Clinical characteristics of autoimmune glial fibrillary acidic protein astrocytopathy in adults: a retrospective analysis of 9 cases

Differentiating GFAP-A from anti-N-methyl-D-aspartate receptor encephalitis based on conventional inflammatory biomarkers remains challenging. Elevated serum C-reactive protein and procalcitonin levels are more suggestive of viral or tuberculous meningoencephalitis. GFAP-A is generally associated with a favourable prognosis and no recurrence within 6 months of follow-up.

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Publication Details

Journal
Internal Medicine Journal
Published
2026-02-22
DOI
https://doi.org/10.1111/imj.70379
Primary Topic
Autoimmune Neurological Disorders and Treatments
Type
article
Field-Weighted Citation Impact
0.00
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article

Clinical characteristics of autoimmune glial fibrillary acidic protein astrocytopathy in adults: a retrospective analysis of 9 cases

Tingting Liu, Jinyu Huang, Siruo Guo, Wu Yang
Internal Medicine Journal
Autoimmune Neurological Disorders and Treatments
article

Clinical characteristics of autoimmune glial fibrillary acidic protein astrocytopathy in adults: a retrospective analysis of 9 cases

Tingting Liu, Jinyu Huang, Siruo Guo, Wu Yang
article en

Abstract

Differentiating GFAP-A from anti-N-methyl-D-aspartate receptor encephalitis based on conventional inflammatory biomarkers remains challenging. Elevated serum C-reactive protein and procalcitonin levels are more suggestive of viral or tuberculous meningoencephalitis. GFAP-A is generally associated with a favourable prognosis and no recurrence within 6 months of follow-up.

Internal Medicine Journal
Integrated Chinese Medicine (China) (HK), First Affiliated Hospital Zhejiang University (CN)
Openalex Percentile: Top 51%
Autoimmune Neurological Disorders and Treatments
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