Quality Control of Motor Unit Number Index (MUNIX) Measurements in 6 Muscles in a Single-Subject "Round-Robin" Setup

PLoS One. 2016 May 2;11(5):e0153948. doi: 10.1371/journal.pone.0153948. eCollection 2016.

Abstract

Background: Motor Unit Number Index (MUNIX) is a neurophysiological measure that provides an index of the number of lower motor neurons in a muscle. Its performance across centres in healthy subjects and patients with Amyotrophic Lateral Sclerosis (ALS) has been established, but inter-rater variability between multiple raters in one single subject has not been investigated.

Objective: To assess reliability in a set of 6 muscles in a single subject among 12 examiners (6 experienced with MUNIX, 6 less experienced) and to determine variables associated with variability of measurements.

Methods: Twelve raters applied MUNIX in six different muscles (abductor pollicis brevis (APB), abductor digiti minimi (ADM), biceps brachii (BB), tibialis anterior (TA), extensor dig. brevis (EDB), abductor hallucis (AH)) twice in one single volunteer on consecutive days. All raters visited at least one training course prior to measurements. Intra- and inter-rater variability as determined by the coefficient of variation (COV) between different raters and their levels of experience with MUNIX were compared.

Results: Mean intra-rater COV of MUNIX was 14.0% (±6.4) ranging from 5.8 (APB) to 30.3% (EDB). Mean inter-rater COV was 18.1 (±5.4) ranging from 8.0 (BB) to 31.7 (AH). No significant differences of variability between experienced and less experienced raters were detected.

Conclusion: We provide evidence that quality control for neurophysiological methods can be performed with similar standards as in laboratory medicine. Intra- and inter-rater variability of MUNIX is muscle-dependent and mainly below 20%. Experienced neurophysiologists can easily adopt MUNIX and adequate teaching ensures reliable utilization of this method.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amyotrophic Lateral Sclerosis / diagnosis
  • Electromyography / methods*
  • Electromyography / standards*
  • Female
  • Healthy Volunteers
  • Humans
  • Male
  • Motor Neurons / physiology*
  • Muscle Strength / physiology
  • Muscle, Skeletal / innervation*
  • Neuromuscular Diseases / diagnosis
  • Reproducibility of Results
  • Sensitivity and Specificity

Grants and funding

Study funded by: CN, CB, and MW were supported by the Swiss ALS Foundation and the Swiss NeRAB Foundation. CB and CN were supported by the “SOPHIA” consortium through the Swiss National Foundation (31ND30_141622) under the aegis of the EU Joint Programme – Neurodegenerative Disease Research (JPND): http://www.jpnd.eu.