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Motor Unit Number Index (Munix) in Patients With Anti-Mag Neuropathy Publisher Pubmed



Fatehi F1, 2 ; Delmont E1, 3 ; Grapperon AM1 ; Salortcampana E1, 4 ; Sevy A1 ; Verschueren A1 ; Boucraut J2, 5 ; Attarian S1, 4
Authors
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Authors Affiliations
  1. 1. Referral Centre for ALS and Neuromuscular Diseases, La Timone University Hospital, Aix-Marseille University, France
  2. 2. Iranian Centre of Neurological Research, Shariati Hospital, Tehran University of Medical Sciences, Iran
  3. 3. Aix-Marseille University, CNR2M, CNRS UMR 7286, Medicine Faculty, Marseille, France
  4. 4. Aix Marseille University, Inserm UMR S 910 Medical Genetics and Functional Genomics, Marseille, France
  5. 5. Immunology Laboratory, Conception University Hospital, Aix-Marseille University, France

Source: Clinical Neurophysiology Published:2017


Abstract

Objective To investigate the relationship between Motor Unit Number Index (MUNIX) and functional scales in patients with anti-Myelin Associated Glycoprotein (MAG) neuropathy and to know if MUNIX is modify after rituximab (RTX) therapy. Methods 17 patients were enrolled, of whom 6 were prospectively evaluated during one year after RTX treatment. MUNIX technique was assessed in abductor digiti mini (ADM), abductor pollicis brevi (APB) and tibialis anterior (TA) muscles. MUNIX sum score was calculated by adding the results of ADM, APB and TA muscles. Results MUNIX sum score was correlated with overall neuropathy limitation scale (ONLS) (r = −0.55, p = 0.02), grip strength in dominant hand (r = 0.63, p = 0.01) MRC testing (r = 0.71, p < 0.001) and CMAP sum score (r = 0.71, p = 0.001). Twelve months after RTX, four patients improved their disability measured on the ONLS score, five patients had improved MUNIX sum score with a median increase of 37% compared to initial evaluation. Conclusions MUNIX is related to motor impairment and disability in anti-MAG neuropathy and MUNIX is modified after immunosuppressive treatment. Significance Considering its advantages, MUNIX may be a suitable test to evaluate anti-MAG neuropathy in clinical trials. © 2017 International Federation of Clinical Neurophysiology