Department of Neurology, Nancy University Hospital, 54035, Nancy, France.
Université de Lorraine, APEMAC, 54000, Nancy, France.
J Neurol. 2024 Jan;271(1):125-133. doi: 10.1007/s00415-023-11905-w. Epub 2023 Aug 31.
Previous cohort studies evaluating the performances of the McDonald criteria suffered from bias regarding real-life conditions. We aimed to evaluate the probability of diagnosing relapsing-remitting multiple sclerosis (MS) at several timepoints from the first medical evaluation and the gain in time-to-diagnosis with the 2017 McDonald criteria compared with the 2001, 2005 and 2010 versions in real life.
Patients with a first demyelinating event suggestive of MS between 2002 and 2020 were included in the ReLSEP, an exhaustive and prospectively incremented registry of MS patients in North-Eastern France. We estimated the probability of being positive at the first medical evaluation and at five timepoints according to the four versions of criteria using Kaplan-Meier estimators and Cox models.
A total of 2220 patients were followed up for a median of 7.1 years. At baseline, 31.7%, 32.1%, 36.6% and 54.0% of patients, respectively, fulfilled the 2001, 2005, 2010 and 2017 McDonald criteria. Using the 2017 criteria, the gain in time-to-diagnosis was 3.7 months compared with the 2010 criteria. The presence of intrathecal synthesis of immunoglobulin G in the McDonald 2017 criteria led to a 1.8-month reduction in median time-to-diagnosis compared to a version of McDonald 2017 without this criteria.
In real-life, the 2017 McDonald criteria revision undoubtedly shortened time-to-diagnosis.
既往评估 McDonald 标准表现的队列研究在现实条件方面存在偏倚。我们旨在评估在现实生活中,从首次医疗评估起的多个时间点诊断复发缓解型多发性硬化症(MS)的概率,以及与 2001、2005 和 2010 版相比,2017 版 McDonald 标准在诊断时间上的获益。
我们纳入了 2002 年至 2020 年间首次出现疑似 MS 的脱髓鞘事件的患者,这些患者纳入了法国东北部详尽且前瞻性递增的 MS 患者登记处 ReLSEP。我们使用 Kaplan-Meier 估计和 Cox 模型,根据四个版本的标准,分别在首次医疗评估时以及五个时间点估计诊断为阳性的概率。
共有 2220 例患者被随访,中位随访时间为 7.1 年。基线时,分别有 31.7%、32.1%、36.6%和 54.0%的患者符合 2001、2005、2010 和 2017 年 McDonald 标准。与 2010 年标准相比,使用 2017 年标准可使诊断时间提前 3.7 个月。McDonald 2017 标准中存在鞘内免疫球蛋白 G 合成,与不包括该标准的 McDonald 2017 版本相比,可使中位诊断时间缩短 1.8 个月。
在现实生活中,2017 年 McDonald 标准修订无疑缩短了诊断时间。