Evidence map›Paper›PMID 39190604›Full record

ArticleeLife2024

Interrogating basal ganglia circuit function in people with Parkinson's disease and dystonia.

Srdjan Sumarac, Kiah A Spencer, Leon A Steiner, Conor Fearon, Emily A Haniff, Andrea A Kühn, Mojgan Hodaie, Suneil K Kalia, Andres Lozano, Alfonso Fasano and 2 more

Abstract read
In one paragraph

Article in eLife, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Pallidal Evoked Resonant Neural Activity as a Candidate Biomarker for Deep Brain Stimulation in Dystonia.Movement disorders : official journal of the Movement Disorder Society · 2026
    Article
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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

12 authors.

Srdjan Sumarac *Institute of Biomedical Engineering, University of Toronto, Toronto, Canada.ORCID https://orcid.org/0000-0002-3840-5957
Kiah A Spencer *Institute of Biomedical Engineering, University of Toronto, Toronto, Canada.
Leon A Steiner *Krembil Brain Institute, University Health Network, Toronto, Canada.
Conor FearonKrembil Brain Institute, University Health Network, Toronto, Canada.
Emily A HaniffKrembil Brain Institute, University Health Network, Toronto, Canada.
Andrea A KühnDepartment of Neurology and Experimental Neurology, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Mojgan HodaieKrembil Brain Institute, University Health Network, Toronto, Canada.
Suneil K KaliaKrembil Brain Institute, University Health Network, Toronto, Canada.
Andres LozanoKrembil Brain Institute, University Health Network, Toronto, Canada.
Alfonso FasanoKrembil Brain Institute, University Health Network, Toronto, Canada.
William Duncan HutchisonKrembil Brain Institute, University Health Network, Toronto, Canada.ORCID https://orcid.org/0000-0002-3866-4940
Luka MilosevicInstitute of Biomedical Engineering, University of Toronto, Toronto, Canada.ORCID https://orcid.org/0000-0002-4051-5397

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The dichotomy between the hypo- versus hyperkinetic nature of Parkinson's disease (PD) and dystonia, respectively, is thought to be reflected in the underlying basal ganglia pathophysiology. In this study, we investigated differences in globus pallidus internus (GPi) neuronal activity, and short- and long-term plasticity of direct pathway projections. Methods: Using microelectrode recording data collected from the GPi during deep brain stimulation surgery, we compared neuronal spiketrain features between people with PD and those with dystonia, as well as correlated neuronal features with respective clinical scores. Additionally, we characterized and compared readouts of short- and long-term synaptic plasticity using measures of inhibitory evoked field potentials. Results: GPi neurons were slower, bustier, and less regular in dystonia. In PD, symptom severity positively correlated with the power of low-beta frequency spiketrain oscillations. In dystonia, symptom severity negatively correlated with firing rate and positively correlated with neuronal variability and the power of theta frequency spiketrain oscillations. Dystonia was moreover associated with less long-term plasticity and slower synaptic depression. Conclusions: We substantiated claims of hyper- versus hypofunctional GPi output in PD versus dystonia, and provided cellular-level validation of the pathological nature of theta and low-beta oscillations in respective disorders. Such circuit changes may be underlain by disease-related differences in plasticity of striato-pallidal synapses. Funding: This project was made possible with the financial support of Health Canada through the Canada Brain Research Fund, an innovative partnership between the Government of Canada (through Health Canada) and Brain Canada, and of the Azrieli Foundation (LM), as well as a grant from the Banting Research Foundation in partnership with the Dystonia Medical Research Foundation (LM).

Indexed as

Basal GangliaDystoniaGlobus PallidusParkinson DiseaseAdultAgedDeep Brain StimulationFemaleHumansMaleMiddle AgedNeuronal PlasticityNeuronsbasal gangliadeep brain stimulationdystoniahumanmedicineneuroscienceParkinson's diseasesingle-neuronsynaptic plasticity

Identifiers

PMID39190604
PMCPMC11349293

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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.