| Literature DB >> 25808373 |
Yumako Miura1, Jérôme J Devaux2, Yuki Fukami1, Constance Manso3, Maya Belghazi3, Anna Hiu Yi Wong1, Nobuhiro Yuki4.
Abstract
A Spanish group recently reported that four patients with chronic inflammatory demyelinating polyneuropathy carrying IgG4 autoantibodies against contactin 1 showed aggressive symptom onset and poor response to intravenous immunoglobulin. We aimed to describe the clinical and serological features of Japanese chronic inflammatory demyelinating polyneuropathy patients displaying the anti-contactin 1 antibodies. Thirteen of 533 (2.4%) patients with chronic inflammatory demyelinating polyneuropathy had anti-contactin 1 IgG4 whereas neither patients from disease or normal control subjects did (P = 0.02). Three of 13 (23%) patients showed subacute symptom onset, but all of the patients presented with sensory ataxia. Six of 10 (60%) anti-contactin 1 antibody-positive patients had poor response to intravenous immunoglobulin, whereas 8 of 11 (73%) antibody-positive patients had good response to corticosteroids. Anti-contactin 1 IgG4 antibodies are a possible biomarker to guide treatment option.Entities:
Keywords: autoantibody; chronic inflammatory demyelinating polyneuropathy; contactin 1; myelin; nodes of Ranvier
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Year: 2015 PMID: 25808373 PMCID: PMC4614146 DOI: 10.1093/brain/awv054
Source DB: PubMed Journal: Brain ISSN: 0006-8950 Impact factor: 13.501