Evidence map›Paper›PMID 31429798›Full record

ArticleBMC research notes2019

Training program-induced skeletal muscle adaptations in two men with myotonic dystrophy type 1.

Marie-Pier Roussel, Marika Morin, Mélina Girardin, Anne-Marie Fortin, Mario Leone, Jean Mathieu, Cynthia Gagnon, Elise Duchesne

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in BMC research notes, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04001920 (Effects of a Multiple Component Training Program on Muscles, Maximal Muscle Strength, Endurance and Functional Performance in Adults With Myotonic Dystrophy Type 1), which is not on this map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 39% 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.

NCT04001920 nacompletednot on this map

Effects of a Multiple Component Training Program on Muscles, Maximal Muscle Strength, Endurance and Functional Performance in Adults With Myotonic Dystrophy Type 1: A Pilot Study

TypeinterventionalSponsorCynthia GagnonRan2013 to 2013Enrolled11ConditionsMyotonic Dystrophy 1ArmsTraining program
3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Myotonic Dystrophy type 2 unmasked by physical activity resumption following COVID-19 lockdown: case discussion and review of the literature.Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology · 2024
    Review
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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

8 authors at 3 institutions in 1 country.

Marie-Pier RousselDépartement des sciences fondamentales, Université du Québec à Chicoutimi, Saguenay, QC, Canada.
Marika MorinDépartement des sciences de la santé, Université du Québec à Chicoutimi, Saguenay, QC, Canada.
Mélina GirardinDépartement des sciences de la santé, Université du Québec à Chicoutimi, Saguenay, QC, Canada.
Anne-Marie FortinGroupe de recherche interdisciplinaire sur les maladies neuromusculaires, Centre intégré universitaire de santé et de services sociaux du Saguenay-Lac-St-Jean, Installations de Jonquière, Saguenay, QC, Canada.
Mario LeoneGroupe de recherche interdisciplinaire sur les maladies neuromusculaires, Centre intégré universitaire de santé et de services sociaux du Saguenay-Lac-St-Jean, Installations de Jonquière, Saguenay, QC, Canada.
Jean MathieuGroupe de recherche interdisciplinaire sur les maladies neuromusculaires, Centre intégré universitaire de santé et de services sociaux du Saguenay-Lac-St-Jean, Installations de Jonquière, Saguenay, QC, Canada.
Cynthia GagnonGroupe de recherche interdisciplinaire sur les maladies neuromusculaires, Centre intégré universitaire de santé et de services sociaux du Saguenay-Lac-St-Jean, Installations de Jonquière, Saguenay, QC, Canada.
Elise DuchesneGroupe de recherche interdisciplinaire sur les maladies neuromusculaires, Centre intégré universitaire de santé et de services sociaux du Saguenay-Lac-St-Jean, Installations de Jonquière, Saguenay, QC, Canada. elise1_duchesne@uqac.ca.ORCID http://orcid.org/0000-0002-9953-8315
Université du Québec à Chicoutimi · CAUniversité de Sherbrooke · CACentre Intégré Universitaire de Santé et de Services Sociaux du Saguenay–Lac-Saint-Jean · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe purpose of this side product of another unpublished research project, was to address the effects of a training program on skeletal muscle adaptations of people with myotonic dystrophy type 1 (DM1), under a multifaceted perspective. The objective of this study was to look at training induced muscular adaptations by evaluating changes in muscle strength, myofiber cross-sectional area (CSA), proportion of myofiber types and with indirect markers of muscle growth [proportion of centrally nucleated fibers (CNF) and density of neutrophils and macrophages]. Two men with DM1 underwent a 12-week strength/endurance training program (18 sessions). Two muscle biopsies were obtained pre- and post-training program.

resultsMuscular adaptations occurred only in Patient 1, who attended 72% of the training sessions compared to 39% for Patient 2. These adaptations included increase in the CSA of type I and II myofibers and changes in their proportion. No changes were observed in the percentage of CNF, infiltration of neutrophils and macrophages and muscle strength. These results illustrate the capacity of skeletal muscle cells to undergo adaptations linked to muscle growth in DM1 patients. Also, these adaptations seem to be dependent on the attendance. Trial registration Clinicaltrials.gov NCT04001920 retrospectively registered on June 26th, 2019.

Indexed as

Adaptation, PhysiologicalAdultHumansLeukocytesMaleMiddle AgedMuscle Fibers, SkeletalMuscle, SkeletalMyotonic DystrophyLeukocytesMuscle growthMuscle plasticityMyogenesisMyotonic dystrophy type 1Training program

Identifiers

PMID31429798
PMCPMC6700834
OpenAlexW2969507580

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.