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

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 ov...

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Autores principales: Wang, Leo H., Shaw, Dennis W. W., Faino, Anna, Budech, Christopher B., Lewis, Leann M., Statland, Jeffrey, Eichinger, Katy, Tapscott, Stephen J., Tawil, Rabi N., Friedman, Seth D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7948347/
https://www.ncbi.nlm.nih.gov/pubmed/33691664
http://dx.doi.org/10.1186/s12891-021-04134-7
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author Wang, Leo H.
Shaw, Dennis W. W.
Faino, Anna
Budech, Christopher B.
Lewis, Leann M.
Statland, Jeffrey
Eichinger, Katy
Tapscott, Stephen J.
Tawil, Rabi N.
Friedman, Seth D.
author_facet Wang, Leo H.
Shaw, Dennis W. W.
Faino, Anna
Budech, Christopher B.
Lewis, Leann M.
Statland, Jeffrey
Eichinger, Katy
Tapscott, Stephen J.
Tawil, Rabi N.
Friedman, Seth D.
author_sort Wang, Leo H.
collection PubMed
description 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12891-021-04134-7.
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spelling pubmed-79483472021-03-11 Longitudinal study of MRI and functional outcome measures in facioscapulohumeral muscular dystrophy Wang, Leo H. Shaw, Dennis W. W. Faino, Anna Budech, Christopher B. Lewis, Leann M. Statland, Jeffrey Eichinger, Katy Tapscott, Stephen J. Tawil, Rabi N. Friedman, Seth D. BMC Musculoskelet Disord Research Article 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12891-021-04134-7. BioMed Central 2021-03-10 /pmc/articles/PMC7948347/ /pubmed/33691664 http://dx.doi.org/10.1186/s12891-021-04134-7 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Wang, Leo H.
Shaw, Dennis W. W.
Faino, Anna
Budech, Christopher B.
Lewis, Leann M.
Statland, Jeffrey
Eichinger, Katy
Tapscott, Stephen J.
Tawil, Rabi N.
Friedman, Seth D.
Longitudinal study of MRI and functional outcome measures in facioscapulohumeral muscular dystrophy
title 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_short 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
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7948347/
https://www.ncbi.nlm.nih.gov/pubmed/33691664
http://dx.doi.org/10.1186/s12891-021-04134-7
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