Department of Neurology, Mayo Clinic, Rochester, Minnesota, USA.
Department of Neurology and Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota, USA.
J Neurol Neurosurg Psychiatry. 2022 Mar;93(3):309-315. doi: 10.1136/jnnp-2021-327302. Epub 2021 Nov 25.
To compare acute treatment responses and long-term outcome in leucine-rich glioma-inactivated 1 (LGI1) antibody encephalitis.
Retrospective case series of 118 patients with LGI1 antibody encephalitis evaluated at Mayo Clinic across all US sites from 1 May 2008 to 31 March 2019. Patient clinical data were identified and analysed through the neuroimmunology laboratory and electronic medical record. LGI1 antibody detection was by cell-based indirect immunofluorescence assay of serum, cerebrospinal fluid or both. Clinical outcomes were faciobrachial dystonic seizure (FBDS) resolution, modified Rankin Scale (mRS) score, Kokmen Short Test of Mental Status (STMS) score (0-38 point scale) and neuropsychometric testing results.
Compared with intravenous immunoglobulin (IVIg) (n=21), patients treated with single-agent acute corticosteroids (intravenous, oral or both) (n=49) were more likely to experience resolution of FBDS (61% vs 7%, p=0.002) and improvements in mRS score (ΔmRS score 2 vs 0, p=0.008) and median Kokmen STMS scores (ΔKokmen STMS score 5 points vs 0 points, p=0.01). In 54 patients with long-term follow-up (≥2 years), the median mRS score was 1 (range 0-6) and the median Kokmen STMS score was 36 (range 24-38) after all combinations of immunotherapy. Neuropsychometric testing in 32 patients with long-term follow-up (≥2 years) demonstrated short-term memory impairments in 37%.
Corticosteroids appeared more effective acutely than IVIg in improving LGI1 antibody encephalitis in this retrospective comparison of immunotherapies. While improvement with immunotherapy is typical and long-term outcome is favourable, short-term memory deficits are noted in approximately a third of the patients.
比较富亮氨酸胶质瘤失活 1 型(LGI1)抗体脑炎的急性治疗反应和长期预后。
回顾性病例系列研究,纳入 2008 年 5 月 1 日至 2019 年 3 月 31 日期间在美国梅奥诊所所有站点接受评估的 118 例 LGI1 抗体脑炎患者。通过神经免疫实验室和电子病历确定并分析患者的临床数据。LGI1 抗体检测采用血清、脑脊液或两者均有的基于细胞的间接免疫荧光分析。临床结局为面臂张力障碍性发作(FBDS)缓解、改良 Rankin 量表(mRS)评分、科克门简易精神状态检查(STMS)评分(0-38 分)和神经心理测试结果。
与静脉注射免疫球蛋白(IVIg)(n=21)相比,接受单药急性皮质类固醇(静脉、口服或两者)治疗的患者更有可能出现 FBDS 缓解(61% vs 7%,p=0.002)和 mRS 评分改善(ΔmRS 评分 2 分 vs 0 分,p=0.008)和科克门 STMS 评分中位数改善(ΔKokmen STMS 评分 5 分 vs 0 分,p=0.01)。在 54 例具有长期随访(≥2 年)的患者中,所有免疫治疗组合后,mRS 评分中位数为 1(范围 0-6),Kokmen STMS 评分中位数为 36(范围 24-38)。在 32 例具有长期随访(≥2 年)的患者中进行的神经心理测试显示,37%的患者存在短期记忆障碍。
在这项免疫治疗的回顾性比较中,皮质类固醇在改善 LGI1 抗体脑炎方面似乎比 IVIg 更有效。虽然免疫治疗的改善是典型的,长期预后是有利的,但大约三分之一的患者存在短期记忆缺陷。