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病例报告:抗代谢型谷氨酸受体1脑炎的临床特征与治疗:病例说明及文献综述

Case Report: Clinical features and management of anti-mGluR1 encephalitis: case illustration and review of the literature.

作者信息

Deng Min, Xiong Jing, Kong Zhaohong, Wang Xufeng, Li Tao

机构信息

Renmin Hospital of Wuhan University, Wuhan, China.

Hubei Provincial Hospital of Traditional Chinese Medicine, Wuhan, Hubei, China.

出版信息

Front Integr Neurosci. 2025 Jul 23;19:1580767. doi: 10.3389/fnint.2025.1580767. eCollection 2025.

Abstract

BACKGROUND

Anti-metabotropic glutamate receptor 1 (mGluR1) encephalitis is a rare autoimmune disease affecting cerebellar Purkinje cells. Only thirty-nine cases have been reported globally, with inconsistent documentation of treatments and outcomes. A systematic review is needed to identify prognostic factors and expand clinical understanding and treatment options.

METHODS

Observational follow-up data of anti-mGluR1 encephalitis cases were collected. All anti-mGluR1 encephalitis cases published in the PubMed and Google Scholar databases in English before November 1, 2024 were included. Clinical information and possible predictive factors from both current and previously reported cases were statistically analyzed.

RESULTS

We present a case of anti-mGluR1 encephalitis successfully treated with ofatumumab. During the patient's initial episode, she partially recovered after first-line treatment. She experienced a relapse 6 months later and was treated with ofatumumab, resulting in complete recovery. Forty cases of anti-mGluR1 encephalitis, including our case, were summarized. The prevalence was similar between men and women, with 50% of patients aged 40-59 years. The most common clinical manifestations were ataxia and dysarthria. Cerebrospinal fluid analysis showed normal white blood cell count and IgG index in 37.1% of patients. Almost half of the patients (48.6%) exhibited cerebellar atrophy on cerebral MRI scans at initial presentation or during follow-up. Only 25% of patients recovered completely. According to the modified Rankin Scale (mRS) scores at the last follow-up, patients with poor outcome ( = 13, 32.5%) had a lower proportion of first-line immunotherapy (62%, = 0.017) and a longer follow-up time (median 36 months, = 0.038).

CONCLUSION

The peak incidence of anti-mGluR1 encephalitis occurs between ages of 40-59 years. More than one-third of patients have normal cell counts and IgG index in the cerebrospinal fluid. Therefore, patients suspected of having this encephalitis should be tested for the presence of anti-mGluR1 antibodies in serum and cerebrospinal fluid. Notably, the first-line immunotherapy may be a critical factor influencing clinical outcomes.

摘要

背景

抗代谢型谷氨酸受体1(mGluR1)脑炎是一种罕见的自身免疫性疾病,会影响小脑浦肯野细胞。全球仅报告了39例病例,治疗方法和结果的记录并不一致。需要进行系统综述以确定预后因素,并扩大临床认识和治疗选择。

方法

收集抗mGluR1脑炎病例的观察性随访数据。纳入了2024年11月1日前在PubMed和谷歌学术数据库中以英文发表的所有抗mGluR1脑炎病例。对当前病例和既往报告病例的临床信息及可能的预测因素进行了统计分析。

结果

我们报告了一例用奥法妥木单抗成功治疗的抗mGluR1脑炎病例。在患者初次发病期间,一线治疗后她部分恢复。6个月后她复发,接受奥法妥木单抗治疗后完全康复。总结了包括我们的病例在内的40例抗mGluR1脑炎病例。男女患病率相似,50%的患者年龄在40 - 59岁之间。最常见的临床表现是共济失调和构音障碍。37.1%的患者脑脊液分析显示白细胞计数和IgG指数正常。几乎一半的患者(48.6%)在初次就诊或随访期间的脑部MRI扫描中显示小脑萎缩。只有25%的患者完全康复。根据最后一次随访时的改良Rankin量表(mRS)评分,预后不良的患者(n = 13,32.5%)接受一线免疫治疗的比例较低(62%,P = 0.017),随访时间较长(中位36个月,P = 0.038)。

结论

抗mGluR1脑炎的发病高峰年龄在40 - 59岁之间。超过三分之一的患者脑脊液细胞计数和IgG指数正常。因此,怀疑患有这种脑炎的患者应检测血清和脑脊液中抗mGluR1抗体的存在。值得注意的是,一线免疫治疗可能是影响临床结果的关键因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13e5/12325280/102ab17eb700/fnint-19-1580767-g001.jpg

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