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Impact of Disease Severity and Disease-Modifying Therapies on Myostatin Levels in SMA Patients
by
Dumonceaux, Julie
, Mackels, Laurane
, Buscemi, Laura
, Servais, Laurent
, Mariot, Virginie
in
Adolescent
/ Catalysis
/ Child
/ Child, Preschool
/ clinical trials
/ Computer Science Applications
/ Disease
/ disease-modifying therapies
/ Female
/ follisatin
/ Follistatin
/ Follistatin - metabolism
/ FSTN
/ GDF8
/ Human health sciences
/ Humans
/ Infant
/ Inorganic Chemistry
/ Male
/ Medical screening
/ Molecular Biology
/ MSTN protein, human
/ Muscular Atrophy, Spinal
/ Muscular Atrophy, Spinal - drug therapy
/ Muscular Atrophy, Spinal - metabolism
/ Musculoskeletal system
/ myostatin
/ Myostatin - antagonists & inhibitors
/ Myostatin - metabolism
/ Nervous system
/ nusinersen
/ Oligonucleotides
/ Oligonucleotides - therapeutic use
/ Organic Chemistry
/ Patients
/ Pediatrics
/ Physical and Theoretical Chemistry
/ Proteins
/ Pédiatrie
/ Retrospective Studies
/ Sciences de la santé humaine
/ Severity of Illness Index
/ Spectroscopy
/ spinal muscular atrophy
2024
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Impact of Disease Severity and Disease-Modifying Therapies on Myostatin Levels in SMA Patients
by
Dumonceaux, Julie
, Mackels, Laurane
, Buscemi, Laura
, Servais, Laurent
, Mariot, Virginie
in
Adolescent
/ Catalysis
/ Child
/ Child, Preschool
/ clinical trials
/ Computer Science Applications
/ Disease
/ disease-modifying therapies
/ Female
/ follisatin
/ Follistatin
/ Follistatin - metabolism
/ FSTN
/ GDF8
/ Human health sciences
/ Humans
/ Infant
/ Inorganic Chemistry
/ Male
/ Medical screening
/ Molecular Biology
/ MSTN protein, human
/ Muscular Atrophy, Spinal
/ Muscular Atrophy, Spinal - drug therapy
/ Muscular Atrophy, Spinal - metabolism
/ Musculoskeletal system
/ myostatin
/ Myostatin - antagonists & inhibitors
/ Myostatin - metabolism
/ Nervous system
/ nusinersen
/ Oligonucleotides
/ Oligonucleotides - therapeutic use
/ Organic Chemistry
/ Patients
/ Pediatrics
/ Physical and Theoretical Chemistry
/ Proteins
/ Pédiatrie
/ Retrospective Studies
/ Sciences de la santé humaine
/ Severity of Illness Index
/ Spectroscopy
/ spinal muscular atrophy
2024
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Impact of Disease Severity and Disease-Modifying Therapies on Myostatin Levels in SMA Patients
by
Dumonceaux, Julie
, Mackels, Laurane
, Buscemi, Laura
, Servais, Laurent
, Mariot, Virginie
in
Adolescent
/ Catalysis
/ Child
/ Child, Preschool
/ clinical trials
/ Computer Science Applications
/ Disease
/ disease-modifying therapies
/ Female
/ follisatin
/ Follistatin
/ Follistatin - metabolism
/ FSTN
/ GDF8
/ Human health sciences
/ Humans
/ Infant
/ Inorganic Chemistry
/ Male
/ Medical screening
/ Molecular Biology
/ MSTN protein, human
/ Muscular Atrophy, Spinal
/ Muscular Atrophy, Spinal - drug therapy
/ Muscular Atrophy, Spinal - metabolism
/ Musculoskeletal system
/ myostatin
/ Myostatin - antagonists & inhibitors
/ Myostatin - metabolism
/ Nervous system
/ nusinersen
/ Oligonucleotides
/ Oligonucleotides - therapeutic use
/ Organic Chemistry
/ Patients
/ Pediatrics
/ Physical and Theoretical Chemistry
/ Proteins
/ Pédiatrie
/ Retrospective Studies
/ Sciences de la santé humaine
/ Severity of Illness Index
/ Spectroscopy
/ spinal muscular atrophy
2024
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Impact of Disease Severity and Disease-Modifying Therapies on Myostatin Levels in SMA Patients
Journal Article
Impact of Disease Severity and Disease-Modifying Therapies on Myostatin Levels in SMA Patients
2024
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Overview
Clinical trials with treatments inhibiting myostatin pathways to increase muscle mass are currently ongoing in spinal muscular atrophy. Given evidence of potential myostatin pathway downregulation in Spinal Muscular Atrophy (SMA), restoring sufficient myostatin levels using disease-modifying treatments (DMTs) might arguably be necessary prior to considering myostatin inhibitors as an add-on treatment. This retrospective study assessed pre-treatment myostatin and follistatin levels’ correlation with disease severity and explored their alteration by disease-modifying treatment in SMA. We retrospectively collected clinical characteristics, motor scores, and mysotatin and follistatin levels between 2018 and 2020 in 25 Belgian patients with SMA (SMA1 (n = 13), SMA2 (n = 6), SMA 3 (n = 6)) and treated by nusinersen. Data were collected prior to treatment and after 2, 6, 10, 18, and 30 months of treatment. Myostatin levels correlated with patients’ age, weight, SMA type, and motor function before treatment initiation. After treatment, we observed correlations between myostatin levels and some motor function scores (i.e., MFM32, HFMSE, 6MWT), but no major effect of nusinersen on myostatin or follistatin levels over time. In conclusion, further research is needed to determine if DMTs can impact myostatin and follistatin levels in SMA, and how this could potentially influence patient selection for ongoing myostatin inhibitor trials.
Publisher
MDPI AG,Multidisciplinary Digital Publishing Institute (MDPI),MDPI
Subject
/ Child
/ Computer Science Applications
/ Disease
/ Female
/ FSTN
/ GDF8
/ Humans
/ Infant
/ Male
/ Muscular Atrophy, Spinal - drug therapy
/ Muscular Atrophy, Spinal - metabolism
/ Myostatin - antagonists & inhibitors
/ Oligonucleotides - therapeutic use
/ Patients
/ Physical and Theoretical Chemistry
/ Proteins
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