Literature DB >> 30080715

Neurophysiological biomarkers in amyotrophic lateral sclerosis.

Steve Vucic1,2, Seward B Rutkove3,4.   

Abstract

PURPOSE OF REVIEW: Amyotrophic lateral sclerosis (ALS) is a rapidly progressive neurodegenerative disorder of the motor neurons, characterized by upper motor neuron (UMN) and lower motor neuron (LMN) dysfunction. There have been significant technological advances in the development of neurophysiological biomarkers of UMN and LMN dysfunction in ALS. In this review, we discuss major advances in development of neurophysiological biomarkers in ALS, critiquing their potential in diagnosis and prognosis of ALS, as well as utility in monitoring treatment effects. RECENT
FINDINGS: The threshold tracking transcranial magnetic stimulation (TMS) technique has established cortical hyperexcitability as an early and specific biomarker of UMN dysfunction in ALS, and associated with neurodegeneration. In addition to establishing cortical hyperexcitability as a pathophysiological mechanism, threshold tracking TMS has enabled an earlier diagnosis of ALS and provided a means of monitoring effects of therapeutic agents. Biomarkers of LMN dysfunction, including motor unit number estimation, the neurophysiological index, electrical impedance myography and axonal excitability techniques, have all exhibited utility in monitoring disease progression.
SUMMARY: In addition to enhancing ALS diagnosis, the development of novel neurophysiological biomarkers has implications for clinical trials research and drug development, enabling the assessment of biological efficacy of agents in early stages of drug development.

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Year:  2018        PMID: 30080715     DOI: 10.1097/WCO.0000000000000593

Source DB:  PubMed          Journal:  Curr Opin Neurol        ISSN: 1350-7540            Impact factor:   5.710


  15 in total

1.  Correlation between clinical phenotype and electromyographic parameters in amyotrophic lateral sclerosis.

Authors:  Eleonora Colombo; Alberto Doretti; Francesco Scheveger; Alessio Maranzano; Giulia Pata; Delia Gagliardi; Megi Meneri; Stefano Messina; Federico Verde; Claudia Morelli; Stefania Corti; Luca Maderna; Vincenzo Silani; Nicola Ticozzi
Journal:  J Neurol       Date:  2022-10-02       Impact factor: 6.682

Review 2.  Considerations for Amyotrophic Lateral Sclerosis (ALS) Clinical Trial Design.

Authors:  Christina N Fournier
Journal:  Neurotherapeutics       Date:  2022-07-11       Impact factor: 6.088

Review 3.  Diagnostics of Amyotrophic Lateral Sclerosis: Up to Date.

Authors:  Ivana Štětkářová; Edvard Ehler
Journal:  Diagnostics (Basel)       Date:  2021-02-03

Review 4.  Recent advances in the diagnosis and prognosis of amyotrophic lateral sclerosis.

Authors:  Stephen A Goutman; Orla Hardiman; Ammar Al-Chalabi; Adriano Chió; Masha G Savelieff; Matthew C Kiernan; Eva L Feldman
Journal:  Lancet Neurol       Date:  2022-03-22       Impact factor: 59.935

Review 5.  Are Circulating Cytokines Reliable Biomarkers for Amyotrophic Lateral Sclerosis?

Authors:  Laura Moreno-Martinez; Ana Cristina Calvo; María Jesús Muñoz; Rosario Osta
Journal:  Int J Mol Sci       Date:  2019-06-05       Impact factor: 5.923

Review 6.  Biomarkers and the Development of a Personalized Medicine Approach in Spinal Muscular Atrophy.

Authors:  Didu S T Kariyawasam; Arlene D'Silva; Cindy Lin; Monique M Ryan; Michelle A Farrar
Journal:  Front Neurol       Date:  2019-08-19       Impact factor: 4.003

7.  Assessing Rat Forelimb and Hindlimb Motor Unit Connectivity as Objective and Robust Biomarkers of Spinal Motor Neuron Function.

Authors:  Markus E Harrigan; Angela R Filous; Andrew P Tosolini; Renee Morris; Jan M Schwab; W David Arnold
Journal:  Sci Rep       Date:  2019-11-13       Impact factor: 4.379

8.  The rise and fall of fasciculations in amyotrophic lateral sclerosis.

Authors:  James A Bashford; Aidan Wickham; Raquel Iniesta; Emmanuel M Drakakis; Martyn G Boutelle; Kerry R Mills; Chris E Shaw
Journal:  Brain Commun       Date:  2020-02-20

9.  Nine Hole Peg Test and Transcranial Magnetic Stimulation: Useful to Evaluate Dexterity of the Hand and Disease Progression in Amyotrophic Lateral Sclerosis.

Authors:  David Czell; Christoph Neuwirth; Markus Weber; Sabine Sartoretti-Schefer; Andreas Gutzeit; Carolin Reischauer
Journal:  Neurol Res Int       Date:  2019-11-07

10.  Median Nerve-Neurophysiological Index Correlates With the Survival of Patients With Amyotrophic Lateral Sclerosis.

Authors:  Liu-Qing Xu; Wei Hu; Qi-Fu Guo; Lu-Lu Lai; Guo-Rong Xu; Wan-Jin Chen; Ning Wang; Qi-Jie Zhang
Journal:  Front Neurol       Date:  2020-10-22       Impact factor: 4.003

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