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Application of oligoclonal bands and other cerebrospinal fluid variables in multiple sclerosis and other neuroimmunological diseases: a narrative review.寡克隆带及其他脑脊液变量在多发性硬化症和其他神经免疫性疾病中的应用:一篇叙述性综述
Ann Transl Med. 2023 Apr 15;11(7):282. doi: 10.21037/atm-21-3073. Epub 2023 Jan 10.
2
Cerebrospinal fluid oligoclonal immunoglobulin gamma bands and long-term disability progression in multiple sclerosis: a retrospective cohort study.脑脊髓液寡克隆免疫球蛋白γ带与多发性硬化症的长期残疾进展:一项回顾性队列研究。
Sci Rep. 2021 Jul 22;11(1):14987. doi: 10.1038/s41598-021-94423-x.
3
Long-term analysis of patients with benign multiple sclerosis: new insights about the disability course.良性多发性硬化症患者的长期分析:对残疾病程的新认识。
J Neurol. 2021 Oct;268(10):3817-3825. doi: 10.1007/s00415-021-10501-0. Epub 2021 Mar 31.
4
Main Role of Antibodies in Demyelination and Axonal Damage in Multiple Sclerosis.抗体在多发性硬化症中的脱髓鞘和轴突损伤中的主要作用。
Cell Mol Neurobiol. 2022 Aug;42(6):1809-1827. doi: 10.1007/s10571-021-01059-6. Epub 2021 Feb 24.
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The frequency and characteristics of MS misdiagnosis in patients referred to the multiple sclerosis centre of Catalonia.在加泰罗尼亚多发性硬化症中心就诊的患者中,多发性硬化症误诊的频率和特征。
Mult Scler. 2021 May;27(6):913-921. doi: 10.1177/1352458520988148. Epub 2021 Feb 10.
6
Intrathecally produced CXCL13: A predictive biomarker in multiple sclerosis.鞘内产生的CXCL13:多发性硬化症的一种预测性生物标志物。
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多发性硬化症中寡克隆带缺失:呼吁进行鉴别诊断。

Absence of Oligoclonal Bands in Multiple Sclerosis: A Call for Differential Diagnosis.

作者信息

Katsarogiannis Evangelos, Landtblom Anne-Marie, Kristoffersson Anna, Wikström Johan, Semnic Robert, Berntsson Shala G

机构信息

Department of Medical Sciences, Neurology, Uppsala University, SE-751 85 Uppsala, Sweden.

Department of Surgical Sciences, Neuroradiology, Uppsala University, SE-751 85 Uppsala, Sweden.

出版信息

J Clin Med. 2023 Jul 13;12(14):4656. doi: 10.3390/jcm12144656.

DOI:10.3390/jcm12144656
PMID:37510771
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10380970/
Abstract

Immunoglobulin gamma (IgG) oligoclonal bands (OCB) in the cerebrospinal fluid (CSF) are absent in a small group of multiple sclerosis (MS) patients. According to previous research, OCB-negative MS patients differ genetically but not clinically from OCB-positive MS patients. However, whether OCB-negative MS is a unique immunological and clinical entity remains unclear. The absence of OCB poses a significant challenge in diagnosing MS. (1) Objective: The objective of this study was twofold: (1) to determine the prevalence of OCB-negative MS patients in the Uppsala region, and (2) to assess the frequency of misdiagnosis in this patient group. (2) Methods: We conducted a retrospective study using data from the Swedish MS registry (SMSreg) covering 83% of prevalent MS cases up to 20 June 2020 to identify all MS patients in the Uppsala region. Subsequently, we collected relevant information from the medical records of all OCB-negative MS cases, including age of onset, gender, presenting symptoms, MRI features, phenotype, Expanded Disability Status Scale (EDSS) scores, and disease-modifying therapies (DMTs). (3) Results: Out of 759 MS patients identified, 69 had an OCB-negative MS diagnosis. Upon re-evaluation, 46 patients had a typical history and MRI findings of MS, while 23 had unusual clinical and/or radiologic features. An alternative diagnosis was established for the latter group, confirming the incorrectness of the initial MS diagnosis. The average EDSS score was 2.0 points higher in the MS group than in the non-MS group ( = 0.001). The overall misdiagnosis rate in the cohort was 33%, with 22% of misdiagnosed patients having received DMTs. (4) Conclusions: Our results confirm that the absence of OCB in the CSF should raise suspicion of possible misdiagnosis in MS patients and prompt a diagnostic reassessment.

摘要

一小部分多发性硬化症(MS)患者的脑脊液(CSF)中不存在免疫球蛋白γ(IgG)寡克隆带(OCB)。根据以往的研究,OCB阴性的MS患者与OCB阳性的MS患者在基因上存在差异,但在临床上并无差异。然而,OCB阴性的MS是否是一种独特的免疫和临床实体仍不清楚。OCB的缺失给MS的诊断带来了重大挑战。(1)目的:本研究的目的有两个:(1)确定乌普萨拉地区OCB阴性MS患者的患病率,(2)评估该患者群体的误诊频率。(2)方法:我们进行了一项回顾性研究,使用瑞典MS登记处(SMSreg)的数据,该数据涵盖了截至2020年6月20日83%的MS现患病例,以确定乌普萨拉地区的所有MS患者。随后,我们从所有OCB阴性MS病例的病历中收集了相关信息,包括发病年龄、性别、首发症状、MRI特征、表型、扩展残疾状态量表(EDSS)评分以及疾病修饰疗法(DMT)。(3)结果:在确定的759例MS患者中,69例被诊断为OCB阴性MS。重新评估后,46例患者有典型的MS病史和MRI表现,而23例有不寻常的临床和/或放射学特征。为后一组患者确立了替代诊断,证实了最初MS诊断的错误。MS组的平均EDSS评分比非MS组高2.0分(=0.001)。该队列的总体误诊率为33%,22%的误诊患者接受了DMT。(4)结论:我们的结果证实,CSF中OCB的缺失应引起对MS患者可能误诊的怀疑,并促使进行诊断重新评估。