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 in | Journal of the peripheral nervous system Vol. 30; no. 1; pp. e70001 - n/a |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
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Malden, USA
Wiley Periodicals, Inc
01.03.2025
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Abstract | 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. |
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AbstractList | 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).BACKGROUND AND AIMSLoss 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).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).METHODSForty-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).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).RESULTSMScanFit 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).MScanFit MUNE could be a useful method for assessing motor axonal loss in CIDP, which correlates with the clinical function and treatment response.INTERPRETATIONMScanFit MUNE could be a useful method for assessing motor axonal loss in CIDP, which correlates with the clinical function and treatment response. 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. Background and AimsLoss 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).MethodsForty‐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).ResultsMScanFit 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).InterpretationMScanFit MUNE could be a useful method for assessing motor axonal loss in CIDP, which correlates with the clinical function and treatment response. 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). 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). 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). MScanFit MUNE could be a useful method for assessing motor axonal loss in CIDP, which correlates with the clinical function and treatment response. |
Author | Mohammed, Abdullahi A. Andersen, Henning Krøigård, Thomas Markvardsen, Lars K. Hansen, Peter N. Tankisi, Hatice Sindrup, Søren H. |
AuthorAffiliation | 2 Department of Neurology Aarhus University Hospital Aarhus Denmark 4 Odense Patient Data Explorative Network (OPEN) Odense University Hospital Odense Denmark 3 Department of Clinical Neurophysiology Aarhus University Hospital Aarhus Denmark 1 Neurology Research Unit, Odense University Hospital, Odense, Denmark University of Southern Denmark Odense Denmark |
AuthorAffiliation_xml | – name: 2 Department of Neurology Aarhus University Hospital Aarhus Denmark – name: 4 Odense Patient Data Explorative Network (OPEN) Odense University Hospital Odense Denmark – name: 3 Department of Clinical Neurophysiology Aarhus University Hospital Aarhus Denmark – name: 1 Neurology Research Unit, Odense University Hospital, Odense, Denmark University of Southern Denmark Odense Denmark |
Author_xml | – sequence: 1 givenname: Peter N. orcidid: 0000-0002-2556-0229 surname: Hansen fullname: Hansen, Peter N. email: peter.norregaard.hansen@rsyd.dk organization: University of Southern Denmark – sequence: 2 givenname: Abdullahi A. surname: Mohammed fullname: Mohammed, Abdullahi A. organization: University of Southern Denmark – sequence: 3 givenname: Lars K. orcidid: 0000-0002-5562-9768 surname: Markvardsen fullname: Markvardsen, Lars K. organization: Aarhus University Hospital – sequence: 4 givenname: Henning surname: Andersen fullname: Andersen, Henning organization: Aarhus University Hospital – sequence: 5 givenname: Hatice surname: Tankisi fullname: Tankisi, Hatice organization: Aarhus University Hospital – sequence: 6 givenname: Søren H. surname: Sindrup fullname: Sindrup, Søren H. organization: Odense University Hospital – sequence: 7 givenname: Thomas orcidid: 0000-0002-1565-6948 surname: Krøigård fullname: Krøigård, Thomas organization: Odense University Hospital |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/39887824$$D View this record in MEDLINE/PubMed |
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Keywords | motor unit number estimation chronic inflammatory demyelinating polyneuropathy immunoglobulin axonal loss MScanFit |
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Notes | Funding This work was supported by Novo Nordisk Foundation, grant no NNF 18OC0053006. ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Funding: This work was supported by Novo Nordisk Foundation, grant no NNF 18OC0053006. |
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Snippet | ABSTRACT
Background and Aims
Loss of motor units in chronic inflammatory demyelinating polyneuropathy is difficult to assess by conventional nerve conduction... Loss of motor units in chronic inflammatory demyelinating polyneuropathy is difficult to assess by conventional nerve conduction due to collateral innervation.... Background and AimsLoss of motor units in chronic inflammatory demyelinating polyneuropathy is difficult to assess by conventional nerve conduction due to... |
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SubjectTerms | Action potential Action Potentials - physiology Adult Aged axonal loss chronic inflammatory demyelinating polyneuropathy Demyelination Electromyography Female Humans immunoglobulin Immunoglobulins Immunoglobulins, Intravenous - pharmacology Immunoglobulins, Intravenous - therapeutic use Immunologic Factors - therapeutic use Inflammation Innervation Intravenous administration Male Medical research Middle Aged Motor Neurons - physiology motor unit number estimation Motor units MScanFit Muscle, Skeletal - physiopathology Nerve conduction Neural Conduction - physiology Neuropathy Patients Polyneuropathy Polyradiculoneuropathy, Chronic Inflammatory Demyelinating - diagnosis Polyradiculoneuropathy, Chronic Inflammatory Demyelinating - drug therapy Polyradiculoneuropathy, Chronic Inflammatory Demyelinating - physiopathology Reinnervation Research Report Statistical analysis |
Title | Association Between MScanFit Motor Unit Number Estimation and Clinical Function and Response to Immunoglobulin Therapy in Chronic Inflammatory Demyelinating Polyneuropathy |
URI | https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fjns.70001 https://www.ncbi.nlm.nih.gov/pubmed/39887824 https://www.proquest.com/docview/3181150344 https://www.proquest.com/docview/3161916980 https://pubmed.ncbi.nlm.nih.gov/PMC11783579 |
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