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

Author:

Pascual-Goñi ElbaORCID,Martín-Aguilar Lorena,Lleixà Cinta,Martínez-Martínez Laura,Simón-Talero Manuel J.,Díaz-Manera Jordi,Cortés-Vicente Elena,Rojas-García Ricard,Moga Esther,Juárez Cándido,Illa Isabel,Querol LuisORCID

Abstract

AbstractAntibodies 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.

Funder

Government of Catalonia | Departament de Salut, Generalitat de Catalunya

Ministry of Economy and Competitiveness | Instituto de Salud Carlos III

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

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