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Early Electrodiagnostic Features of Upper Extremity Sensory Nerves Can Differentiate Axonal Guillain-Barré Syndrome from Acute Inflammatory Demyelinating Polyneuropathy
BACKGROUND AND PURPOSE: Serial nerve conduction studies (NCSs) are recommended for differentiating axonal and demyelinating Guillain-Barré syndrome (GBS), but this approach is not suitable for early diagnoses. This study was designed to identify possible NCS parameters for differentiating GBS subtyp...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Neurological Association
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5063878/ https://www.ncbi.nlm.nih.gov/pubmed/27819421 http://dx.doi.org/10.3988/jcn.2016.12.4.495 |
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author | Koo, Yong Seo Shin, Ha Young Kim, Jong Kuk Nam, Tai-Seung Shin, Kyong Jin Bae, Jong-Seok Suh, Bum Chun Oh, Jeeyoung Yoon, Byeol-A Kim, Byung-Jo |
author_facet | Koo, Yong Seo Shin, Ha Young Kim, Jong Kuk Nam, Tai-Seung Shin, Kyong Jin Bae, Jong-Seok Suh, Bum Chun Oh, Jeeyoung Yoon, Byeol-A Kim, Byung-Jo |
author_sort | Koo, Yong Seo |
collection | PubMed |
description | BACKGROUND AND PURPOSE: Serial nerve conduction studies (NCSs) are recommended for differentiating axonal and demyelinating Guillain-Barré syndrome (GBS), but this approach is not suitable for early diagnoses. This study was designed to identify possible NCS parameters for differentiating GBS subtypes. METHODS: We retrospectively reviewed the medical records of 70 patients with GBS who underwent NCS within 10 days of symptom onset. Patients with axonal GBS and acute inflammatory demyelinating polyneuropathy (AIDP) were selected based on clinical characteristics and serial NCSs. An antiganglioside antibody study was used to increase the diagnostic certainty. RESULTS: The amplitudes of median and ulnar nerve sensory nerve action potentials (SNAPs) were significantly smaller in the AIDP group than in the axonal-GBS group. Classification and regression-tree analysis revealed that the distal ulnar sensory nerve SNAP amplitude was the best predictor of axonal GBS. CONCLUSIONS: Early upper extremity sensory NCS findings are helpful in differentiating axonal-GBS patients with antiganglioside antibodies from AIDP patients. |
format | Online Article Text |
id | pubmed-5063878 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Korean Neurological Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-50638782016-10-17 Early Electrodiagnostic Features of Upper Extremity Sensory Nerves Can Differentiate Axonal Guillain-Barré Syndrome from Acute Inflammatory Demyelinating Polyneuropathy Koo, Yong Seo Shin, Ha Young Kim, Jong Kuk Nam, Tai-Seung Shin, Kyong Jin Bae, Jong-Seok Suh, Bum Chun Oh, Jeeyoung Yoon, Byeol-A Kim, Byung-Jo J Clin Neurol Original Article BACKGROUND AND PURPOSE: Serial nerve conduction studies (NCSs) are recommended for differentiating axonal and demyelinating Guillain-Barré syndrome (GBS), but this approach is not suitable for early diagnoses. This study was designed to identify possible NCS parameters for differentiating GBS subtypes. METHODS: We retrospectively reviewed the medical records of 70 patients with GBS who underwent NCS within 10 days of symptom onset. Patients with axonal GBS and acute inflammatory demyelinating polyneuropathy (AIDP) were selected based on clinical characteristics and serial NCSs. An antiganglioside antibody study was used to increase the diagnostic certainty. RESULTS: The amplitudes of median and ulnar nerve sensory nerve action potentials (SNAPs) were significantly smaller in the AIDP group than in the axonal-GBS group. Classification and regression-tree analysis revealed that the distal ulnar sensory nerve SNAP amplitude was the best predictor of axonal GBS. CONCLUSIONS: Early upper extremity sensory NCS findings are helpful in differentiating axonal-GBS patients with antiganglioside antibodies from AIDP patients. Korean Neurological Association 2016-10 2016-09-30 /pmc/articles/PMC5063878/ /pubmed/27819421 http://dx.doi.org/10.3988/jcn.2016.12.4.495 Text en Copyright © 2016 Korean Neurological Association http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Koo, Yong Seo Shin, Ha Young Kim, Jong Kuk Nam, Tai-Seung Shin, Kyong Jin Bae, Jong-Seok Suh, Bum Chun Oh, Jeeyoung Yoon, Byeol-A Kim, Byung-Jo Early Electrodiagnostic Features of Upper Extremity Sensory Nerves Can Differentiate Axonal Guillain-Barré Syndrome from Acute Inflammatory Demyelinating Polyneuropathy |
title | Early Electrodiagnostic Features of Upper Extremity Sensory Nerves Can Differentiate Axonal Guillain-Barré Syndrome from Acute Inflammatory Demyelinating Polyneuropathy |
title_full | Early Electrodiagnostic Features of Upper Extremity Sensory Nerves Can Differentiate Axonal Guillain-Barré Syndrome from Acute Inflammatory Demyelinating Polyneuropathy |
title_fullStr | Early Electrodiagnostic Features of Upper Extremity Sensory Nerves Can Differentiate Axonal Guillain-Barré Syndrome from Acute Inflammatory Demyelinating Polyneuropathy |
title_full_unstemmed | Early Electrodiagnostic Features of Upper Extremity Sensory Nerves Can Differentiate Axonal Guillain-Barré Syndrome from Acute Inflammatory Demyelinating Polyneuropathy |
title_short | Early Electrodiagnostic Features of Upper Extremity Sensory Nerves Can Differentiate Axonal Guillain-Barré Syndrome from Acute Inflammatory Demyelinating Polyneuropathy |
title_sort | early electrodiagnostic features of upper extremity sensory nerves can differentiate axonal guillain-barré syndrome from acute inflammatory demyelinating polyneuropathy |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5063878/ https://www.ncbi.nlm.nih.gov/pubmed/27819421 http://dx.doi.org/10.3988/jcn.2016.12.4.495 |
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