Myostatin and follistatin as monitoring and prognostic biomarkers in dysferlinopathy

Myostatin is a myokine which acts upon skeletal muscle to inhibit growth and regeneration. Myostatin is endogenously antagonised by follistatin. This study assessed serum myostatin and follistatin concentrations as monitoring or prognostic biomarkers in dysferlinopathy, an autosomal recessively inhe...

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Detalles Bibliográficos
Autores: Moore, Ursula|||0000-0002-0643-5596, Fernández Simón, Esther|||0000-0003-4804-6553, Schiava, Marianela|||0000-0002-2709-265X, Cox, Dan, Gordish-Dressman, Heather|||0000-0002-2330-5427, James, Meredith K.|||0000-0001-8078-7744, Mayhew, Anna G.|||0000-0001-7085-9011, Wilson, Ian, Guglieri, Michela|||0000-0002-8455-0637, Rufibach, Laura E.|||0000-0001-8208-0574, Blamire, Andrew|||0000-0002-8749-1257, Carlier, Pierre G.|||0000-0002-2315-6927, Mori-Yoshimura, Madoka|||0000-0003-4312-9114, Day, John W.|||0000-0002-0086-9529, Jones, Kristi J., Bharucha-Goebel, Diana|||0000-0002-7437-0982, Salort-Campana, Emmanuelle|||0000-0002-1846-3017, Pestronk, Alan|||0000-0002-8991-5770, Walter, Maggie C.|||0000-0002-7611-4827, Paradas, Carmen|||0000-0002-6917-2236, Stojkovic, Tanya|||0000-0002-4054-2838, Bravver, Elena, Pegoraro, Elena|||0000-0002-7740-4156, Mendell, Jerry R.|||0000-0002-2691-0200, Bushby, Kate|||0000-0001-8818-4008, Diaz-Manera, Jordi|||0000-0003-2941-7988, Straub, Volker|||0000-0001-9046-3540
Tipo de recurso: artículo
Fecha de publicación:2023
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:303442
Acceso en línea:https://ddd.uab.cat/record/303442
https://dx.doi.org/urn:doi:10.1016/j.nmd.2023.01.001
Access Level:acceso abierto
Palabra clave:Dysferlinopathy
Follistatin
Limb girdle muscular dystrophy R2
Miyoshi myopathy
Muscular dystrophy
Myostatin
Descripción
Sumario:Myostatin is a myokine which acts upon skeletal muscle to inhibit growth and regeneration. Myostatin is endogenously antagonised by follistatin. This study assessed serum myostatin and follistatin concentrations as monitoring or prognostic biomarkers in dysferlinopathy, an autosomal recessively inherited muscular dystrophy. Myostatin was quantified twice with a three-year interval in 76 patients with dysferlinopathy and 38 controls. Follistatin was quantified in 62 of these patients at the same timepoints, and in 31 controls. Correlations with motor function, muscle fat fraction and contractile cross-sectional area were performed. A regression model was used to account for confounding variables. Baseline myostatin, but not follistatin, correlated with baseline function and MRI measures. However, in individual patients, three-year change in myostatin did not correlate with functional or MRI changes. Linear modelling demonstrated that function, serum creatine kinase and C-reactive protein, but not age, were independently related to myostatin concentration. Baseline myostatin concentration predicted loss of ambulation but not rate of change of functional or MRI measures, even when relative inhibition with follistatin was considered. With adjustment for extra-muscular causes of variation, myostatin could form a surrogate measure of functional ability or muscle mass, however myostatin inhibition does not form a promising treatment target in dysferlinopathy.