eISSN: 2300-6722
ISSN: 1899-1874
Medical Studies/Studia Medyczne
Current issue Archive Manuscripts accepted About the journal Supplements Editorial board Abstracting and indexing Subscription Contact Instructions for authors Publication charge Ethical standards and procedures
Editorial System
Submit your Manuscript
1/2019
vol. 35
 
Share:
Share:
abstract:
Original paper

Electromyographic parameters in abnormal gait in patients suffering from amyotrophic lateral sclerosis

Ilona A. Hübner
,
Jacek Hübner
,
Sławomir Kroczka

Medical Studies/Studia Medyczne 2019; 35 (1): 23–31
Online publish date: 2019/03/30
View full text Get citation
 
PlumX metrics:
Introduction
Amyotrophic lateral sclerosis (ALS) is a terminal neurodegenerative disease, which gradually damages motor neurons in the cortex, brainstem, and spinal cord, leading to a progressive deterioration in patients’ fitness and their dependence on others.

Aim of the research
To assess electromyographic parameters and abnormal gait in the course of ALS.

Material and methods
The study covered 20 people with clinically proven or probable ALS diagnosed, determined according to the El Escorial criteria. In the study group, 10 patients were affected by the limb onset of the disorder, and the remaining 10 people by the bulbar onset. The analysis covered electromyography and test results: 6-minute walk test and 10-metre walk test performed three times within 6 months.

Results
The results of electromyographic parameters and tests were analysed for the whole group and separately for the group with bulbar-onset and limb-onset ALS. The statistical analysis of the results has shown that the duration of motor unit potential (MUP) is the most useful electromyographic parameter in early diagnosis and monitoring of the course of the disease. The increasing abnormal gait in the course of ALS was a clinical reflection of gradually prolonging MUP.

Conclusions
The progressing loss of nerve and muscle function as a result of motor neuron loss is reflected in walking deterioration in ALS patients. 2. The gradually increasing MUP duration of particular muscles is concomitant to the increasing abnormal gait. The assessment of the MUP duration of particular muscles may serve to monitor the ALS progression.

keywords:

amyotrophic lateral sclerosis, motor unit potential, abnormal gait, electromyographic parameters

Quick links
© 2024 Termedia Sp. z o.o.
Developed by Bentus.