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Efficacy of steroid therapy for Fukuyama congenital muscular dystrophy

Although there is only symptomatic treatment for Fukuyama congenital muscular dystrophy (FCMD), several reports have suggested that steroid therapy could be effective for FCMD; however, no independent intervention studies have been conducted. This study aimed to evaluate the efficacy of steroid ther...

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Autores principales: Murakami, Terumi, Sato, Takatoshi, Adachi, Michiru, Ishiguro, Kumiko, Shichiji, Minobu, Tachimori, Hisateru, Nagata, Satoru, Ishigaki, Keiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8688455/
https://www.ncbi.nlm.nih.gov/pubmed/34930981
http://dx.doi.org/10.1038/s41598-021-03781-z
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author Murakami, Terumi
Sato, Takatoshi
Adachi, Michiru
Ishiguro, Kumiko
Shichiji, Minobu
Tachimori, Hisateru
Nagata, Satoru
Ishigaki, Keiko
author_facet Murakami, Terumi
Sato, Takatoshi
Adachi, Michiru
Ishiguro, Kumiko
Shichiji, Minobu
Tachimori, Hisateru
Nagata, Satoru
Ishigaki, Keiko
author_sort Murakami, Terumi
collection PubMed
description Although there is only symptomatic treatment for Fukuyama congenital muscular dystrophy (FCMD), several reports have suggested that steroid therapy could be effective for FCMD; however, no independent intervention studies have been conducted. This study aimed to evaluate the efficacy of steroid therapy for restoring motor functions in FCMD patients. This study involved 3-to-10-year-old FCMD patients who exhibited a decline in motor functions, requested steroid therapy. Patients with consent started oral administration of 0.5-mg/kg prednisolone every alternate day, which was increased to 1.0 mg/kg if the response was inadequate. We used the Gross Motor Function Measure (GMFM) to evaluate and compare the motor functions of all patients. Wilcoxon signed-rank test (significance level, P ≤ 0.05) was used for statistical analysis. At the onset of steroid therapy, 8.10 years (SD, 2.14 years) was the mean age of FCMD patients. The mean GMFM difference between before and after the steroid therapy was + 1.23 (SD, 1.10), and a P value of 0.015 represented significant improvement in GMFM. Our results indicate that steroid therapy may contribute to the maintenance and improvement of the motor functions of advanced-stage FCMD patients. Clinical Trial Registration Registration Number: UMIN000020715, Registration Date: Feb 1st, 2016 (01/02/2016).
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spelling pubmed-86884552021-12-22 Efficacy of steroid therapy for Fukuyama congenital muscular dystrophy Murakami, Terumi Sato, Takatoshi Adachi, Michiru Ishiguro, Kumiko Shichiji, Minobu Tachimori, Hisateru Nagata, Satoru Ishigaki, Keiko Sci Rep Article Although there is only symptomatic treatment for Fukuyama congenital muscular dystrophy (FCMD), several reports have suggested that steroid therapy could be effective for FCMD; however, no independent intervention studies have been conducted. This study aimed to evaluate the efficacy of steroid therapy for restoring motor functions in FCMD patients. This study involved 3-to-10-year-old FCMD patients who exhibited a decline in motor functions, requested steroid therapy. Patients with consent started oral administration of 0.5-mg/kg prednisolone every alternate day, which was increased to 1.0 mg/kg if the response was inadequate. We used the Gross Motor Function Measure (GMFM) to evaluate and compare the motor functions of all patients. Wilcoxon signed-rank test (significance level, P ≤ 0.05) was used for statistical analysis. At the onset of steroid therapy, 8.10 years (SD, 2.14 years) was the mean age of FCMD patients. The mean GMFM difference between before and after the steroid therapy was + 1.23 (SD, 1.10), and a P value of 0.015 represented significant improvement in GMFM. Our results indicate that steroid therapy may contribute to the maintenance and improvement of the motor functions of advanced-stage FCMD patients. Clinical Trial Registration Registration Number: UMIN000020715, Registration Date: Feb 1st, 2016 (01/02/2016). Nature Publishing Group UK 2021-12-20 /pmc/articles/PMC8688455/ /pubmed/34930981 http://dx.doi.org/10.1038/s41598-021-03781-z Text en © The Author(s) 2021, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/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 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Murakami, Terumi
Sato, Takatoshi
Adachi, Michiru
Ishiguro, Kumiko
Shichiji, Minobu
Tachimori, Hisateru
Nagata, Satoru
Ishigaki, Keiko
Efficacy of steroid therapy for Fukuyama congenital muscular dystrophy
title Efficacy of steroid therapy for Fukuyama congenital muscular dystrophy
title_full Efficacy of steroid therapy for Fukuyama congenital muscular dystrophy
title_fullStr Efficacy of steroid therapy for Fukuyama congenital muscular dystrophy
title_full_unstemmed Efficacy of steroid therapy for Fukuyama congenital muscular dystrophy
title_short Efficacy of steroid therapy for Fukuyama congenital muscular dystrophy
title_sort efficacy of steroid therapy for fukuyama congenital muscular dystrophy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8688455/
https://www.ncbi.nlm.nih.gov/pubmed/34930981
http://dx.doi.org/10.1038/s41598-021-03781-z
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