Use of Bayesian MUNE to show differing rate of loss of motor units in subgroups of ALS


Autoria(s): Baumann, F.; Henderson, R.D.; Ridall, G.; Pettitt, A.N.; McCombe, P.A.
Data(s)

17/04/2012

Resumo

Objectives To evaluate differences among patients with different clinical features of ALS, we used our Bayesian method of motor unit number estimation (MUNE). Methods We performed serial MUNE studies on 42 subjects who fulfilled the diagnostic criteria for ALS during the course of their illness. Subjects were classified into three subgroups according to whether they had typical ALS (with upper and lower motor neurone signs) or had predominantly upper motor neurone weakness with only minor LMN signs, or predominantly lower motor neurone weakness with only minor UMN signs. In all subjects we calculated the half life of MUs, defined as the expected time for the number of MUs to halve, in one or more of the abductor digiti minimi (ADM), abductor pollicis brevis (APB) and extensor digitorum brevis (EDB) muscles. Results The mean half life of MUs was less in subjects who had typical ALS with both upper and lower motor neurone signs than in those with predominantly upper motor neurone weakness or predominantly lower motor neurone weakness. In 18 subjects we analysed the estimated size of the MUs and demonstrated the appearance of large MUs in subjects with upper or lower motor neurone predominant weakness. We found that the appearance of large MUs was correlated with the half life of MUs. Conclusions Patients with different clinical features of ALS have different rates of loss and different sizes of MUs. Significance: These findings could indicate differences in disease pathogenesis.

Identificador

http://eprints.qut.edu.au/50638/

Publicador

Elsevier Ireland Ltd

Relação

DOI:10.1016/j.clinph.2012.04.022

Baumann, F., Henderson, R.D., Ridall, G., Pettitt, A.N., & McCombe, P.A. (2012) Use of Bayesian MUNE to show differing rate of loss of motor units in subgroups of ALS. Clinical Neurophysiology, 123(12), pp. 2446-2453.

Direitos

Copyright 2012 International Federation of Clinical Neurophysiology and Elsevier Ireland Ltd.

This is the author’s version of a work that was accepted for publication in Clinical Neurophysiology. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Clinical Neurophysiology, [VOL 123, ISSUE 12, (2012)] DOI: 10.1016/j.clinph.2012.04.022

Fonte

School of Mathematical Sciences; Science & Engineering Faculty

Palavras-Chave #ALS #Disease phenotypes #Exponential decay #Motor unit #MUNE
Tipo

Journal Article