Modulation of spontaneous motor unit potentials by a new motor cortical magnetic stimulation method in amyotrophic lateral sclerosis

Background Patients with amyotrophic lateral sclerosis (ALS) show altered cortical excitability. In this study, we measure modulation of spontaneous motor unit potentials (sMUPs) in hand muscles by multifocal cortical stimulation with a newly developed wearable transcranial rotating permanent magnet...

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Veröffentlicht in:Journal of neurology 2022-10, Vol.269 (10), p.5487-5496
Hauptverfasser: Helekar, Santosh A., Thonhoff, Jason, John, Blessy S., Nguyen, Lisa, Rosenfield, David B., Appel, Stanley H.
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container_end_page 5496
container_issue 10
container_start_page 5487
container_title Journal of neurology
container_volume 269
creator Helekar, Santosh A.
Thonhoff, Jason
John, Blessy S.
Nguyen, Lisa
Rosenfield, David B.
Appel, Stanley H.
description Background Patients with amyotrophic lateral sclerosis (ALS) show altered cortical excitability. In this study, we measure modulation of spontaneous motor unit potentials (sMUPs) in hand muscles by multifocal cortical stimulation with a newly developed wearable transcranial rotating permanent magnet stimulator (TRPMS). Methods We conducted cross-sectional and longitudinal electromyographic assessments in 40 and 20 ALS patients, respectively, of the stimulation-induced peak increase in the count of sMUPs in two hand muscles modulated by unilateral TRPMS stimulation of the primary motor cortex. We measured peak sMUP counts during several short sessions consisting of 10 stimuli over 60 s and 30 s post-stimulation periods. The longitudinal component involved an initial assessment at an early stage of the disease and up to five follow-up assessments at least 3 months apart. Results TRPMS stimulation produced no device-related adverse effects. It showed an inverted V -shaped modulation of the peak sMUP counts as a function of ALS functional rating scale revised scores. The ratios of ALS subjects showing peak sMUP count increases between early and intermediate stages ( χ 2 = 4.086, df = 1, p  = 0.043) and intermediate and late stages ( χ 2 = 4.29, df = 1, p  = 0.038) in cross-sectional data were significantly different. Longitudinal assessment also produced a significant ( z  = 2.31, p  = 0.021) result, with all subjects showing a post-initial visit increase in peak sMUP counts. Conclusions These results are consistent with delayed onset of upper motor neuronal dysfunction with respect to onset of clinical features. However, the above results need to be confirmed in a larger sample of patients and with multiple lines of evidence.
doi_str_mv 10.1007/s00415-022-11214-8
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In this study, we measure modulation of spontaneous motor unit potentials (sMUPs) in hand muscles by multifocal cortical stimulation with a newly developed wearable transcranial rotating permanent magnet stimulator (TRPMS). Methods We conducted cross-sectional and longitudinal electromyographic assessments in 40 and 20 ALS patients, respectively, of the stimulation-induced peak increase in the count of sMUPs in two hand muscles modulated by unilateral TRPMS stimulation of the primary motor cortex. We measured peak sMUP counts during several short sessions consisting of 10 stimuli over 60 s and 30 s post-stimulation periods. The longitudinal component involved an initial assessment at an early stage of the disease and up to five follow-up assessments at least 3 months apart. Results TRPMS stimulation produced no device-related adverse effects. It showed an inverted V -shaped modulation of the peak sMUP counts as a function of ALS functional rating scale revised scores. The ratios of ALS subjects showing peak sMUP count increases between early and intermediate stages ( χ 2 = 4.086, df = 1, p  = 0.043) and intermediate and late stages ( χ 2 = 4.29, df = 1, p  = 0.038) in cross-sectional data were significantly different. Longitudinal assessment also produced a significant ( z  = 2.31, p  = 0.021) result, with all subjects showing a post-initial visit increase in peak sMUP counts. Conclusions These results are consistent with delayed onset of upper motor neuronal dysfunction with respect to onset of clinical features. However, the above results need to be confirmed in a larger sample of patients and with multiple lines of evidence.</description><identifier>ISSN: 0340-5354</identifier><identifier>EISSN: 1432-1459</identifier><identifier>DOI: 10.1007/s00415-022-11214-8</identifier><identifier>PMID: 35704101</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Amyotrophic lateral sclerosis ; Cohort analysis ; Cortex (motor) ; Electromyography ; Excitability ; Magnetic fields ; Medicine ; Medicine &amp; Public Health ; Muscles ; Neurology ; Neuroradiology ; Neurosciences ; Original Communication ; Patients</subject><ispartof>Journal of neurology, 2022-10, Vol.269 (10), p.5487-5496</ispartof><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany 2022</rights><rights>2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany.</rights><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany 2022.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c256t-8e0d9cb16fd40689fb303ae4fc2abb10d0ad98c7f67e7511ccd6cb29148ca8c53</cites><orcidid>0000-0002-9264-0966</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00415-022-11214-8$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00415-022-11214-8$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,778,782,27907,27908,41471,42540,51302</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35704101$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Helekar, Santosh A.</creatorcontrib><creatorcontrib>Thonhoff, Jason</creatorcontrib><creatorcontrib>John, Blessy S.</creatorcontrib><creatorcontrib>Nguyen, Lisa</creatorcontrib><creatorcontrib>Rosenfield, David B.</creatorcontrib><creatorcontrib>Appel, Stanley H.</creatorcontrib><title>Modulation of spontaneous motor unit potentials by a new motor cortical magnetic stimulation method in amyotrophic lateral sclerosis</title><title>Journal of neurology</title><addtitle>J Neurol</addtitle><addtitle>J Neurol</addtitle><description>Background Patients with amyotrophic lateral sclerosis (ALS) show altered cortical excitability. In this study, we measure modulation of spontaneous motor unit potentials (sMUPs) in hand muscles by multifocal cortical stimulation with a newly developed wearable transcranial rotating permanent magnet stimulator (TRPMS). Methods We conducted cross-sectional and longitudinal electromyographic assessments in 40 and 20 ALS patients, respectively, of the stimulation-induced peak increase in the count of sMUPs in two hand muscles modulated by unilateral TRPMS stimulation of the primary motor cortex. We measured peak sMUP counts during several short sessions consisting of 10 stimuli over 60 s and 30 s post-stimulation periods. The longitudinal component involved an initial assessment at an early stage of the disease and up to five follow-up assessments at least 3 months apart. Results TRPMS stimulation produced no device-related adverse effects. It showed an inverted V -shaped modulation of the peak sMUP counts as a function of ALS functional rating scale revised scores. The ratios of ALS subjects showing peak sMUP count increases between early and intermediate stages ( χ 2 = 4.086, df = 1, p  = 0.043) and intermediate and late stages ( χ 2 = 4.29, df = 1, p  = 0.038) in cross-sectional data were significantly different. Longitudinal assessment also produced a significant ( z  = 2.31, p  = 0.021) result, with all subjects showing a post-initial visit increase in peak sMUP counts. Conclusions These results are consistent with delayed onset of upper motor neuronal dysfunction with respect to onset of clinical features. However, the above results need to be confirmed in a larger sample of patients and with multiple lines of evidence.</description><subject>Amyotrophic lateral sclerosis</subject><subject>Cohort analysis</subject><subject>Cortex (motor)</subject><subject>Electromyography</subject><subject>Excitability</subject><subject>Magnetic fields</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Muscles</subject><subject>Neurology</subject><subject>Neuroradiology</subject><subject>Neurosciences</subject><subject>Original Communication</subject><subject>Patients</subject><issn>0340-5354</issn><issn>1432-1459</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kUtP3DAUhS1UBMPjD7BAlrrpJnD9SJws0YgC0lRs2rXlOM6MUWKntqNq9v3huM1QJBZd2db5zrm-OghdEbghAOI2AnBSFkBpQQglvKiP0Ipwlp-8bD6hFTAORclKforOYnwBgDoLJ-iUlSJbgazQ72--mweVrHfY9zhO3iXljJ8jHn3yAc_OJjz5ZFyyaoi43WOFnfl1kLUPyWo14FFtnclXHJMd3xJHk3a-w9ZhNe59Cn7aZSKLJmRL1IMJPtp4gY77nG0uD-c5-vH1_vv6sdg8Pzyt7zaFpmWVitpA1-iWVH3HoaqbvmXAlOG9pqptCXSguqbWoq-EESUhWneVbmlDeK1VrUt2jr4suVPwP2cTkxxt1GYYlo0lrUTVUCpAZPTzB_TFz8Hl30kqCIOG0QYyRRdK5z1iML2cgh1V2EsC8k9HculI5o7k345knU3Xh-i5HU33z_JWSgbYAsQsua0J77P_E_sKucyf1w</recordid><startdate>20221001</startdate><enddate>20221001</enddate><creator>Helekar, Santosh A.</creator><creator>Thonhoff, Jason</creator><creator>John, Blessy S.</creator><creator>Nguyen, Lisa</creator><creator>Rosenfield, David B.</creator><creator>Appel, Stanley H.</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-9264-0966</orcidid></search><sort><creationdate>20221001</creationdate><title>Modulation of spontaneous motor unit potentials by a new motor cortical magnetic stimulation method in amyotrophic lateral sclerosis</title><author>Helekar, Santosh A. ; Thonhoff, Jason ; John, Blessy S. ; Nguyen, Lisa ; Rosenfield, David B. ; Appel, Stanley H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c256t-8e0d9cb16fd40689fb303ae4fc2abb10d0ad98c7f67e7511ccd6cb29148ca8c53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Amyotrophic lateral sclerosis</topic><topic>Cohort analysis</topic><topic>Cortex (motor)</topic><topic>Electromyography</topic><topic>Excitability</topic><topic>Magnetic fields</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Muscles</topic><topic>Neurology</topic><topic>Neuroradiology</topic><topic>Neurosciences</topic><topic>Original Communication</topic><topic>Patients</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Helekar, Santosh A.</creatorcontrib><creatorcontrib>Thonhoff, Jason</creatorcontrib><creatorcontrib>John, Blessy S.</creatorcontrib><creatorcontrib>Nguyen, Lisa</creatorcontrib><creatorcontrib>Rosenfield, David B.</creatorcontrib><creatorcontrib>Appel, Stanley H.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Health &amp; 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In this study, we measure modulation of spontaneous motor unit potentials (sMUPs) in hand muscles by multifocal cortical stimulation with a newly developed wearable transcranial rotating permanent magnet stimulator (TRPMS). Methods We conducted cross-sectional and longitudinal electromyographic assessments in 40 and 20 ALS patients, respectively, of the stimulation-induced peak increase in the count of sMUPs in two hand muscles modulated by unilateral TRPMS stimulation of the primary motor cortex. We measured peak sMUP counts during several short sessions consisting of 10 stimuli over 60 s and 30 s post-stimulation periods. The longitudinal component involved an initial assessment at an early stage of the disease and up to five follow-up assessments at least 3 months apart. Results TRPMS stimulation produced no device-related adverse effects. It showed an inverted V -shaped modulation of the peak sMUP counts as a function of ALS functional rating scale revised scores. The ratios of ALS subjects showing peak sMUP count increases between early and intermediate stages ( χ 2 = 4.086, df = 1, p  = 0.043) and intermediate and late stages ( χ 2 = 4.29, df = 1, p  = 0.038) in cross-sectional data were significantly different. Longitudinal assessment also produced a significant ( z  = 2.31, p  = 0.021) result, with all subjects showing a post-initial visit increase in peak sMUP counts. Conclusions These results are consistent with delayed onset of upper motor neuronal dysfunction with respect to onset of clinical features. However, the above results need to be confirmed in a larger sample of patients and with multiple lines of evidence.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>35704101</pmid><doi>10.1007/s00415-022-11214-8</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-9264-0966</orcidid></addata></record>
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subjects Amyotrophic lateral sclerosis
Cohort analysis
Cortex (motor)
Electromyography
Excitability
Magnetic fields
Medicine
Medicine & Public Health
Muscles
Neurology
Neuroradiology
Neurosciences
Original Communication
Patients
title Modulation of spontaneous motor unit potentials by a new motor cortical magnetic stimulation method in amyotrophic lateral sclerosis
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