Current and emerging treatments for amyotrophic lateral sclerosis

Stefano Zoccolella1, Andrea Santamato2, Paolo Lamberti31Azienda Ospedaliero-UniversitariaOspedali Riuniti, Department of Medical and Neurological Sciences, Clinic of Nervous System Diseases, University of Foggia, Italy; 2Department of Physical Medicine and Rehabilitation, University of Foggia, OORR,...

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Autores principales: Stefano Zoccolella, Andrea Santamato, Paolo Lamberti
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Publicado: Dove Medical Press 2009
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spelling oai:doaj.org-article:8c7354c611d24e3fa1f71f95ba79cd212021-12-02T00:48:16ZCurrent and emerging treatments for amyotrophic lateral sclerosis1176-63281178-2021https://doaj.org/article/8c7354c611d24e3fa1f71f95ba79cd212009-11-01T00:00:00Zhttp://www.dovepress.com/current-and-emerging-treatments-for-amyotrophic-lateral-sclerosis-a3691https://doaj.org/toc/1176-6328https://doaj.org/toc/1178-2021Stefano Zoccolella1, Andrea Santamato2, Paolo Lamberti31Azienda Ospedaliero-UniversitariaOspedali Riuniti, Department of Medical and Neurological Sciences, Clinic of Nervous System Diseases, University of Foggia, Italy; 2Department of Physical Medicine and Rehabilitation, University of Foggia, OORR, Italy; 3Department of Neurology and Psychiatry, University of Bari, ItalyBackground: Amyotrophic lateral sclerosis (ALS) is a relatively rare neurodegenerative disorder of both upper and lower motoneurons. Currently, the management of ALS is essentially symptoms-based, and riluzole, an antiglutamatergic agent, is the only drug for the treatment of ALS approved by the food and drug administration.Objective: We reviewed current literature concerning emerging treatments for amyotrophic lateral sclerosis.Methods: A Medline literature search was performed to identify all studies on ALS treatment published from January 1st, 1986 through August 31st, 2009. We selected papers concerning only disease-modifying therapy.Results: Forty-eight compounds were identified and reviewed in this study.Conclusions: Riluzole is the only compound that demonstrated a beneficial effect on ALS patients, but with only modest increase in survival. Although several drugs showed effective results in the animal models for ALS, none of them significantly prolonged survival or improved quality of life of ALS patients. Several factors have been implicated in explaining the predominantly negative results of numerous randomized clinical trials in ALS, including methodological problems in the use of animal-drug screening, the lack of assessment of pharmacokinetic profile of the drugs, and methodological pitfalls of clinical trials in ALS patients.Keywords: amyotrophic lateral sclerosis, therapy, drug, survival Stefano ZoccolellaAndrea SantamatoPaolo LambertiDove Medical PressarticleNeurosciences. Biological psychiatry. NeuropsychiatryRC321-571Neurology. Diseases of the nervous systemRC346-429ENNeuropsychiatric Disease and Treatment, Vol 2009, Iss default, Pp 577-595 (2009)
institution DOAJ
collection DOAJ
language EN
topic Neurosciences. Biological psychiatry. Neuropsychiatry
RC321-571
Neurology. Diseases of the nervous system
RC346-429
spellingShingle Neurosciences. Biological psychiatry. Neuropsychiatry
RC321-571
Neurology. Diseases of the nervous system
RC346-429
Stefano Zoccolella
Andrea Santamato
Paolo Lamberti
Current and emerging treatments for amyotrophic lateral sclerosis
description Stefano Zoccolella1, Andrea Santamato2, Paolo Lamberti31Azienda Ospedaliero-UniversitariaOspedali Riuniti, Department of Medical and Neurological Sciences, Clinic of Nervous System Diseases, University of Foggia, Italy; 2Department of Physical Medicine and Rehabilitation, University of Foggia, OORR, Italy; 3Department of Neurology and Psychiatry, University of Bari, ItalyBackground: Amyotrophic lateral sclerosis (ALS) is a relatively rare neurodegenerative disorder of both upper and lower motoneurons. Currently, the management of ALS is essentially symptoms-based, and riluzole, an antiglutamatergic agent, is the only drug for the treatment of ALS approved by the food and drug administration.Objective: We reviewed current literature concerning emerging treatments for amyotrophic lateral sclerosis.Methods: A Medline literature search was performed to identify all studies on ALS treatment published from January 1st, 1986 through August 31st, 2009. We selected papers concerning only disease-modifying therapy.Results: Forty-eight compounds were identified and reviewed in this study.Conclusions: Riluzole is the only compound that demonstrated a beneficial effect on ALS patients, but with only modest increase in survival. Although several drugs showed effective results in the animal models for ALS, none of them significantly prolonged survival or improved quality of life of ALS patients. Several factors have been implicated in explaining the predominantly negative results of numerous randomized clinical trials in ALS, including methodological problems in the use of animal-drug screening, the lack of assessment of pharmacokinetic profile of the drugs, and methodological pitfalls of clinical trials in ALS patients.Keywords: amyotrophic lateral sclerosis, therapy, drug, survival
format article
author Stefano Zoccolella
Andrea Santamato
Paolo Lamberti
author_facet Stefano Zoccolella
Andrea Santamato
Paolo Lamberti
author_sort Stefano Zoccolella
title Current and emerging treatments for amyotrophic lateral sclerosis
title_short Current and emerging treatments for amyotrophic lateral sclerosis
title_full Current and emerging treatments for amyotrophic lateral sclerosis
title_fullStr Current and emerging treatments for amyotrophic lateral sclerosis
title_full_unstemmed Current and emerging treatments for amyotrophic lateral sclerosis
title_sort current and emerging treatments for amyotrophic lateral sclerosis
publisher Dove Medical Press
publishDate 2009
url https://doaj.org/article/8c7354c611d24e3fa1f71f95ba79cd21
work_keys_str_mv AT stefanozoccolella currentandemergingtreatmentsforamyotrophiclateralsclerosis
AT andreasantamato currentandemergingtreatmentsforamyotrophiclateralsclerosis
AT paololamberti currentandemergingtreatmentsforamyotrophiclateralsclerosis
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