Evidence map›Paper›PMID 32877421›Full record

ArticlePloS one2020

Muscle weakness has a limited effect on motor control of gait in Duchenne muscular dystrophy.

Ines Vandekerckhove, Nathalie De Beukelaer, Marleen Van den Hauwe, Benjamin R Shuman, Katherine M Steele, Anja Van Campenhout, Nathalie Goemans, Kaat Desloovere, Marije Goudriaan

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 27% of its field
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

7 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
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  4. Review
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  7. One more time about motor (and non-motor) synergies.Experimental brain research · 2021
    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

9 authors at 3 institutions in 3 countries.

Ines VandekerckhoveDepartment of Rehabilitation Sciences, KU Leuven, Leuven, Belgium.ORCID 0000-0002-6023-3004
Nathalie De BeukelaerDepartment of Rehabilitation Sciences, KU Leuven, Leuven, Belgium.ORCID 0000-0002-7800-3354
Marleen Van den HauweDepartment of Rehabilitation Sciences, KU Leuven, Leuven, Belgium.
Benjamin R ShumanMechanical Engineering, University of Washington, Seattle, Washington, United States of America.
Katherine M SteeleMechanical Engineering, University of Washington, Seattle, Washington, United States of America.
Anja Van CampenhoutDepartment of Development and Regeneration, KU Leuven, Leuven, Belgium.
Nathalie GoemansDepartment of Child Neurology, University Hospitals, Leuven, Belgium.
Kaat DesloovereDepartment of Rehabilitation Sciences, KU Leuven, Leuven, Belgium.
Marije GoudriaanDepartment of Rehabilitation Sciences, KU Leuven, Leuven, Belgium.ORCID 0000-0001-6162-3867
KU Leuven · BEUniversity of Washington · USVrije Universiteit Amsterdam · NL

Funding

Quantifying patient-specific changes in neuromuscular control in cerebral palsyR01NS091056 · NINDS · UNIVERSITY OF WASHINGTON · PI Michael Hart Schwartz, Katherine M Steele · 2015 to 2026
$3.4M
NINDS NIH HHS R01 NS091056
6 · The paper itself

Abstract

aimOur aim was to determine if synergy weights and activations are altered in Duchenne muscular dystrophy (DMD) and if these alterations could be linked to muscle weakness.

methodsIn 22 children with DMD and 22 typical developing (TD) children of a similar age, surface electromyography (sEMG) of the gluteus medius, rectus femoris (REF), medial hamstrings, tibialis anterior, and medial gastrocnemius (GAS) were recorded during gait. Muscle weakness was assessed with maximal voluntary isometric contractions (MVIC). Synergies were calculated with non-negative matrix factorization. The number of synergies explaining ≥90% of the variance in the sEMG signals (N90), were extracted and grouped with k-means cluster analysis. We verified differences in weights with a Mann-Whitney U test. Statistical non-parametric mapping (Hotelling's T2 test and two-tailed t-test) was used to assess group differences in synergy activations. We used Spearman's rank correlation coefficients and canonical correlation analysis to assess if weakness was related to modifications in weights and activations, respectively.

resultsFor both groups, average N90 was three. In synergy one, characterized by activity at the beginning of stance, the DMDs showed an increased REF weight (p = 0.001) and decreased GAS weight (p = 0.007). Synergy activations were similar, with only a small difference detected in mid-swing in the combined activations (p<0.001). Weakness was not associated with these differences.

conclusionDespite the apparent weakness in DMD, synergy weights and activations were similar between the two groups. Our findings are in line with previous research suggesting non-neural alterations have limited influence on muscle synergies.

Indexed as

Biomechanical PhenomenaChildElectromyographyFemaleGaitGait Disorders, NeurologicHumansIsometric ContractionMaleMuscle, SkeletalMuscle StrengthMuscle WeaknessMuscular Dystrophy, Duchenne

Identifiers

PMID32877421
PMCPMC7467330
OpenAlexW3081695602

What OpenQuestion holds

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LicenceCC BY
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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.