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Validation of MRC Centre MRI calf muscle fat fraction protocol as an outcome measure in CMT1A

OBJECTIVE: To translate the quantitative MRC Centre MRI protocol in Charcot-Marie-Tooth disease type 1A (CMT1A) to a second site; validate its responsiveness in an independent cohort; and test the benefit of participant stratification to increase outcome measure responsiveness. METHODS: Three health...

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Autores principales: Morrow, Jasper M., Evans, Matthew R.B., Grider, Tiffany, Sinclair, Christopher D.J., Thedens, Daniel, Shah, Sachit, Yousry, Tarek A., Hanna, Michael G., Nopoulos, Peggy, Thornton, John S., Shy, Michael E., Reilly, Mary M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6161551/
https://www.ncbi.nlm.nih.gov/pubmed/30120135
http://dx.doi.org/10.1212/WNL.0000000000006214
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author Morrow, Jasper M.
Evans, Matthew R.B.
Grider, Tiffany
Sinclair, Christopher D.J.
Thedens, Daniel
Shah, Sachit
Yousry, Tarek A.
Hanna, Michael G.
Nopoulos, Peggy
Thornton, John S.
Shy, Michael E.
Reilly, Mary M.
author_facet Morrow, Jasper M.
Evans, Matthew R.B.
Grider, Tiffany
Sinclair, Christopher D.J.
Thedens, Daniel
Shah, Sachit
Yousry, Tarek A.
Hanna, Michael G.
Nopoulos, Peggy
Thornton, John S.
Shy, Michael E.
Reilly, Mary M.
author_sort Morrow, Jasper M.
collection PubMed
description OBJECTIVE: To translate the quantitative MRC Centre MRI protocol in Charcot-Marie-Tooth disease type 1A (CMT1A) to a second site; validate its responsiveness in an independent cohort; and test the benefit of participant stratification to increase outcome measure responsiveness. METHODS: Three healthy volunteers were scanned for intersite standardization. For the longitudinal patient study, 11 patients with CMT1A were recruited with 10 patients rescanned at a 12-month interval. Three-point Dixon MRI of leg muscles was performed to generate fat fraction (FF) maps, transferred to a central site for quality control and analysis. Clinical data collected included CMT Neuropathy Score. RESULTS: Test-retest reliability of FF within individual healthy calf muscles at the remote site was excellent: intraclass correlation coefficient 0.79, limits of agreement −0.67 to +0.85 %FF. In patients, mean calf muscle FF was 21.0% and correlated strongly with disease severity and age. Calf muscle FF significantly increased over 12 months (+1.8 ± 1.7 %FF, p = 0.009). Patients with baseline FF >10% showed a 12-month FF increase of 2.9% ± 1.3% (standardized response mean = 2.19). CONCLUSIONS: We have validated calf muscle FF as an outcome measure in an independent cohort of patients with CMT1A. Responsiveness is significantly improved by enrolling a stratified patient cohort with baseline calf FF >10%.
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spelling pubmed-61615512018-10-01 Validation of MRC Centre MRI calf muscle fat fraction protocol as an outcome measure in CMT1A Morrow, Jasper M. Evans, Matthew R.B. Grider, Tiffany Sinclair, Christopher D.J. Thedens, Daniel Shah, Sachit Yousry, Tarek A. Hanna, Michael G. Nopoulos, Peggy Thornton, John S. Shy, Michael E. Reilly, Mary M. Neurology Article OBJECTIVE: To translate the quantitative MRC Centre MRI protocol in Charcot-Marie-Tooth disease type 1A (CMT1A) to a second site; validate its responsiveness in an independent cohort; and test the benefit of participant stratification to increase outcome measure responsiveness. METHODS: Three healthy volunteers were scanned for intersite standardization. For the longitudinal patient study, 11 patients with CMT1A were recruited with 10 patients rescanned at a 12-month interval. Three-point Dixon MRI of leg muscles was performed to generate fat fraction (FF) maps, transferred to a central site for quality control and analysis. Clinical data collected included CMT Neuropathy Score. RESULTS: Test-retest reliability of FF within individual healthy calf muscles at the remote site was excellent: intraclass correlation coefficient 0.79, limits of agreement −0.67 to +0.85 %FF. In patients, mean calf muscle FF was 21.0% and correlated strongly with disease severity and age. Calf muscle FF significantly increased over 12 months (+1.8 ± 1.7 %FF, p = 0.009). Patients with baseline FF >10% showed a 12-month FF increase of 2.9% ± 1.3% (standardized response mean = 2.19). CONCLUSIONS: We have validated calf muscle FF as an outcome measure in an independent cohort of patients with CMT1A. Responsiveness is significantly improved by enrolling a stratified patient cohort with baseline calf FF >10%. Lippincott Williams & Wilkins 2018-09-18 /pmc/articles/PMC6161551/ /pubmed/30120135 http://dx.doi.org/10.1212/WNL.0000000000006214 Text en Copyright © 2018 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Morrow, Jasper M.
Evans, Matthew R.B.
Grider, Tiffany
Sinclair, Christopher D.J.
Thedens, Daniel
Shah, Sachit
Yousry, Tarek A.
Hanna, Michael G.
Nopoulos, Peggy
Thornton, John S.
Shy, Michael E.
Reilly, Mary M.
Validation of MRC Centre MRI calf muscle fat fraction protocol as an outcome measure in CMT1A
title Validation of MRC Centre MRI calf muscle fat fraction protocol as an outcome measure in CMT1A
title_full Validation of MRC Centre MRI calf muscle fat fraction protocol as an outcome measure in CMT1A
title_fullStr Validation of MRC Centre MRI calf muscle fat fraction protocol as an outcome measure in CMT1A
title_full_unstemmed Validation of MRC Centre MRI calf muscle fat fraction protocol as an outcome measure in CMT1A
title_short Validation of MRC Centre MRI calf muscle fat fraction protocol as an outcome measure in CMT1A
title_sort validation of mrc centre mri calf muscle fat fraction protocol as an outcome measure in cmt1a
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6161551/
https://www.ncbi.nlm.nih.gov/pubmed/30120135
http://dx.doi.org/10.1212/WNL.0000000000006214
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