Three-year quantitative magnetic resonance imaging and phosphorus magnetic resonance spectroscopy study in lower limb muscle in dysferlinopathy.


Journal

Journal of cachexia, sarcopenia and muscle
ISSN: 2190-6009
Titre abrégé: J Cachexia Sarcopenia Muscle
Pays: Germany
ID NLM: 101552883

Informations de publication

Date de publication:
06 2022
Historique:
revised: 10 02 2022
received: 28 07 2021
accepted: 28 02 2022
pubmed: 5 4 2022
medline: 11 6 2022
entrez: 4 4 2022
Statut: ppublish

Résumé

Natural history studies in neuromuscular disorders are vital to understand the disease evolution and to find sensitive outcome measures. We performed a longitudinal assessment of quantitative magnetic resonance imaging (MRI) and phosphorus magnetic resonance spectroscopy ( Quantitative MRI/ Posterior muscles in thigh and leg showed the highest FF values. FF at baseline was highly heterogeneous across patients. In ambulant patients, median annual increases in global thigh and leg segment FF values were 4.1% and 3.0%, respectively (P < 0.001). After 3 years, global thigh and leg FF increases were 9.6% and 8.4%, respectively (P < 0.001). SRM values for global thigh FF were over 0.8 for all years. Vastus lateralis muscle showed the highest SRM values across all time points. cCSA decreased significantly after 3 years with median values of 11.0% and 12.8% in global thigh and global leg, respectively (P < 0.001). Water T This multi-centre study has shown that quantitative MRI/

Sections du résumé

BACKGROUND
Natural history studies in neuromuscular disorders are vital to understand the disease evolution and to find sensitive outcome measures. We performed a longitudinal assessment of quantitative magnetic resonance imaging (MRI) and phosphorus magnetic resonance spectroscopy (
METHODS
Quantitative MRI/
RESULTS
Posterior muscles in thigh and leg showed the highest FF values. FF at baseline was highly heterogeneous across patients. In ambulant patients, median annual increases in global thigh and leg segment FF values were 4.1% and 3.0%, respectively (P < 0.001). After 3 years, global thigh and leg FF increases were 9.6% and 8.4%, respectively (P < 0.001). SRM values for global thigh FF were over 0.8 for all years. Vastus lateralis muscle showed the highest SRM values across all time points. cCSA decreased significantly after 3 years with median values of 11.0% and 12.8% in global thigh and global leg, respectively (P < 0.001). Water T
CONCLUSIONS
This multi-centre study has shown that quantitative MRI/

Identifiants

pubmed: 35373496
doi: 10.1002/jcsm.12987
pmc: PMC9178361
doi:

Substances chimiques

Water 059QF0KO0R
Phosphorus 27YLU75U4W

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1850-1863

Subventions

Organisme : Jain Foundation

Informations de copyright

© 2022 The Authors. Journal of Cachexia, Sarcopenia and Muscle published by John Wiley & Sons Ltd on behalf of Society on Sarcopenia, Cachexia and Wasting Disorders.

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Auteurs

Harmen Reyngoudt (H)

NMR Laboratory, Neuromuscular Investigation Center, Institute of Myology, Paris, France.
NMR Laboratory, CEA/DRF/IBFJ/MIRCen, Paris, France.

Fiona E Smith (FE)

Magnetic Resonance Centre, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK.

Ericky Caldas de Almeida Araújo (E)

NMR Laboratory, Neuromuscular Investigation Center, Institute of Myology, Paris, France.
NMR Laboratory, CEA/DRF/IBFJ/MIRCen, Paris, France.

Ian Wilson (I)

Magnetic Resonance Centre, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK.

Roberto Fernández-Torrón (R)

The John Walton Muscular Dystrophy Research Centre, Translational and Clinical Research Institute, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
Neuromuscular Area, Biodonostia Health Research Institute, Neurology Service, Donostia University Hospital, Donostia-San Sebastian, Spain.

Meredith K James (MK)

The John Walton Muscular Dystrophy Research Centre, Translational and Clinical Research Institute, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.

Ursula R Moore (UR)

The John Walton Muscular Dystrophy Research Centre, Translational and Clinical Research Institute, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.

Jordi Díaz-Manera (J)

The John Walton Muscular Dystrophy Research Centre, Translational and Clinical Research Institute, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.
Neuromuscular Disorders Unit, Neurology Department, Hospital Santa Creu i Sant Pau, Barcelona, Spain.
Centro de Investigación Biomédica en Red en Enfermedades Raras (CIBERER), Valencia, Spain.

Benjamin Marty (B)

NMR Laboratory, Neuromuscular Investigation Center, Institute of Myology, Paris, France.
NMR Laboratory, CEA/DRF/IBFJ/MIRCen, Paris, France.

Noura Azzabou (N)

NMR Laboratory, Neuromuscular Investigation Center, Institute of Myology, Paris, France.
NMR Laboratory, CEA/DRF/IBFJ/MIRCen, Paris, France.

Heather Gordish (H)

Center for Translational Science, Division of Biostatistics and Study Methodology, Children's National Health System, Washington, DC, USA.
Pediatrics, Epidemiology and Biostatistics, George Washington University, Washington, DC, USA.

Laura Rufibach (L)

The JAIN Foundation, Seattle, WA, USA.

Tim Hodgson (T)

Magnetic Resonance Centre, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK.

Dorothy Wallace (D)

Magnetic Resonance Centre, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK.

Louise Ward (L)

Magnetic Resonance Centre, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK.

Jean-Marc Boisserie (JM)

NMR Laboratory, Neuromuscular Investigation Center, Institute of Myology, Paris, France.
NMR Laboratory, CEA/DRF/IBFJ/MIRCen, Paris, France.

Julien Le Louër (J)

NMR Laboratory, Neuromuscular Investigation Center, Institute of Myology, Paris, France.
NMR Laboratory, CEA/DRF/IBFJ/MIRCen, Paris, France.

Heather Hilsden (H)

The John Walton Muscular Dystrophy Research Centre, Translational and Clinical Research Institute, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.

Helen Sutherland (H)

The John Walton Muscular Dystrophy Research Centre, Translational and Clinical Research Institute, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.

Aurélie Canal (A)

Neuromuscular Physiology and Evaluation Laboratory, Neuromuscular Investigation Center, Institute of Myology, Paris, France.

Jean-Yves Hogrel (JY)

Neuromuscular Physiology and Evaluation Laboratory, Neuromuscular Investigation Center, Institute of Myology, Paris, France.

Marni Jacobs (M)

Center for Translational Science, Division of Biostatistics and Study Methodology, Children's National Health System, Washington, DC, USA.
Pediatrics, Epidemiology and Biostatistics, George Washington University, Washington, DC, USA.

Tanya Stojkovic (T)

Neuromuscular Reference Center, Institute of Myology, Pitié-Salpêtrière Hospital (AP-HP), Paris, France.

Kate Bushby (K)

The John Walton Muscular Dystrophy Research Centre, Translational and Clinical Research Institute, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.

Anna Mayhew (A)

The John Walton Muscular Dystrophy Research Centre, Translational and Clinical Research Institute, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.

Volker Straub (V)

The John Walton Muscular Dystrophy Research Centre, Translational and Clinical Research Institute, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.

Pierre G Carlier (PG)

University Paris-Saclay, CEA, DRF, SHFJ, Orsay, France.

Andrew M Blamire (AM)

Magnetic Resonance Centre, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, UK.

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