Evidence map›Paper›PMID 40172076›Full record

ArticleMovement disorders : official journal of the Movement Disorder Society2025

Trajectories of Pontine Volume in Patients with Multiple System Atrophy.

Kazuya Kawabata, Florian Krismer, Mizuki Ito, Kazuhiro Hara, Epifanio Bagarinao, Vincent Beliveau, Patrice Péran, Germain Arribarat, Anne Pavy-Le Traon, Wassilios G Meissner and 10 more

Abstract read
In one paragraph

Article in Movement disorders : official journal of the Movement Disorder Society, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Glymphatic dysfunction in cerebellar neurodegeneration: mechanistic insights and emerging clinical implications.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
    Review
  2. The role of neuro-imaging in multiple system atrophy.Journal of neural transmission (Vienna, Austria : 1996) · 2026
    Review
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

20 authors.

Kazuya KawabataDepartment of Neurology, Medical University Innsbruck, Innsbruck, Austria.ORCID https://orcid.org/0000-0002-8851-4377
Florian KrismerDepartment of Neurology, Medical University Innsbruck, Innsbruck, Austria.ORCID https://orcid.org/0000-0002-4493-5073
Mizuki ItoDepartment of Neurology, Fujita Health University School of Medicine, Toyoake, Japan.
Kazuhiro HaraDepartment of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Epifanio BagarinaoDepartment of Integrated Health Sciences, Nagoya University Graduate School of Medicine, Nagoya, Japan.ORCID https://orcid.org/0000-0001-5000-6943
Vincent BeliveauDepartment of Neurology, Medical University Innsbruck, Innsbruck, Austria.ORCID https://orcid.org/0000-0001-7805-279X
Patrice PéranToNIC, Toulouse NeuroImaging Center, Université de Toulouse, INSERM, UPS, Toulouse, France.ORCID https://orcid.org/0000-0001-7200-0139
Germain ArribaratToNIC, Toulouse NeuroImaging Center, Université de Toulouse, INSERM, UPS, Toulouse, France.ORCID https://orcid.org/0000-0002-8754-8110
Anne Pavy-Le TraonFrench Reference Center for MSA, Neurology Department, University Hospital of Toulouse and INSERM-Institute of Cardiovascular and Metabolic Diseases (I2MC) UMR1297, Toulouse, France.
Wassilios G MeissnerCHU Bordeaux, Service de Neurologie des Maladies Neurodégénératives, IMNc, CRMR AMS, Bordeaux, France.ORCID https://orcid.org/0000-0003-2172-7527
Alexandra Foubert-SamierCHU Bordeaux, Service de Neurologie des Maladies Neurodégénératives, IMNc, CRMR AMS, Bordeaux, France.
Margherita FabbriFrench Reference Center for MSA, Clinical Investigation Center CIC1436, Department of Clinical Pharmacology and Neurosciences, NS-Park/FCRIN Network and NeuroToul Center of Excellence for Neurodegeneration, INSERM, University Hospital of Toulouse and University of Toulouse, Toulouse, France.ORCID https://orcid.org/0000-0001-7250-592X
Mark Forrest GordonTeva Pharmaceuticals, West Chester, Pennsylvania, USA.
Aya OguraDepartment of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Masahisa KatsunoDepartment of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan.ORCID https://orcid.org/0000-0001-9453-9311
Olivier RascolFrench Reference Center for MSA, Clinical Investigation Center CIC1436, Department of Clinical Pharmacology and Neurosciences, NS-Park/FCRIN Network and NeuroToul Center of Excellence for Neurodegeneration, INSERM, University Hospital of Toulouse and University of Toulouse, Toulouse, France.ORCID https://orcid.org/0000-0002-1410-6397
Christoph ScherflerDepartment of Neurology, Medical University Innsbruck, Innsbruck, Austria.ORCID https://orcid.org/0000-0002-4885-5265
Klaus SeppiDepartment of Neurology, Medical University Innsbruck, Innsbruck, Austria.ORCID https://orcid.org/0000-0001-6503-1455
Hirohisa WatanabeDepartment of Neurology, Fujita Health University School of Medicine, Toyoake, Japan.ORCID https://orcid.org/0000-0001-8553-8536
Werner PoeweDepartment of Neurology, Medical University Innsbruck, Innsbruck, Austria.ORCID https://orcid.org/0000-0003-4367-0971

Funding

Japan Society for the Promotion of ScienceResearch Committee of Ataxia, Health Labour Sciences Research, Ministry of Health, Labour and Welfare, Japan JPMH20FC1041
6 · The paper itself

Abstract

objectivesTo investigate trajectories of regional brain volume changes in multiple system atrophy (MSA) and their potential utility as surrogate markers of disease progression in the cerebellar subtype (MSA-C).

backgroundReliable biomarkers for tracking disease progression in MSA are urgently needed. Although several studies have explored neuroimaging markers, imaging measures that are reliable and reproducible at the individual-level are lacking.

methodsLongitudinal three-dimensional (3D)-T1 images from multiple cohorts of 21 subjects with probable MSA-C, 19 with probable MSA-parkinsonian subtype (MSA-P), 113 with Parkinson's disease, and 227 healthy controls were processed using the FreeSurfer longitudinal pipeline. Extracted volumes were assessed for individual longitudinal trajectories, intra-individual variability, and pontine regional volume decline.

resultsPontine volumes showed lower intra-individual variability in measurements compared with other infratentorial brain regions. All probable MSA-C patients exhibited a decline in pontine volume, ranging from -3.6% to -16.8% per year (mean: -9.1%), falling more than two standard deviations below the mean of healthy controls. In MSA-C, the temporal dynamics of pontine volumes exhibited nonlinear changes, characterized by progressive atrophy in the earlier period of the disease, followed by a pre-plateau phase associated with advanced disability in the later period. Predictive modeling suggests that pontine atrophy may begin before symptom onset of MSA-C.

conclusionsPontine volume is a sensitive marker of disease progression, exhibiting a nonlinear decline with low intra-individual variability in measurements and greater volume loss in the earlier stages, reaching a pre-plateau phase in the later stages with advanced disability. © 2025 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Indexed as

Multiple System AtrophyPonsAgedDisease ProgressionFemaleHumansImaging, Three-DimensionalLongitudinal StudiesMagnetic Resonance ImagingMaleMiddle AgedParkinson Disease

Identifiers

PMID40172076
PMCPMC12273624

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.