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Muscle & nerve · 2018

Guillain-BarrÉ syndrome subtype diagnosis: A prospective multicentric European study.

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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, University of Louvain GBS Electrodiagnosis Study Group

Аннотация

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, 2018.

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

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