Guillain‐BarrÉ syndrome subtype diagnosis: A prospective multicentric European study

ABSTRACT Introduction: There is uncertainty as to whether the Guillain‐Barré syndrome (GBS) subtypes, acute inflammatory demyelinating polyradiculoneuropathy (AIDP) and acute motor axonal neuropathy (AMAN), can be diagnosed electrophysiologically. Methods: We prospectively included 58 GBS patients....

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Published inMuscle & nerve Vol. 58; no. 1; pp. 23 - 28
Main Authors Van den Bergh, Peter Y. K., Piéret, Françoise, Woodard, John L., Attarian, Shahram, Grapperon, Aude‐Marie, Nicolas, Guillaume, Brisset, Marion, Cassereau, Julien, Rajabally, Yusuf A., Van Parijs, Vinciane, Verougstraete, Donatienne, Jacquerye, Philippe, Raymackers, Jean‐Marc, Redant, Céline, Michel, Claure, Delmont, Emilien
Format Journal Article
LanguageEnglish
Published United States Wiley Subscription Services, Inc 01.07.2018
Wiley
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ISSN0148-639X
1097-4598
1097-4598
DOI10.1002/mus.26056

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Summary:ABSTRACT Introduction: There is uncertainty as to whether the Guillain‐Barré syndrome (GBS) subtypes, acute inflammatory demyelinating polyradiculoneuropathy (AIDP) and acute motor axonal neuropathy (AMAN), can be diagnosed electrophysiologically. Methods: We prospectively included 58 GBS patients. Electrodiagnostic testing (EDX) was performed at means of 5 and 33 days after disease onset. Two traditional and one recent criteria sets were used to classify studies as demyelinating or axonal. Results were correlated with anti‐ganglioside antibodies and reversible conduction failure (RCF). Results: No classification shifts were observed, but more patients were classified as axonal with recent criteria. RCF and anti‐ganglioside antibodies were present in both subtypes, more frequently in the axonal subtype. Discussion: Serial EDX has no effect on GBS subtype proportions. The absence of exclusive correlation with RCF and anti‐ganglioside antibodies may challenge the concept of demyelinating and axonal GBS subtypes based upon electrophysiological criteria. Frequent RCF indicates that nodal/paranodal alterations may represent the main pathophysiology. Muscle Nerve 58: 23–28, 2018.
Bibliography:Conflicts of Interest
1–3
Neuromuscular Disorders
this issue.
Journal of the International Neuropsychological Society
The other authors have nothing to disclose.
John L. Woodard is associate editor of
Peter Y. K. Van den Bergh is executive associate editor of
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ISSN:0148-639X
1097-4598
1097-4598
DOI:10.1002/mus.26056