Cargando…

Towards the Identification of Biomarkers for Muscle Function Improvement in Myotonic Dystrophy Type 1

BACKGROUND: Myotonic dystrophy type 1 (DM1) is the most common muscular dystrophy in adults. In DM1 patients, skeletal muscle is severely impaired, even atrophied and patients experience a progressive decrease in maximum strength. Strength training for these individuals can improve their muscle func...

Descripción completa

Detalles Bibliográficos
Autores principales: Aoussim, Amira, Légaré, Cécilia, Roussel, Marie-Pier, Madore, Anne-Marie, Morissette, Mathieu C., Laprise, Catherine, Duchesne, Elise
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10657677/
https://www.ncbi.nlm.nih.gov/pubmed/37694373
http://dx.doi.org/10.3233/JND-221645
_version_ 1785148189365501952
author Aoussim, Amira
Légaré, Cécilia
Roussel, Marie-Pier
Madore, Anne-Marie
Morissette, Mathieu C.
Laprise, Catherine
Duchesne, Elise
author_facet Aoussim, Amira
Légaré, Cécilia
Roussel, Marie-Pier
Madore, Anne-Marie
Morissette, Mathieu C.
Laprise, Catherine
Duchesne, Elise
author_sort Aoussim, Amira
collection PubMed
description BACKGROUND: Myotonic dystrophy type 1 (DM1) is the most common muscular dystrophy in adults. In DM1 patients, skeletal muscle is severely impaired, even atrophied and patients experience a progressive decrease in maximum strength. Strength training for these individuals can improve their muscle function and mass, however, the biological processes involved in these improvements remain unknown. OBJECTIVE: This exploratory study aims at identifying the proteomic biomarkers and variables associated with the muscle proteome changes induced by training in DM1 individuals. METHODS: An ion library was developed from liquid chromatography-tandem mass spectrometry proteomic analyses of Vastus Lateralis muscle biopsies collected in 11 individuals with DM1 pre-and post-training. RESULTS: The proteomic analysis showed that the levels of 44 proteins were significantly modulated. A literature review (PubMed, UniProt, PANTHER, REACTOME) classified these proteins into biological sub-classes linked to training-induced response, including immunity, energy metabolism, apoptosis, insulin signaling, myogenesis and muscle contraction. Linear models identified key variables explaining the proteome modulation, including atrophy and hypertrophy factors. Finally, six proteins of interest involved in myogenesis, muscle contraction and insulin signaling were identified: calpain-3 (CAN3; Muscle development, positive regulation of satellite cell activation), 14-3-3 protein epsilon (1433E; Insulin/Insulin-like growth factor, PI3K/Akt signaling), myosin-binding protein H (MYBPH; Regulation of striated muscle contraction), four and a half LIM domains protein 3 (FHL3; Muscle organ development), filamin-C (FLNC; Muscle fiber development) and Cysteine and glycine-rich protein 3 (CSRP3). CONCLUSION: These findings may lead to the identification for DM1 individuals of novel muscle biomarkers for clinical improvement induced by rehabilitation, which could eventually be used in combination with a targeted pharmaceutical approach to improving muscle function, but further studies are needed to confirm those results.
format Online
Article
Text
id pubmed-10657677
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher IOS Press
record_format MEDLINE/PubMed
spelling pubmed-106576772023-11-19 Towards the Identification of Biomarkers for Muscle Function Improvement in Myotonic Dystrophy Type 1 Aoussim, Amira Légaré, Cécilia Roussel, Marie-Pier Madore, Anne-Marie Morissette, Mathieu C. Laprise, Catherine Duchesne, Elise J Neuromuscul Dis Research Report BACKGROUND: Myotonic dystrophy type 1 (DM1) is the most common muscular dystrophy in adults. In DM1 patients, skeletal muscle is severely impaired, even atrophied and patients experience a progressive decrease in maximum strength. Strength training for these individuals can improve their muscle function and mass, however, the biological processes involved in these improvements remain unknown. OBJECTIVE: This exploratory study aims at identifying the proteomic biomarkers and variables associated with the muscle proteome changes induced by training in DM1 individuals. METHODS: An ion library was developed from liquid chromatography-tandem mass spectrometry proteomic analyses of Vastus Lateralis muscle biopsies collected in 11 individuals with DM1 pre-and post-training. RESULTS: The proteomic analysis showed that the levels of 44 proteins were significantly modulated. A literature review (PubMed, UniProt, PANTHER, REACTOME) classified these proteins into biological sub-classes linked to training-induced response, including immunity, energy metabolism, apoptosis, insulin signaling, myogenesis and muscle contraction. Linear models identified key variables explaining the proteome modulation, including atrophy and hypertrophy factors. Finally, six proteins of interest involved in myogenesis, muscle contraction and insulin signaling were identified: calpain-3 (CAN3; Muscle development, positive regulation of satellite cell activation), 14-3-3 protein epsilon (1433E; Insulin/Insulin-like growth factor, PI3K/Akt signaling), myosin-binding protein H (MYBPH; Regulation of striated muscle contraction), four and a half LIM domains protein 3 (FHL3; Muscle organ development), filamin-C (FLNC; Muscle fiber development) and Cysteine and glycine-rich protein 3 (CSRP3). CONCLUSION: These findings may lead to the identification for DM1 individuals of novel muscle biomarkers for clinical improvement induced by rehabilitation, which could eventually be used in combination with a targeted pharmaceutical approach to improving muscle function, but further studies are needed to confirm those results. IOS Press 2023-11-07 /pmc/articles/PMC10657677/ /pubmed/37694373 http://dx.doi.org/10.3233/JND-221645 Text en © 2023 – The authors. Published by IOS Press https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC 4.0) License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Report
Aoussim, Amira
Légaré, Cécilia
Roussel, Marie-Pier
Madore, Anne-Marie
Morissette, Mathieu C.
Laprise, Catherine
Duchesne, Elise
Towards the Identification of Biomarkers for Muscle Function Improvement in Myotonic Dystrophy Type 1
title Towards the Identification of Biomarkers for Muscle Function Improvement in Myotonic Dystrophy Type 1
title_full Towards the Identification of Biomarkers for Muscle Function Improvement in Myotonic Dystrophy Type 1
title_fullStr Towards the Identification of Biomarkers for Muscle Function Improvement in Myotonic Dystrophy Type 1
title_full_unstemmed Towards the Identification of Biomarkers for Muscle Function Improvement in Myotonic Dystrophy Type 1
title_short Towards the Identification of Biomarkers for Muscle Function Improvement in Myotonic Dystrophy Type 1
title_sort towards the identification of biomarkers for muscle function improvement in myotonic dystrophy type 1
topic Research Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10657677/
https://www.ncbi.nlm.nih.gov/pubmed/37694373
http://dx.doi.org/10.3233/JND-221645
work_keys_str_mv AT aoussimamira towardstheidentificationofbiomarkersformusclefunctionimprovementinmyotonicdystrophytype1
AT legarececilia towardstheidentificationofbiomarkersformusclefunctionimprovementinmyotonicdystrophytype1
AT rousselmariepier towardstheidentificationofbiomarkersformusclefunctionimprovementinmyotonicdystrophytype1
AT madoreannemarie towardstheidentificationofbiomarkersformusclefunctionimprovementinmyotonicdystrophytype1
AT morissettemathieuc towardstheidentificationofbiomarkersformusclefunctionimprovementinmyotonicdystrophytype1
AT laprisecatherine towardstheidentificationofbiomarkersformusclefunctionimprovementinmyotonicdystrophytype1
AT duchesneelise towardstheidentificationofbiomarkersformusclefunctionimprovementinmyotonicdystrophytype1