Rate of familial amyotrophic lateral sclerosis: a systematic review and meta-analysis

肌萎缩侧索硬化 荟萃分析 人口 医学 前瞻性队列研究 入射(几何) 系统回顾 人口学 梅德林 内科学 疾病 生物 环境卫生 光学 物理 社会学 生物化学
作者
Susan Byrne,Cathal Walsh,Conor C. Lynch,Peter Bede,Marwa Elamin,Kevin P. Kenna,Russell L. McLaughlin,Orla Hardiman
出处
期刊:Journal of Neurology, Neurosurgery, and Psychiatry [BMJ]
卷期号:82 (6): 623-627 被引量:333
标识
DOI:10.1136/jnnp.2010.224501
摘要

Background

The population rate of familial amyotrophic lateral sclerosis (FALS) is frequently reported as 10%. However, a systematic review and meta-analysis of the true population based frequency of FALS has never been performed.

Method

A Medline literature review identified all original articles reporting a rate of FALS. Studies were grouped according to the type of data presented and examined for sources of case ascertainment. A systematic review and meta-analysis of reported rates of FALS was then conducted to facilitate comparison between studies and calculate a pooled rate of FALS.

Results

38 papers reported a rate of FALS. Thirty-three papers were included in analysis and the rate of FALS for all studies was 4.6% (95% CI 3.9% to 5.5%). Restricting the analysis to prospective population based registry data revealed a rate of 5.1% (95% CI 4.1% to 6.1%). The incidence of FALS was lower in southern Europe. There was no correlation between rate of FALS and reported SOD1 mutation rates.

Conclusion

The rate of FALS among prospective population based registries is 5.1% (CI 4.1 to 6.1%), and not 10% as is often stated. Further detailed prospective population based studies of familial ALS are required to confirm this rate.

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