Evidence map›Paper›PMID 41716855›Full record

ArticleClinical parkinsonism & related disorders2026

Effects of deep brain stimulation on non motor fluctuations in Parkinson's disease (assessed with the NMF severity scale).

Christian Matta, Camille Comet, Corentin Gaillard, Florent Faggianelli, Stephan Grimaldi, Tatiana Witjas, Solène Ansquer, Cécile Hubsch, Mathieu Anheim, Caroline Moreau and 21 more

Abstract read
In one paragraph

Article in Clinical parkinsonism & related disorders, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

31 authors.

Christian MattaDepartment of Neurology, Saint Joseph University, Beirut, Lebanon.
Camille CometDepartment of Neurology, University Hospital Timone, Marseille, France.
Corentin GaillardDepartment of Neurology, University Hospital Timone, Marseille, France.
Florent FaggianelliDepartment of Neurology, University Hospital Timone, Marseille, France.
Stephan GrimaldiDepartment of Neurology, University Hospital Timone, Marseille, France.
Tatiana WitjasDepartment of Neurology, University Hospital Timone, Marseille, France.
Solène AnsquerCentre Hospitalier Universitaire de Poitiers, France - Centre d'investigation clinique CIC INSERM 1402, France.
Cécile HubschService of Neurology, Department of Clinical Neurosciences, Lausanne University Hospital (CHUV) and University of Lausanne (UNIL), Lausanne, Switzerland.
Mathieu AnheimFrench Clinical Research Network for Parkinson's Disease and Movement Disorders (NS-PARK), France.
Caroline MoreauDD and ASR Department of Medical Pharmacology, Neurology and Movement Disorders Department, Referent Center of Parkinson's Disease, CHU of Lille, Univ. Lille Neuroscience & Cognition, Inserm, UMR-S1172, NS-Park Network France, Lille, France.
Elodie HainqueDépartement de Neurologie, APHP, Paris, France.
Sophie DrapierNeurologie, CHU Pontchaillou, Rennes, France.
Béchir JarrayaNeuroscience, Hospital Foch, Suresnes, Île-de-France, France.
Chloé LaurencinCNRS UMR 5229, Bron, France.
Dominique GuehlPôle de Neurosciences Cliniques, CHU de Bordeaux, Bordeaux, France.
Lucie HopesNeurology, Centre Hospitalier Universitaire de Nancy, Nancy, Lorraine, France.
Christine Brefel-CourbonDepartment of Clinical Pharmacology and Neurosciences, Parkinson Expert Centre, Centre d'Investigation Clinique CIC1436, University Hospital of Toulouse, NeuroToul COEN Centre Inserm UMR-1214, NS-PARK Network, Toulouse, France.
Melissa TirNeurology, CHU Amiens-Picardie, Amiens, Hauts-de-France, France.
Ana MarquesDepartment of Neurology, Clermont-Ferrand University Hospital, Université Clermont Auvergne, Clermont-Ferrand, France.
Tiphaine RouaudDepartment of Neurology, Nantes University Hospital, Nantes, France.
David MalteteDepartment of Neurology, Rouen University Hospital and University of Rouen, France.
Caroline GiordanaNeurology Department, Centre, Nice, France.
Karine BaumstarckAix Marseille Université, EA 3279 Self-Perceived Health Assessment Research Unit, Marseille, France.
Olivier RascolUniversity Hospital of Toulouse, INSERM, University of Toulouse 3, Toulouse, France.
Jean-Christophe CorvolDépartement de Neurologie, CIC Neurosciences, Sorbonne Université, Assistance Publique Hôpitaux de Paris, Paris Brain Institute (ICM), Inserm, CNRS, Hôpital Pitié-Salpêtrière, NS-PARK/FCRIN Network, Paris, France.
Fabienne Ory-MagneFrench Clinical Research Network for Parkinson's Disease and Movement Disorders (NS-PARK), France.
Anne-Sophie RollandDepartment of Medical Pharmacology, Neurology and Movement Disorders Department, Referent Center of Parkinson's Disease, CHU of Lille, Univ. Lille Neuroscience & Cognition, Inserm, UMR-S1172, Lille, France.
David DevosMedical Pharmacology, Lille University Medical Center, Lille, France University of Lille, Inserm, CHU Lille, UMR-S1172 Lille Neuroscience & Cognition (LilNCog), Lille, France.
J-P AzulayDepartment of Neurology, University Hospital Timone, Marseille, France.
Alexandre EusebioDepartment of Neurology, University Hospital Timone, Marseille, France.
PREDISTIM Study Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Deep Brain Stimulation (DBS) of the subthalamic nucleus (STN) is a well-established treatment for motor fluctuations (MF) in Parkinson's disease (PD), but its impact on non-motor fluctuations (NMF) remains unclear. As NMFs are frequent, disabling, and affect quality of life, understanding their response to DBS is critical. Objectives: To assess the presence of NMF after STN-DBS, identify preoperative factors of improvement, and compare NMF responses to DBS and levodopa. Methods: This project is an ancillary study of the French multicenter PREDISTIM cohort. We used the validated Non-Motor Fluctuation Severity Scale (NMF2S) to evaluate NMFs one year after STN-DBS and before surgery when data were available. Evaluations were performed under standardized conditions (OFF-Dopa/OFF-Stim vs. OFF-Dopa/ON-Stim). Results: We included 284 PD patients assessed one year after STN-DBS using the NMF2S scale. Preoperative data were available for 153 patients. Evaluations were performed under standardized stimulation conditions (OFF-Dopa/OFF-Stim vs. OFF-Dopa/ON-Stim).STN-DBS led to a 41.1% reduction in NMF severity, with anxiety, concentration difficulties, and pain showing the most improvement. However, DBS effects were less pronounced than those of levodopa, especially for psychiatric symptoms. NMF improvement did not correlate with motor improvement. Among all preoperative variables, only the levodopa response in the cognitive domain was associated with post-DBS NMF benefit. Conclusions: STN-DBS significantly improves NMFs, although to a lesser extent than levodopa. The dissociation between motor and non-motor responses underscores the need for specific markers to predict NMF outcomes. These findings support the integration of NMF assessment into DBS indications and patient selection.

Indexed as

Deep brain stimulationNon-motor fluctuationsParkinson’s diseasePredictive factors of DBS responseSubthalamic nucleus

Identifiers

PMID41716855
PMCPMC12915265

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.