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Fatigue in adults with spinal muscular atrophy under treatment with nusinersen

5q-Associated spinal muscular atrophy is a hereditary neuromuscular disease leading to progressive muscle weakness in which fatigue occurs and affects quality of life. Treatment with the antisense oligonucleotide nusinersen has been shown to improve motor function. Fatigue can be measured within the...

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Autores principales: Kizina, K., Stolte, B., Totzeck, A., Bolz, S., Schlag, M., Ose, C., von Velsen, O., Kleinschnitz, C., Hagenacker, Tim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7338415/
https://www.ncbi.nlm.nih.gov/pubmed/32632203
http://dx.doi.org/10.1038/s41598-020-68051-w
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author Kizina, K.
Stolte, B.
Totzeck, A.
Bolz, S.
Schlag, M.
Ose, C.
von Velsen, O.
Kleinschnitz, C.
Hagenacker, Tim
author_facet Kizina, K.
Stolte, B.
Totzeck, A.
Bolz, S.
Schlag, M.
Ose, C.
von Velsen, O.
Kleinschnitz, C.
Hagenacker, Tim
author_sort Kizina, K.
collection PubMed
description 5q-Associated spinal muscular atrophy is a hereditary neuromuscular disease leading to progressive muscle weakness in which fatigue occurs and affects quality of life. Treatment with the antisense oligonucleotide nusinersen has been shown to improve motor function. Fatigue can be measured within the Fatigue Severity Scale (FSS). FSS is a self-reported questionnaire consisting of nine items to quantify fatigue severity within the last week. Higher values indicating a higher severity. Using the FSS, fatigue was measured in 28 adult patients, subdivided into ambulatory and non-ambulatory, suffering from a genetically confirmed 5q-SMA under treatment with nusinersen in accordance with the label. Correlations were performed among FSS and motor scales, 6-minute walk test (6MWT) and Hammersmiths Functional Motor Scale Expanded (HFMSE). Evaluation was performed prior to treatment initiation and after 6 and 10 months. The mean FSS score for all 28 patients at baseline was 4.61 ± 1.44. After 6 months mean FSS score significantly reduced to 3.92 ± 1.35. After 10 months mean FSS score had not differed from baseline, 3.84 ± 1.25. A moderate negative correlation of the difference of FSS and 6MWT after 6 months compared to baseline conditions was measured. Nusinersen reduces fatigue as measured by the FSS in adult patients with 5q-SMA transiently after initiation of treatment. There was no reduction of FSS 10 months after the beginning of treatment when compared to baseline.
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spelling pubmed-73384152020-07-07 Fatigue in adults with spinal muscular atrophy under treatment with nusinersen Kizina, K. Stolte, B. Totzeck, A. Bolz, S. Schlag, M. Ose, C. von Velsen, O. Kleinschnitz, C. Hagenacker, Tim Sci Rep Article 5q-Associated spinal muscular atrophy is a hereditary neuromuscular disease leading to progressive muscle weakness in which fatigue occurs and affects quality of life. Treatment with the antisense oligonucleotide nusinersen has been shown to improve motor function. Fatigue can be measured within the Fatigue Severity Scale (FSS). FSS is a self-reported questionnaire consisting of nine items to quantify fatigue severity within the last week. Higher values indicating a higher severity. Using the FSS, fatigue was measured in 28 adult patients, subdivided into ambulatory and non-ambulatory, suffering from a genetically confirmed 5q-SMA under treatment with nusinersen in accordance with the label. Correlations were performed among FSS and motor scales, 6-minute walk test (6MWT) and Hammersmiths Functional Motor Scale Expanded (HFMSE). Evaluation was performed prior to treatment initiation and after 6 and 10 months. The mean FSS score for all 28 patients at baseline was 4.61 ± 1.44. After 6 months mean FSS score significantly reduced to 3.92 ± 1.35. After 10 months mean FSS score had not differed from baseline, 3.84 ± 1.25. A moderate negative correlation of the difference of FSS and 6MWT after 6 months compared to baseline conditions was measured. Nusinersen reduces fatigue as measured by the FSS in adult patients with 5q-SMA transiently after initiation of treatment. There was no reduction of FSS 10 months after the beginning of treatment when compared to baseline. Nature Publishing Group UK 2020-07-06 /pmc/articles/PMC7338415/ /pubmed/32632203 http://dx.doi.org/10.1038/s41598-020-68051-w Text en © The Author(s) 2020 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kizina, K.
Stolte, B.
Totzeck, A.
Bolz, S.
Schlag, M.
Ose, C.
von Velsen, O.
Kleinschnitz, C.
Hagenacker, Tim
Fatigue in adults with spinal muscular atrophy under treatment with nusinersen
title Fatigue in adults with spinal muscular atrophy under treatment with nusinersen
title_full Fatigue in adults with spinal muscular atrophy under treatment with nusinersen
title_fullStr Fatigue in adults with spinal muscular atrophy under treatment with nusinersen
title_full_unstemmed Fatigue in adults with spinal muscular atrophy under treatment with nusinersen
title_short Fatigue in adults with spinal muscular atrophy under treatment with nusinersen
title_sort fatigue in adults with spinal muscular atrophy under treatment with nusinersen
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7338415/
https://www.ncbi.nlm.nih.gov/pubmed/32632203
http://dx.doi.org/10.1038/s41598-020-68051-w
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