Anti-Myelin-Associated Glycoprotein Neuropathy: Recent Developments.

IF 2.3 Q3 CLINICAL NEUROLOGY Neurology. Clinical practice Pub Date : 2025-02-01 Epub Date: 2024-10-08 DOI:10.1212/CPJ.0000000000200368
Jennifer Morganroth, Chafic Karam
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Abstract

Background: The purpose of this review is to give an update on myelin-associated glycoprotein (MAG) neuropathy.

Recent findings: There are several recent developments in anti-MAG neuropathy, with the major one being the retrospective analysis of 50 clinical trials that showed that at least a 50% reduction in anti-MAG levels is associated with a therapeutic response. Other updates address antibody levels needed for a positive test, response, and exacerbations to therapy and the type of antibody more associated with malignancy.

Implications for practice: Anti-MAG neuropathy is heterogeneous, and the natural history of the disease continues to be refined. Treatment options are being explored for refractory disease.

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抗髓鞘相关糖蛋白神经病:最新进展。
背景:本综述旨在介绍髓鞘相关糖蛋白(MAG)神经病变的最新进展:抗 MAG 神经病变方面有几项最新进展,其中最主要的是对 50 项临床试验的回顾性分析,分析表明抗 MAG 水平至少降低 50%与治疗反应相关。其他更新还涉及阳性检测所需的抗体水平、对治疗的反应和加重,以及与恶性肿瘤更相关的抗体类型:抗 MAG 神经病变具有异质性,该病的自然史仍在不断完善。目前正在探索针对难治性疾病的治疗方案。
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来源期刊
Neurology. Clinical practice
Neurology. Clinical practice CLINICAL NEUROLOGY-
CiteScore
4.00
自引率
0.00%
发文量
77
期刊介绍: Neurology® Genetics is an online open access journal publishing peer-reviewed reports in the field of neurogenetics. The journal publishes original articles in all areas of neurogenetics including rare and common genetic variations, genotype-phenotype correlations, outlier phenotypes as a result of mutations in known disease genes, and genetic variations with a putative link to diseases. Articles include studies reporting on genetic disease risk, pharmacogenomics, and results of gene-based clinical trials (viral, ASO, etc.). Genetically engineered model systems are not a primary focus of Neurology® Genetics, but studies using model systems for treatment trials, including well-powered studies reporting negative results, are welcome.
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