Bradykinesia induced by pallidal neurostimulation in dystonia: clinical risk factors and anatomical mapping

Pallidal deep brain stimulation (DBS) for dystonia can induce bradykinesia. We analyzed retrospective (n = 55) and prospective (n = 11) cohorts to identify risks and anatomical substrates for this side effect. Bradykinesia was prevalent (60-72%), with female sex, older dystonia onset, shorter disease duration, and crucially, stimulation pulse width identified as key predictive factors. Probabilistic mapping isolated a posterolateral globus pallidus internus "sour spot" for bradykinesia, which was spatially distinct from therapeutic "sweet spots" and demonstrated patient-level predictive power in cross-validation (R² = 0.16, p = 0.0013). Kinematic analysis showed reducing stimulation selectively improved movement frequency without altering amplitude. The effect appears mediated by local grey-matter modulation, not major white matter tracts. These findings suggest programming strategies using shorter pulse widths while avoiding the identified sour spot can mitigate bradykinesia without sacrificing antidystonic benefit.

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Publication Details

Journal
npj Parkinson s Disease
Published
2025-10-23
DOI
https://doi.org/10.1038/s41531-025-01177-8
Citations
1
Primary Topic
Neurological disorders and treatments
Type
article
Field-Weighted Citation Impact
1.39

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article

Bradykinesia induced by pallidal neurostimulation in dystonia: clinical risk factors and anatomical mapping

Andrea A. Kühn, Florian Lange, Diego L. Guarín, Christine Daniels et al.
1 citations
npj Parkinson s Disease
Neurological disorders and treatments
1.39
article

Bradykinesia induced by pallidal neurostimulation in dystonia: clinical risk factors and anatomical mapping

Andrea A. Kühn, Florian Lange, Diego L. Guarín, Christine Daniels, Benedikt Weigl, Martin M. Reich, Jonas Roothans, Jens Volkmann, Günther Deuschl, Robert L. Peach, Thorsten Odorfer, Philipp Mahlknecht, Joachim K. Krauss, Gregor A. Brandt, Joachim Runge, Pavel Navratil, Stella Mosert, Berenike Karrasch
article en
1 citations

Abstract

Pallidal deep brain stimulation (DBS) for dystonia can induce bradykinesia. We analyzed retrospective (n = 55) and prospective (n = 11) cohorts to identify risks and anatomical substrates for this side effect. Bradykinesia was prevalent (60-72%), with female sex, older dystonia onset, shorter disease duration, and crucially, stimulation pulse width identified as key predictive factors. Probabilistic mapping isolated a posterolateral globus pallidus internus "sour spot" for bradykinesia, which was spatially distinct from therapeutic "sweet spots" and demonstrated patient-level predictive power in cross-validation (R² = 0.16, p = 0.0013). Kinematic analysis showed reducing stimulation selectively improved movement frequency without altering amplitude. The effect appears mediated by local grey-matter modulation, not major white matter tracts. These findings suggest programming strategies using shorter pulse widths while avoiding the identified sour spot can mitigate bradykinesia without sacrificing antidystonic benefit.

npj Parkinson s DiseaseVol. 11(1)
Innsbruck Medical University (AT), University of Würzburg (DE), Christian-Albrechts-Universität zu Kiel (DE), University of Florida (US), Medizinische Hochschule Hannover (DE), University Hospital Cologne (DE), Imperial College London (GB), Charité - Universitätsmedizin Berlin (DE)
Deutsche Forschungsgemeinschaft, Interdisziplinäres Zentrum für Klinische Forschung, Universitätsklinikum Würzburg
Openalex Percentile: Top 15%
Neurological disorders and treatments
1.39
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