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Chronic demyelinating neuropathy with anti-myelin-associated glycoprotein antibody without any detectable M-protein

Overview of attention for article published in Neurological Sciences, October 2017
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Title
Chronic demyelinating neuropathy with anti-myelin-associated glycoprotein antibody without any detectable M-protein
Published in
Neurological Sciences, October 2017
DOI 10.1007/s10072-017-3133-0
Pubmed ID
Authors

Yuki Sakamoto, Toshio Shimizu, Shinsuke Tobisawa, Eiji Isozaki

Abstract

Previous case reports and studies have shown that anti-myelin-associated glycoprotein (MAG) antibody can be detected in patients with polyneuropathy without any detectable M-protein. Nevertheless, the frequency of and related factors have not yet been adequately investigated. The objectives of this study are to examine the prevalence of anti-MAG antibody in patients with demyelinating neuropathy without M-protein and to determine their clinical characteristics. From January, 2004, to September, 2016, consecutive patients with chronic demyelinating neuropathy were recruited. Anti-MAG antibody presence was tested at the first evaluation. We determined the prevalence of anti-MAG antibody without M-protein among included patients and evaluated the clinical characteristics. A total of 44 patients were included in the present study (12 women; median age at first visit 60 years [interquartile range 47-67 years]; median duration between onset and first visit 9 months [3-26 months]). M-protein was found in eight patients (18%) at the first evaluation. Anti-MAG antibody was present in 2 of remaining 36 (5.6 [95% confidence interval 0-13.0] %) patients without M-protein. Patients with anti-MAG antibody exhibited slowly progressive and distal dominant neuropathy with elevated serum IgM levels and refractory to immunotherapy. There were no differences in clinical features between patients having anti-MAG antibody without M-protein, and those with M-protein. One patient with the anti-MAG antibody showed a delayed appearance of M-protein during a 4-year follow-up after diagnosis. The prevalence of the anti-MAG antibody in chronic demyelinating neuropathy without any detectable M-protein was 5.6%. Anti-MAG antibody may be detectable earlier than M-protein.

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Geographical breakdown

Country Count As %
Unknown 20 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 5 25%
Student > Ph. D. Student 3 15%
Student > Bachelor 2 10%
Other 2 10%
Student > Postgraduate 2 10%
Other 2 10%
Unknown 4 20%
Readers by discipline Count As %
Medicine and Dentistry 8 40%
Neuroscience 4 20%
Agricultural and Biological Sciences 1 5%
Psychology 1 5%
Unknown 6 30%