Evidence map›Paper›PMID 40595525›Full record

ArticleNature communications2025

Boundary complexity of cortical and subcortical areas predicts deep brain stimulation outcomes in Parkinson's disease.

Devin Schoen, Skyler Deutsch, Juhi Mehta, Sarah Wang, John Kornak, Philip A Starr, Doris D Wang, Jill L Ostrem, Ian O Bledsoe, Melanie A Morrison

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Preoperative Functional Connectivity Predicts Antiparkinson Drug Change after Deep Brain Stimulation.Movement disorders : official journal of the Movement Disorder Society · 2026
    Article
  5. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Devin SchoenDepartment of Radiology and Biomedical Imaging, University of California, San Francisco, USA.ORCID http://orcid.org/0000-0002-7797-4431
Skyler DeutschDepartment of Radiology and Biomedical Imaging, University of California, San Francisco, USA.ORCID http://orcid.org/0000-0003-2261-5885
Juhi MehtaDepartment of Radiology and Biomedical Imaging, University of California, San Francisco, USA.ORCID http://orcid.org/0009-0008-3690-1683
Sarah WangDepartment of Neurology, University of California, San Francisco, USA.
John KornakDepartment of Epidemiology and Biostatistics, University of California, San Francisco, USA.
Philip A StarrUCSF-UC Berkeley Joint PhD Program in Bioengineering, Berkeley, USA.ORCID http://orcid.org/0000-0003-2733-4003
Doris D WangUCSF-UC Berkeley Joint PhD Program in Bioengineering, Berkeley, USA.ORCID http://orcid.org/0000-0001-6112-3002
Jill L OstremDepartment of Neurology, University of California, San Francisco, USA.
Ian O BledsoeDepartment of Neurology, University of California, San Francisco, USA.
Melanie A MorrisonDepartment of Radiology and Biomedical Imaging, University of California, San Francisco, USA. melanie.morrison@ucsf.edu.ORCID http://orcid.org/0000-0002-5993-0515

Funding

MULTIMODAL MRI TO PREDICT DBS MOTOR AND COGNITIVE OUTCOMES IN PARKINSON’S DISEASER01NS130066 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Melanie A Morrison · 2022 to 2026
$3.3M
NINDS NIH HHS R01 NS130066U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01NS130066
6 · The paper itself

Abstract

While deep brain stimulation (DBS) remains an effective therapy for Parkinson's disease (PD), sources of variance in patient outcomes are still not fully understood, underscoring a need for better prognostic criteria. Here, we leveraged routinely collected T1-weighted (T1-w) magnetic resonance imaging (MRI) data to derive patient-specific measures of brain structure and evaluate their usefulness in predicting changes in PD medications in response to DBS. Preoperative T1-w MRI data from 231 patients with PD were used to extract regional measures of fractal dimension (FD), sensitive to the structural complexities of cortical and subcortical brain. FD was validated as a biomarker of PD progression through comparison of patients with PD and healthy controls (HCs). This analysis revealed significant group differences in FD across nine brain regions, including frontal, occipital, insular, and basal ganglia areas, which supports its utility as a marker of PD. We evaluated the impact of adding imaging features (FD) to a clinical model that included demographics and clinical parameters (age, sex, total number and location of DBS electrodes), and preoperative motor response to levodopa. This model aimed to explain variance and predict changes in medication following DBS. Regression analysis revealed that inclusion of the FD of distributed brain areas correlated with post-DBS reductions in medication burden, explaining an additional 13.6% of outcome variance (R

Indexed as

BrainDeep Brain StimulationParkinson DiseaseAgedFemaleFractalsHumansLevodopaMagnetic Resonance ImagingMaleMiddle AgedTreatment OutcomeLevodopa

Identifiers

PMID40595525
PMCPMC12219618

What OpenQuestion holds

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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.