Lower motor neuron involvement in ALS assessed by motor unit number index (MUNIX): Long-term changes and reproducibility
•The reproducibility of MUNIX was tested in a large number of ALS-patients by three different statistical methods.•There was a significant decrease of MUNIX values in ALS-patients as compared to healthy controls and also during ALS progression.•Intra-rater reproducibility of MUNIX in ALS-patients in...
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Published in | Clinical neurophysiology Vol. 127; no. 4; pp. 1984 - 1988 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier B.V
01.04.2016
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Online Access | Get full text |
ISSN | 1388-2457 1872-8952 1872-8952 |
DOI | 10.1016/j.clinph.2015.12.023 |
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Abstract | •The reproducibility of MUNIX was tested in a large number of ALS-patients by three different statistical methods.•There was a significant decrease of MUNIX values in ALS-patients as compared to healthy controls and also during ALS progression.•Intra-rater reproducibility of MUNIX in ALS-patients in the course of the disorder was high, rendering MUNIX a reliable clinical biomarker.
Motor unit number estimation (MUNE) techniques such as motor unit number index (MUNIX) have been used to quantify lower motor neuron loss and disease progression in amyotrophic lateral sclerosis (ALS). We investigated the consistency of reproducibility of MUNIX in 30 ALS-patients during the course of the disorder.
MUNIX was recorded in abductor pollicis brevis and tibialis anterior muscles bilaterally in ALS-patients by two measurements at the first and at one follow-up visit and once in healthy controls. Intra-rater reproducibility was evaluated by three statistical methods: interclass correlation coefficient (ICC), correlation coefficient analysis (CCA), and coefficient of variation (CV).
We found significant correlation between the first and second measurement of MUNIX in all tested muscles and at the follow-up visit (r⩾0.891, p<0.01) and good statistically significant reproducibility of MUNIX in all four measured muscles at the follow-up visit (ICC⩾0.946, p<0.01). The CV of MUNIX at the follow-up visit ranged from 13.90% to 32.95%.
This study shows good consistency of reproducibility of MUNIX in the course of ALS.
This study suggests that MUNIX can be used to track the progression of the disorder both in clinical routine and in treatment trials. |
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AbstractList | Motor unit number estimation (MUNE) techniques such as motor unit number index (MUNIX) have been used to quantify lower motor neuron loss and disease progression in amyotrophic lateral sclerosis (ALS). We investigated the consistency of reproducibility of MUNIX in 30 ALS-patients during the course of the disorder.
MUNIX was recorded in abductor pollicis brevis and tibialis anterior muscles bilaterally in ALS-patients by two measurements at the first and at one follow-up visit and once in healthy controls. Intra-rater reproducibility was evaluated by three statistical methods: interclass correlation coefficient (ICC), correlation coefficient analysis (CCA), and coefficient of variation (CV).
We found significant correlation between the first and second measurement of MUNIX in all tested muscles and at the follow-up visit (r⩾0.891, p<0.01) and good statistically significant reproducibility of MUNIX in all four measured muscles at the follow-up visit (ICC⩾0.946, p<0.01). The CV of MUNIX at the follow-up visit ranged from 13.90% to 32.95%.
This study shows good consistency of reproducibility of MUNIX in the course of ALS.
This study suggests that MUNIX can be used to track the progression of the disorder both in clinical routine and in treatment trials. Highlights • The reproducibility of MUNIX was tested in a large number of ALS-patients by three different statistical methods. • There was a significant decrease of MUNIX values in ALS-patients as compared to healthy controls and also during ALS progression. • Intra-rater reproducibility of MUNIX in ALS-patients in the course of the disorder was high, rendering MUNIX a reliable clinical biomarker. •The reproducibility of MUNIX was tested in a large number of ALS-patients by three different statistical methods.•There was a significant decrease of MUNIX values in ALS-patients as compared to healthy controls and also during ALS progression.•Intra-rater reproducibility of MUNIX in ALS-patients in the course of the disorder was high, rendering MUNIX a reliable clinical biomarker. Motor unit number estimation (MUNE) techniques such as motor unit number index (MUNIX) have been used to quantify lower motor neuron loss and disease progression in amyotrophic lateral sclerosis (ALS). We investigated the consistency of reproducibility of MUNIX in 30 ALS-patients during the course of the disorder. MUNIX was recorded in abductor pollicis brevis and tibialis anterior muscles bilaterally in ALS-patients by two measurements at the first and at one follow-up visit and once in healthy controls. Intra-rater reproducibility was evaluated by three statistical methods: interclass correlation coefficient (ICC), correlation coefficient analysis (CCA), and coefficient of variation (CV). We found significant correlation between the first and second measurement of MUNIX in all tested muscles and at the follow-up visit (r⩾0.891, p<0.01) and good statistically significant reproducibility of MUNIX in all four measured muscles at the follow-up visit (ICC⩾0.946, p<0.01). The CV of MUNIX at the follow-up visit ranged from 13.90% to 32.95%. This study shows good consistency of reproducibility of MUNIX in the course of ALS. This study suggests that MUNIX can be used to track the progression of the disorder both in clinical routine and in treatment trials. Motor unit number estimation (MUNE) techniques such as motor unit number index (MUNIX) have been used to quantify lower motor neuron loss and disease progression in amyotrophic lateral sclerosis (ALS). We investigated the consistency of reproducibility of MUNIX in 30 ALS-patients during the course of the disorder.OBJECTIVEMotor unit number estimation (MUNE) techniques such as motor unit number index (MUNIX) have been used to quantify lower motor neuron loss and disease progression in amyotrophic lateral sclerosis (ALS). We investigated the consistency of reproducibility of MUNIX in 30 ALS-patients during the course of the disorder.MUNIX was recorded in abductor pollicis brevis and tibialis anterior muscles bilaterally in ALS-patients by two measurements at the first and at one follow-up visit and once in healthy controls. Intra-rater reproducibility was evaluated by three statistical methods: interclass correlation coefficient (ICC), correlation coefficient analysis (CCA), and coefficient of variation (CV).METHODSMUNIX was recorded in abductor pollicis brevis and tibialis anterior muscles bilaterally in ALS-patients by two measurements at the first and at one follow-up visit and once in healthy controls. Intra-rater reproducibility was evaluated by three statistical methods: interclass correlation coefficient (ICC), correlation coefficient analysis (CCA), and coefficient of variation (CV).We found significant correlation between the first and second measurement of MUNIX in all tested muscles and at the follow-up visit (r⩾0.891, p<0.01) and good statistically significant reproducibility of MUNIX in all four measured muscles at the follow-up visit (ICC⩾0.946, p<0.01). The CV of MUNIX at the follow-up visit ranged from 13.90% to 32.95%.RESULTSWe found significant correlation between the first and second measurement of MUNIX in all tested muscles and at the follow-up visit (r⩾0.891, p<0.01) and good statistically significant reproducibility of MUNIX in all four measured muscles at the follow-up visit (ICC⩾0.946, p<0.01). The CV of MUNIX at the follow-up visit ranged from 13.90% to 32.95%.This study shows good consistency of reproducibility of MUNIX in the course of ALS.CONCLUSIONSThis study shows good consistency of reproducibility of MUNIX in the course of ALS.This study suggests that MUNIX can be used to track the progression of the disorder both in clinical routine and in treatment trials.SIGNIFICANCEThis study suggests that MUNIX can be used to track the progression of the disorder both in clinical routine and in treatment trials. |
Author | Kollewe, Katja Mohammadi, Bahram Dengler, Reinhard Böselt, Sebastian Petri, Susanne Fathi, Davood |
Author_xml | – sequence: 1 givenname: Davood surname: Fathi fullname: Fathi, Davood organization: Brain and Spinal Cord Injury Research Center, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran – sequence: 2 givenname: Bahram surname: Mohammadi fullname: Mohammadi, Bahram organization: International Neuroscience Institute, Hannover, Germany – sequence: 3 givenname: Reinhard surname: Dengler fullname: Dengler, Reinhard organization: Department of Neurology, Hannover Medical School, Hannover, Germany – sequence: 4 givenname: Sebastian surname: Böselt fullname: Böselt, Sebastian organization: Department of Neurology, Hannover Medical School, Hannover, Germany – sequence: 5 givenname: Susanne surname: Petri fullname: Petri, Susanne organization: Department of Neurology, Hannover Medical School, Hannover, Germany – sequence: 6 givenname: Katja surname: Kollewe fullname: Kollewe, Katja email: kollewe.katja@mh-hannover.de organization: Department of Neurology, Hannover Medical School, Hannover, Germany |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/26971480$$D View this record in MEDLINE/PubMed |
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Keywords | Amyotrophic lateral sclerosis (ALS) Reproducibility Motor unit number index (MUNIX) Consistency |
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Snippet | •The reproducibility of MUNIX was tested in a large number of ALS-patients by three different statistical methods.•There was a significant decrease of MUNIX... Highlights • The reproducibility of MUNIX was tested in a large number of ALS-patients by three different statistical methods. • There was a significant... Motor unit number estimation (MUNE) techniques such as motor unit number index (MUNIX) have been used to quantify lower motor neuron loss and disease... |
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SubjectTerms | Aged Amyotrophic lateral sclerosis (ALS) Amyotrophic Lateral Sclerosis - diagnosis Amyotrophic Lateral Sclerosis - physiopathology Consistency Electromyography - standards Female Follow-Up Studies Humans Male Middle Aged Motor Neurons - physiology Motor unit number index (MUNIX) Neurology Recruitment, Neurophysiological - physiology Reproducibility Reproducibility of Results Time Factors |
Title | Lower motor neuron involvement in ALS assessed by motor unit number index (MUNIX): Long-term changes and reproducibility |
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