From the Department of Neurology (Y.X., L.Y., J.S., Y.Y., Y.W., H.C., H.W., T.S., F.-D.S., X.Z., D.-C.T.), China National Clinical Research Center for Neurological Diseases, Beijing Tiantan Hospital, Capital Medical University; Department of Neurology (H.M.), First Hospital of Shanxi Medical University, Taiyuan; Department of Neurology (M.F., C.-S.Y., F.-D.S.), Tianjin Neurological Institute, Tianjin Medical University General Hospital; and Department of Neurology (J.F.), The First Affiliated Hospital of Chongqing Medical University, China.
Neurol Neuroimmunol Neuroinflamm. 2024 Nov;11(6):e200309. doi: 10.1212/NXI.0000000000200309. Epub 2024 Sep 9.
To identify predictors for relapse in patients with myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) and to develop and validate a simple risk score for predicting relapse.
In China National Registry of Neuro-Inflammatory Diseases (CNRID), we identified patients with MOGAD from March 2023 and followed up prospectively to September 2023. The primary endpoint was MOGAD relapse, confirmed by an independent panel. Patients were randomly divided into model development (75%) and internal validation (25%) cohorts. Prediction models were constructed and internally validated using Andersen-Gill models. Nomogram and relapse risk score were generated based on the final prediction models.
A total of 188 patients (comprising 612 treatment episodes) were included in cohorts. Female (HR: 0.687, 95% CI 0.524-0.899, = 0.006), onset age 45 years or older (HR: 1.621, 95% CI 1.242-2.116, < 0.001), immunosuppressive therapy (HR: 0.338, 95% CI 0.239-0.479, < 0.001), oral corticosteroids >3 months (HR 0.449, 95% CI 0.326-0.620, < 0.001), and onset phenotype ( < 0.001) were identified as factors associated with MOGAD relapse. A predictive score, termed MOG-AR (Immunosuppressive therapy, oral Corticosteroids, Onset Age, Sex, Attack phenotype), derived in prediction model, demonstrated strong predictive ability for MOGAD relapse. MOG-AR score of 13-16 indicates a higher risk of relapse (HR: 3.285, 95% CI 1.473-7.327, = 0.004).
The risk of MOGAD relapse seems to be predictable. Further validation of MOG-AR score developed from this cohort to determine appropriate treatment and monitoring frequency is warranted.
CNRID, NCT05154370, registered December 13, 2021, first enrolled December 15, 2021.
识别髓鞘少突胶质细胞糖蛋白抗体相关性疾病(MOGAD)患者复发的预测因素,并建立和验证一种简单的预测复发风险的评分。
在中国神经免疫疾病注册研究(CNRID)中,我们从 2023 年 3 月开始纳入 MOGAD 患者,并前瞻性随访至 2023 年 9 月。主要终点是由独立专家组确认的 MOGAD 复发。患者被随机分为模型建立(75%)和内部验证(25%)队列。使用 Andersen-Gill 模型构建和内部验证预测模型。基于最终预测模型生成列线图和复发风险评分。
共纳入 188 例患者(包含 612 个治疗周期)进入队列。女性(HR:0.687,95%CI 0.524-0.899, = 0.006)、45 岁及以上起病年龄(HR:1.621,95%CI 1.242-2.116, < 0.001)、免疫抑制治疗(HR:0.338,95%CI 0.239-0.479, < 0.001)、口服皮质类固醇 >3 个月(HR 0.449,95%CI 0.326-0.620, < 0.001)和起病表型( < 0.001)与 MOGAD 复发相关。在预测模型中,一个预测评分,称为 MO-GAR(免疫抑制治疗、口服皮质类固醇、起病年龄、性别、发作表型),可以很好地预测 MOGAD 复发。MO-GAR 评分 13-16 预示着更高的复发风险(HR:3.285,95%CI 1.473-7.327, = 0.004)。
MOGAD 的复发风险似乎是可以预测的。需要进一步验证从该队列中开发的 MO-GAR 评分,以确定适当的治疗和监测频率。
CNRID,NCT05154370,于 2021 年 12 月 13 日注册,于 2021 年 12 月 15 日首次入组。