Evidence map›Paper›PMID 42329964›Full record

SynthesisPloS one2026

Applications of electromyography in Amyotrophic Lateral Sclerosis: A systematic review.

Ana Paula Mendonça Fernandes, Luiz Henrique Bertucci Borges, Ledycnarf Januário de Holanda, Bruno Henrique E Silva Bezerra, Anna Clara Sales Miranda Lopes, Maria Clara Fernandes da Silva, Ricardo A de M Valentim, Laurent Bougrain, Gabriel Alves Mendes Vasiljevic, Ana Raquel Rodrigues Lindquist

Abstract readSystematic Review
In one paragraph

Synthesis in PloS one, 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

10 authors.

Ana Paula Mendonça FernandesDepartment of Physical Therapy, Federal University of Rio Grande do Norte, Natal, Brazil.ORCID https://orcid.org/0000-0002-0100-8026
Luiz Henrique Bertucci BorgesDepartment of Physical Therapy, Federal University of Rio Grande do Norte, Natal, Brazil.
Ledycnarf Januário de HolandaBloorview Research Institute, Holland Bloorview Kids Rehabilitation Hospital, Toronto, Canada.
Bruno Henrique E Silva BezerraDepartment of Physical Therapy, Federal University of Rio Grande do Norte, Natal, Brazil.ORCID https://orcid.org/0000-0002-6713-4738
Anna Clara Sales Miranda LopesDepartment of Physical Therapy, Federal University of Rio Grande do Norte, Natal, Brazil.ORCID https://orcid.org/0009-0005-3792-3794
Maria Clara Fernandes da SilvaDepartment of Physical Therapy, Federal University of Rio Grande do Norte, Natal, Brazil.
Ricardo A de M ValentimLaboratory of Technological Innovation in Health, Federal University of Rio Grande do Norte, Natal, Brazil.ORCID https://orcid.org/0000-0002-9216-8593
Laurent BougrainDepartment of Complex System, Intelligence and Robotics at Loria, University of Lorraine, Nancy, France.
Gabriel Alves Mendes VasiljevicEdmond and Lily Safra International Institute of Neuroscience, Santos Dumont Institute (ISD), Macaíba, Brazil.
Ana Raquel Rodrigues LindquistDepartment of Physical Therapy, Federal University of Rio Grande do Norte, Natal, Brazil.ORCID https://orcid.org/0000-0001-9628-7891

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This systematic review examined the use of surface electromyography (sEMG) for the neuromuscular assessment of individuals with Amyotrophic Lateral Sclerosis (ALS), focusing on clinical parameters, the muscle groups evaluated, acquisition protocols, technical properties of the recording systems, integration with other technologies, and signal processing strategies. We included observational studies that applied sEMG to individuals diagnosed with ALS, with or without comparison to healthy controls, and without restrictions on publication year. The analyses included signals recorded at rest and during voluntary contractions, with or without the use of biofeedback. Most studies employed conventional or high-density surface electrodes, with sampling frequencies ranging from 500 Hz to 3000 Hz. The results showed that the primary parameters assessed were muscle fatigue, fasciculation patterns, the number of motor units (MUNE/MUNIX), motor unit firing rates, and signal complexity. These parameters demonstrated sensitivity to disease progression and may contribute to early diagnosis, phenotypic stratification, and functional monitoring of ALS. Additionally, the studies highlighted the increasing use of advanced computational approaches, such as machine learning, for feature extraction and automated classification. In conclusion, sEMG is a promising tool for functional assessment in ALS, with the potential to improve diagnostic accuracy and support new therapeutic strategies based on electrophysiological biomarkers. However, despite technological advances, the included studies displayed substantial methodological heterogeneity and limited protocol standardization. Integration with other neurophysiological modalities also remains underexplored, despite its significant clinical potential.

Indexed as

Amyotrophic Lateral SclerosisElectromyographyHumansMotor NeuronsMuscle, Skeletal

Identifiers

PMID42329964
PMCPMC13286138

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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.