Literature DB >> 18484797

Management of amyotrophic lateral sclerosis.

Philippe Corcia1, Vincent Meininger.   

Abstract

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease affecting the motor neurons, in both the spinal cord and medulla (lower motor neurons) and cerebral cortex (upper motor neurons). Even though ALS remains fatal, several advances have been made during the last decade in improving the consequences of motor dysfunction, quality of life and survival time of patients. Treatment of ALS cannot be restricted to riluzole, the only molecule that has been proved to modify the evolution of the disease. Symptomatic treatments have an important role in controlling the major consequences of the disease, such as pain, sleep disorders, spasticity, hypersialhorroea, emotional lability, depression and digestive disorders (constipation and reflux). All these symptoms need to be recognized and their possible causes identified in order to provide the most appropriate management of patients with ALS. However, an advance in the daily care of patients is the identification of two important phenomena that occur during the evolution of the disease: swallowing difficulties and the occurrence of diaphragmatic dysfunction. For both, specific medical interventions have been developed to allow correction of the consequences (i.e. weight loss and respiratory insufficiency). Although no controlled trials have been performed, observational studies suggest that gastrostomy and non-invasive ventilation may improve at least quality of life and survival. All of these various approaches, pharmaceutical and non-pharmaceutical therapies, are prescribed according to individual symptoms and require the involvement of a large range of health professionals. This multidisciplinary approach in ALS clinics is considered to be one of the more important factors impacting on survival rate and appears to be the gold standard of medical care of ALS patients. Important findings have been made in understanding the nature of the degenerative process that affects the motor neurons. All these data have allowed new therapeutic molecules to be tested alone or in combination with riluzole. Despite the negative results obtained until now, we hope to demonstrate very soon a greater improvement in therapy.

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Year:  2008        PMID: 18484797     DOI: 10.2165/00003495-200868080-00003

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  91 in total

1.  Hospitalization in amyotrophic lateral sclerosis: causes, costs, and outcomes.

Authors:  N Lechtzin; C M Wiener; L Clawson; V Chaudhry; G B Diette
Journal:  Neurology       Date:  2001-03-27       Impact factor: 9.910

Review 2.  Management of motor neurone disease.

Authors:  R S Howard; R W Orrell
Journal:  Postgrad Med J       Date:  2002-12       Impact factor: 2.401

3.  Autologous mesenchymal stem cells: clinical applications in amyotrophic lateral sclerosis.

Authors:  Letizia Mazzini; Katia Mareschi; Ivana Ferrero; Elena Vassallo; Giuseppe Oliveri; Riccardo Boccaletti; Lucia Testa; Sergio Livigni; Franca Fagioli
Journal:  Neurol Res       Date:  2006-07       Impact factor: 2.448

4.  The course of the terminal phase in patients with amyotrophic lateral sclerosis.

Authors:  C Neudert; D Oliver; M Wasner; G D Borasio
Journal:  J Neurol       Date:  2001-07       Impact factor: 4.849

5.  Hypermetabolism in ALS: correlations with clinical and paraclinical parameters.

Authors:  Jean-Claude Desport; Frédéric Torny; Mathieu Lacoste; Pierre-Marie Preux; Philippe Couratier
Journal:  Neurodegener Dis       Date:  2005       Impact factor: 2.977

6.  Efficacy of pramipexole in restless legs syndrome: a six-week, multicenter, randomized, double-blind study (effect-RLS study).

Authors:  Wolfgang H Oertel; Karin Stiasny-Kolster; Bettina Bergtholdt; Yngve Hallström; Jaan Albo; Lena Leissner; Thomas Schindler; Juergen Koester; Juergen Reess
Journal:  Mov Disord       Date:  2007-01-15       Impact factor: 10.338

7.  Efficacy of minocycline in patients with amyotrophic lateral sclerosis: a phase III randomised trial.

Authors:  Paul H Gordon; Dan H Moore; Robert G Miller; Julaine M Florence; Joseph L Verheijde; Carolyn Doorish; Joan F Hilton; G Mark Spitalny; Robert B MacArthur; Hiroshi Mitsumoto; Hans E Neville; Kevin Boylan; Tahseen Mozaffar; Jerry M Belsh; John Ravits; Richard S Bedlack; Michael C Graves; Leo F McCluskey; Richard J Barohn; Rup Tandan
Journal:  Lancet Neurol       Date:  2007-11-05       Impact factor: 44.182

8.  A rare Cu/Zn superoxide dismutase mutation causing familial amyotrophic lateral sclerosis with variable age of onset, incomplete penetrance and a sensory neuropathy.

Authors:  Kourosh Rezania; Jianhua Yan; Lisa Dellefave; Han-Xiang Deng; Nailah Siddique; Robert T Pascuzzi; Teepu Siddique; Raymond P Roos
Journal:  Amyotroph Lateral Scler Other Motor Neuron Disord       Date:  2003-09

9.  Trial of baclofen in amyotrophic lateral sclerosis.

Authors:  F H Norris; K S U; B Sachais; M Carey
Journal:  Arch Neurol       Date:  1979-11

Review 10.  Amyotrophic lateral sclerosis: recent advances and future therapies.

Authors:  Niranjanan Nirmalananthan; Linda Greensmith
Journal:  Curr Opin Neurol       Date:  2005-12       Impact factor: 5.710

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  9 in total

1.  Evidence-based drug treatment in amyotrophic lateral sclerosis and upcoming clinical trials.

Authors:  Albert C Ludolph; Sarah Jesse
Journal:  Ther Adv Neurol Disord       Date:  2009-09       Impact factor: 6.570

Review 2.  Trends in Research Literature Describing Dysphagia in Motor Neuron Diseases (MND): A Scoping Review.

Authors:  Ashley A Waito; Teresa J Valenzano; Melanie Peladeau-Pigeon; Catriona M Steele
Journal:  Dysphagia       Date:  2017-06-29       Impact factor: 3.438

3.  Respiratory and nutritional support in amyotrophic lateral sclerosis.

Authors:  Namita A Goyal; Tahseen Mozaffar
Journal:  Curr Treat Options Neurol       Date:  2014-02       Impact factor: 3.598

4.  Pain in amyotrophic lateral sclerosis: a neglected aspect of disease.

Authors:  Chalonda R Handy; Christina Krudy; Nicholas Boulis; Thais Federici
Journal:  Neurol Res Int       Date:  2011-05-03

5.  CNS-targeted glucocorticoid reduces pathology in mouse model of amyotrophic lateral sclerosis.

Authors:  Matthew C Evans; Pieter J Gaillard; Marco de Boer; Chantal Appeldoorn; Rick Dorland; Nicola R Sibson; Martin R Turner; Daniel C Anthony; Helen B Stolp
Journal:  Acta Neuropathol Commun       Date:  2014-06-13       Impact factor: 7.801

Review 6.  The efficacy and safety of riluzole for neurodegenerative movement disorders: a systematic review with meta-analysis.

Authors:  Jia Liu; Lu-Ning Wang
Journal:  Drug Deliv       Date:  2018-11       Impact factor: 6.419

7.  Association Between Premorbid Body Mass Index and Amyotrophic Lateral Sclerosis: Causal Inference Through Genetic Approaches.

Authors:  Ping Zeng; Xinghao Yu; Haibo Xu
Journal:  Front Neurol       Date:  2019-05-24       Impact factor: 4.003

8.  Young-onset Amyotrophic Lateral Sclerosis with Rare Skin Manifestation: Case Report and Literature Review.

Authors:  Aamna Qazi; Farheen Malik; Lubna Shafi; Saqib Basar; Azka Qazi
Journal:  Cureus       Date:  2020-04-27

9.  Causal effects of blood lipids on amyotrophic lateral sclerosis: a Mendelian randomization study.

Authors:  Ping Zeng; Xiang Zhou
Journal:  Hum Mol Genet       Date:  2019-02-15       Impact factor: 6.150

  9 in total

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