Longitudinal study of MRI and functional outcome measures in facioscapulohumeral muscular dystrophy

Abstract Background Facioscapulohumeral muscular dystrophy (FSHD) is a patchy and slowly progressive disease of skeletal muscle. For MRI to be a useful biomarker in an FSHD clinical trial, it should reliably detect changes over relatively short time-intervals (~ 1 year). We hypothesized that fatty c...

Full description

Bibliographic Details
Main Authors: Leo H. Wang, Dennis W. W. Shaw, Anna Faino, Christopher B. Budech, Leann M. Lewis, Jeffrey Statland, Katy Eichinger, Stephen J. Tapscott, Rabi N. Tawil, Seth D. Friedman
Format: Article
Language:English
Published: BMC 2021-03-01
Series:BMC Musculoskeletal Disorders
Subjects:
MRI
Online Access:https://doi.org/10.1186/s12891-021-04134-7
id doaj-d70451aa6ae64c5697fa216d037e6492
record_format Article
spelling doaj-d70451aa6ae64c5697fa216d037e64922021-03-11T11:43:46ZengBMCBMC Musculoskeletal Disorders1471-24742021-03-0122111110.1186/s12891-021-04134-7Longitudinal study of MRI and functional outcome measures in facioscapulohumeral muscular dystrophyLeo H. Wang0Dennis W. W. Shaw1Anna Faino2Christopher B. Budech3Leann M. Lewis4Jeffrey Statland5Katy Eichinger6Stephen J. Tapscott7Rabi N. Tawil8Seth D. Friedman9Department of Neurology, University of WashingtonDepartment of Radiology, University of WashingtonChildren’s Core for Biomedical Statistics, Seattle Children’s Research InstituteDepartment of Radiology, University of WashingtonDepartment of Neurology, University of RochesterDepartment of Neurology, Kansas University Medical CenterDepartment of Neurology, University of RochesterHuman Biology Division, Fred Hutchinson Research CenterDepartment of Neurology, University of RochesterDepartment of Radiology, University of WashingtonAbstract Background Facioscapulohumeral muscular dystrophy (FSHD) is a patchy and slowly progressive disease of skeletal muscle. For MRI to be a useful biomarker in an FSHD clinical trial, it should reliably detect changes over relatively short time-intervals (~ 1 year). We hypothesized that fatty change over the study course would be most likely in muscles already demonstrating disease progression, and that the degree of MRI burden would be correlated with function. Methods We studied 36 patients with FSHD and lower-extremity weakness at baseline. Thirty-two patients returned in our 12-month longitudinal observational study. We analyzed DIXON MRI images of 16 lower-extremity muscles in each patient and compared them to quantitative strength measurement and ambulatory functional outcome measures. Results There was a small shift to higher fat fractions in the summed muscle data for each patient, however individual muscles demonstrated much larger magnitudes of change. The greatest increase in fat fraction was observed in muscles having an intermediate fat replacement at baseline, with minimally (baseline fat fraction < 0.10) or severely (> 0.70) affected muscles less likely to progress. Functional outcome measures did not demonstrate marked change over the interval; however, overall MRI disease burden was correlated with functional outcome measures. Direct comparison of the tibialis anterior (TA) fat fraction and quantitative strength measurement showed a sigmoidal relationship, with steepest drop being when the muscle gets more than ~ 20% fatty replaced. Conclusions Assessing MRI changes in 16 lower-extremity muscles across 1 year demonstrated that those muscles having an intermediate baseline fat fraction were more likely to progress. Ambulatory functional outcome measures are generally related to overall muscle MRI burden but remain unchanged in the short term. Quantitative strength measurement of the TA showed a steep loss of strength when more fatty infiltration is present suggesting that MRI may be preferable for following incremental change or modulation with drug therapy.https://doi.org/10.1186/s12891-021-04134-7MRIAll neuromuscular diseaseMuscle diseaseFacioscapulohumeral muscular dystrophy (FSHD)Outcome measures
collection DOAJ
language English
format Article
sources DOAJ
author Leo H. Wang
Dennis W. W. Shaw
Anna Faino
Christopher B. Budech
Leann M. Lewis
Jeffrey Statland
Katy Eichinger
Stephen J. Tapscott
Rabi N. Tawil
Seth D. Friedman
spellingShingle Leo H. Wang
Dennis W. W. Shaw
Anna Faino
Christopher B. Budech
Leann M. Lewis
Jeffrey Statland
Katy Eichinger
Stephen J. Tapscott
Rabi N. Tawil
Seth D. Friedman
Longitudinal study of MRI and functional outcome measures in facioscapulohumeral muscular dystrophy
BMC Musculoskeletal Disorders
MRI
All neuromuscular disease
Muscle disease
Facioscapulohumeral muscular dystrophy (FSHD)
Outcome measures
author_facet Leo H. Wang
Dennis W. W. Shaw
Anna Faino
Christopher B. Budech
Leann M. Lewis
Jeffrey Statland
Katy Eichinger
Stephen J. Tapscott
Rabi N. Tawil
Seth D. Friedman
author_sort Leo H. Wang
title Longitudinal study of MRI and functional outcome measures in facioscapulohumeral muscular dystrophy
title_short Longitudinal study of MRI and functional outcome measures in facioscapulohumeral muscular dystrophy
title_full Longitudinal study of MRI and functional outcome measures in facioscapulohumeral muscular dystrophy
title_fullStr Longitudinal study of MRI and functional outcome measures in facioscapulohumeral muscular dystrophy
title_full_unstemmed Longitudinal study of MRI and functional outcome measures in facioscapulohumeral muscular dystrophy
title_sort longitudinal study of mri and functional outcome measures in facioscapulohumeral muscular dystrophy
publisher BMC
series BMC Musculoskeletal Disorders
issn 1471-2474
publishDate 2021-03-01
description Abstract Background Facioscapulohumeral muscular dystrophy (FSHD) is a patchy and slowly progressive disease of skeletal muscle. For MRI to be a useful biomarker in an FSHD clinical trial, it should reliably detect changes over relatively short time-intervals (~ 1 year). We hypothesized that fatty change over the study course would be most likely in muscles already demonstrating disease progression, and that the degree of MRI burden would be correlated with function. Methods We studied 36 patients with FSHD and lower-extremity weakness at baseline. Thirty-two patients returned in our 12-month longitudinal observational study. We analyzed DIXON MRI images of 16 lower-extremity muscles in each patient and compared them to quantitative strength measurement and ambulatory functional outcome measures. Results There was a small shift to higher fat fractions in the summed muscle data for each patient, however individual muscles demonstrated much larger magnitudes of change. The greatest increase in fat fraction was observed in muscles having an intermediate fat replacement at baseline, with minimally (baseline fat fraction < 0.10) or severely (> 0.70) affected muscles less likely to progress. Functional outcome measures did not demonstrate marked change over the interval; however, overall MRI disease burden was correlated with functional outcome measures. Direct comparison of the tibialis anterior (TA) fat fraction and quantitative strength measurement showed a sigmoidal relationship, with steepest drop being when the muscle gets more than ~ 20% fatty replaced. Conclusions Assessing MRI changes in 16 lower-extremity muscles across 1 year demonstrated that those muscles having an intermediate baseline fat fraction were more likely to progress. Ambulatory functional outcome measures are generally related to overall muscle MRI burden but remain unchanged in the short term. Quantitative strength measurement of the TA showed a steep loss of strength when more fatty infiltration is present suggesting that MRI may be preferable for following incremental change or modulation with drug therapy.
topic MRI
All neuromuscular disease
Muscle disease
Facioscapulohumeral muscular dystrophy (FSHD)
Outcome measures
url https://doi.org/10.1186/s12891-021-04134-7
work_keys_str_mv AT leohwang longitudinalstudyofmriandfunctionaloutcomemeasuresinfacioscapulohumeralmusculardystrophy
AT denniswwshaw longitudinalstudyofmriandfunctionaloutcomemeasuresinfacioscapulohumeralmusculardystrophy
AT annafaino longitudinalstudyofmriandfunctionaloutcomemeasuresinfacioscapulohumeralmusculardystrophy
AT christopherbbudech longitudinalstudyofmriandfunctionaloutcomemeasuresinfacioscapulohumeralmusculardystrophy
AT leannmlewis longitudinalstudyofmriandfunctionaloutcomemeasuresinfacioscapulohumeralmusculardystrophy
AT jeffreystatland longitudinalstudyofmriandfunctionaloutcomemeasuresinfacioscapulohumeralmusculardystrophy
AT katyeichinger longitudinalstudyofmriandfunctionaloutcomemeasuresinfacioscapulohumeralmusculardystrophy
AT stephenjtapscott longitudinalstudyofmriandfunctionaloutcomemeasuresinfacioscapulohumeralmusculardystrophy
AT rabintawil longitudinalstudyofmriandfunctionaloutcomemeasuresinfacioscapulohumeralmusculardystrophy
AT sethdfriedman longitudinalstudyofmriandfunctionaloutcomemeasuresinfacioscapulohumeralmusculardystrophy
_version_ 1724225330142511104