Department of Neurology and Neurosciences, Hospital of the University of Pennsylvania, Perelman School of Medicine, Philadelphia, PA, USA.
Lancet Neurol. 2013 Feb;12(2):157-65. doi: 10.1016/S1474-4422(12)70310-1. Epub 2013 Jan 3.
Anti-NMDA receptor (NMDAR) encephalitis is an autoimmune disorder in which the use of immunotherapy and the long-term outcome have not been defined. We aimed to assess the presentation of the disease, the spectrum of symptoms, immunotherapies used, timing of improvement, and long-term outcome.
In this multi-institutional observational study, we tested for the presence of NMDAR antibodies in serum or CSF samples of patients with encephalitis between Jan 1, 2007, and Jan 1, 2012. All patients who tested positive for NMDAR antibodies were included in the study; patients were assessed at symptom onset and at months 4, 8, 12, 18, and 24, by use of the modified Rankin scale (mRS). Treatment included first-line immunotherapy (steroids, intravenous immunoglobulin, plasmapheresis), second-line immunotherapy (rituximab, cyclophosphamide), and tumour removal. Predictors of outcome were determined at the Universities of Pennsylvania (PA, USA) and Barcelona (Spain) by use of a generalised linear mixed model with binary distribution.
We enrolled 577 patients (median age 21 years, range 8 months to 85 years), 211 of whom were children (<18 years). Treatment effects and outcome were assessable in 501 (median follow-up 24 months, range 4-186): 472 (94%) underwent first-line immunotherapy or tumour removal, resulting in improvement within 4 weeks in 251 (53%). Of 221 patients who did not improve with first-line treatment, 125 (57%) received second-line immunotherapy that resulted in a better outcome (mRS 0-2) than those who did not (odds ratio [OR] 2·69, CI 1·24-5·80; p=0·012). During the first 24 months, 394 of 501 patients achieved a good outcome (mRS 0-2; median 6 months, IQR 2-12) and 30 died. At 24 months' follow-up, 203 (81%) of 252 patients had good outcome. Outcomes continued to improve for up to 18 months after symptom onset. Predictors of good outcome were early treatment (0·62, 0·50-0·76; p<0·0001) and no admission to an intensive care unit (0·12, 0·06-0·22; p<0·0001). 45 patients had one or multiple relapses (representing a 12% risk within 2 years); 46 (67%) of 69 relapses were less severe than initial episodes (p<0·0001). In 177 children, predictors of good outcome and the magnitude of effect of second-line immunotherapy were similar to those of the entire cohort.
Most patients with anti-NMDAR encephalitis respond to immunotherapy. Second-line immunotherapy is usually effective when first-line treatments fail. In this cohort, the recovery of some patients took up to 18 months.
The Dutch Cancer Society, the National Institutes of Health, the McKnight Neuroscience of Brain Disorders award, The Fondo de Investigaciones Sanitarias, and Fundació la Marató de TV3.
抗 N- 甲基-D- 天冬氨酸受体(NMDAR)脑炎是一种自身免疫性疾病,其免疫治疗的使用和长期预后尚未明确。我们旨在评估该疾病的表现、症状谱、使用的免疫疗法、改善的时间和长期预后。
在这项多机构观察性研究中,我们在 2007 年 1 月 1 日至 2012 年 1 月 1 日期间检测了血清或脑脊液中存在 NMDAR 抗体的脑炎患者。所有 NMDAR 抗体检测阳性的患者均纳入研究;使用改良 Rankin 量表(mRS)在症状出现时和第 4、8、12、18 和 24 个月进行评估。治疗包括一线免疫疗法(类固醇、静脉注射免疫球蛋白、血浆置换)、二线免疫疗法(利妥昔单抗、环磷酰胺)和肿瘤切除。在宾夕法尼亚大学(美国宾夕法尼亚州)和巴塞罗那大学(西班牙巴塞罗那),通过使用二项分布的广义线性混合模型来确定预后的预测因素。
我们纳入了 577 名患者(中位年龄 21 岁,范围 8 个月至 85 岁),其中 211 名为儿童(<18 岁)。501 名(中位随访 24 个月,范围 4-186)可评估治疗效果和预后:472 名(94%)接受了一线免疫治疗或肿瘤切除,其中 251 名(53%)在 4 周内得到改善。在 221 名未接受一线治疗改善的患者中,125 名(57%)接受了二线免疫治疗,其预后(mRS 0-2)优于未接受二线治疗的患者(比值比[OR] 2.69,95%CI 1.24-5.80;p=0.012)。在最初的 24 个月内,501 名患者中有 394 名(mRS 0-2;中位数 6 个月,IQR 2-12)获得了良好的结局,30 名患者死亡。在 24 个月的随访中,252 名患者中有 203 名(81%)有良好的结局。症状出现后长达 18 个月,预后仍在持续改善。良好预后的预测因素是早期治疗(0.62,0.50-0.76;p<0.0001)和未入住重症监护病房(0.12,0.06-0.22;p<0.0001)。45 名患者有一次或多次复发(2 年内的风险为 12%);69 次复发中的 46 次(67%)比初次发作轻(p<0.0001)。在 177 名儿童中,良好预后的预测因素和二线免疫治疗的影响程度与整个队列相似。
大多数抗 NMDAR 脑炎患者对免疫治疗有反应。一线治疗失败时,二线免疫治疗通常有效。在本队列中,一些患者的恢复需要长达 18 个月。
荷兰癌症协会、美国国立卫生研究院、麦克奈特神经科学脑疾病奖、西班牙卫生研究基金会和 TV3 马拉松基金会。