precise field mapping, and adaptive DBS paradigms may promote individualized care that optimizes speech and motor function in precision DBS therapy. © 2026 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Indexed as

Deep Brain StimulationDystoniaEssential TremorParkinson DiseaseSpeechSpeech DisordersHumansSubthalamic Nucleusdeep brain stimulationdystoniaessential tremorParkinson's diseasespeech

Identifiers

PMID42059110
PMCPMC13518292

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.