Clinical and laboratory features of anti-MAG neuropathy without monoclonal gammopathy

Autor: Pascual-Goñi, Elba, Martín-Aguilar, Lorena, Lleixà, Cinta, Martinez-Martinez, Laura, Simón-Talero, Manuel J., Diaz-Manera, Jordi., Cortés-Vicente, Elena, Rojas-Garcia, Ricard, Moga, Esther, Juarez, Candido, Illa, Isabel, Querol, Luis, Universitat Autònoma de Barcelona
Jazyk: angličtina
Rok vydání: 2019
Předmět:
Zdroj: Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Scientific Reports
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Scientific Reports, Vol 9, Iss 1, Pp 1-5 (2019)
ISSN: 2045-2322
Popis: Antibodies against myelin-associated glycoprotein (MAG) almost invariably appear in the context of an IgM monoclonal gammopathy associated neuropathy. Very few cases of anti-MAG neuropathy lacking IgM-monoclonal gammopathy have been reported. We investigated the presence of anti-MAG antibodies in 69 patients fulfilling diagnostic criteria for CIDP. Anti-MAG antibodies were tested by ELISA and confirmed by immunohistochemistry. We identified four (5.8%) anti-MAG positive patients without detectable IgM-monoclonal gammopathy. In two of them, IgM-monoclonal gammopathy was detected at 3 and 4-year follow-up coinciding with an increase in anti-MAG antibodies titers. In conclusion, anti-MAG antibody testing should be considered in chronic demyelinating neuropathies, even if IgM-monoclonal gammopathy is not detectable.
Databáze: OpenAIRE