An estimate of amyotrophic lateral sclerosis heritability using twin data

被引:219
作者
Al-Chalabi, A. [1 ]
Fang, F. [2 ]
Hanby, M. F. [1 ]
Leigh, P. N. [1 ]
Shaw, C. E. [1 ]
Ye, W. [2 ]
Rijsdijk, F. [3 ]
机构
[1] Kings Coll London, Inst Psychiat, MRC Ctr Neurodegenerat Res, London SE5 8AF, England
[2] Karolinska Inst, Dept Med Epidemiol & Biostat, Stockholm, Sweden
[3] Kings Coll London, NIHR Biomed Res Ctr Mental Hlth, MRC Ctr Social Genet & Dev Psychiat, London SE5 8AF, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
PATH-ANALYSIS; MUTATIONS; EPIDEMIOLOGY; ALS; PROTEIN; ONSET; GENE;
D O I
10.1136/jnnp.2010.207464
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background Causative gene mutations have been identified in about 2% of those with amyotrophic lateral sclerosis (ALS), often, but not always, when there is a strong family history. There is an assumption that there is a genetic component to all ALS, but genome-wide association studies have yet to produce a robustly replicated result. A definitive estimate of ALS heritability is therefore required to determine whether ongoing efforts to find susceptibility genes are worth while. Methods The authors performed two twin studies, one population-and one clinic-based. The authors used structural equation modelling to perform a meta-analysis of data from these studies and an existing twin study to estimate ALS heritability, and identified 171 twin pairs in which at least one twin had ALS. Results and discussion Five monozygotic twin pairs were concordant-affected, and 44 discordant-affected. No dizygotic twin pairs were concordant-affected, and 122 discordant-affected. The heritability of sporadic ALS was estimated as 0.61 (0.38 to 0.78) with the unshared environmental component 0.39 (0.22 to 0.62). ALS has a high heritability, and efforts to find causative genes should continue.
引用
收藏
页码:1324 / 1326
页数:3
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