Evidence map›Paper›PMID 37143180›Full record

ArticleCerebral cortex (New York, N.Y. : 1991)2023

Cortico-muscular coherence in primary lateral sclerosis reveals abnormal cortical engagement during motor function beyond primary motor areas.

Saroj Bista, Amina Coffey, Antonio Fasano, Teresa Buxo, Matthew Mitchell, Eileen Rose Giglia, Stefan Dukic, Mark Heverin, Muthuraman Muthuraman, Richard G Carson and 4 more

Abstract read
In one paragraph

Article in Cerebral cortex (New York, N.Y. : 1991), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. 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

14 authors.

Saroj BistaAcademic Unit of Neurology, Trinity Biomedical Science Institute, Trinity College Dublin, Dublin 2, Ireland.ORCID 0000-0003-0763-6864
Amina CoffeyAcademic Unit of Neurology, Trinity Biomedical Science Institute, Trinity College Dublin, Dublin 2, Ireland.
Antonio FasanoAcademic Unit of Neurology, Trinity Biomedical Science Institute, Trinity College Dublin, Dublin 2, Ireland.ORCID 0000-0002-8727-9141
Teresa BuxoAcademic Unit of Neurology, Trinity Biomedical Science Institute, Trinity College Dublin, Dublin 2, Ireland.ORCID 0009-0006-6349-5129
Matthew MitchellAcademic Unit of Neurology, Trinity Biomedical Science Institute, Trinity College Dublin, Dublin 2, Ireland.ORCID 0000-0002-9363-4170
Eileen Rose GigliaAcademic Unit of Neurology, Trinity Biomedical Science Institute, Trinity College Dublin, Dublin 2, Ireland.ORCID 0000-0002-2244-0803
Stefan DukicAcademic Unit of Neurology, Trinity Biomedical Science Institute, Trinity College Dublin, Dublin 2, Ireland.ORCID 0000-0001-7867-2876
Mark HeverinAcademic Unit of Neurology, Trinity Biomedical Science Institute, Trinity College Dublin, Dublin 2, Ireland.ORCID 0000-0002-7326-4432
Muthuraman MuthuramanNeural Engineering with Signal Analytics and Artificial Intelligence, Department of Neurology, University Hospital Würzburg, Würzburg 97080, Germany.ORCID 0000-0001-6158-2663
Richard G CarsonTrinity College Institute of Neuroscience and School of Psychology, Trinity College Dublin,, Dublin 2, Ireland.ORCID 0000-0002-1190-2814
Madeleine LowerySchool of Electrical and Electronic Engineering, University College Dublin, Dublin 4, Ireland.ORCID 0000-0001-6743-360X
Orla HardimanAcademic Unit of Neurology, Trinity Biomedical Science Institute, Trinity College Dublin, Dublin 2, Ireland.ORCID 0000-0003-2610-1291
Lara McManusAcademic Unit of Neurology, Trinity Biomedical Science Institute, Trinity College Dublin, Dublin 2, Ireland.ORCID 0000-0002-2255-7382
Bahman NasseroleslamiAcademic Unit of Neurology, Trinity Biomedical Science Institute, Trinity College Dublin, Dublin 2, Ireland.ORCID 0000-0002-2227-2176

Funding

Wellcome Trust
6 · The paper itself

Abstract

Primary lateral sclerosis (PLS) is a slowly progressing disorder, which is characterized primarily by the degeneration of upper motor neurons (UMNs) in the primary motor area (M1). It is not yet clear how the function of sensorimotor networks beyond M1 are affected by PLS. The aim of this study was to use cortico-muscular coherence (CMC) to characterize the oscillatory drives between cortical regions and muscles during a motor task in PLS and to examine the relationship between CMC and the level of clinical impairment. We recorded EEG and EMG from hand muscles in 16 participants with PLS and 18 controls during a pincer-grip task. In PLS, higher CMC was observed over contralateral-M1 (α- and γ-band) and ipsilateral-M1 (β-band) compared with controls. Significant correlations between clinically assessed UMN scores and CMC measures showed that higher clinical impairment was associated with lower CMC over contralateral-M1/frontal areas, higher CMC over parietal area, and both higher and lower CMC (in different bands) over ipsilateral-M1. The results suggest an atypical engagement of both contralateral and ipsilateral M1 during motor activity in PLS, indicating the presence of pathogenic and/or adaptive/compensatory alterations in neural activity. The findings demonstrate the potential of CMC for identifying dysfunction within the sensorimotor networks in PLS.

Indexed as

Motor CortexMotor Neuron DiseaseElectromyographyHandHumansMuscle, Skeletalcortico-muscular coherenceEMGneurodegeneration EEGprimary lateral sclerosis (PLS)upper motor neuron

Identifiers

PMID37143180
PMCPMC10321081

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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.