Literature DB >> 23418210

Fasciculation potentials and earliest changes in motor unit physiology in ALS.

Mamede de Carvalho1, Michael Swash.   

Abstract

BACKGROUND: There is little information on the earliest changes in motor unit (MU) physiology in amyotrophic lateral sclerosis (ALS) and the development of the classical neurophysiological features of ALS over time.
OBJECTIVE: We studied the earliest abnormalities in MU physiology in ALS and changes over time.
DESIGN: Observational, cross-sectional and longitudinal study. POPULATION AND METHODS: We studied the tibialis anterior (TA) muscle in three groups of subjects; 73 patients with ALS, 10 with benign fasciculation and 37 healthy control subjects. In the ALS group, 61 had normal strength in the TA muscle and 12 had TA muscle strength of 4 on the medical research council scale. In all subjects we evaluated the presence of fasciculation potentials (FPs) and fibrillation/sharp-waves (fibs-sw), and quantified MU potentials (MUPs) and jitter. Twenty-six ALS patients with TA muscle of normal strength were investigated in serial studies.
RESULTS: FPs were recorded in TA muscles (medical research council 5) of 21 ALS patients with normal MUPs. Longitudinal studies confirmed that the patients presenting with FPs as the only abnormality progressed to MUP instability before large MUPs associated with fibs-sw were detected. FPs from ALS patients with no other neurophysiological change were simpler than in patients in whom there were also fibs-sw and neurogenic MUPs. The complexity of FPs in patients with weak TA muscle was greater than in the latter group. FPs in patients with benign fasciculations were simpler than FPs in ALS patients with normal TA muscle strength.
CONCLUSIONS: FPs are a very early marker of ALS and anticipate MUP instability or reinnervation, consistent with a very early phase of increased axonal excitability. Later, widespread neuronal dysfunction causes widespread fibs-sw and loss of MUPs with compensatory reinnervation. Our results confirm the importance of FP morphology analysis in the differential diagnosis of ALS and other disorders, and indicate that benign FPs represent a different phenomenon.

Entities:  

Keywords:  EMG; MOTOR NEURON DISEASE; NEUROMUSCULAR; NEUROPHYSIOLOGY; NEUROPHYSIOLOGY, MOTOR

Mesh:

Year:  2013        PMID: 23418210     DOI: 10.1136/jnnp-2012-304545

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN: 0022-3050            Impact factor:   10.154


  20 in total

1.  Physiology of the fasciculation potentials in amyotrophic lateral sclerosis: which motor units fasciculate?

Authors:  Mamede de Carvalho; Michael Swash
Journal:  J Physiol Sci       Date:  2016-09-16       Impact factor: 2.781

Review 2.  Impairments in Motor Neurons, Interneurons and Astrocytes Contribute to Hyperexcitability in ALS: Underlying Mechanisms and Paths to Therapy.

Authors:  Dzung Do-Ha; Yossi Buskila; Lezanne Ooi
Journal:  Mol Neurobiol       Date:  2017-02-03       Impact factor: 5.590

3.  Fasciculation score: a sensitive biomarker in amyotrophic lateral sclerosis.

Authors:  Jing Ma; Qi Wen; Xiaomin Pang; Shan Huang; Jing Zhang; Juan Wang; Xueli Chang; Junhong Guo; Wei Zhang
Journal:  Neurol Sci       Date:  2021-03-11       Impact factor: 3.307

4.  Intravenous injection of l-BMAA induces a rat model with comprehensive characteristics of amyotrophic lateral sclerosis/Parkinson-dementia complex.

Authors:  Ke-Wei Tian; Hong Jiang; Bei-Bei Wang; Fan Zhang; Shu Han
Journal:  Toxicol Res (Camb)       Date:  2015-11-10       Impact factor: 3.524

5.  Spike sorting paradigm for classification of multi-channel recorded fasciculation potentials.

Authors:  Faezeh Jahanmiri-Nezhad; Paul E Barkhaus; William Zev Rymer; Ping Zhou
Journal:  Comput Biol Med       Date:  2014-10-05       Impact factor: 4.589

6.  Quantitative analysis of the features of fasciculation potentials and their relation with muscle strength in amyotrophic lateral sclerosis.

Authors:  Kota Bokuda; Toshio Shimizu; Hideki Kimura; Toshihiro Yamazaki; Tsutomu Kamiyama; Kazuhiko Watabe; Akihiro Kawata; Masaharu Hayashi; Eiji Isozaki
Journal:  Neurol Sci       Date:  2016-08-19       Impact factor: 3.307

7.  Motor unit firing pattern: evidence for motoneuronal or axonal discharge origin?

Authors:  Lydia P Kudina; Regina E Andreeva
Journal:  Neurol Sci       Date:  2015-08-04       Impact factor: 3.307

Review 8.  Another Perspective on Fasciculations: When is it not Caused by the Classic form of Amyotrophic Lateral Sclerosis or Progressive Spinal Atrophy?

Authors:  Marco Antonio Araujo Leite; Marco Orsini; Marcos R G de Freitas; João Santos Pereira; Fábio Henrique Porto Gobbi; Victor Hugo Bastos; Dionis de Castro Machado; Sergio Machado; Oscar Arrias-Carrion; Jano Alves de Souza; Acary Bulle Oliveira
Journal:  Neurol Int       Date:  2014-08-08

Review 9.  Diagnostics of Amyotrophic Lateral Sclerosis: Up to Date.

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

Review 10.  Mimics and chameleons in motor neurone disease.

Authors:  Martin R Turner; Kevin Talbot
Journal:  Pract Neurol       Date:  2013-04-24
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