Evidence map›Paper›PMID 41108486›Full record

ArticleNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology2025

Is gaitrite system sensitive in discriminating gait pattern of subjects affected by Charcot Marie tooth? A pilot study.

Cristina Schenone, Maria Lagostina, Marta Ponzano, Chiara Avanti, Cecilia Contenti, Mehrnaz Hamedani, Marina Grandis, Chiara Gemelli, Sara Massucco, Lucio Marinelli and 4 more

Abstract read
In one paragraph

Article in Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Commentary on "Is gaitrite system sensitive in discriminating gait pattern of subjects affected by Charcot Marie tooth? A pilot study".Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors.

Cristina SchenoneDepartment of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DINOGMI), University of Genoa, Genoa, Italy. cristina.schenone@edu.unige.it.ORCID http://orcid.org/0009-0009-0442-3549
Maria LagostinaDepartment of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DINOGMI), University of Genoa, Genoa, Italy.
Marta PonzanoDepartment of Health Sciences (DISSAL), Biostatistics Unit, University of Genoa, Genoa, Italy.
Chiara AvantiSC Recupero e Rieducazione Funzionale ASL 3 Genovese, Genoa, Italy.
Cecilia ContentiIRCCS Ospedale Policlinico San Martino IRCCS, Genoa, Italy.
Mehrnaz HamedaniDepartment of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DINOGMI), University of Genoa, Genoa, Italy.
Marina GrandisDepartment of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DINOGMI), University of Genoa, Genoa, Italy.
Chiara GemelliIRCCS Ospedale Policlinico San Martino IRCCS, Genoa, Italy.
Sara MassuccoDepartment of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DINOGMI), University of Genoa, Genoa, Italy.
Lucio MarinelliDepartment of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DINOGMI), University of Genoa, Genoa, Italy.
Edoardo RovetaIRCCS Ospedale Policlinico San Martino IRCCS, Genoa, Italy.
Angelo SchenoneDepartment of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DINOGMI), University of Genoa, Genoa, Italy.
Carlo TrompettoDepartment of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DINOGMI), University of Genoa, Genoa, Italy.
Mori LauraDepartment of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health (DINOGMI), University of Genoa, Genoa, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCharcot-Marie-Tooth (CMT) disease is the most common hereditary neuropathy, characterized by progressive distal muscle weakness and gait abnormalities, impacting patients mobility and quality of life. Despite efforts to develop effective treatments, pharmacological options remain limited. Evaluation of gait function is crucial for assessing disease progression and treatment efficacy.

aimThis study compared the sensitivity of clinical and instrumental outcome measures (OM) in discriminating CMT patients and identifying key spatio-temporal gait parameters and their correlations with clinical measures.

methodsEighteen CMT patients and 18 healthy age-matched subjects (HS) were evaluated using clinical scales and instrumental gait analysis. Clinical measures included the 10 m walk test (10MWT), 6-minutes walk test (6MWT), Berg balance scale (BBS), Short Physical Performance Battery (SPPB), CMT Examination Score (CMTES), and Walk12 scale. Instrumental evaluation utilized the GAITRite electronic walkway system to assess spatio-temporal parameters. Correlations between clinical and instrumental parameters were examined.

resultsCMT patients exhibited significantly lower performance in clinical scales compared to HS. Instrumental evaluation revealed significant differences in stride length, velocity, stance percentage, and swing percentage between CMT patients and HS. Correlation analysis demonstrated associations between clinical and instrumental measures, particularly with stride length, gait speed, and balance assessments.

conclusionThe GAITRite system demonstrated sensitivity in discriminating CMT patients and controls, highlighting gait abnormalities consistent with previous literature findings. Correlations between instrumental and clinical measures suggest potential for objective gait assessment in CMT management. Further research with larger cohorts is warranted to validate these findings and assess longitudinal gait changes in CMT.

Indexed as

Charcot-Marie-Tooth DiseaseGaitGait AnalysisGait Disorders, NeurologicAdultFemaleHumansMaleMiddle AgedPilot ProjectsWalk TestYoung AdultBalanceGaitHereditary neuropathyOutcome measures

Identifiers

PMID41108486
PMCPMC12678515

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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.