Evidence map›Paper›PMID 41524211›Full record

ArticleAnnals of neurology2026

Probabilistic Lesion Mapping to Optimize Thalamotomy Targets for Focal Hand Dystonia.

Masahiko Nishitani, Shiro Horisawa, Konstantin Butenko, Hiroki Togo, Arun Garimella, William Drew, Melissa Chua, Esraa Shaban, Takakazu Kawamata, Takaomi Taira and 3 more

Abstract read
In one paragraph

Article in Annals of neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

13 authors.

Masahiko NishitaniDepartment of Neurosurgery, Tokyo Women's Medical University, Tokyo, Japan.ORCID 0009-0003-8214-0305
Shiro HorisawaDepartment of Neurosurgery, Tokyo Women's Medical University, Tokyo, Japan.
Konstantin ButenkoCenter for Brain Circuit Therapeutics, Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Hiroki TogoDepartment of Integrated Neuroanatomy and Neuroimaging, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Arun GarimellaCenter for Brain Circuit Therapeutics, Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
William DrewCenter for Brain Circuit Therapeutics, Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Melissa ChuaCenter for Brain Circuit Therapeutics, Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.ORCID 0000-0002-2832-4002
Esraa ShabanCenter for Brain Circuit Therapeutics, Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Takakazu KawamataDepartment of Neurosurgery, Tokyo Women's Medical University, Tokyo, Japan.
Takaomi TairaDepartment of Neurosurgery, Tokyo Women's Medical University, Tokyo, Japan.
Andreas HornCenter for Brain Circuit Therapeutics, Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Michael D FoxCenter for Brain Circuit Therapeutics, Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.ORCID 0000-0001-8848-6399
Takashi HanakawaDepartment of Integrated Neuroanatomy and Neuroimaging, Kyoto University Graduate School of Medicine, Kyoto, Japan.ORCID 0000-0003-3267-8214

Funding

Deutsche Forschungsgemeinschaft 424778381-TRR 295Japan Agency for Medical Research and Development 18dm0307003Japan Agency for Medical Research and Development 23wm0625001
6 · The paper itself

Abstract

objectiveFocal hand dystonia (FHD) severely impairs task-specific motor control, yet the optimal surgical target for stereotactic intervention remains uncertain. This study aimed to identify the precise thalamic lesion site associated with symptomatic improvement and to clarify its network connectivity.

methodsWe retrospectively analyzed 164 patients with FHD (mean age = 42.0 years, 26.2% women) who underwent stereotactic thalamotomy of the ventral lateral thalamus. Voxel-wise probabilistic lesion mapping was applied to relate lesion locations to clinical outcomes. Structural connectivity analyses assessed fiber tracts linked to the optimal lesion site. Model performance was evaluated by 10-fold cross-validation, validation in an out-of-sample cohort, and testing in reoperation cases.

resultsWe identified that lesioning the border zone between the ventralis oralis posterior (Vop) and ventralis intermedius (Vim) nuclei was associated with improvement of FHD. The predictive model achieved high accuracy in cross-validation (area under the curve [AUC] = 0.836) and performed robustly in independent validation. Connectivity analyses showed that the Vop-Vim border zone was linked to cerebellothalamic and pallidothalamic afferents as well as thalamocortical projections to the supplementary motor area and premotor cortex. In contrast, lesions extending into the ventralis oralis anterior nucleus were associated with an increased risk of motor complications.

interpretationPrecise targeting of the Vop-Vim border maximizes clinical benefit while minimizing adverse effects in FHD thalamotomy. These findings establish the first evidence-based thalamic target for FHD, offering practical guidance for stereotactic interventions and advancing understanding of dystonia pathophysiology. ANN NEUROL 2026;99:1227-1238.

Indexed as

Brain MappingDystonic DisordersHandThalamusVentral Thalamic NucleiAdultFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedRetrospective StudiesStereotaxic Techniques

Identifiers

PMID41524211
PMCPMC13092777

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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.