Prognostic Usefulness of Motor Unit Number Index (MUNIX) in Patients Newly Diagnosed with Amyotrophic Lateral Sclerosis

Author:

Risi Barbara123,Cotti Piccinelli Stefano13,Gazzina Stefano4,Labella Beatrice12ORCID,Caria Filomena3,Damioli Simona3,Poli Loris2ORCID,Padovani Alessandro12,Filosto Massimiliano13ORCID

Affiliation:

1. Department of Clinical and Experimental Sciences, University of Brescia, 25121 Brescia, Italy

2. Unit of Neurology, ASST Spedali Civili, 25123 Brescia, Italy

3. NeMO-Brescia Clinical Center for Neuromuscular Diseases, 25064 Gussago, Italy

4. Unit of Neurophysiology, ASST Spedali Civili, 25123 Brescia, Italy

Abstract

The MUNIX technique allows us to estimate the number and size of surviving motor units (MUs). Previous studies on ALS found correlations between MUNIX and several clinical measures, but its potential role as a predictor of disease progression rate (DPR) has not been thoroughly evaluated to date. We aimed to investigate MUNIX’s ability to predict DPR at a six-month follow up. Methods: 24 ALS patients with short disease duration (<24 months from symptoms’ onset) were enrolled and divided according to their baseline DPR into two groups (normal [DPR-N] and fast [DPR-F] progressors). MUNIX values were obtained from five muscles (TA, APB, ADM, FDI, Trapezius) and averaged for each subject. Results: MUNIX was found to predict DPR at follow up in a multivariable linear regression model; namely, patients with lower MUNIX values were at risk of showing greater DPR scores at follow up. The result was replicated in a simple logistic regression analysis, with the dichotomic category “MUNIX-Low” as the independent variable and the outcome “DPR-F” as the dependent variable. Conclusions: our results pave the way for the use of the MUNIX method as a prognostic tool in early ALS, enabling patients’ stratification according to their rates of future decline.

Publisher

MDPI AG

Subject

General Medicine

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