Evidence map›Paper›PMID 36782059›Full record

ArticleScientific reports2023

Muscle fat replacement and contractility in patients with skeletal muscle sodium channel disorders.

Jonas Jalili Pedersen, Mads Godtfeldt Stemmerik, Laura Nørager Jacobsen, Sofie Vinther Skriver, Gustav Rhode Wilms, Morten Duno, John Vissing

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04808388 (Using MRI to Quantify Fatty Infiltration in Muscle Tissue, and Compare it to Isometric Muscle Strength Measurements and), which is not on this map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.5field-weighted citation impact, top 18% 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.

NCT04808388 unknown statusnot on this map

Using MRI to Quantify Fatty Infiltration in Muscle Tissue, and Compare it to Isometric Muscle Strength Measurements and (2) Use Questionnaires, Systemic Interview and Simple Myotonic Bed-side Tests to Describe the Phenotype.

TypeobservationalSponsorRigshospitalet, DenmarkRan2021 to 2021Enrolled25ConditionsParamyotonia Congenita, Nondystrophic MyotoniaArmsMRI
3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 10 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

Jonas Jalili PedersenCopenhagen Neuromuscular Center, Department of Neurology, Rigshospitalet, University of Copenhagen, Inge Lehmanns Vej 7-9, 2100, Copenhagen, Denmark. Jalilijonas@gmail.com.ORCID 0000-0002-9496-7655
Mads Godtfeldt StemmerikCopenhagen Neuromuscular Center, Department of Neurology, Rigshospitalet, University of Copenhagen, Inge Lehmanns Vej 7-9, 2100, Copenhagen, Denmark.
Laura Nørager JacobsenCopenhagen Neuromuscular Center, Department of Neurology, Rigshospitalet, University of Copenhagen, Inge Lehmanns Vej 7-9, 2100, Copenhagen, Denmark.
Sofie Vinther SkriverCopenhagen Neuromuscular Center, Department of Neurology, Rigshospitalet, University of Copenhagen, Inge Lehmanns Vej 7-9, 2100, Copenhagen, Denmark.
Gustav Rhode WilmsCopenhagen Neuromuscular Center, Department of Neurology, Rigshospitalet, University of Copenhagen, Inge Lehmanns Vej 7-9, 2100, Copenhagen, Denmark.
Morten DunoClinical Genetic Laboratory, Department of Biochemical Genetics, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
John VissingCopenhagen Neuromuscular Center, Department of Neurology, Rigshospitalet, University of Copenhagen, Inge Lehmanns Vej 7-9, 2100, Copenhagen, Denmark.
University of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Skeletal muscle sodium channel disorders give rise to episodic symptoms such as myotonia and/or periodic paralysis. Chronic symptoms with permanent weakness are not considered characteristic of the phenotypes. Muscle fat replacement represents irreversible damage that inevitably will impact on muscle strength. This study investigates muscle fat replacement and contractility in patients with pathogenic SCN4A variants compared to healthy controls. T1-weighted and 2-point Dixon MRI of the legs were conducted to assess fat replacement. Stationary dynamometry was used to assess muscle strength. Contractility was determined by maximal muscle contraction divided by cross-sectional muscle area. The average cross-sectional intramuscular fat fraction was greater in patients compared with controls by 2.5% in the calves (95% CI 0.74-4.29%, p = 0.007) and by 2.0% in the thighs (95% CI 0.75-3.2%, p = 0.003). Muscle contractility was less in patients vs. controls by 14-27% (p < 0.05). Despite greater fat fraction and less contractility, absolute strength was not significantly less. This study quantitatively documents greater fat fraction and additionally describes difference in muscle contractility in a large cohort of patients with skeletal muscle sodium channel disorders. The clinical impact of these abnormal findings is likely limited as muscle hypertrophy in the patients served to preserve absolute muscle strength. Subgroup analysis indicated significant difference in phenotype by genotype, however these findings lack statistical significance and serve as inspiration for future researchers to probe into the geno- phenotype relationship in these disorders.Trial registration: The study was registered at http://clinicaltrials.gov (identifier: NCT04808388).

Indexed as

ChannelopathiesMuscular DiseasesMyotoniaCross-Sectional StudiesHumansMuscle, SkeletalNAV1.4 Voltage-Gated Sodium ChannelSodium ChannelsNAV1.4 Voltage-Gated Sodium ChannelSCN4A protein, humanSodium Channels

Identifiers

PMID36782059
PMCPMC9925746
OpenAlexW4320557284

What OpenQuestion holds

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Registered trials

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.