• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

以自主神经功能障碍为表现的自身免疫性胶质纤维酸性蛋白星形细胞病的临床分析与病例系列报告

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

作者信息

Wu Xiao Ke, Zhai Guojie, Zhang Jin Ru, Du Hua Ping, Hu Lan, Yu Shu Ye, Hang Hai Lun, Han Sirui, Zhang Yanlin, Xu Yuan

机构信息

Suzhou Ninth People's Hospital, Suzhou, China.

Department of Neurology, The Second Affiliated Hospital of Soochow University, Suzhou, China.

出版信息

Front Neurol. 2025 Jan 31;15:1464891. doi: 10.3389/fneur.2024.1464891. eCollection 2024.

DOI:10.3389/fneur.2024.1464891
PMID:39975853
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11837777/
Abstract

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.

摘要

背景与目的

自身免疫性胶质纤维酸性蛋白星形细胞病(GFAP-A)患者自主神经功能障碍的发生率常常被低估且常被忽视。本研究全面分析了GFAP-A累及自主神经系统患者的临床表现、实验室及影像学检查结果以及治疗方式。本文主要阐述了各种自主神经系统症状的发生率和预后情况,同时研究了相关的实验室及影像学指标。这些研究结果旨在为此类患者的个性化诊断和治疗策略奠定基础。

方法

我们对苏州大学附属第二医院和苏州市第九人民医院2020年至2023年3例GFAP-A累及自主神经的病例进行了回顾性数据分析。在广泛查阅文献后,我们确定了39例涉及GFAP-A和自主神经功能障碍的病例。我们还全面分析了患者的临床表现、实验室生物标志物和影像学检查结果。

结果

该研究共纳入42例患者,其中女性15例,男性27例。自主神经功能障碍的主要表现包括膀胱功能障碍(41/42例)、胃肠功能障碍(18/42例)、心率变异性(4/42例)、异常出汗(2/42例)和血压波动(1/42例)。其他神经症状包括头痛(12/42例)、肢体无力表现(30/42例)。血压变异性与脑脊液压力和惊厥发作有关。心率变异性与意识障碍有关。异常出汗与年龄、性别、脑脊液蛋白含量和惊厥发作有关。胃肠功能障碍与性别、睡眠障碍、脑脊液蛋白含量和脑MRI病变有关。自主神经功能障碍的预后与睡眠障碍和脑脊液蛋白含量有关。脑脊液蛋白水平越高,自主神经系统的预后越差。

结论

膀胱功能障碍和胃肠功能障碍是GFAP-A患者自主神经功能障碍的主要表现,部分患者还存在心率、血压和出汗异常。这些额外症状对预后有影响,临床医生需要对GFAP-A患者给予更多关注。

相似文献

1
Clinical analysis and case series report on autoimmune glial fibrillary acidic protein astrocytopathy presenting with autonomic dysfunction.以自主神经功能障碍为表现的自身免疫性胶质纤维酸性蛋白星形细胞病的临床分析与病例系列报告
Front Neurol. 2025 Jan 31;15:1464891. doi: 10.3389/fneur.2024.1464891. eCollection 2024.
2
Autoimmune glial fibrillary acidic protein astrocytopathy misdiagnosed as intracranial infectious diseases: case reports and literature review.被误诊为颅内感染性疾病的自身免疫性胶质纤维酸性蛋白星形细胞病:病例报告及文献综述
Front Immunol. 2025 Jan 22;16:1519700. doi: 10.3389/fimmu.2025.1519700. eCollection 2025.
3
A case report of autoimmune GFAP astrocytopathy presenting with abnormal heart rate variability and blood pressure variability.自身免疫性 GFAP 星形胶质细胞病伴异常心率变异性和血压变异性病例报告。
BMC Neurol. 2023 Jan 17;23(1):24. doi: 10.1186/s12883-023-03070-4.
4
Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy in Children: A Retrospective Analysis of 35 Cases.儿童自身免疫性胶质纤维酸性蛋白星形胶质细胞病:35 例回顾性分析。
Front Immunol. 2021 Nov 22;12:761354. doi: 10.3389/fimmu.2021.761354. eCollection 2021.
5
A rare case of glial fibrillary acidic protein astrocytopathy that resolved spontaneously within a self-limited course.一例罕见的胶质纤维酸性蛋白星形细胞病,在自限性病程中自发缓解。
Heliyon. 2023 Oct 12;9(10):e20912. doi: 10.1016/j.heliyon.2023.e20912. eCollection 2023 Oct.
6
Clinical characteristics of autoimmune glial fibrillary acidic protein (GFAP) astrocytopathy in children: A case series of 16 patients.儿童自身免疫性神经丝酸性蛋白(GFAP)星形胶质细胞病的临床特征:16 例病例系列研究。
J Neuroimmunol. 2023 Sep 15;382:578176. doi: 10.1016/j.jneuroim.2023.578176. Epub 2023 Aug 7.
7
Case report: Excessive daytime sleepiness as a presenting manifestation of autoimmune glial fibrillary acidic protein astrocytopathy.病例报告:自身免疫性神经胶质纤维酸性蛋白星形胶质细胞病的首发表现为日间过度嗜睡。
Front Immunol. 2023 Dec 20;14:1302514. doi: 10.3389/fimmu.2023.1302514. eCollection 2023.
8
Review of clinical and imaging findings in autoimmune glial fibrillary acidic protein astrocytopathy to aid in early diagnosis.自身免疫性胶质纤维酸性蛋白星形细胞病的临床及影像学表现回顾以助早期诊断
Front Immunol. 2024 Dec 10;15:1466847. doi: 10.3389/fimmu.2024.1466847. eCollection 2024.
9
Epstein-Barr virus: To be a trigger of autoimmune glial fibrillary acidic protein astrocytopathy?爱泼斯坦-巴尔病毒:是否为自身免疫性胶质纤维酸性蛋白星形胶质细胞病的触发因素?
CNS Neurosci Ther. 2023 Dec;29(12):4139-4146. doi: 10.1111/cns.14336. Epub 2023 Jul 17.
10
Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy Presenting with Area Postrema Syndrome-Like Symptoms without Medulla Oblongata Lesions.表现为类似最后区综合征症状且无延髓病变的自身免疫性胶质纤维酸性蛋白星形细胞病
Neuroimmunomodulation. 2022;29(4):433-438. doi: 10.1159/000524344. Epub 2022 Apr 14.

本文引用的文献

1
Autoimmune encephalitis in glial fibrillary acidic protein astrocytopathy.胶质纤维酸性蛋白星形胶质细胞病中的自身免疫性脑炎。
BMJ Case Rep. 2024 May 9;17(5):e260628. doi: 10.1136/bcr-2024-260628.
2
Clinical and neuroimaging phenotypes of autoimmune glial fibrillary acidic protein astrocytopathy: A systematic review and meta-analysis.自身免疫性胶质纤维酸性蛋白星形胶质细胞病的临床和神经影像学表型:系统评价和荟萃分析。
Eur J Neurol. 2024 Jul;31(7):e16284. doi: 10.1111/ene.16284. Epub 2024 Mar 20.
3
New insights into neuropathology and pathogenesis of autoimmune glial fibrillary acidic protein meningoencephalomyelitis.自身免疫性胶质纤维酸性蛋白性脑膜脑炎的神经病理学和发病机制的新见解。
Acta Neuropathol. 2024 Feb 3;147(1):31. doi: 10.1007/s00401-023-02678-7.
4
Clinical characteristics and prognostic factors for short-term outcomes of autoimmune glial fibrillary acidic protein astrocytopathy: a retrospective analysis of 33 patients.自身免疫性胶质纤维酸性蛋白星形胶质细胞病的临床特征和短期预后的影响因素:33 例回顾性分析。
Front Immunol. 2023 Jun 7;14:1136955. doi: 10.3389/fimmu.2023.1136955. eCollection 2023.
5
A case report of autoimmune GFAP astrocytopathy presenting with abnormal heart rate variability and blood pressure variability.自身免疫性 GFAP 星形胶质细胞病伴异常心率变异性和血压变异性病例报告。
BMC Neurol. 2023 Jan 17;23(1):24. doi: 10.1186/s12883-023-03070-4.
6
Hybrid F-florbetapir PET/MRI for assessing myelin recovery in GFAP-A patients.用于评估GFAP-A患者髓鞘恢复情况的混合F-氟代硼替吡咯PET/MRI
Transl Neurosci. 2022 Jun 9;13(1):120-124. doi: 10.1515/tnsci-2022-0223. eCollection 2022 Jan 1.
7
Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy: To Identify Its Diagnosis, Management and Prognosis (GFAP-AID) Registry: Study Protocol for an Ambispective, Multicenter Registry in China.自身免疫性胶质纤维酸性蛋白星形细胞病:确定其诊断、管理和预后(GFAP-AID)注册研究:中国一项前瞻性-回顾性多中心注册研究方案
Neuropsychiatr Dis Treat. 2022 Jun 1;18:1099-1105. doi: 10.2147/NDT.S364246. eCollection 2022.
8
[Recurrent autoimmune glial fibrillary acidic protein (GFAP) astrocytopathy with long cervical cord lesions: a case report].[复发性自身免疫性胶质纤维酸性蛋白(GFAP)星形细胞病伴颈髓长节段病变:一例报告]
Rinsho Shinkeigaku. 2022 May 31;62(5):386-390. doi: 10.5692/clinicalneurol.cn-001713. Epub 2022 Apr 26.
9
Clinical, neuroradiological, diagnostic and prognostic profile of autoimmune glial fibrillary acidic protein astrocytopathy: A pooled analysis of 324 cases from published data and a single-center retrospective study.自身免疫性胶质纤维酸性蛋白星形胶质细胞病的临床、神经放射学、诊断和预后特征:来自已发表数据的 324 例病例的汇总分析和单中心回顾性研究。
J Neuroimmunol. 2021 Nov 15;360:577718. doi: 10.1016/j.jneuroim.2021.577718. Epub 2021 Sep 10.
10
Paroxysmal Sympathetic Hyperactivity in Severe Anti-N-Methyl-d-Aspartate Receptor Encephalitis: A Single Center Retrospective Observational Study.抗 N-甲基-D-天冬氨酸受体脑炎中阵发性交感神经兴奋:单中心回顾性观察研究。
Front Immunol. 2021 Apr 12;12:665183. doi: 10.3389/fimmu.2021.665183. eCollection 2021.