Frequency of anti-MOG antibodies in serum and CSF of patients with possible autoimmune encephalitis: Results from a Brazilian multicentric study

IF 2.9 3区 医学 Q2 CLINICAL NEUROLOGY Multiple sclerosis and related disorders Pub Date : 2024-11-14 DOI:10.1016/j.msard.2024.106171
Bruna de Freitas Dias , Fabio Fieni Toso , Maria Eduarda Slhessarenko Fraife Barreto , Alessandra Dellavance , Rodrigo Barbosa Thomaz , Pedro André Kowacs , Hélio Teive , Mariana Spitz , Aline Freire Borges Juliano , Letícia Januzi de Almeida Rocha , Valéria Nogueira Tobias Granja , Pedro Braga-Neto , Paulo Ribeiro Nóbrega , Jamary Oliveira-Filho , Ronaldo Maciel Dias , Jaene Andrade Pacheco Amoras , Renata Brasileiro Reis Pereira , Clécio de Oliveira Godeiro Júnior , Fernanda Martins Maia , Mara Lúcia Santos , Lívia Almeida Dutra
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Abstract

Introduction

MOGAD encephalitis and ADEM share several clinical features with autoimmune encephalitis (AE) associated with antineuronal antibodies (ANeA); nonetheless, treatment and prognosis differ. Anti-MOG antibodies (abs) are not routinely tested in possible AE, and epidemiological studies on MOGAD encephalitis are scarce.

Objectives

To determine the frequency of anti-MOG abs in the serum and CSF in a cohort of possible AE and to compare the clinical characteristics of MOGAD patients and those with seropositive AE.

Methods

481 patients with possible AE from the Brazilian Autoimmune Encephalitis Network underwent tissue-based assay and cell-based assay (CBA) for ANeA. Anti-MOG abs were assessed in serum and CSF with in-house CBA. Clinical and laboratory characteristics of MOGAD and seropositive AE patients were compared.

Results

Of the 481 patients, 87 (18 %) had ANeA, and 17 (3.5 %) had anti-MOG abs. Three AE patients with anti-MOG abs and ANeA were excluded from further analysis. Anti-MOG abs were detected in 4 (1.2 %) of the 328 adults and 10 (6.5 %) of the 153 children. Of the 14 patients with MOGAD, nine had ADEM (mostly children), and five had encephalitis (including three adults). Only one patient with ADEM had anti-MOG abs exclusively in CSF. All patients with MOGAD encephalitis were seropositive for anti-MOG abs, and three had normal brain MRI. Patients with MOGAD had fewer behavioral changes (MOGAD 21 % x AE 96 %, p ≤ 0.0001) and movement disorders (MOGAD 42 % x AE 81 %, p = 0.0017) and more demyelinating symptoms, such as myelitis and optic neuritis (MOGAD 14 % x AE 0 %, p = 0.013).

Conclusion

Approximately 3.5 % of patients with possible AE harbor anti-MOG abs, and 0.9 % of the adults had MOGAD encephalitis. Anti-MOG abs were more frequent than other ANeAs regularly tested in AE. We provide evidence that MOGAD is a differential diagnosis in possible AE, even in adult patients with normal brain MRI, and that serum anti-MOG should be considered as an add-on diagnostic tool in AE among adults and pediatric patients.
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可能患有自身免疫性脑炎的患者血清和脑脊液中抗 MOG 抗体的频率:巴西一项多中心研究的结果。
导言:MOGAD 脑炎和 ADEM 与伴有抗神经元抗体(ANeA)的自身免疫性脑炎(AE)有一些共同的临床特征,但治疗和预后却不同。抗 MOG 抗体(abs)不是可能的 AE 的常规检测项目,而且有关 MOGAD 脑炎的流行病学研究也很少:方法:巴西自身免疫性脑炎网络的 481 名可能患有自身免疫性脑炎的患者接受了组织检测和细胞检测(CBA)。通过内部 CBA 评估血清和脑脊液中的抗 MOG abs。比较了 MOGAD 和血清阳性 AE 患者的临床和实验室特征:结果:在 481 名患者中,87 人(18%)有 ANeA,17 人(3.5%)有抗 MOG abs。进一步分析中排除了 3 名既有抗 MOG abs 又有 ANeA 的 AE 患者。在 328 名成人和 153 名儿童中,分别有 4 人(1.2%)和 10 人(6.5%)检测到抗 MOG abs。在 14 名 MOGAD 患者中,9 人患有 ADEM(多数为儿童),5 人患有脑炎(包括 3 名成人)。只有一名 ADEM 患者的抗 MOG abs 完全存在于 CSF 中。所有 MOGAD 脑炎患者的抗 MOG abs 血清均呈阳性,其中三人的脑磁共振成像正常。MOGAD患者的行为改变(MOGAD 21 % x AE 96 %,p ≤ 0.0001)和运动障碍(MOGAD 42 % x AE 81 %,p = 0.0017)较少,而脊髓炎和视神经炎等脱髓鞘症状较多(MOGAD 14 % x AE 0 %,p = 0.013):结论:可能患有AE的患者中约有3.5%携带抗MOG抗体,0.9%的成人患有MOGAD脑炎。抗 MOG abs 比 AE 中定期检测的其他 ANeAs 更为常见。我们提供的证据表明,即使在脑磁共振成像正常的成人患者中,MOGAD 也是可能的 AE 的鉴别诊断之一,血清抗 MOG 应被视为成人和儿童患者 AE 的附加诊断工具。
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来源期刊
CiteScore
5.80
自引率
20.00%
发文量
814
审稿时长
66 days
期刊介绍: Multiple Sclerosis is an area of ever expanding research and escalating publications. Multiple Sclerosis and Related Disorders is a wide ranging international journal supported by key researchers from all neuroscience domains that focus on MS and associated disease of the central nervous system. The primary aim of this new journal is the rapid publication of high quality original research in the field. Important secondary aims will be timely updates and editorials on important scientific and clinical care advances, controversies in the field, and invited opinion articles from current thought leaders on topical issues. One section of the journal will focus on teaching, written to enhance the practice of community and academic neurologists involved in the care of MS patients. Summaries of key articles written for a lay audience will be provided as an on-line resource. A team of four chief editors is supported by leading section editors who will commission and appraise original and review articles concerning: clinical neurology, neuroimaging, neuropathology, neuroepidemiology, therapeutics, genetics / transcriptomics, experimental models, neuroimmunology, biomarkers, neuropsychology, neurorehabilitation, measurement scales, teaching, neuroethics and lay communication.
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