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ORIGINAL RESEARCH article

Front. Neurol.
Sec. Multiple Sclerosis and Neuroimmunology
Volume 16 - 2025 | doi: 10.3389/fneur.2025.1538602
This article is part of the Research Topic Neuroimaging Innovations for Encephalitis, Neuroinfectious Diseases, and Neuroinflammation View all 4 articles

Area postrema syndrome in patients with autoimmune glial fibrillary acidic protein astrocytopathy

Provisionally accepted
  • Department of Neurology, First Affiliated Hospital of Zhengzhou University, Zhengzhou, China

The final, formatted version of the article will be published soon.

    Objective: Area postrema syndrome (APS) is a relatively rare symptom of autoimmune glial fibrillary acidic protein astrocytopathy (A-GFAP-A). This study aimed to report the APS in GFAP-immunoglobulin G (GFAP-IgG) positive patients.We retrospectively analyzed the clinical data of APS in GFAP-IgG positive patients and reviewed relevant literature. Moreover, we compared the these data with APS patients in aquaporin-4-IgG-positive neuromyelitis optica spectrum disorders (AQP4-IgG+ NMOSD).Results: 7 of 75 (9.3%) GFAP-IgG positive patients experienced APS, including 4 females and 3 males. The median age of onset was 42 years (range, 12-71 years). All patients presented with APS as their initial manifestation. Nausea and vomiting were observed in all 7 patients, while hiccups occurred in 5 patients. The median duration of APS episodes was 12 days (range, 6-40 days). None of the patients experienced isolated APS episodes during their illness. AQP4-IgG was positive in 2 patients. 5 patients had dorsal medulla oblongata lesions, while 3 patients showed an "inverted V" sign on axial images. In addition, 5 patients presented with longitudinally extensive linear or patchy lesions in cervical spinal cord extending to area postrema on sagittal images. All APS attacks completely disappeared after immunotherapy.Compared with the APS in AQP4+NMOSD, APS in A-GFAP-A had a lower proportion of females (33.3% vs. 80%, P=0.003), more hiccups (81% vs. 50%, P=0.037), more leptomeningeal enhancement (61.9% vs. 5%, P=0.000), higher CSF white blood cell count (median 120 vs. 10 cells/mm 3 , P=0.000) and protein (median 0.949 vs. 0.407 g/L, P=0.000). Furthermore, fewer patients with A-GFAP-A received long-term immunotherapy (19% vs. 65%, P=0.003).Conclusions: APS often occurs as an initial manifestation of A-GFAP-A. MRI examination and antibody testing should be performed in suspected patients to avoid

    Keywords: Glial Fibrillary Acidic Protein, Area postrema syndrome, Encephalitis, Magnetic Resonance Imaging, aquaporin-4

    Received: 03 Dec 2024; Accepted: 16 Jan 2025.

    Copyright: © 2025 Li and Teng. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

    * Correspondence: Junfang Teng, Department of Neurology, First Affiliated Hospital of Zhengzhou University, Zhengzhou, China

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