Cargando…
GEMALS: A promising therapy for amyotrophic lateral sclerosis
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease that currently has no cure. At present, the only approved treatment for ALS is Riluzole, a glutamate release blocker that improves life expectancy by 3–6 months. ALS-Endotherapia (GEMALS) is a novel therapeutic approach to treat ALS...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5841048/ https://www.ncbi.nlm.nih.gov/pubmed/29545836 http://dx.doi.org/10.3892/etm.2018.5868 |
_version_ | 1783304690454233088 |
---|---|
author | Geffard, Michel Mangas, Arturo Bedat, Denis Coveñas, Rafael |
author_facet | Geffard, Michel Mangas, Arturo Bedat, Denis Coveñas, Rafael |
author_sort | Geffard, Michel |
collection | PubMed |
description | Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease that currently has no cure. At present, the only approved treatment for ALS is Riluzole, a glutamate release blocker that improves life expectancy by 3–6 months. ALS-Endotherapia (GEMALS) is a novel therapeutic approach to treat ALS and the aim of the present study was to investigate the potential beneficial effects of this novel treatment. A total of 31 patients with ALS were assessed in the current study. Deceleration of the disease was observed in 83.87% (P<0.0001) of patients and mean life expectancy was increased by 38 months. Motor functions, including breathing, walking, salivation, speech, swallowing and writing, were also improved in patients treated with GEMALS. The results of the present study demonstrate that long-term treatment with GEMALS has a curative effect in patients with ALS. Furthermore, the overall effectiveness of GEMALS was assessed using the ALS Assessment Questionnaire. The score improvement was 76.2 and 100% for men and women, respectively (P<0.0001), compared with the worldwide reference score. The present study provides a promising basis for the use of GEMALS as a therapeutic treatment for patients with ALS; however, these results must be confirmed in a double-blinded and randomized clinical trial. |
format | Online Article Text |
id | pubmed-5841048 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-58410482018-03-15 GEMALS: A promising therapy for amyotrophic lateral sclerosis Geffard, Michel Mangas, Arturo Bedat, Denis Coveñas, Rafael Exp Ther Med Articles Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease that currently has no cure. At present, the only approved treatment for ALS is Riluzole, a glutamate release blocker that improves life expectancy by 3–6 months. ALS-Endotherapia (GEMALS) is a novel therapeutic approach to treat ALS and the aim of the present study was to investigate the potential beneficial effects of this novel treatment. A total of 31 patients with ALS were assessed in the current study. Deceleration of the disease was observed in 83.87% (P<0.0001) of patients and mean life expectancy was increased by 38 months. Motor functions, including breathing, walking, salivation, speech, swallowing and writing, were also improved in patients treated with GEMALS. The results of the present study demonstrate that long-term treatment with GEMALS has a curative effect in patients with ALS. Furthermore, the overall effectiveness of GEMALS was assessed using the ALS Assessment Questionnaire. The score improvement was 76.2 and 100% for men and women, respectively (P<0.0001), compared with the worldwide reference score. The present study provides a promising basis for the use of GEMALS as a therapeutic treatment for patients with ALS; however, these results must be confirmed in a double-blinded and randomized clinical trial. D.A. Spandidos 2018-04 2018-02-14 /pmc/articles/PMC5841048/ /pubmed/29545836 http://dx.doi.org/10.3892/etm.2018.5868 Text en Copyright: © Geffard et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Geffard, Michel Mangas, Arturo Bedat, Denis Coveñas, Rafael GEMALS: A promising therapy for amyotrophic lateral sclerosis |
title | GEMALS: A promising therapy for amyotrophic lateral sclerosis |
title_full | GEMALS: A promising therapy for amyotrophic lateral sclerosis |
title_fullStr | GEMALS: A promising therapy for amyotrophic lateral sclerosis |
title_full_unstemmed | GEMALS: A promising therapy for amyotrophic lateral sclerosis |
title_short | GEMALS: A promising therapy for amyotrophic lateral sclerosis |
title_sort | gemals: a promising therapy for amyotrophic lateral sclerosis |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5841048/ https://www.ncbi.nlm.nih.gov/pubmed/29545836 http://dx.doi.org/10.3892/etm.2018.5868 |
work_keys_str_mv | AT geffardmichel gemalsapromisingtherapyforamyotrophiclateralsclerosis AT mangasarturo gemalsapromisingtherapyforamyotrophiclateralsclerosis AT bedatdenis gemalsapromisingtherapyforamyotrophiclateralsclerosis AT covenasrafael gemalsapromisingtherapyforamyotrophiclateralsclerosis |