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用于诊断和预测髓鞘少突胶质细胞糖蛋白抗体相关疾病的生物标志物——综述文章

Biomarkers for diagnosis and prognosis of myelin oligodendrocyte glycoprotein antibody-associated disease - review article.

作者信息

Sapana Tamang, Zhuo Zhihong

机构信息

Department of Pediatrics, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.

Henan Provincial Key Laboratory of Childhood Epilepsy and Immunology, Zhengzhou, Henan, China.

出版信息

Front Immunol. 2025 Jun 6;16:1594960. doi: 10.3389/fimmu.2025.1594960. eCollection 2025.

DOI:10.3389/fimmu.2025.1594960
PMID:40547008
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12178866/
Abstract

Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) is a complex inflammatory central nervous system disorder affecting mainly children and young adults. Its diverse clinical spectrum often resembles other neurological diseases like multiple sclerosis (MS) or neuromyelitis optica spectrum disorder (NMOSD). Accurate diagnosis and monitoring are challenging due to its heterogeneous presentation and lack of specific biomarkers. In addition, disease-modifying therapies are well-established for treating MS and NMOSD. In contrast, the absence of approved therapies for MOGAD remains a significant challenge in clinical management and should become a priority in future research efforts. This review explores existing literature on biomarkers in MOGAD, including clinical, radiological, and laboratory parameters along with novel biomarkers and the future challenges that can facilitate personalized therapeutic approaches in MOGAD. A comprehensive understanding of these biomarker profiles is crucial for optimizing patient care and advancing therapeutic strategies in neuroinflammatory disorders.

摘要

髓鞘少突胶质细胞糖蛋白抗体相关疾病(MOGAD)是一种复杂的炎症性中枢神经系统疾病,主要影响儿童和年轻人。其多样的临床谱常类似于其他神经系统疾病,如多发性硬化症(MS)或视神经脊髓炎谱系障碍(NMOSD)。由于其表现异质性且缺乏特异性生物标志物,准确诊断和监测具有挑战性。此外,针对MS和NMOSD的疾病修饰疗法已确立。相比之下,MOGAD缺乏获批疗法仍是临床管理中的重大挑战,应成为未来研究工作的重点。本综述探讨了关于MOGAD生物标志物的现有文献,包括临床、放射学和实验室参数以及新型生物标志物,以及有助于MOGAD个性化治疗方法的未来挑战。全面了解这些生物标志物概况对于优化患者护理和推进神经炎症性疾病的治疗策略至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8db8/12178866/c6a403e149c3/fimmu-16-1594960-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8db8/12178866/c6a403e149c3/fimmu-16-1594960-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8db8/12178866/c6a403e149c3/fimmu-16-1594960-g001.jpg

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引用本文的文献

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本文引用的文献

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Serum NfL and EGFR/NfL ratio mRNAs as biomarkers for phenotype and disease severity of myelin oligodendrocyte glycoprotein IgG-associated disease.血清 NfL 和 EGFR/NfL 比值 mRNA 作为髓鞘少突胶质细胞糖蛋白 IgG 相关疾病表型和疾病严重程度的生物标志物。
Front Immunol. 2024 May 14;15:1388734. doi: 10.3389/fimmu.2024.1388734. eCollection 2024.
2
Oral corticosteroid dosage and taper duration at onset in myelin oligodendrocyte glycoprotein antibody-associated disease influences time to first relapse.髓鞘少突胶质细胞糖蛋白抗体相关疾病发病时的口服皮质类固醇剂量和减量持续时间影响首次复发的时间。
J Neurol Neurosurg Psychiatry. 2024 Oct 16;95(11):1054-1063. doi: 10.1136/jnnp-2024-333463.
3
Aberrant white matter microstructure detected by automatic fiber quantification in pediatric myelin oligodendrocyte glycoprotein antibody-associated disease.
自动纤维定量检测到小儿髓鞘少突胶质细胞糖蛋白抗体相关性疾病中的异常白质微观结构。
Mult Scler Relat Disord. 2024 Apr;84:105483. doi: 10.1016/j.msard.2024.105483. Epub 2024 Feb 9.
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The MOG antibody non-P42 epitope is predictive of a relapsing course in MOG antibody-associated disease.MOG 抗体非 P42 表位可预测 MOG 抗体相关性疾病的复发病程。
J Neurol Neurosurg Psychiatry. 2024 May 14;95(6):544-553. doi: 10.1136/jnnp-2023-332851.
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Neurol Sci. 2024 Apr;45(4):1429-1436. doi: 10.1007/s10072-023-07189-7. Epub 2023 Nov 27.
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Mult Scler Relat Disord. 2023 Jun;74:104704. doi: 10.1016/j.msard.2023.104704. Epub 2023 Apr 3.
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Lancet Neurol. 2023 Mar;22(3):268-282. doi: 10.1016/S1474-4422(22)00431-8. Epub 2023 Jan 24.