Neurology. 2024 Oct 8;103(7_Supplement_1):S83-S84. doi: 10.1212/01.wnl.0001051560.74390.09.
To characterize the long-term outcomes of patients with "possible only" or "probable" autoimmune encephalitis (AE).
Despite comprising one-third of AE cases, antibody-negative cases lacking typical AE-defining features are understudied.
DESIGN/METHODS: We conducted a retrospective analysis of adult patients evaluated at a tertiary center neuroimmunology practice from 2006 to 2020, meeting diagnostic criteria for "possible only" or "probable but antibody-negative" AE, with at least one year of follow-up. All patients underwent neural antibody testing.
Forty-five patients (median age, 61 years [range, 20-88]; female, 21 [47%]) were included, with a median follow-up of 36 months (range, 12-174). A change in diagnosis was noted in six additional patients, who were excluded from further analysis, with only two receiving a non-autoimmune diagnosis during follow-up. The majority (41/45 [91%]) presented with significant disability (modified Rankin Scale [mRS] ≥3) at baseline. CSF was inflammatory in 20/44 (45%) and MRI was abnormal in 21/45 (47%). Unclassified neural-specific IgG staining on tissue-based assay was detected in five (11%). Two cases (4%) had a paraneoplastic cause. The median time from onset to immunotherapy initiation was two months (range, 0-21), resulting in at least partial improvement in all 44 (98%) treated cases. Clinical relapses occurred in 14/45 (31%). At last follow-up, the most common symptoms were memory dysfunction (31/45 [69%]), attention deficits (17/45 [38%]), gait instability (13/45 [29%]), and visuospatial dysfunction (10/45 [22%]). Most patients achieved independence (median mRS, 2 [range, 0-6]); however, 11 patients had poor neurological outcome (mRS ≥3). Higher mRS score and gait assistance requirement at three months were predictive of poor outcome (P ≤0.01).
Despite significant disability at initial stages, patients with antibody-negative but clinically presumed AE show potential for improvement with immunotherapy, highlighting the importance of early intervention. Early functional status and gait assistance requirements may assist in predicting long-term prognosis.
描述“可能仅有”或“可能但抗体阴性”自身免疫性脑炎(AE)患者的长期预后。
尽管抗体阴性病例缺乏典型的 AE 定义特征,但占 AE 病例的三分之一,此类病例研究较少。
设计/方法:我们对 2006 年至 2020 年在一家三级神经免疫中心接受评估的成年患者进行了回顾性分析,这些患者符合“可能仅有”或“可能但抗体阴性”AE 的诊断标准,且至少有一年的随访。所有患者均接受神经抗体检测。
共纳入 45 例患者(中位年龄 61 岁[范围 20-88];女性 21 例[47%]),中位随访时间为 36 个月(范围 12-174)。另外 6 例患者的诊断发生变化,这些患者被排除在进一步分析之外,仅有 2 例在随访期间被诊断为非自身免疫性疾病。大多数(41/45[91%])患者在基线时存在显著的残疾(改良 Rankin 量表[mRS]≥3)。20/44(45%)例患者的脑脊液呈炎症性,21/45(47%)例患者的 MRI 异常。组织检测中发现 5 例(11%)存在未分类的神经特异性 IgG 染色。2 例(4%)患者存在副肿瘤性病因。从发病到免疫治疗开始的中位时间为 2 个月(范围 0-21),所有 44 例(98%)接受治疗的患者均至少部分改善。14/45(31%)例患者出现临床复发。末次随访时,最常见的症状是记忆功能障碍(31/45[69%])、注意力缺陷(17/45[38%])、步态不稳(13/45[29%])和视空间功能障碍(10/45[22%])。大多数患者达到独立状态(中位 mRS 为 2[范围 0-6]),但 11 例患者的神经功能预后较差(mRS≥3)。3 个月时的 mRS 评分较高和需要步态辅助是预后不良的预测因素(P≤0.01)。
尽管在初始阶段存在显著的残疾,但具有临床推定的抗体阴性但可能患有 AE 的患者经免疫治疗后具有改善的潜力,这凸显了早期干预的重要性。早期的功能状态和步态辅助需求可能有助于预测长期预后。