Cree Bruce A C, Gourraud Pierre-Antoine, Oksenberg Jorge R, Bevan Carolyn, Crabtree-Hartman Elizabeth, Gelfand Jeffrey M, Goodin Douglas S, Graves Jennifer, Green Ari J, Mowry Ellen, Okuda Darin T, Pelletier Daniel, von Büdingen H-Christian, Zamvil Scott S, Agrawal Alisha, Caillier Stacy, Ciocca Caroline, Gomez Refujia, Kanner Rachel, Lincoln Robin, Lizee Antoine, Qualley Pamela, Santaniello Adam, Suleiman Leena, Bucci Monica, Panara Valentina, Papinutto Nico, Stern William A, Zhu Alyssa H, Cutter Gary R, Baranzini Sergio, Henry Roland G, Hauser Stephen L
Department of Neurology, University of California, San Francisco, San Francisco, CA.
Department of Neurology, University of Texas Southwestern Medical Center, Dallas, TX.
Ann Neurol. 2016 Oct;80(4):499-510. doi: 10.1002/ana.24747. Epub 2016 Aug 13.
To characterize the accrual of long-term disability in a cohort of actively treated multiple sclerosis (MS) patients and to assess whether clinical and magnetic resonance imaging (MRI) data used in clinical trials have long-term prognostic value.
This is a prospective study of 517 actively managed MS patients enrolled at a single center.
More than 91% of patients were retained, with data ascertained up to 10 years after the baseline visit. At this last assessment, neurologic disability as measured by the Expanded Disability Status Scale (EDSS) was stable or improved compared to baseline in 41% of patients. Subjects with no evidence of disease activity (NEDA) by clinical and MRI criteria during the first 2 years had long-term outcomes that were no different from those of the cohort as a whole. 25-OH vitamin D serum levels were inversely associated with short-term MS disease activity; however, these levels had no association with long-term disability. At a median time of 16.8 years after disease onset, 10.7% (95% confidence interval [CI] = 7.2-14%) of patients reached an EDSS ≥ 6, and 18.1% (95% CI = 13.5-22.5%) evolved from relapsing MS to secondary progressive MS (SPMS).
Rates of worsening and evolution to SPMS were substantially lower when compared to earlier natural history studies. Notably, the NEDA 2-year endpoint was not a predictor of long-term stability. Finally, the data call into question the utility of annual MRI assessments as a treat-to-target approach for MS care. Ann Neurol 2016;80:499-510.
描述一组接受积极治疗的多发性硬化症(MS)患者长期残疾的累积情况,并评估临床试验中使用的临床和磁共振成像(MRI)数据是否具有长期预后价值。
这是一项对在单一中心登记的517例接受积极管理的MS患者进行的前瞻性研究。
超过91%的患者被随访,在基线访视后长达10年的数据得以确定。在最后一次评估时,41%的患者根据扩展残疾状态量表(EDSS)测量的神经功能残疾与基线相比保持稳定或有所改善。在前两年中根据临床和MRI标准无疾病活动证据(NEDA)的受试者,其长期预后与整个队列无异。25-羟基维生素D血清水平与MS短期疾病活动呈负相关;然而,这些水平与长期残疾无关。在疾病发作后的中位时间16.8年时,10.7%(95%置信区间[CI]=7.2-14%)的患者EDSS≥6,18.1%(95%CI=13.5-22.5%)从复发型MS转变为继发进展型MS(SPMS)。
与早期自然史研究相比,病情恶化和转变为SPMS的发生率显著降低。值得注意的是,NEDA 2年终点并非长期稳定性的预测指标。最后,这些数据对每年进行MRI评估作为MS治疗达标方法的实用性提出了质疑。《神经病学纪事》2016年;80:499-510。