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多发性硬化在时间和空间上——病因的地理线索

Multiple sclerosis in time and space--geographic clues to cause.

作者信息

Kurtzke J F

机构信息

Neuroepidemiology Section, Veterans Affairs Medical Center, Washington DC, USA.

出版信息

J Neurovirol. 2000 May;6 Suppl 2:S134-40.

Abstract

Geographically MS describes three frequency zones. High frequency areas (prevalence 30+ per 100 000) now comprise most of Europe, Israel, Canada, northern US, southeastern Australia, New Zealand, and easternmost Russia. Medium frequency areas include southern US, most of Australia, South Africa, the southern Mediterranean basin, Russia into Siberia, the Ukraine and parts of Latin America. Prevalence rates under 5 per 100 000 are found in the rest of Asia, Africa and northern South America. Migrants from high to lower risk areas retain the MS risk of their birth place only if they are at least age 15 at migration. Those from low to high increase their risk even beyond that of the natives, with susceptibility extending from about age 11 to 45. Thus MS is ordinarily acquired in early adolescence with a lengthy latency before symptom onset. MS occurred in epidemic form in North Atlantic islands: probably in Iceland and the Shetland-Orkneys; clearly in the Faroe Islands. In the Faroes first symptom onset was in 1943, heralding the first of four successive epidemics at 13 year intervals. The disease was presumably introduced by occupying British troops during World War II, with the postwar occurrences representing later transmissions to and from consecutive cohorts of Faroese. What was transmitted is thought to be a specific, widespread, persistent infection called PMSA (the primary multiple sclerosis affection) which only rarely leads years later to clinical MS. Search for PMSA is best attempted on the Faroes where there are regions still free of MS after 50 years.

摘要

从地理分布来看,多发性硬化症呈现出三个发病频率区域。高频区域(每10万人中患病率达30及以上)如今涵盖了欧洲大部分地区、以色列、加拿大、美国北部、澳大利亚东南部、新西兰以及俄罗斯最东部地区。中频区域包括美国南部、澳大利亚大部分地区、南非、地中海盆地南部、俄罗斯直至西伯利亚、乌克兰以及拉丁美洲部分地区。在亚洲其他地区、非洲以及南美洲北部,每10万人中患病率低于5。从高风险区域迁移至低风险区域的移民,只有在15岁及以上移民时才会保留其出生地患多发性硬化症的风险。从低风险区域迁移至高风险区域的移民,其患病风险甚至会超过当地居民,易感性从11岁左右持续至45岁左右。因此,多发性硬化症通常在青春期早期感染,在症状出现前有很长的潜伏期。多发性硬化症曾在北大西洋岛屿呈流行形式出现:可能在冰岛以及设得兰群岛 - 奥克尼群岛;在法罗群岛则很明显。在法罗群岛,首例症状出现在1943年,随后每隔13年出现一次连续四次的流行疫情。据推测,这种疾病是在第二次世界大战期间由占领该地的英国军队传入的,战后的病例代表了法罗群岛连续几代人之间的后续传播。据认为传播的是一种特定的、广泛存在且持续的感染,称为PMSA(原发性多发性硬化症感染源),这种感染很少在数年之后导致临床多发性硬化症。在法罗群岛进行寻找PMSA的研究最为适宜,那里有一些地区在50年后仍未出现多发性硬化症病例。

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