Association Between MScanFit Motor Unit Number Estimation and Clinical Function and Response to Immunoglobulin Therapy in Chronic Inflammatory Demyelinating Polyneuropathy

ABSTRACT Background and Aims Loss of motor units in chronic inflammatory demyelinating polyneuropathy is difficult to assess by conventional nerve conduction due to collateral innervation. We aimed to assess the association between a motor unit number estimate (MUNE) derived from the compound muscle...

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Published inJournal of the peripheral nervous system Vol. 30; no. 1; pp. e70001 - n/a
Main Authors Hansen, Peter N., Mohammed, Abdullahi A., Markvardsen, Lars K., Andersen, Henning, Tankisi, Hatice, Sindrup, Søren H., Krøigård, Thomas
Format Journal Article
LanguageEnglish
Published Malden, USA Wiley Periodicals, Inc 01.03.2025
Wiley Subscription Services, Inc
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Summary:ABSTRACT Background and Aims Loss of motor units in chronic inflammatory demyelinating polyneuropathy is difficult to assess by conventional nerve conduction due to collateral innervation. We aimed to assess the association between a motor unit number estimate (MUNE) derived from the compound muscle action potential (CMAP) scan using MScanFit and hand function and the clinical response to intravenous immunoglobulin (IVIG). Methods Forty‐nine CIDP patients and 52 control subjects were included. CMAP scan recordings were obtained from the right abductor pollicis brevis muscle. The primary outcome was the correlation between MUNE and the duration of the nine‐hole‐peg test (9‐HPT) at baseline and the change in the duration of the 9‐HPT following treatment with IVIG. Secondary outcomes were grip strength, 10‐m‐walk test, six‐spot‐step test, medical research council sum score, inflammatory neuropathy cause and treatment sensory sum score, overall neuropathy limitations scale, and the Rasch‐built overall disability scale (R‐ODS). Results MScanFit analysis suggested both loss of motor units (reduced MUNE (p = 0.022) and N50 (p < 0.0001)) and collateral reinnervation (increased median amplitude (p < 0.0001) and size of the largest unit (p < 0.0001)) in CIDP patients compared to controls. In CIDP patients, there was a statistically significant correlation between MUNE and the duration of the 9‐HPT (Spearman's r = −0.342; p = 0.016). Further, patients with a low MUNE had the largest reduction in the duration of the 9‐HPT following IVIG treatment (r = −0.577; p = 0.043). MUNE also correlated significantly with R‐ODS (r = −0.722; p = 0.007). Interpretation MScanFit MUNE could be a useful method for assessing motor axonal loss in CIDP, which correlates with the clinical function and treatment response.
Bibliography:Funding
This work was supported by Novo Nordisk Foundation, grant no NNF 18OC0053006.
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Funding: This work was supported by Novo Nordisk Foundation, grant no NNF 18OC0053006.
ISSN:1085-9489
1529-8027
1529-8027
DOI:10.1111/jns.70001