Autoimmune GFAP Astrocytopathy—Beyond the Known Horizon, India’s First Multifaceted Institutional Experience

IF 1.8 Q4 NEUROSCIENCES
Safwan Ahmed, Vimala Christina Colaco K., S. Kannoth, Fathima Raeesa, Z. Misri, Don G. Mascarenhas, Sindhu Nair
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引用次数: 0

Abstract

Background: Autoimmune glial fibrillary acidic protein (GFAP) astrocytopathy is an immune-mediated inflammatory disease of the central nervous system, the clinical phenotype of which includes meningoencephalitis, myelitis, optic neuritis, seizures, movement disorders, autonomic dysfunction among others, affecting people across all ages. Due to its recent discovery, there is a paucity of literature on this topic and an absolute lack of Indian case series. Purpose: This study aims to shed light on the variable presentations of anti-GFAP astrocytopathy and review the existing literature on the topic. Methods: This was a retrospective study that included all patients who tested positive in the cerebrospinal fluid(CSF) and/or serum for GFAP immunoglobulin G between February 2023 and August 2023, after obtaining ethical clearance. Relevant clinical, demographic data was collected from the electronic medical records. A descriptive analysis of data was done and the current available literature was reviewed. Results: Our case series included four patients (F:M::3:1) with a median age of 28 years at symptom onset. Two of the cases had a relapsing-remitting disease pattern, while the other two had monophasic illnesses. The clinical spectrum we encountered included ataxia, tremors, myoclonus, seizures, recurrent myelitis, brain stem syndromes, autonomic dysfunction and psychiatric manifestations. All four patients responded remarkably to steroids and two patients are on rituximab therapy. Conclusion: Autoimmune GFAP astrocytopathy encompasses an expanding clinical spectrum and should be considered in the context of myelitis, optic neuritis, ataxia, papillitis, seizures, autonomic dysfunction and movement disorders occurring in isolation or more commonly in varying combinations. Our case series, the first in India, shows a favourable clinical profile and the primary hurdle encountered in all four cases was to establish a diagnosis, further stressing the need for a predictive diagnostic algorithm.
自身免疫性 GFAP 星形细胞病变--超越已知范围,印度首个多层面机构经验
背景:自身免疫性胶质纤维酸性蛋白(GFAP)星形胶质细胞病是一种免疫介导的中枢神经系统炎症性疾病,其临床表现包括脑膜脑炎、脊髓炎、视神经炎、癫痫发作、运动障碍、自主神经功能障碍等,影响各个年龄段的人群。由于该病是最近才被发现的,因此有关该主题的文献很少,而且绝对缺乏印度病例系列。目的:本研究旨在揭示抗-GFAP 星形细胞病的不同表现形式,并回顾现有的相关文献。研究方法这是一项回顾性研究,在获得伦理许可后,纳入了 2023 年 2 月至 2023 年 8 月间所有脑脊液(CSF)和/或血清中 GFAP 免疫球蛋白 G 检测呈阳性的患者。从电子病历中收集了相关的临床和人口统计学数据。对数据进行了描述性分析,并查阅了现有文献。结果我们的病例系列包括四名患者(女:男::3:1),发病时的中位年龄为 28 岁。其中两例为复发-缓解型,另外两例为单相型。临床表现包括共济失调、震颤、肌阵挛、癫痫发作、复发性脊髓炎、脑干综合征、自主神经功能障碍和精神症状。四名患者均对类固醇治疗有显著反应,其中两名患者正在接受利妥昔单抗治疗。结论自身免疫性GFAP星形胶质细胞病的临床范围不断扩大,应结合脊髓炎、视神经炎、共济失调、乳头炎、癫痫发作、自主神经功能障碍和运动障碍等疾病单独或更常见地以不同的组合形式出现。我们的病例系列是印度的首例,显示出良好的临床特征,而所有四例病例遇到的主要障碍是确定诊断,这进一步强调了对预测性诊断算法的需求。
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来源期刊
Annals of Neurosciences
Annals of Neurosciences NEUROSCIENCES-
CiteScore
2.40
自引率
0.00%
发文量
39
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