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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2019
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.
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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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