Evidence map›Paper›PMID 40962905›Full record

ArticleScientific reports2025

Phenotyping and characterising gait profiles of people with multiple sclerosis.

Katrin Trentzsch, Dirk Schriefer, Heidi Stölzer-Hutsch, Hernan Inojosa, Tjalf Ziemssen

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. 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

5 authors.

Katrin TrentzschCenter of Clinical Neuroscience - Neurological Clinic, Faculty of Medicine and University Hospital Carl Gustav Carus, TUD Dresden University of Technology, 01307, Dresden, Germany.ORCID http://orcid.org/0000-0003-2832-4640
Dirk SchrieferCenter of Clinical Neuroscience - Neurological Clinic, Faculty of Medicine and University Hospital Carl Gustav Carus, TUD Dresden University of Technology, 01307, Dresden, Germany.ORCID http://orcid.org/0000-0002-7524-7628
Heidi Stölzer-HutschCenter of Clinical Neuroscience - Neurological Clinic, Faculty of Medicine and University Hospital Carl Gustav Carus, TUD Dresden University of Technology, 01307, Dresden, Germany.ORCID http://orcid.org/0000-0002-1656-501X
Hernan InojosaCenter of Clinical Neuroscience - Neurological Clinic, Faculty of Medicine and University Hospital Carl Gustav Carus, TUD Dresden University of Technology, 01307, Dresden, Germany.ORCID http://orcid.org/0000-0002-1377-836X
Tjalf ZiemssenCenter of Clinical Neuroscience - Neurological Clinic, Faculty of Medicine and University Hospital Carl Gustav Carus, TUD Dresden University of Technology, 01307, Dresden, Germany. tjalf.ziemssen@ukdd.de.ORCID http://orcid.org/0000-0001-8799-8202

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gait disorders are among the most disabling symptoms in people with multiple sclerosis (pwMS), substantially affecting quality of life, autonomy, and participation. The Expanded Disability Status Scale (EDSS) captures impairments -particularly pyramidal, cerebellar and sensory- that influence gait patterns. Quantitative gait analysis enables objective exploration of these patterns supporting personalised strategies. This study aimed to characterise gait profiles in pwMS based on EDSS-derived functional scores. In this cross-sectional study at University Hospital Dresden, 204 pwMS and 237 healthy controls underwent instrumented gait assessments under self-selected, fast, and dual-task conditions. PwMS were categorised into pyramidal, cerebellar, or sensory gait pattern groups based on EDSS functional system scores. Spatiotemporal gait parameters were analysed using generalised linear models adjusted for age, gender, and body mass index. Sensory gait patterns were observed in 57.8% of pwMS, pyramidal in 27.9%, and cerebellar in 14.2%. Significant group differences emerged across all walking conditions. Ataxic gait showed reduced speed and increased step and stride variability. Sensory patterns featured higher speed, longer steps, and increased cadence. Pyramidal patterns resembled ataxic ones but differed under fast walking. EDSS-based functional deficits correspond to distinct MS-specific gait profiles. Multidimensional clinical gait phenotyping provides actionable insights for tailoring rehabilitation and monitoring mobility outcomes in pwMS.

Indexed as

GaitGait Disorders, NeurologicMultiple SclerosisAdultCase-Control StudiesCross-Sectional StudiesDisability EvaluationFemaleGait AnalysisHumansMaleMiddle AgedPhenotypeGaitGait or walking classificationMultiple sclerosisPattern detectionPhenotyping

Identifiers

PMID40962905
PMCPMC12443981

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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.