Evidence map›Paper›PMID 42741215›Full record

ArticleFrontiers in immunology2026

Case Report: Efficacy of efgartigimod for autonomic dysfunction in patients with autoimmune glial fibrillary acidic protein astrocytopathy: a case series of 3 patients.

Huayi Ma, Bingying Xie, Yi Wu, Houshi Zhou, Feiyu Ma, Chuming Huang, Xiujun Zheng

Abstract readCase Reports
In one paragraph

Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Huayi Ma *Department of Neurology, Shantou Central Hospital, Shantou, China.
Bingying Xie *Department of Nephrology, Shantou Central Hospital, Shantou, China.
Yi Wu *Department of Neurology, Shantou Central Hospital, Shantou, China.
Houshi ZhouDepartment of Neurology, Shantou Central Hospital, Shantou, China.
Feiyu MaDepartment of Neurology, Shantou Central Hospital, Shantou, China.
Chuming HuangDepartment of Neurology, Shantou Central Hospital, Shantou, China.
Xiujun ZhengDepartment of Neurology, Shantou Central Hospital, Shantou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Efgartigimod can rapidly reduce serum IgG antibody levels and decrease antibody-mediated neuroinflammation and damage. It is primarily used to treat autoimmune diseases. Glial fibrillary acidic protein astrocytopathy (GFAP-A) is a disease of the central nervous system characterized by GFAP antibodies. It has a high incidence of autonomic dysfunction in patients and there is currently no effective treatment plan. It is not known whether efgartigimod can improve autonomic dysfunction in GFAP-A. Case presentation: All three patients with GFAP-A presented with autonomic dysfunction, which manifested as urinary and defecatory disorders. Marked remission of corticosteroid-refractory autonomic dysfunction was observed following combined treatment with efgartigimod and corticosteroids. All three patients presented with autonomic dysfunction. Patient 1 experienced marked improvement in autonomic function after the addition of efgartigimod, despite showing no significant improvement after high-dose pulse steroid therapy. Patient 2 showed no significant improvement after treatment with low-dose steroids, but achieved complete recovery of autonomic dysfunction after efgartigimod treatment. Patient 3 initially received low-dose steroids, with no significant improvement in autonomic dysfunction. After switching to a high dose of steroids combined with efgartigimod, the patient's autonomic dysfunction gradually improved. Conclusion: We observed that after combined treatment with efgartigimod and corticosteroids, the corticosteroid-refractory autonomic dysfunction in GFAP-A patients was significantly alleviated, providing a new clinical treatment option. However, this article is based on a small sample size and requires further validation through larger-scale studies.

Indexed as

AstrocytesAutonomic Nervous System DiseasesGlial Fibrillary Acidic ProteinAgedAutoantibodiesHumansMaleMiddle AgedTreatment OutcomeYoung AdultAutoantibodiesGFAP protein, humanGlial Fibrillary Acidic Proteinautonomic neurological dysfunctioncase seriesefgartigimodGFAP-Aurinary and defecation disorders

Identifiers

PMID42741215
PMCPMC13572910

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.