一组迟发性多发性硬化症患者的治疗反应
Response to therapy in a cohort of patients with late-onset multiple sclerosis.
作者信息
Ahmad Sophie, Graham Edith L, Lancki Nicola, Caldito Natalia Gonzalez, Perez-Giraldo Gina, Cohen Bruce A
机构信息
Kirk Kerkorian School of Medicine at UNLV, Las Vegas, NV, USA.
Department of Neurology, Multiple Sclerosis and Neuroimmunology, Northwestern University, Chicago, IL, USA.
出版信息
Mult Scler J Exp Transl Clin. 2025 Jul 29;11(3):20552173251360357. doi: 10.1177/20552173251360357. eCollection 2025 Jul-Sep.
BACKGROUND AND OBJECTIVES
Late-onset MS (LOMS, symptom onset after age 50) remains underrepresented in clinical trials, leading to a gap in knowledge about the efficacy of disease-modifying therapies (DMTs). This study aims to evaluate treatment outcomes in relapsing LOMS.
METHODS
A retrospective electronic medical record study at Northwestern University analyzed patients with LOMS presenting between 2004 and 2021. Demographic, clinical, DMT, and MRI data were extracted. Statistical analyses evaluated progression based on DMT efficacy.
RESULTS
Overall, 63 patients (63% female, 76% white, median onset 55 years) were followed for a median of 7.6 years. Most patients (73%) were started on low/moderate efficacy DMTs (LET/MET). Increasing baseline EDSS was associated with an increased risk of reaching EDSS 6 ( < .001), but increasing age at diagnosis/treatment was not associated with increasing disability attainment ( = .527). Patients on LET/MET had no difference in progression to EDSS 6.0 compared to no DMT ( = .354) or change in Age-Related Multiple Sclerosis Severity Score (ARMSS) from the start of treatment/diagnosis to last follow-up ( = .477).
DISCUSSION
The effect of LET/MET DMTs is less pronounced in older adults and may not significantly impact long-term disability outcomes.
背景与目的
迟发性多发性硬化症(LOMS,症状在50岁之后出现)在临床试验中的代表性仍然不足,导致在疾病修正疗法(DMTs)疗效方面存在知识空白。本研究旨在评估复发型LOMS的治疗结果。
方法
西北大学的一项回顾性电子病历研究分析了2004年至2021年间出现症状的LOMS患者。提取了人口统计学、临床、DMT和MRI数据。基于DMT疗效进行的统计分析评估了疾病进展情况。
结果
总体而言,63例患者(63%为女性,76%为白人,中位发病年龄55岁)接受了中位时间为7.6年的随访。大多数患者(73%)开始使用低/中效DMTs(LET/MET)。基线扩展残疾状态量表(EDSS)升高与达到EDSS 6的风险增加相关(P<0.001),但诊断/治疗时年龄增加与残疾程度增加无关(P=0.527)。与未使用DMT的患者相比,使用LET/MET的患者进展至EDSS 6.0的情况无差异(P=0.354),从治疗/诊断开始到最后一次随访的年龄相关多发性硬化严重程度评分(ARMSS)变化也无差异(P=0.4
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