Clinical analysis and case series report on autoimmune glial fibrillary acidic protein astrocytopathy presenting with autonomic dysfunction

被引:0
|
作者
Wu, Xiao Ke [1 ]
Zhai, Guojie [2 ]
Zhang, Jin Ru [2 ]
Du, Hua Ping [1 ]
Hu, Lan [1 ]
Yu, Shu Ye [1 ]
Hang, Hai Lun [1 ]
Han, Sirui [3 ]
Zhang, Yanlin [2 ]
Xu, Yuan [1 ]
机构
[1] Suzhou Ninth Peoples Hosp, Suzhou, Peoples R China
[2] Soochow Univ, Affiliated Hosp 2, Dept Neurol, Suzhou, Peoples R China
[3] Nanjing Med Univ, Kang da Coll, Lianyungang, Peoples R China
来源
FRONTIERS IN NEUROLOGY | 2025年 / 15卷
关键词
GFAP-A; autonomic dysfunction; prognosis; urinary bladder dysfunction; autoimmune glial fibrillary acidic protein astrocytopathy;
D O I
10.3389/fneur.2024.1464891
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and purpose The incidence of autonomic dysfunction is frequently underestimated and often overlooked in patients with autoimmune glial fibrillary acidic protein astrocytopathy (GFAP-A). This study comprehensively analyzes the clinical manifestations, laboratory and imaging findings, and treatment modalities for patients demonstrating GFAP-A involvement in the autonomic nervous system. The present article primarily elucidates the prevalence and prognosis of diverse autonomic system symptoms while examining the associated laboratory and imaging indicators. These findings aim to establish a foundation for personalized diagnosis and treatment strategies in such patients.Method We performed a retrospective data analysis from three cases of GFAP-A involvement in autonomic nerves from the Ninth People's Hospital of Suzhou and the Second Affiliated Hospital of Soochow University from 2020 to 2023. After an extensive literature review, we identified 39 cases involving GFAP-A and autonomic nervous system dysfunction. We also comprehensively analyzed the patient's clinical manifestations, laboratory biomarkers, and imaging findings.Result The study included a total of 42 patients, consisting of 15 females and 27 males. The primary manifestations of autonomic dysfunction included bladder dysfunction (41/42 cases), gastrointestinal dysfunction (18 /42 cases), heart rate variability (4/42 cases), unusual sweating (2/42 cases), and blood pressure fluctuations (1/42 cases). Other neurological symptoms comprised headache (12 /42 cases), limb weakness presentation (30/42 cases). Blood pressure variability is related to cerebrospinal fluid pressure and convulsive seizures. Heart rate variability is related to disorders of consciousness. unusual sweating was associated to age, gender, cerebrospinal fluid protein content and convulsive seizures. Gastrointestinal disorders have associations with gender, sleep disturbances, protein content in the cerebrospinal fluid, and brain MRI lesions. The prognosis of autonomic nerve dysfunction is associated to sleep disorder and cerebrospinal fluid protein content. The higher the cerebrospinal fluid protein level, the worse the prognosis of autonomic nervous system.Conclusion Bladder dysfunction and gastrointestinal dysfunction are the primary manifestations of autonomic dysfunction in GFAP-A patients, with a subset also experiencing abnormalities in heart rate, blood pressure, and sweating. These additional symptoms have implications for prognosis, necessitating heightened attention from clinicians toward GFAP-A patients.
引用
收藏
页数:10
相关论文
共 50 条
  • [31] Autoimmune glial fibrillary acidic protein astrocytopathy masquerading as tuberculosis of the central nervous system: a case series
    Quek, Amy M. L.
    Tang, David
    Chin, Amanda
    Ng, Kay W. P.
    Lin, Hazel
    Seet, Raymond C. S.
    INTERNATIONAL JOURNAL OF INFECTIOUS DISEASES, 2022, 124 : 164 - 167
  • [32] Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy: A Review of the Literature
    Shan, Fulan
    Long, Youming
    Qiu, Wei
    FRONTIERS IN IMMUNOLOGY, 2018, 9
  • [33] Glial fibrillary acidic protein astrocytopathy presented as meningitis: A case report
    Guo, Ya
    Guo, Jiamin
    Wang, Xueyu
    Ma, Aihua
    Gao, Yuxing
    Chen, Jiacheng
    Nie, Cuili
    Chen, Na
    HELIYON, 2024, 10 (05)
  • [34] A case of Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy(GFAP) Meningo encephalomyelitis
    Sivalingam, Ambihai
    NEUROLOGY, 2018, 90
  • [35] Area Postrema Syndrome in Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy A Case Series and Literature Review
    Deng, Bo
    Wang, Jingguo
    Yu, Hai
    Jin, Lei
    Qiu, Yue
    Liu, Xiaoni
    Wang, Pengyu
    Zhang, Xiang
    Chen, Xiangjun
    NEUROLOGY-NEUROIMMUNOLOGY & NEUROINFLAMMATION, 2022, 9 (06):
  • [36] Case report: Headache as the sole neurological symptom in autoimmune glial fibrillary acidic protein (GFAP) astrocytopathy
    Shosha, Eslam
    Connolly, Colleen
    Budhram, Adrian
    FRONTIERS IN NEUROLOGY, 2024, 15
  • [37] Autoimmune glial fibrillary acidic protein astrocytopathy: case report of a treatable cause of rapidly progressive dementia
    Carlos Toledano-Illán
    Inés Esparragosa Vázquez
    María Victoria Zelaya Huerta
    Juan José Rosales Castillo
    Alberto Paternain Nuin
    Javier Arbizu Lostao
    María Reyes García de Eulate
    Mario Riverol Fernández
    Journal of Neurology, 2021, 268 : 2256 - 2258
  • [38] A case of autoimmune glial fibrillary acidic protein astrocytopathy presenting with magnetic resonance imaging mimics of multiple sclerosis
    Sakashita, Yasuhiro
    Nozaki, Ichiro
    Hamaguchi, Tsuyoshi
    Kimura, Akio
    Shimohata, Takayoshi
    Ono, Kenjiro
    CLINICAL NEUROLOGY AND NEUROSURGERY, 2022, 218
  • [39] Autoimmune glial fibrillary acidic protein astrocytopathy: case report of a treatable cause of rapidly progressive dementia
    Toledano-Illan, Carlos
    Esparragosa Vazquez, Ines
    Zelaya Huerta, Maria Victoria
    Rosales Castillo, Juan Jose
    Paternain Nuin, Alberto
    Arbizu Lostao, Javier
    Garcia de Eulate, Maria Reyes
    Riverol Fernandez, Mario
    JOURNAL OF NEUROLOGY, 2021, 268 (06) : 2256 - 2258
  • [40] Failure of IVIG in steroid-responsive autoimmune glial fibrillary acidic protein astrocytopathy: A case report
    Heide, Elena S.
    Chaudhari, Amit
    Pirverdian, Ateena
    Lai, Samuel
    Courtney, Ardith
    MULTIPLE SCLEROSIS AND RELATED DISORDERS, 2021, 51