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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.

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。

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