Yamout B, Barada W, Tohme R A, Mehio-Sibai A, Khalifeh R, El-Hajj T
Department of Internal Medicine, Faculty of Medicine, American University of Beirut Medical Center, Lebanon.
J Neurol Sci. 2008 Jul 15;270(1-2):88-93. doi: 10.1016/j.jns.2008.02.009. Epub 2008 Mar 25.
The epidemiologic, clinical, radiological and laboratory characterization of multiple sclerosis (MS) is very well documented in Caucasian and Japanese populations, but very little is known about MS in the Arab world. Such knowledge is becoming of paramount importance, with the recent advances in therapies, MRI techniques and other diagnostic procedures. We report a cohort of Lebanese MS patients, including details of their clinical and laboratory characteristics. The medical records of 202 patients fulfilling the Mc Donald's diagnostic criteria, and followed in our tertiary care center were reviewed. This cohort is highly representative of the disease in Lebanon where the number of MS patients is estimated to be between 1200 and 1700. The peak age of onset of MS in our cohort was in the third decade with 62.4% of patients developing their first symptoms between 20 and 39 years. The female/male ratio was 1.8/1.0. A positive family history for MS was present in 5% of patients. The most frequent presenting symptoms were brainstem-cerebellar (46.2%) followed by sensory (42.5%), motor (33.9%) and visual (29.6%). Of the total number of patients, 85.1% had relapsing remitting MS at onset, and 7.9% primary progressive MS. Benign MS defined as EDSS<=2.0 after 10 years from onset was present in 20% of patients. The mean time from onset to secondary progressive MS was around 9 years. Visual, brainstem, and somatosensory evoked potentials were abnormal in 65.6%, 27.8%, and 50.7% of patients tested respectively. Cerebrospinal fluid showed pleocytosis in 32.6%, increased IgG synthesis in 45.2%, positive oligoclonal bands in 40%, and elevated protein in 34% of patients tested. Although some of the clinical characteristics of our MS population were different compared to western series, the natural history of the disease was similar.
多发性硬化症(MS)的流行病学、临床、放射学和实验室特征在白种人和日本人群中有详尽记录,但在阿拉伯世界对MS却知之甚少。随着近期治疗方法、MRI技术及其他诊断程序的进展,此类知识变得至关重要。我们报告了一组黎巴嫩MS患者,包括其临床和实验室特征的详细情况。回顾了在我们三级医疗中心就诊的202例符合麦克唐纳诊断标准的患者的病历。该队列高度代表了黎巴嫩的这种疾病,据估计黎巴嫩MS患者数量在1200至1700人之间。我们队列中MS发病的高峰年龄在第三个十年,62.4%的患者在20至39岁之间出现首发症状。女性/男性比例为1.8/1.0。5%的患者有MS的阳性家族史。最常见的首发症状是脑干 - 小脑症状(46.2%),其次是感觉症状(42.5%)、运动症状(33.9%)和视觉症状(29.6%)。在所有患者中,85.1%在发病时为复发缓解型MS,7.9%为原发进展型MS。定义为发病10年后扩展残疾状态量表(EDSS)<=2.0的良性MS在20%的患者中出现。从发病到继发进展型MS的平均时间约为9年。分别有65.6%、27.8%和50.7%接受测试的患者视觉、脑干和体感诱发电位异常。脑脊液检查显示,32.6%的患者有细胞数增多,45.2%的患者有IgG合成增加,40%的患者有寡克隆带阳性,34%接受测试的患者有蛋白升高。尽管我们的MS人群的一些临床特征与西方系列不同,但该疾病的自然史相似。