Ben-Shlomo Y, Wenning G K, Tison F, Quinn N P
Department of Social Medicine, Bristol University, UK.
Neurology. 1997 Feb;48(2):384-93. doi: 10.1212/wnl.48.2.384.
A systematic review of the neurologic literature identified 433 cases of pathologically proven multiple system atrophy over a 100-year period. Earlier case reports included patients younger in age with more frequent cerebellar involvement. Mean age of onset was 54.2 years (range 31 to 78) and survival was 6.2 years (range 0.5 to 24). Survival analysis showed a secular trend from a median duration of 4.9 years for publications between 1887 and 1970 to 6.8 years between 1991 and 1994. Older age of onset was associated with shorter survival; the hazard ratio for patients with onset after 60 years was 1.8 (95% CI 1.4 to 2.3) compared with patients between 31 and 49 years. Cerebellar features were associated with marginally increased survival (6.1 years versus 5.4 years; p = 0.04). There were no difference in survival according to gender, parkinsonian, or pyramidal features or whether the patient was classified as striatonigral degeneration or olivopontocerebellar atrophy type. These results demonstrate the poor prognosis for patients with multiple system atrophy but may be biased toward the worst cases. Future research needs to recruit more representative samples.
一项对神经学文献的系统综述在100年期间确定了433例经病理证实的多系统萎缩病例。早期的病例报告包括年龄较小、小脑受累更频繁的患者。平均发病年龄为54.2岁(范围31至78岁),生存期为6.2年(范围0.5至24年)。生存分析显示出一种长期趋势,即1887年至1970年期间发表的文献中生存期的中位数为4.9年,而1991年至1994年期间为6.8年。发病年龄较大与生存期较短相关;60岁以后发病的患者与31至49岁的患者相比,风险比为1.8(95%置信区间1.4至2.3)。小脑特征与生存期略有增加相关(6.1年对5.4年;p = 0.04)。根据性别、帕金森样或锥体束征特征,或者患者被归类为纹状体黑质变性或橄榄脑桥小脑萎缩型,生存期没有差异。这些结果表明多系统萎缩患者预后较差,但可能偏向于最严重的病例。未来的研究需要招募更具代表性的样本。