Detection of early motor involvement in diabetic polyneuropathy using a novel MUNE method - MScanFit MUNE.
Action Potentials
/ physiology
Adult
Aged
Aged, 80 and over
Cohort Studies
Diabetes Mellitus, Type 2
/ diagnosis
Diabetic Neuropathies
/ diagnosis
Female
Humans
Male
Middle Aged
Motor Neurons
/ physiology
Muscle, Skeletal
/ physiology
Neural Conduction
/ physiology
Recruitment, Neurophysiological
/ physiology
CMAP amplitude
DPN
Diabetic polyneuropathy
MScanFit MUNE
Motor involvement
Mscan
Nerve conduction studies
Journal
Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology
ISSN: 1872-8952
Titre abrégé: Clin Neurophysiol
Pays: Netherlands
ID NLM: 100883319
Informations de publication
Date de publication:
10 2019
10 2019
Historique:
received:
15
04
2019
revised:
05
07
2019
accepted:
12
08
2019
pubmed:
3
9
2019
medline:
13
5
2020
entrez:
3
9
2019
Statut:
ppublish
Résumé
Detection of motor involvement in diabetic polyneuropathy (DPN) by nerve conduction studies (NCS) does not occur until there is substantial loss of motor units, because collateral reinnervation maintains compound muscle action potential (CMAP) amplitude. Motor unit number estimation (MUNE) methods may therefore be more sensitive. This study was undertaken to test whether the novel method, MScanFit MUNE (MScan) can detect motor involvement in DPN despite normal NCS. Fifty-two type-2 diabetic patients and 38 healthy controls were included. The median nerve was examined in all participants using standard NCS and a detailed CMAP scan, used for MScan. Additional lower extremity NCS in patients were used for DPN diagnosis. Of 52 diabetic patients, 21 had NCS-defined DPN while lower extremity NCS were normal in 31 patients. MScan motor unit number and size showed higher sensitivity and incidence of abnormality than motor NCS parameters, and a similar sensitivity to sensory NCS. MScan is able to detect motor axonal damage at times when collateral reinnervation limits NCS changes. MScan is a sensitive method to detect motor involvement in DPN, which our data suggests is present as early as sensory.
Identifiants
pubmed: 31476704
pii: S1388-2457(19)31189-7
doi: 10.1016/j.clinph.2019.08.003
pii:
doi:
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1981-1987Informations de copyright
Copyright © 2019 International Federation of Clinical Neurophysiology. Published by Elsevier B.V. All rights reserved.