Electrophysiology of Guillain-Barré syndrome in Bangladesh: A prospective study of 312 patients

Objective: To describe the electrophysiological features in relation to clinical and serological findings of Guillain-Barré syndrome (GBS) in the national neuroscience hospital in Bangladesh. This is one of the few studies that investigated GBS patients using standardized electrophysiology in low-in...

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Main Authors: Badrul Islam, Zhahirul Islam, Hubert P. Endtz, Israt Jahan, Bart C. Jacobs, Quazi D. Mohammad, Hessel Franssen
Format: Article
Language:English
Published: Elsevier 2021-01-01
Series:Clinical Neurophysiology Practice
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2467981X21000202
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spelling doaj-8270d822da224ac68b6e73ce376358562021-05-14T04:19:34ZengElsevierClinical Neurophysiology Practice2467-981X2021-01-016155163Electrophysiology of Guillain-Barré syndrome in Bangladesh: A prospective study of 312 patientsBadrul Islam0Zhahirul Islam1Hubert P. Endtz2Israt Jahan3Bart C. Jacobs4Quazi D. Mohammad5Hessel Franssen6Laboratory Sciences and Services Division, icddr,b, Dhaka, Bangladesh; Corresponding author at: Laboratory Sciences and Services Division (LSSD), International Center for Diarrheal Disease Research, Bangladesh (icddr,b), Dhaka, Bangladesh.Laboratory Sciences and Services Division, icddr,b, Dhaka, BangladeshDepartment of Medical Microbiology and Infectious Diseases, Erasmus University Medical Center, Rotterdam, the NetherlandsLaboratory Sciences and Services Division, icddr,b, Dhaka, BangladeshDepartment of Immunology, Erasmus University Medical Center, Rotterdam, the Netherlands; Department of Neurology, Erasmus University Medical Center, Rotterdam, the NetherlandsNational Institute of Neurosciences and Hospital, Dhaka, BangladeshDepartment of Neuromuscular Disorders, Utrecht Brain Center, the NetherlandsObjective: To describe the electrophysiological features in relation to clinical and serological findings of Guillain-Barré syndrome (GBS) in the national neuroscience hospital in Bangladesh. This is one of the few studies that investigated GBS patients using standardized electrophysiology in low-income countries. Methods: In a prospective and observational study, we investigated 312 GBS patients by standardized clinical, serological and electrophysiological methods. Unilateral motor and sensory nerve conduction studies (NCS) were performed within two weeks of onset of weakness. Follow up NCS were performed in 189 patients and classified according to eight sets of established GBS criteria. Serology included assessment of anti-GM1 antibodies and anti-campylobacter jejuni lipo-oligosaccharide (LOS) antibodies. Results: Depending on the criteria used, 44–59% patients had axonal GBS with anti-GM1 antibodies being present in 55–58% and 9–42% patients had demyelinating GBS with anti-GM1 antibodies being present in 7–35%. Conduction block (CB) with demyelinative slowing in the same nerve segment was found in 24% (74/312) patients, and CB without demyelinative slowing in the same nerve segment was found in 18% (56/312) patients, of whom anti-GM1 antibodies were found in 27% and 57% patients respectively. Follow-up NCS showed a change in GBS classification in 11–26% of patients, mainly from demyelinating to axonal GBS. Conclusions: The predominant subtype of GBS in Bangladesh is axonal but demyelinating GBS also occurs with classification being strongly dependent on the applied criteria. Significance: The present study demonstrates the importance of reaching international agreement on GBS criteria that should be based on the best evidence.http://www.sciencedirect.com/science/article/pii/S2467981X21000202Guillain-Barré syndromeCriteriaConduction blockDemyelinationAxon lossAnti-GM1 antibody
collection DOAJ
language English
format Article
sources DOAJ
author Badrul Islam
Zhahirul Islam
Hubert P. Endtz
Israt Jahan
Bart C. Jacobs
Quazi D. Mohammad
Hessel Franssen
spellingShingle Badrul Islam
Zhahirul Islam
Hubert P. Endtz
Israt Jahan
Bart C. Jacobs
Quazi D. Mohammad
Hessel Franssen
Electrophysiology of Guillain-Barré syndrome in Bangladesh: A prospective study of 312 patients
Clinical Neurophysiology Practice
Guillain-Barré syndrome
Criteria
Conduction block
Demyelination
Axon loss
Anti-GM1 antibody
author_facet Badrul Islam
Zhahirul Islam
Hubert P. Endtz
Israt Jahan
Bart C. Jacobs
Quazi D. Mohammad
Hessel Franssen
author_sort Badrul Islam
title Electrophysiology of Guillain-Barré syndrome in Bangladesh: A prospective study of 312 patients
title_short Electrophysiology of Guillain-Barré syndrome in Bangladesh: A prospective study of 312 patients
title_full Electrophysiology of Guillain-Barré syndrome in Bangladesh: A prospective study of 312 patients
title_fullStr Electrophysiology of Guillain-Barré syndrome in Bangladesh: A prospective study of 312 patients
title_full_unstemmed Electrophysiology of Guillain-Barré syndrome in Bangladesh: A prospective study of 312 patients
title_sort electrophysiology of guillain-barré syndrome in bangladesh: a prospective study of 312 patients
publisher Elsevier
series Clinical Neurophysiology Practice
issn 2467-981X
publishDate 2021-01-01
description Objective: To describe the electrophysiological features in relation to clinical and serological findings of Guillain-Barré syndrome (GBS) in the national neuroscience hospital in Bangladesh. This is one of the few studies that investigated GBS patients using standardized electrophysiology in low-income countries. Methods: In a prospective and observational study, we investigated 312 GBS patients by standardized clinical, serological and electrophysiological methods. Unilateral motor and sensory nerve conduction studies (NCS) were performed within two weeks of onset of weakness. Follow up NCS were performed in 189 patients and classified according to eight sets of established GBS criteria. Serology included assessment of anti-GM1 antibodies and anti-campylobacter jejuni lipo-oligosaccharide (LOS) antibodies. Results: Depending on the criteria used, 44–59% patients had axonal GBS with anti-GM1 antibodies being present in 55–58% and 9–42% patients had demyelinating GBS with anti-GM1 antibodies being present in 7–35%. Conduction block (CB) with demyelinative slowing in the same nerve segment was found in 24% (74/312) patients, and CB without demyelinative slowing in the same nerve segment was found in 18% (56/312) patients, of whom anti-GM1 antibodies were found in 27% and 57% patients respectively. Follow-up NCS showed a change in GBS classification in 11–26% of patients, mainly from demyelinating to axonal GBS. Conclusions: The predominant subtype of GBS in Bangladesh is axonal but demyelinating GBS also occurs with classification being strongly dependent on the applied criteria. Significance: The present study demonstrates the importance of reaching international agreement on GBS criteria that should be based on the best evidence.
topic Guillain-Barré syndrome
Criteria
Conduction block
Demyelination
Axon loss
Anti-GM1 antibody
url http://www.sciencedirect.com/science/article/pii/S2467981X21000202
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