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Assessment of disease progression in dysferlinopathy: A 1-year cohort study
OBJECTIVE: To assess the ability of functional measures to detect disease progression in dysferlinopathy over 6 months and 1 year. METHODS: One hundred ninety-three patients with dysferlinopathy were recruited to the Jain Foundation's International Clinical Outcome Study for Dysferlinopathy. Ba...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6369904/ https://www.ncbi.nlm.nih.gov/pubmed/30626655 http://dx.doi.org/10.1212/WNL.0000000000006858 |
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author | Moore, Ursula Jacobs, Marni James, Meredith K. Mayhew, Anna G. Fernandez-Torron, Roberto Feng, Jia Cnaan, Avital Eagle, Michelle Bettinson, Karen Rufibach, Laura E. Lofra, Robert Muni Blamire, Andrew M. Carlier, Pierre G. Mittal, Plavi Lowes, Linda Pax Alfano, Lindsay Rose, Kristy Duong, Tina Berry, Katherine M. Montiel-Morillo, Elena Pedrosa-Hernández, Irene Holsten, Scott Sanjak, Mohammed Ashida, Ai Sakamoto, Chikako Tateishi, Takayuki Yajima, Hiroyuki Canal, Aurélie Ollivier, Gwenn Decostre, Valerie Mendez, Juan Bosco Sánchez-Aguilera Praxedes, Nieves Thiele, Simone Siener, Catherine Shierbecker, Jeanine Florence, Julaine M. Vandevelde, Bruno DeWolf, Brittney Hutchence, Meghan Gee, Richard Prügel, Juliana Maron, Elke Hilsden, Heather Lochmüller, Hanns Grieben, Ulrike Spuler, Simone Tesi Rocha, Carolina Day, John W. Jones, Kristi J. Bharucha-Goebel, Diana X. Salort-Campana, Emmanuelle Harms, Matthew Pestronk, Alan Krause, Sabine Schreiber-Katz, Olivia Walter, Maggie C. Paradas, Carmen Hogrel, Jean-Yves Stojkovic, Tanya Takeda, Shin'ichi Mori-Yoshimura, Madoka Bravver, Elena Sparks, Susan Díaz-Manera, Jordi Bello, Luca Semplicini, Claudio Pegoraro, Elena Mendell, Jerry R. Bushby, Kate Straub, Volker |
author_facet | Moore, Ursula Jacobs, Marni James, Meredith K. Mayhew, Anna G. Fernandez-Torron, Roberto Feng, Jia Cnaan, Avital Eagle, Michelle Bettinson, Karen Rufibach, Laura E. Lofra, Robert Muni Blamire, Andrew M. Carlier, Pierre G. Mittal, Plavi Lowes, Linda Pax Alfano, Lindsay Rose, Kristy Duong, Tina Berry, Katherine M. Montiel-Morillo, Elena Pedrosa-Hernández, Irene Holsten, Scott Sanjak, Mohammed Ashida, Ai Sakamoto, Chikako Tateishi, Takayuki Yajima, Hiroyuki Canal, Aurélie Ollivier, Gwenn Decostre, Valerie Mendez, Juan Bosco Sánchez-Aguilera Praxedes, Nieves Thiele, Simone Siener, Catherine Shierbecker, Jeanine Florence, Julaine M. Vandevelde, Bruno DeWolf, Brittney Hutchence, Meghan Gee, Richard Prügel, Juliana Maron, Elke Hilsden, Heather Lochmüller, Hanns Grieben, Ulrike Spuler, Simone Tesi Rocha, Carolina Day, John W. Jones, Kristi J. Bharucha-Goebel, Diana X. Salort-Campana, Emmanuelle Harms, Matthew Pestronk, Alan Krause, Sabine Schreiber-Katz, Olivia Walter, Maggie C. Paradas, Carmen Hogrel, Jean-Yves Stojkovic, Tanya Takeda, Shin'ichi Mori-Yoshimura, Madoka Bravver, Elena Sparks, Susan Díaz-Manera, Jordi Bello, Luca Semplicini, Claudio Pegoraro, Elena Mendell, Jerry R. Bushby, Kate Straub, Volker |
author_sort | Moore, Ursula |
collection | PubMed |
description | OBJECTIVE: To assess the ability of functional measures to detect disease progression in dysferlinopathy over 6 months and 1 year. METHODS: One hundred ninety-three patients with dysferlinopathy were recruited to the Jain Foundation's International Clinical Outcome Study for Dysferlinopathy. Baseline, 6-month, and 1-year assessments included adapted North Star Ambulatory Assessment (a-NSAA), Motor Function Measure (MFM-20), timed function tests, 6-minute walk test (6MWT), Brooke scale, Jebsen test, manual muscle testing, and hand-held dynamometry. Patients also completed the ACTIVLIM questionnaire. Change in each measure over 6 months and 1 year was calculated and compared between disease severity (ambulant [mild, moderate, or severe based on a-NSAA score] or nonambulant [unable to complete a 10-meter walk]) and clinical diagnosis. RESULTS: The functional a-NSAA test was the most sensitive to deterioration for ambulant patients overall. The a-NSAA score was the most sensitive test in the mild and moderate groups, while the 6MWT was most sensitive in the severe group. The 10-meter walk test was the only test showing significant change across all ambulant severity groups. In nonambulant patients, the MFM domain 3, wrist flexion strength, and pinch grip were most sensitive. Progression rates did not differ by clinical diagnosis. Power calculations determined that 46 moderately affected patients are required to determine clinical effectiveness for a hypothetical 1-year clinical trial based on the a-NSAA as a clinical endpoint. CONCLUSION: Certain functional outcome measures can detect changes over 6 months and 1 year in dysferlinopathy and potentially be useful in monitoring progression in clinical trials. CLINICALTRIALS.GOV IDENTIFIER: NCT01676077. |
format | Online Article Text |
id | pubmed-6369904 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-63699042019-02-20 Assessment of disease progression in dysferlinopathy: A 1-year cohort study Moore, Ursula Jacobs, Marni James, Meredith K. Mayhew, Anna G. Fernandez-Torron, Roberto Feng, Jia Cnaan, Avital Eagle, Michelle Bettinson, Karen Rufibach, Laura E. Lofra, Robert Muni Blamire, Andrew M. Carlier, Pierre G. Mittal, Plavi Lowes, Linda Pax Alfano, Lindsay Rose, Kristy Duong, Tina Berry, Katherine M. Montiel-Morillo, Elena Pedrosa-Hernández, Irene Holsten, Scott Sanjak, Mohammed Ashida, Ai Sakamoto, Chikako Tateishi, Takayuki Yajima, Hiroyuki Canal, Aurélie Ollivier, Gwenn Decostre, Valerie Mendez, Juan Bosco Sánchez-Aguilera Praxedes, Nieves Thiele, Simone Siener, Catherine Shierbecker, Jeanine Florence, Julaine M. Vandevelde, Bruno DeWolf, Brittney Hutchence, Meghan Gee, Richard Prügel, Juliana Maron, Elke Hilsden, Heather Lochmüller, Hanns Grieben, Ulrike Spuler, Simone Tesi Rocha, Carolina Day, John W. Jones, Kristi J. Bharucha-Goebel, Diana X. Salort-Campana, Emmanuelle Harms, Matthew Pestronk, Alan Krause, Sabine Schreiber-Katz, Olivia Walter, Maggie C. Paradas, Carmen Hogrel, Jean-Yves Stojkovic, Tanya Takeda, Shin'ichi Mori-Yoshimura, Madoka Bravver, Elena Sparks, Susan Díaz-Manera, Jordi Bello, Luca Semplicini, Claudio Pegoraro, Elena Mendell, Jerry R. Bushby, Kate Straub, Volker Neurology Article OBJECTIVE: To assess the ability of functional measures to detect disease progression in dysferlinopathy over 6 months and 1 year. METHODS: One hundred ninety-three patients with dysferlinopathy were recruited to the Jain Foundation's International Clinical Outcome Study for Dysferlinopathy. Baseline, 6-month, and 1-year assessments included adapted North Star Ambulatory Assessment (a-NSAA), Motor Function Measure (MFM-20), timed function tests, 6-minute walk test (6MWT), Brooke scale, Jebsen test, manual muscle testing, and hand-held dynamometry. Patients also completed the ACTIVLIM questionnaire. Change in each measure over 6 months and 1 year was calculated and compared between disease severity (ambulant [mild, moderate, or severe based on a-NSAA score] or nonambulant [unable to complete a 10-meter walk]) and clinical diagnosis. RESULTS: The functional a-NSAA test was the most sensitive to deterioration for ambulant patients overall. The a-NSAA score was the most sensitive test in the mild and moderate groups, while the 6MWT was most sensitive in the severe group. The 10-meter walk test was the only test showing significant change across all ambulant severity groups. In nonambulant patients, the MFM domain 3, wrist flexion strength, and pinch grip were most sensitive. Progression rates did not differ by clinical diagnosis. Power calculations determined that 46 moderately affected patients are required to determine clinical effectiveness for a hypothetical 1-year clinical trial based on the a-NSAA as a clinical endpoint. CONCLUSION: Certain functional outcome measures can detect changes over 6 months and 1 year in dysferlinopathy and potentially be useful in monitoring progression in clinical trials. CLINICALTRIALS.GOV IDENTIFIER: NCT01676077. Lippincott Williams & Wilkins 2019-01-29 /pmc/articles/PMC6369904/ /pubmed/30626655 http://dx.doi.org/10.1212/WNL.0000000000006858 Text en Copyright © 2019 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Article Moore, Ursula Jacobs, Marni James, Meredith K. Mayhew, Anna G. Fernandez-Torron, Roberto Feng, Jia Cnaan, Avital Eagle, Michelle Bettinson, Karen Rufibach, Laura E. Lofra, Robert Muni Blamire, Andrew M. Carlier, Pierre G. Mittal, Plavi Lowes, Linda Pax Alfano, Lindsay Rose, Kristy Duong, Tina Berry, Katherine M. Montiel-Morillo, Elena Pedrosa-Hernández, Irene Holsten, Scott Sanjak, Mohammed Ashida, Ai Sakamoto, Chikako Tateishi, Takayuki Yajima, Hiroyuki Canal, Aurélie Ollivier, Gwenn Decostre, Valerie Mendez, Juan Bosco Sánchez-Aguilera Praxedes, Nieves Thiele, Simone Siener, Catherine Shierbecker, Jeanine Florence, Julaine M. Vandevelde, Bruno DeWolf, Brittney Hutchence, Meghan Gee, Richard Prügel, Juliana Maron, Elke Hilsden, Heather Lochmüller, Hanns Grieben, Ulrike Spuler, Simone Tesi Rocha, Carolina Day, John W. Jones, Kristi J. Bharucha-Goebel, Diana X. Salort-Campana, Emmanuelle Harms, Matthew Pestronk, Alan Krause, Sabine Schreiber-Katz, Olivia Walter, Maggie C. Paradas, Carmen Hogrel, Jean-Yves Stojkovic, Tanya Takeda, Shin'ichi Mori-Yoshimura, Madoka Bravver, Elena Sparks, Susan Díaz-Manera, Jordi Bello, Luca Semplicini, Claudio Pegoraro, Elena Mendell, Jerry R. Bushby, Kate Straub, Volker Assessment of disease progression in dysferlinopathy: A 1-year cohort study |
title | Assessment of disease progression in dysferlinopathy: A 1-year cohort study |
title_full | Assessment of disease progression in dysferlinopathy: A 1-year cohort study |
title_fullStr | Assessment of disease progression in dysferlinopathy: A 1-year cohort study |
title_full_unstemmed | Assessment of disease progression in dysferlinopathy: A 1-year cohort study |
title_short | Assessment of disease progression in dysferlinopathy: A 1-year cohort study |
title_sort | assessment of disease progression in dysferlinopathy: a 1-year cohort study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6369904/ https://www.ncbi.nlm.nih.gov/pubmed/30626655 http://dx.doi.org/10.1212/WNL.0000000000006858 |
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