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Serum neurofilament light chain for individual prognostication of disease activity in people with multiple sclerosis: a retrospective modelling and validation study.血清神经丝轻链对多发性硬化症患者疾病活动的个体预后预测:一项回顾性建模和验证研究。
Lancet Neurol. 2022 Mar;21(3):246-257. doi: 10.1016/S1474-4422(22)00009-6.
2
OCT retinal nerve fiber layer thickness differentiates acute optic neuritis from MOG antibody-associated disease and Multiple Sclerosis: RNFL thickening in acute optic neuritis from MOGAD vs MS.光学相干断层扫描(OCT)测量的视网膜神经纤维层厚度可区分急性视神经炎与MOG抗体相关疾病及多发性硬化症:MOG抗体相关疾病与多发性硬化症所致急性视神经炎的视网膜神经纤维层增厚情况比较
Mult Scler Relat Disord. 2022 Feb;58:103525. doi: 10.1016/j.msard.2022.103525. Epub 2022 Jan 11.
3
Serum Neurofilament Light and GFAP Are Associated With Disease Severity in Inflammatory Disorders With Aquaporin-4 or Myelin Oligodendrocyte Glycoprotein Antibodies.血清神经丝轻链和 GFAP 与水通道蛋白 4 或髓鞘少突胶质细胞糖蛋白抗体阳性的炎症性疾病的严重程度相关。
Front Immunol. 2021 Mar 16;12:647618. doi: 10.3389/fimmu.2021.647618. eCollection 2021.
4
Serum Glial Fibrillary Acidic Protein: A Neuromyelitis Optica Spectrum Disorder Biomarker.血清神经丝酸性蛋白:视神经脊髓炎谱系疾病生物标志物。
Ann Neurol. 2021 May;89(5):895-910. doi: 10.1002/ana.26067. Epub 2021 Mar 30.
5
Association of Spectral-Domain OCT With Long-term Disability Worsening in Multiple Sclerosis.频域光学相干断层扫描与多发性硬化症长期残疾恶化的关联
Neurology. 2021 Apr 20;96(16):e2058-e2069. doi: 10.1212/WNL.0000000000011788. Epub 2021 Mar 2.
6
Prevalence of neuromyelitis optica spectrum disorder in Belo Horizonte, Southeast Brazil.巴西东南部贝洛奥里藏特视神经脊髓炎谱系障碍的患病率。
Mult Scler Relat Disord. 2021 May;50:102807. doi: 10.1016/j.msard.2021.102807. Epub 2021 Feb 3.
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Recent developments in MOG-IgG associated neurological disorders.髓鞘少突胶质细胞糖蛋白免疫球蛋白G相关神经系统疾病的最新进展
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8
Serum GFAP and neurofilament light as biomarkers of disease activity and disability in NMOSD.血清 GFAP 和神经丝轻链作为 NMOSD 疾病活动和残疾的生物标志物。
Neurology. 2019 Sep 24;93(13):e1299-e1311. doi: 10.1212/WNL.0000000000008160. Epub 2019 Aug 30.
9
Blood neurofilament light chain as a biomarker of MS disease activity and treatment response.血液神经丝轻链作为 MS 疾病活动和治疗反应的生物标志物。
Neurology. 2019 Mar 5;92(10):e1007-e1015. doi: 10.1212/WNL.0000000000007032. Epub 2019 Feb 8.
10
Live-cell based assays are the gold standard for anti-MOG-Ab testing.基于活细胞的检测方法是抗髓鞘少突胶质细胞糖蛋白抗体(MOG-Ab)检测的金标准。
Neurology. 2019 Mar 12;92(11):501-502. doi: 10.1212/WNL.0000000000007077. Epub 2019 Feb 6.

脱髓鞘疾病的鉴别诊断:有哪些新进展?

Differential diagnosis of demyelinating diseases: what's new?

机构信息

Universidade de São Paulo, Faculdade de Medicina, Hospital das Clínicas, Departamento de Neurologia, São Paulo SP, Brazil.

Hospital Sírio-Libanês, Centro de Esclerose Múltipla, São Paulo SP, Brazil.

出版信息

Arq Neuropsiquiatr. 2022 May;80(5 Suppl 1):137-142. doi: 10.1590/0004-282X-ANP-2022-S109.

DOI:10.1590/0004-282X-ANP-2022-S109
PMID:35976299
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9491438/
Abstract

BACKGROUND

Acquired demyelinating disorders lead to overlapping visual, pyramidal, sensory, autonomic, and cerebellar deficits and may lead to severe disability. Early diagnosis and start of treatment are fundamental towards preventing further attacks and halting disability.

OBJECTIVE

In this paper we provide an updated overview of the differential diagnoses of acquired demyelinating disorders.

METHODS

We performed a critical targeted review of the diagnoses of the most prevalent demyelinating disorders: multiple sclerosis (MS), neuromyelitis optica spectrum disorders (NMOSD) and myelin oligodendrocyte glycoprotein antibody disease (MOGAD).

RESULTS

We discuss the workup, diagnostic criteria and new biomarkers currently being used for the diagnosis of these disease entities taking into account the particularities of the Brazilian population and healthcare system.

CONCLUSION

A comprehensive analysis of medical history, physical examination, biomedical and imaging data should be performed to obtain differential diagnosis. Diagnostic criteria should be mindfully employed considering ethnic and environmental particularities of each patient.

摘要

背景

获得性脱髓鞘疾病导致视觉、锥体、感觉、自主和小脑功能缺陷重叠,并可能导致严重残疾。早期诊断和开始治疗对于预防进一步发作和阻止残疾至关重要。

目的

本文提供了对获得性脱髓鞘疾病的鉴别诊断的最新概述。

方法

我们对最常见的脱髓鞘疾病(多发性硬化症[MS]、视神经脊髓炎谱系障碍[NMOSD]和髓鞘少突胶质细胞糖蛋白抗体病[MOGAD])的诊断进行了批判性的靶向综述。

结果

我们讨论了目前用于这些疾病实体诊断的检查、诊断标准和新的生物标志物,同时考虑了巴西人群和医疗保健系统的特点。

结论

应全面分析病史、体检、生物医学和影像学数据以获得鉴别诊断。在考虑每个患者的种族和环境特点时,应慎重使用诊断标准。