Literature DB >> 28446118

Motor neurone disease: progress and challenges.

Thanuja Dharmadasa1, Robert D Henderson2, Paul S Talman3, Richard Al Macdonell4, Susan Mathers5, David W Schultz6, Merrillee Needham7, Margaret Zoing8, Steve Vucic9, Matthew C Kiernan8.   

Abstract

Major progress has been made over the past decade in the understanding of motor neurone disease (MND), changing the landscape of this complex disease. Through identifying positive prognostic factors, new evidence-based standards of care have been established that improve patient survival, reduce burden of disease for patients and their carers, and enhance quality of life. These factors include early management of respiratory dysfunction with non-invasive ventilation, maintenance of weight and nutritional status, as well as instigation of a multidisciplinary team including neurologists, general practitioners and allied health professionals. Advances in technology have enhanced our understanding of the genetic architecture of MND considerably, with implications for patients, their families and clinicians. Recognition of extra-motor involvement, particularly cognitive dysfunction, has identified a spectrum of disease from MND through to frontotemporal dementia. Although riluzole remains the only disease-modifying medication available in clinical practice in Australia, several new therapies are undergoing clinical trials nationally and globally, representing a shift in treatment paradigms. Successful translation of this clinical research through growth in community funding, awareness and national MND research organisations has laid the foundation for closing the research-practice gap on this debilitating disease. In this review, we highlight these recent developments, which have transformed treatment, augmented novel therapeutic platforms, and established a nexus between research and the MND community. This era of change is of significant relevance to both specialists and general practitioners who remain integral to the care of patients with MND.

Entities:  

Mesh:

Year:  2017        PMID: 28446118     DOI: 10.5694/mja16.01063

Source DB:  PubMed          Journal:  Med J Aust        ISSN: 0025-729X            Impact factor:   7.738


  12 in total

1.  Amyotrophic Lateral Sclerosis Mortality in the United States, 2011-2014.

Authors:  Theodore C Larson; Wendy Kaye; Paul Mehta; D Kevin Horton
Journal:  Neuroepidemiology       Date:  2018-07-10       Impact factor: 3.282

2.  The Impact of Next-Generation Sequencing on the Diagnosis, Treatment, and Prevention of Hereditary Neuromuscular Disorders.

Authors:  Sarah J Beecroft; Phillipa J Lamont; Samantha Edwards; Hayley Goullée; Mark R Davis; Nigel G Laing; Gianina Ravenscroft
Journal:  Mol Diagn Ther       Date:  2020-09-30       Impact factor: 4.074

3.  Commentary: Amyotrophic Lateral Sclerosis and Myasthenia Gravis Overlap Syndrome: A Review of Two Cases and the Associated Literature.

Authors:  Ian Paul Johnson; Patrizia Longone
Journal:  Front Neurol       Date:  2017-07-27       Impact factor: 4.003

Review 4.  Pathophysiology and Diagnosis of ALS: Insights from Advances in Neurophysiological Techniques.

Authors:  Mehdi A J van den Bos; Nimeshan Geevasinga; Mana Higashihara; Parvathi Menon; Steve Vucic
Journal:  Int J Mol Sci       Date:  2019-06-10       Impact factor: 5.923

5.  Cortical inexcitability defines an adverse clinical profile in amyotrophic lateral sclerosis.

Authors:  T Dharmadasa; J Howells; J M Matamala; N G Simon; D Burke; S Vucic; M C Kiernan
Journal:  Eur J Neurol       Date:  2020-10-09       Impact factor: 6.089

6.  Aluminum dust exposure and risk of neurodegenerative diseases in a cohort of male miners in Ontario, Canada.

Authors:  Xiaoke Zeng; Jill Macleod; Colin Berriault; Nathan L DeBono; Victoria H Arrandale; Anne M Harris; Paul A Demers
Journal:  Scand J Work Environ Health       Date:  2021-09-30       Impact factor: 5.024

Review 7.  Cortical Excitability across the ALS Clinical Motor Phenotypes.

Authors:  Thanuja Dharmadasa
Journal:  Brain Sci       Date:  2021-05-28

8.  Phase 2 randomized placebo controlled double blind study to assess the efficacy and safety of tecfidera in patients with amyotrophic lateral sclerosis (TEALS Study): Study protocol clinical trial (SPIRIT Compliant).

Authors:  Steve Vucic; Julie Ryder; Linda Mekhael; Henderson Rd; Susan Mathers; Merilee Needham; Schultz Dw; Kiernan Mc
Journal:  Medicine (Baltimore)       Date:  2020-02       Impact factor: 1.817

9.  Structural Variants May Be a Source of Missing Heritability in sALS.

Authors:  Frances Theunissen; Loren L Flynn; Ryan S Anderton; Frank Mastaglia; Julia Pytte; Leanne Jiang; Stuart Hodgetts; Daniel K Burns; Ann Saunders; Sue Fletcher; Steve D Wilton; Patrick Anthony Akkari
Journal:  Front Neurosci       Date:  2020-01-31       Impact factor: 4.677

10.  Sex-dependent effects of amyloid precursor-like protein 2 in the SOD1-G37R transgenic mouse model of MND.

Authors:  Phan H Truong; Peter J Crouch; James B W Hilton; Catriona A McLean; Roberto Cappai; Giuseppe D Ciccotosto
Journal:  Cell Mol Life Sci       Date:  2021-09-02       Impact factor: 9.261

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