Bafrani Melika Arab, Asadigandomani Hassan, Kasbi Naghmeh Abbasi, Heidari Hora, Eskandarieh Sharareh
Multiple Sclerosis Research Center, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran.
Neurol Sci. 2025 Jan;46(1):351-364. doi: 10.1007/s10072-024-07746-8. Epub 2024 Sep 4.
Multiple sclerosis (MS) is a chronic, disabling neurodegenerative disease, leads to reduced quality of life. The increasing prevalence of MS around the world and its comorbidities increase its burden. Primary vasculitis subtypes, one of autoimmune diseases with different prevalence in different ages and genders, should be considered one of the important differential diagnosis in patients with MS. This study aims to verify the relationship between MS and primary vasculitis by conducting a systematic review.
We searched PubMed, Scopus, EMBASE, Web of Science, and Google Scholar, from January 1974 to July 2023. We included original articles that reported characteristics of patients involved with any type of Primary Vasculitis with MS.
From an initial 816 publications, 18 studies consisting of 18 individual patients from 14 countries with confirmed MS and one of different subtypes of primary vasculitis met the inclusion criteria. The female/male ratio was 0.38:1, the mean (SD) age was 40.44 (14.37) years with the range of 16 to 70 years old, and the relapsing/progressive ratio was 1.57:1. Most of them, 14 (77%) experienced MS before vasculitis, and mostly received Corticosteroids, interferon, cyclophosphamide, Glatiramer acetate as MS treatment. The concurrence of Takayasu Arteritis (2 cases), Polyarteritis Nodosa (2 cases), Churg-Strauss Syndrome (1 case), Wegener's Granulomatosis (2 cases), Microscopic Polyangiitis (1 case), Cutaneous leukocytoclastic vasculitis (5 cases), Good pasture's disease (5 cases) were reported with MS.
Our study suggested that different primary vasculitis can be an important comorbidity of MS and can mimic its symptoms and MRI. Any atypical syndrome for PwMS, whether clinical or radiological, must be evaluated in terms of other differential diagnoses including vasculitis.
多发性硬化症(MS)是一种慢性致残性神经退行性疾病,会导致生活质量下降。全球范围内MS患病率的上升及其合并症增加了其负担。原发性血管炎亚型是一种在不同年龄和性别中患病率不同的自身免疫性疾病,应被视为MS患者重要的鉴别诊断之一。本研究旨在通过系统评价来验证MS与原发性血管炎之间的关系。
我们检索了1974年1月至2023年7月期间的PubMed、Scopus、EMBASE、Web of Science和谷歌学术。我们纳入了报告患有任何类型原发性血管炎合并MS患者特征的原创文章。
从最初的816篇出版物中,18项研究(包括来自14个国家的18例确诊MS患者以及一种不同亚型的原发性血管炎)符合纳入标准。女性/男性比例为0.38:1,平均(标准差)年龄为40.44(14.37)岁,年龄范围为16至70岁,复发/进展比例为1.57:1。其中大多数(14例,77%)在血管炎之前就患有MS,并且大多接受了皮质类固醇、干扰素、环磷酰胺、醋酸格拉替雷作为MS治疗。报告了与MS并发的高安动脉炎(2例)、结节性多动脉炎(2例)、变应性肉芽肿性血管炎(1例)、韦格纳肉芽肿(2例)、显微镜下多血管炎(1例)、皮肤白细胞破碎性血管炎(5例)、肺出血肾炎综合征(5例)。
我们的研究表明,不同的原发性血管炎可能是MS的重要合并症,并且可以模仿其症状和MRI表现。对于MS患者的任何非典型综合征,无论是临床还是放射学方面,都必须从包括血管炎在内的其他鉴别诊断角度进行评估。