Pathological spontaneous activity as a prognostic marker in chronic inflammatory demyelinating polyneuropathy
Background and purpose Monitoring of the disease course of patients with chronic inflammatory demyelinating polyneuropathy (CIDP) remains challenging because nerve conduction studies do not adequately correlate with functional disability. The prognostic value of pathological spontaneous activity (PS...
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Veröffentlicht in: | European journal of neurology 2020-12, Vol.27 (12), p.2595-2603 |
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creator | Grüter, T. Motte, J. Fisse, A. L. Bulut, Y. Köse, N. Athanasopoulos, D. Otto, S. Yoon, M. ‐S. Schneider‐Gold, C. Gold, R. Pitarokoili, K. |
description | Background and purpose
Monitoring of the disease course of patients with chronic inflammatory demyelinating polyneuropathy (CIDP) remains challenging because nerve conduction studies do not adequately correlate with functional disability. The prognostic value of pathological spontaneous activity (PSA) in needle electromyography (EMG) in different CIDP subgroups in a longitudinal context has, to date, not been analysed. We aimed to determine whether PSA was a prognostic marker or a marker of disease activity in a cohort of patients with CIDP.
Methods
A total of 127 patients with CIDP spectrum disorder were retrospectively analysed over 57 ± 47 months regarding the occurrence of PSA (fibrillations and positive sharp waves). The presence of PSA at diagnosis, newly occurring PSA, and continuously present PSA were longitudinally correlated with clinical disability using the Inflammatory Neuropathy Cause and Treatment Overall Disability Sum Score (INCAT‐ODSS) and CIDP subtype.
Results
Pathological spontaneous activity occurred in 49.6% of all CIDP patients at first diagnosis. More frequent evidence of PSA was significantly associated with a higher INCAT‐ODSS at the last follow‐up. Continuous and new occurrence of PSA were associated with higher degree of disability at the last follow‐up. The majority of patients with sustained evidence of PSA were characterized by an atypical phenotype, higher degree of disability, and the need for escalation of treatment.
Conclusions
Pathological spontaneous activity was associated with a higher degree of disability and occurred more frequently in atypical CIDP variants according to the longitudinal data of a large cohort of patients with CIDP. Our results showed that EMG examination was an adequate marker for disease progression and should be evaluated during the disease course. |
doi_str_mv | 10.1111/ene.14476 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2434484690</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2434484690</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3886-bffac60110ae4bfbc638521d48f4652d8f2513992ab4c01b90bc2fd097fa93e33</originalsourceid><addsrcrecordid>eNp1kctOxCAUhonReF_4AobEjS6q3NqhSzMZL4lRF7puKIURpVCh1fTtZezowkQ2nJAvH-ecH4AjjM5xOhfKqXPM2KzYALuYFTzDlOLNVNMcZzlGeAfsxfiKECIzgrbBDiWzkpGc74L2UfQv3vqlkcLC2HnXC6f8EKGQvfkw_QhFqmEX_NL52BsJWxHeVIDGQfkSvEsvxmkr2lb0PoywUe2orHGiN24JO29Hp4bgu_TPeAC2tLBRHa7vffB8tXia32R3D9e388u7TFLOi6zWWsgCYYyEYrWuZUF5TnDDuGZFThquSY5pWRJRM4lwXaJaEt2gcqZFSRWl--B08qa23wcV-6o1USprp9kqwihjnBUlSujJH_TVD8Gl7hKVJ4YzshKeTZQMPsagdNUFkxYxVhhVqwyqlEH1nUFij9fGoW5V80v-LD0BFxPwaawa_zdVi_vFpPwCHIqSoA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2458468423</pqid></control><display><type>article</type><title>Pathological spontaneous activity as a prognostic marker in chronic inflammatory demyelinating polyneuropathy</title><source>Wiley Journals</source><creator>Grüter, T. ; Motte, J. ; Fisse, A. L. ; Bulut, Y. ; Köse, N. ; Athanasopoulos, D. ; Otto, S. ; Yoon, M. ‐S. ; Schneider‐Gold, C. ; Gold, R. ; Pitarokoili, K.</creator><creatorcontrib>Grüter, T. ; Motte, J. ; Fisse, A. L. ; Bulut, Y. ; Köse, N. ; Athanasopoulos, D. ; Otto, S. ; Yoon, M. ‐S. ; Schneider‐Gold, C. ; Gold, R. ; Pitarokoili, K.</creatorcontrib><description>Background and purpose
Monitoring of the disease course of patients with chronic inflammatory demyelinating polyneuropathy (CIDP) remains challenging because nerve conduction studies do not adequately correlate with functional disability. The prognostic value of pathological spontaneous activity (PSA) in needle electromyography (EMG) in different CIDP subgroups in a longitudinal context has, to date, not been analysed. We aimed to determine whether PSA was a prognostic marker or a marker of disease activity in a cohort of patients with CIDP.
Methods
A total of 127 patients with CIDP spectrum disorder were retrospectively analysed over 57 ± 47 months regarding the occurrence of PSA (fibrillations and positive sharp waves). The presence of PSA at diagnosis, newly occurring PSA, and continuously present PSA were longitudinally correlated with clinical disability using the Inflammatory Neuropathy Cause and Treatment Overall Disability Sum Score (INCAT‐ODSS) and CIDP subtype.
Results
Pathological spontaneous activity occurred in 49.6% of all CIDP patients at first diagnosis. More frequent evidence of PSA was significantly associated with a higher INCAT‐ODSS at the last follow‐up. Continuous and new occurrence of PSA were associated with higher degree of disability at the last follow‐up. The majority of patients with sustained evidence of PSA were characterized by an atypical phenotype, higher degree of disability, and the need for escalation of treatment.
Conclusions
Pathological spontaneous activity was associated with a higher degree of disability and occurred more frequently in atypical CIDP variants according to the longitudinal data of a large cohort of patients with CIDP. Our results showed that EMG examination was an adequate marker for disease progression and should be evaluated during the disease course.</description><identifier>ISSN: 1351-5101</identifier><identifier>EISSN: 1468-1331</identifier><identifier>DOI: 10.1111/ene.14476</identifier><identifier>PMID: 32794258</identifier><language>eng</language><publisher>England: John Wiley & Sons, Inc</publisher><subject>chronic inflammatory demyelinating polyneuropathy ; Correlation analysis ; Demyelination ; Diagnosis ; Electromyography ; Health services ; Inflammation ; Markers ; Nerve conduction ; Neuropathy ; pathological spontaneous activity ; Patients ; Phenotypes ; Polyneuropathy ; prognosis ; Subgroups</subject><ispartof>European journal of neurology, 2020-12, Vol.27 (12), p.2595-2603</ispartof><rights>2020 The Authors. published by John Wiley & Sons Ltd on behalf of European Academy of Neurology</rights><rights>2020 The Authors. European Journal of Neurology published by John Wiley & Sons Ltd on behalf of European Academy of Neurology.</rights><rights>2020. This article is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3886-bffac60110ae4bfbc638521d48f4652d8f2513992ab4c01b90bc2fd097fa93e33</citedby><cites>FETCH-LOGICAL-c3886-bffac60110ae4bfbc638521d48f4652d8f2513992ab4c01b90bc2fd097fa93e33</cites><orcidid>0000-0001-8927-9818 ; 0000-0002-6624-8565 ; 0000-0003-0493-8656</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fene.14476$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fene.14476$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32794258$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Grüter, T.</creatorcontrib><creatorcontrib>Motte, J.</creatorcontrib><creatorcontrib>Fisse, A. L.</creatorcontrib><creatorcontrib>Bulut, Y.</creatorcontrib><creatorcontrib>Köse, N.</creatorcontrib><creatorcontrib>Athanasopoulos, D.</creatorcontrib><creatorcontrib>Otto, S.</creatorcontrib><creatorcontrib>Yoon, M. ‐S.</creatorcontrib><creatorcontrib>Schneider‐Gold, C.</creatorcontrib><creatorcontrib>Gold, R.</creatorcontrib><creatorcontrib>Pitarokoili, K.</creatorcontrib><title>Pathological spontaneous activity as a prognostic marker in chronic inflammatory demyelinating polyneuropathy</title><title>European journal of neurology</title><addtitle>Eur J Neurol</addtitle><description>Background and purpose
Monitoring of the disease course of patients with chronic inflammatory demyelinating polyneuropathy (CIDP) remains challenging because nerve conduction studies do not adequately correlate with functional disability. The prognostic value of pathological spontaneous activity (PSA) in needle electromyography (EMG) in different CIDP subgroups in a longitudinal context has, to date, not been analysed. We aimed to determine whether PSA was a prognostic marker or a marker of disease activity in a cohort of patients with CIDP.
Methods
A total of 127 patients with CIDP spectrum disorder were retrospectively analysed over 57 ± 47 months regarding the occurrence of PSA (fibrillations and positive sharp waves). The presence of PSA at diagnosis, newly occurring PSA, and continuously present PSA were longitudinally correlated with clinical disability using the Inflammatory Neuropathy Cause and Treatment Overall Disability Sum Score (INCAT‐ODSS) and CIDP subtype.
Results
Pathological spontaneous activity occurred in 49.6% of all CIDP patients at first diagnosis. More frequent evidence of PSA was significantly associated with a higher INCAT‐ODSS at the last follow‐up. Continuous and new occurrence of PSA were associated with higher degree of disability at the last follow‐up. The majority of patients with sustained evidence of PSA were characterized by an atypical phenotype, higher degree of disability, and the need for escalation of treatment.
Conclusions
Pathological spontaneous activity was associated with a higher degree of disability and occurred more frequently in atypical CIDP variants according to the longitudinal data of a large cohort of patients with CIDP. Our results showed that EMG examination was an adequate marker for disease progression and should be evaluated during the disease course.</description><subject>chronic inflammatory demyelinating polyneuropathy</subject><subject>Correlation analysis</subject><subject>Demyelination</subject><subject>Diagnosis</subject><subject>Electromyography</subject><subject>Health services</subject><subject>Inflammation</subject><subject>Markers</subject><subject>Nerve conduction</subject><subject>Neuropathy</subject><subject>pathological spontaneous activity</subject><subject>Patients</subject><subject>Phenotypes</subject><subject>Polyneuropathy</subject><subject>prognosis</subject><subject>Subgroups</subject><issn>1351-5101</issn><issn>1468-1331</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><recordid>eNp1kctOxCAUhonReF_4AobEjS6q3NqhSzMZL4lRF7puKIURpVCh1fTtZezowkQ2nJAvH-ecH4AjjM5xOhfKqXPM2KzYALuYFTzDlOLNVNMcZzlGeAfsxfiKECIzgrbBDiWzkpGc74L2UfQv3vqlkcLC2HnXC6f8EKGQvfkw_QhFqmEX_NL52BsJWxHeVIDGQfkSvEsvxmkr2lb0PoywUe2orHGiN24JO29Hp4bgu_TPeAC2tLBRHa7vffB8tXia32R3D9e388u7TFLOi6zWWsgCYYyEYrWuZUF5TnDDuGZFThquSY5pWRJRM4lwXaJaEt2gcqZFSRWl--B08qa23wcV-6o1USprp9kqwihjnBUlSujJH_TVD8Gl7hKVJ4YzshKeTZQMPsagdNUFkxYxVhhVqwyqlEH1nUFij9fGoW5V80v-LD0BFxPwaawa_zdVi_vFpPwCHIqSoA</recordid><startdate>202012</startdate><enddate>202012</enddate><creator>Grüter, T.</creator><creator>Motte, J.</creator><creator>Fisse, A. L.</creator><creator>Bulut, Y.</creator><creator>Köse, N.</creator><creator>Athanasopoulos, D.</creator><creator>Otto, S.</creator><creator>Yoon, M. ‐S.</creator><creator>Schneider‐Gold, C.</creator><creator>Gold, R.</creator><creator>Pitarokoili, K.</creator><general>John Wiley & Sons, Inc</general><scope>24P</scope><scope>WIN</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7U7</scope><scope>C1K</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-8927-9818</orcidid><orcidid>https://orcid.org/0000-0002-6624-8565</orcidid><orcidid>https://orcid.org/0000-0003-0493-8656</orcidid></search><sort><creationdate>202012</creationdate><title>Pathological spontaneous activity as a prognostic marker in chronic inflammatory demyelinating polyneuropathy</title><author>Grüter, T. ; Motte, J. ; Fisse, A. L. ; Bulut, Y. ; Köse, N. ; Athanasopoulos, D. ; Otto, S. ; Yoon, M. ‐S. ; Schneider‐Gold, C. ; Gold, R. ; Pitarokoili, K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3886-bffac60110ae4bfbc638521d48f4652d8f2513992ab4c01b90bc2fd097fa93e33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>chronic inflammatory demyelinating polyneuropathy</topic><topic>Correlation analysis</topic><topic>Demyelination</topic><topic>Diagnosis</topic><topic>Electromyography</topic><topic>Health services</topic><topic>Inflammation</topic><topic>Markers</topic><topic>Nerve conduction</topic><topic>Neuropathy</topic><topic>pathological spontaneous activity</topic><topic>Patients</topic><topic>Phenotypes</topic><topic>Polyneuropathy</topic><topic>prognosis</topic><topic>Subgroups</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Grüter, T.</creatorcontrib><creatorcontrib>Motte, J.</creatorcontrib><creatorcontrib>Fisse, A. L.</creatorcontrib><creatorcontrib>Bulut, Y.</creatorcontrib><creatorcontrib>Köse, N.</creatorcontrib><creatorcontrib>Athanasopoulos, D.</creatorcontrib><creatorcontrib>Otto, S.</creatorcontrib><creatorcontrib>Yoon, M. ‐S.</creatorcontrib><creatorcontrib>Schneider‐Gold, C.</creatorcontrib><creatorcontrib>Gold, R.</creatorcontrib><creatorcontrib>Pitarokoili, K.</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Wiley Online Library (Open Access Collection)</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Grüter, T.</au><au>Motte, J.</au><au>Fisse, A. L.</au><au>Bulut, Y.</au><au>Köse, N.</au><au>Athanasopoulos, D.</au><au>Otto, S.</au><au>Yoon, M. ‐S.</au><au>Schneider‐Gold, C.</au><au>Gold, R.</au><au>Pitarokoili, K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pathological spontaneous activity as a prognostic marker in chronic inflammatory demyelinating polyneuropathy</atitle><jtitle>European journal of neurology</jtitle><addtitle>Eur J Neurol</addtitle><date>2020-12</date><risdate>2020</risdate><volume>27</volume><issue>12</issue><spage>2595</spage><epage>2603</epage><pages>2595-2603</pages><issn>1351-5101</issn><eissn>1468-1331</eissn><abstract>Background and purpose
Monitoring of the disease course of patients with chronic inflammatory demyelinating polyneuropathy (CIDP) remains challenging because nerve conduction studies do not adequately correlate with functional disability. The prognostic value of pathological spontaneous activity (PSA) in needle electromyography (EMG) in different CIDP subgroups in a longitudinal context has, to date, not been analysed. We aimed to determine whether PSA was a prognostic marker or a marker of disease activity in a cohort of patients with CIDP.
Methods
A total of 127 patients with CIDP spectrum disorder were retrospectively analysed over 57 ± 47 months regarding the occurrence of PSA (fibrillations and positive sharp waves). The presence of PSA at diagnosis, newly occurring PSA, and continuously present PSA were longitudinally correlated with clinical disability using the Inflammatory Neuropathy Cause and Treatment Overall Disability Sum Score (INCAT‐ODSS) and CIDP subtype.
Results
Pathological spontaneous activity occurred in 49.6% of all CIDP patients at first diagnosis. More frequent evidence of PSA was significantly associated with a higher INCAT‐ODSS at the last follow‐up. Continuous and new occurrence of PSA were associated with higher degree of disability at the last follow‐up. The majority of patients with sustained evidence of PSA were characterized by an atypical phenotype, higher degree of disability, and the need for escalation of treatment.
Conclusions
Pathological spontaneous activity was associated with a higher degree of disability and occurred more frequently in atypical CIDP variants according to the longitudinal data of a large cohort of patients with CIDP. Our results showed that EMG examination was an adequate marker for disease progression and should be evaluated during the disease course.</abstract><cop>England</cop><pub>John Wiley & Sons, Inc</pub><pmid>32794258</pmid><doi>10.1111/ene.14476</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-8927-9818</orcidid><orcidid>https://orcid.org/0000-0002-6624-8565</orcidid><orcidid>https://orcid.org/0000-0003-0493-8656</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | chronic inflammatory demyelinating polyneuropathy Correlation analysis Demyelination Diagnosis Electromyography Health services Inflammation Markers Nerve conduction Neuropathy pathological spontaneous activity Patients Phenotypes Polyneuropathy prognosis Subgroups |
title | Pathological spontaneous activity as a prognostic marker in chronic inflammatory demyelinating polyneuropathy |
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