Department of Neurology, Beijing Tongren Hospital, Capital Medical University, Beijing, China.
Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing, China.
BMC Neurol. 2024 Aug 9;24(1):276. doi: 10.1186/s12883-024-03724-x.
Recognizing the predictors of poor short-term prognosis after first-line immunotherapy in patients with anti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis is essential for individualized treatment strategy. The objective of this study was to ascertain the factors that forecast short-term prognosis in patients with anti-NMDAR encephalitis, develop a prognostic prediction model, and authenticate its efficacy in an external validation cohort. Further, all patients were followed-up long-term to assess the factors of long-term outcome and relapses.
A prospective enrollment of patients diagnosed with anti-NMDAR encephalitis was conducted across five clinical centers in China from June 2014 to Mar 2022. The enrolled patients were divided into the derivation and validation sets based on enrollment time. The short-term prognostic model was visualized using a nomogram. Further, all patients were followed-up long-term to assess the factors of long-term outcome.
This study found that poor short-term prognosis was a risk factor for poor long-term outcome (6-month prognosis, OR 29.792, 95%CI 6.507-136.398, p < 0.001; 12-month prognosis, OR 15.756, 95%CI 3.384-73.075, p < 0.001; 24-month prognosis, OR 5.500, 95%CI 1.045-28.955, p = 0.044). Abnormal behavior or cognitive dysfunction (OR 8.57, 95%CI 1.48-49.79, p = 0.017), consciousness impairment (OR19.32, 95%CI 3.03-123.09, p = 0.002), autonomic dysfunction or central hypoventilation (OR 5.66, 95%CI 1.25-25.75, p = 0.025), CSF pleocytosis (OR 4.33, 95%CI 1.48-12.65, p = 0.007), abnormal EEG (OR 5.48, 95% CI 1.09-27.54, p = 0.039) were independent predictors for a poor short-term prognosis after first-line immunotherapy. A nomogram that incorporated those factors showed good discrimination and calibration abilities. The area under the curve (AUC) for the prognostic model were 0.866 (95%CI: 0.798-0.934) with a sensitivity of 0.761 and specificity of 0.869.
We established and validated a prognostic model that can provide individual prediction of short-term prognosis after first-line immunotherapy for patients with anti-NMDAR encephalitis. This practical prognostic model may help neurologists to predict the short-term prognosis early and potentially assist in adjusting appropriate treatment timely.
识别抗 N-甲基-D-天冬氨酸受体(抗 NMDAR)脑炎患者一线免疫治疗后短期预后不良的预测因素对于个体化治疗策略至关重要。本研究旨在确定预测抗 NMDAR 脑炎患者短期预后的因素,制定预后预测模型,并在外部验证队列中验证其疗效。此外,所有患者均进行长期随访,以评估长期结局和复发的相关因素。
本研究前瞻性纳入了 2014 年 6 月至 2022 年 3 月期间中国五家临床中心诊断为抗 NMDAR 脑炎的患者。根据入组时间将入组患者分为推导组和验证组。使用列线图可视化短期预后模型。此外,所有患者均进行长期随访,以评估长期结局的相关因素。
本研究发现,短期预后不良是长期预后不良的危险因素(6 个月预后,OR 29.792,95%CI 6.507-136.398,p<0.001;12 个月预后,OR 15.756,95%CI 3.384-73.075,p<0.001;24 个月预后,OR 5.500,95%CI 1.045-28.955,p=0.044)。异常行为或认知功能障碍(OR 8.57,95%CI 1.48-49.79,p=0.017)、意识障碍(OR 19.32,95%CI 3.03-123.09,p=0.002)、自主神经功能障碍或中枢性通气不足(OR 5.66,95%CI 1.25-25.75,p=0.025)、CSF 细胞增多(OR 4.33,95%CI 1.48-12.65,p=0.007)、异常脑电图(OR 5.48,95%CI 1.09-27.54,p=0.039)是一线免疫治疗后短期预后不良的独立预测因素。纳入这些因素的列线图显示出良好的区分度和校准能力。该预测模型的曲线下面积(AUC)为 0.866(95%CI:0.798-0.934),灵敏度为 0.761,特异性为 0.869。
我们建立并验证了一个预测模型,可以对接受抗 NMDAR 脑炎一线免疫治疗的患者的短期预后进行个体化预测。这个实用的预后模型可以帮助神经科医生早期预测短期预后,并有可能及时调整适当的治疗方案。