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 |
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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 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2676922707</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2676922707</sourcerecordid><originalsourceid>FETCH-LOGICAL-c256t-8e0d9cb16fd40689fb303ae4fc2abb10d0ad98c7f67e7511ccd6cb29148ca8c53</originalsourceid><addsrcrecordid>eNp9kUtP3DAUhS1UBMPjD7BAlrrpJnD9SJws0YgC0lRs2rXlOM6MUWKntqNq9v3huM1QJBZd2db5zrm-OghdEbghAOI2AnBSFkBpQQglvKiP0Ipwlp-8bD6hFTAORclKforOYnwBgDoLJ-iUlSJbgazQ72--mweVrHfY9zhO3iXljJ8jHn3yAc_OJjz5ZFyyaoi43WOFnfl1kLUPyWo14FFtnclXHJMd3xJHk3a-w9ZhNe59Cn7aZSKLJmRL1IMJPtp4gY77nG0uD-c5-vH1_vv6sdg8Pzyt7zaFpmWVitpA1-iWVH3HoaqbvmXAlOG9pqptCXSguqbWoq-EESUhWneVbmlDeK1VrUt2jr4suVPwP2cTkxxt1GYYlo0lrUTVUCpAZPTzB_TFz8Hl30kqCIOG0QYyRRdK5z1iML2cgh1V2EsC8k9HculI5o7k345knU3Xh-i5HU33z_JWSgbYAsQsua0J77P_E_sKucyf1w</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2713093290</pqid></control><display><type>article</type><title>Modulation of spontaneous motor unit potentials by a new motor cortical magnetic stimulation method in amyotrophic lateral sclerosis</title><source>SpringerLink Journals - AutoHoldings</source><creator>Helekar, Santosh A. ; Thonhoff, Jason ; John, Blessy S. ; Nguyen, Lisa ; Rosenfield, David B. ; Appel, Stanley H.</creator><creatorcontrib>Helekar, Santosh A. ; Thonhoff, Jason ; John, Blessy S. ; Nguyen, Lisa ; Rosenfield, David B. ; Appel, Stanley H.</creatorcontrib><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><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 & 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 & 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 & 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 & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Helekar, Santosh A.</au><au>Thonhoff, Jason</au><au>John, Blessy S.</au><au>Nguyen, Lisa</au><au>Rosenfield, David B.</au><au>Appel, Stanley H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Modulation of spontaneous motor unit potentials by a new motor cortical magnetic stimulation method in amyotrophic lateral sclerosis</atitle><jtitle>Journal of neurology</jtitle><stitle>J Neurol</stitle><addtitle>J Neurol</addtitle><date>2022-10-01</date><risdate>2022</risdate><volume>269</volume><issue>10</issue><spage>5487</spage><epage>5496</epage><pages>5487-5496</pages><issn>0340-5354</issn><eissn>1432-1459</eissn><abstract>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.</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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source | SpringerLink Journals - AutoHoldings |
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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