Literature DB >> 28074267

Reduced serum myostatin concentrations associated with genetic muscle disease progression.

Peter M Burch1, Oksana Pogoryelova2, Joe Palandra3, Richard Goldstein4, Donald Bennett5, Lori Fitz5, Michela Guglieri2, Chiara Marini Bettolo2, Volker Straub2, Teresinha Evangelista2, Hendrik Neubert3, Hanns Lochmüller2, Carl Morris5,6.   

Abstract

Myostatin is a highly conserved protein secreted primarily from skeletal muscle that can potently suppress muscle growth. This ability to regulate skeletal muscle mass has sparked intense interest in the development of anti-myostatin therapies for a wide array of muscle disorders including sarcopenia, cachexia and genetic neuromuscular diseases. While a number of studies have examined the circulating myostatin concentrations in healthy and sarcopenic populations, very little data are available from inherited muscle disease patients. Here, we have measured the myostatin concentration in serum from seven genetic neuromuscular disorder patient populations using immunoaffinity LC-MS/MS. Average serum concentrations of myostatin in all seven muscle disease patient groups were significantly less than those measured in healthy controls. Furthermore, circulating myostatin concentrations correlated with clinical measures of disease progression for five of the muscle disease patient populations. These findings greatly expand the understanding of myostatin in neuromuscular disease and suggest its potential utility as a biomarker of disease progression.

Entities:  

Keywords:  Biomarker; Mass spectrometry; Myostatin; Neuromuscular disease

Mesh:

Substances:

Year:  2017        PMID: 28074267     DOI: 10.1007/s00415-016-8379-6

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


  44 in total

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5.  Systemic myostatin inhibition via liver-targeted gene transfer in normal and dystrophic mice.

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Journal:  PLoS One       Date:  2010-02-11       Impact factor: 3.240

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Review 7.  Limb-girdle muscular dystrophies--from genetics to molecular pathology.

Authors:  S H Laval; K M D Bushby
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8.  Myostatin as a mediator of sarcopenia versus homeostatic regulator of muscle mass: insights using a new mass spectrometry-based assay.

Authors:  H Robert Bergen; Joshua N Farr; Patrick M Vanderboom; Elizabeth J Atkinson; Thomas A White; Ravinder J Singh; Sundeep Khosla; Nathan K LeBrasseur
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9.  Affinity proteomics within rare diseases: a BIO-NMD study for blood biomarkers of muscular dystrophies.

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Journal:  PLoS One       Date:  2013-11-25       Impact factor: 3.240

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  18 in total

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Authors:  Roula Tsonaka; Mirko Signorelli; Ekrem Sabir; Alexandre Seyer; Kristina Hettne; Annemieke Aartsma-Rus; Pietro Spitali
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Review 2.  Inhibition of myostatin and related signaling pathways for the treatment of muscle atrophy in motor neuron diseases.

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3.  A mouse anti-myostatin antibody increases muscle mass and improves muscle strength and contractility in the mdx mouse model of Duchenne muscular dystrophy and its humanized equivalent, domagrozumab (PF-06252616), increases muscle volume in cynomolgus monkeys.

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Review 4.  GNE myopathy: from clinics and genetics to pathology and research strategies.

Authors:  Oksana Pogoryelova; José Andrés González Coraspe; Nikoletta Nikolenko; Hanns Lochmüller; Andreas Roos
Journal:  Orphanet J Rare Dis       Date:  2018-05-02       Impact factor: 4.123

Review 5.  Targeting the myostatin signaling pathway to treat muscle loss and metabolic dysfunction.

Authors:  Se-Jin Lee
Journal:  J Clin Invest       Date:  2021-05-03       Impact factor: 14.808

6.  Platelet Derived Growth Factor-AA Correlates With Muscle Function Tests and Quantitative Muscle Magnetic Resonance in Dystrophinopathies.

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7.  Downregulation of myostatin pathway in neuromuscular diseases may explain challenges of anti-myostatin therapeutic approaches.

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8.  MRC Centre Neuromuscular Biobank (Newcastle and London): Supporting and facilitating rare and neuromuscular disease research worldwide.

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9.  Specific inhibition of myostatin activation is beneficial in mouse models of SMA therapy.

Authors:  Kimberly K Long; Karen M O'Shea; Ramzi J Khairallah; Kelly Howell; Sergey Paushkin; Karen S Chen; Shaun M Cote; Micah T Webster; Joseph P Stains; Erin Treece; Alan Buckler; Adriana Donovan
Journal:  Hum Mol Genet       Date:  2019-04-01       Impact factor: 6.150

10.  Myostatin: a Circulating Biomarker Correlating with Disease in Myotubular Myopathy Mice and Patients.

Authors:  Catherine Koch; Suzie Buono; Alexia Menuet; Anne Robé; Sarah Djeddi; Christine Kretz; Raquel Gomez-Oca; Marion Depla; Arnaud Monseur; Leen Thielemans; Laurent Servais; Jocelyn Laporte; Belinda S Cowling
Journal:  Mol Ther Methods Clin Dev       Date:  2020-05-04       Impact factor: 6.698

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