Department of Neurology, Medical University of Innsbruck, Anichstrasse 35, 6020, Innsbruck, Austria.
Department of Medical Statistics, Informatics and Health Economics, Medical University Innsbruck, Innsbruck, Austria.
J Neurol. 2024 Feb;271(2):674-687. doi: 10.1007/s00415-023-12041-1. Epub 2023 Oct 19.
There is a lack of knowledge of disease course, prognosis, comorbidities and potential treatments of elderly MS patients.
To characterize the disease course including disability progression and relapses, to quantify the use of DMTs and to identify comorbidities and risk factors for progression in elderly multiple sclerosis (MS) patients.
This is a retrospective study of 1200 Austrian MS patients older than 55 years as of May 1st, 2017 representing roughly one-third of all the MS patients of this age in Austria. Data were collected from 15 MS centers including demographics, first symptom at onset, number of relapses, evolvement of disability, medication, and comorbidities.
Median observation time was 17.1 years with 957 (80%) relapsing and 243 (20%) progressive onsets. Average age at diagnosis was 45 years with a female predominance of 71%. Three-hundred and twenty-six (27%) patients were never treated with a DMT, while most treated patients received interferons (496; 41%) at some point. At last follow-up, 420 (35%) patients were still treated with a DMT. No difference was found between treated and never-treated patients in terms of clinical outcome; however, patients with worse disability progression had significantly more DMT switches. Pyramidal onset, number of comorbidities, dementia, epilepsy, and psychiatric conditions as well as a higher number of relapses were associated with worse outcome. The risk of reaching EDSS 6 rose with every additional comorbidity by 22%. In late and very-late-onset MS (LOMS, VLOMS) time to diagnosis took nearly twice the time compared to adult and early onset (AEOMS). The overall annualized relapse rate (ARR) decreased over time and patients with AEOMS had significantly higher ARR compared to LOMS and VLOMS. Four percent of MS patients had five medications or more fulfilling criteria of polypharmacy and 20% of psychiatric drugs were administered without a matching diagnosis.
In this study, we identified number of comorbidities, pyramidal and cerebellar signs, and a higher number of relapses as unfavorable prognostic factors in elderly MS patients filling gaps of knowledge in patients usually underrepresented in clinical trials and may guide future therapeutic studies.
老年人多发性硬化症(MS)患者对疾病进程、预后、合并症和潜在治疗方法的了解有限。
描述疾病进程,包括残疾进展和复发,量化疾病修正治疗(DMT)的使用情况,并确定老年多发性硬化症患者的进展相关合并症和风险因素。
这是一项回顾性研究,纳入了 1200 名 2017 年 5 月 1 日年龄在 55 岁以上的奥地利多发性硬化症患者,占奥地利该年龄段所有多发性硬化症患者的约三分之一。数据来自 15 个多发性硬化症中心,包括人口统计学资料、首发症状、复发次数、残疾演变、药物治疗和合并症。
中位观察时间为 17.1 年,957 名(80%)患者为复发型,243 名(20%)为进展型。诊断时的平均年龄为 45 岁,女性占 71%。326 名(27%)患者从未接受过疾病修正治疗,而大多数接受过治疗的患者在某个阶段接受过干扰素治疗(496 名;41%)。在最后一次随访时,420 名(35%)患者仍在接受疾病修正治疗。在临床结局方面,治疗组和未治疗组之间无差异;然而,残疾进展更严重的患者疾病修正治疗转换次数明显更多。锥体束征、合并症数量、痴呆、癫痫和精神疾病以及更多的复发与更差的结局相关。每增加一种合并症,达到扩展残疾状况量表(EDSS)6 分的风险增加 22%。在晚发性和极晚发性多发性硬化症(LOMS、VLOMS)中,诊断所需的时间几乎是成人和早发性多发性硬化症(AEOMS)的两倍。总的年复发率(ARR)随时间推移而降低,AEOMS 患者的 ARR 显著高于 LOMS 和 VLOMS。4%的多发性硬化症患者接受了五种或更多药物治疗,符合药物治疗过多的标准,20%的精神药物在没有匹配诊断的情况下使用。
在这项研究中,我们确定了合并症数量、锥体束和小脑征以及更多的复发是老年多发性硬化症患者的不利预后因素,填补了临床试验中通常代表性不足的患者的知识空白,可能为未来的治疗研究提供指导。