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Genome scan in familial late-onset Alzheimer’s disease: a locus on chromosome 6 contributes to age at onset

机译:基因组扫描在家庭晚期疾病的疾病中:染色体6的轨迹有助于发病时的年龄

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摘要

Alzheimer’s disease (AD) is a common, genetically complex, fatal neurodegenerative disorder of late life. Although several genes are known to play a role in early-onset AD, identification of the genetic basis of late onset AD (LOAD) has been challenging, with only the APOE gene known to have a high contribution to both AD risk and age-at-onset. Here we present the first genome-scan analysis of the complete, well-characterized University of Washington LOAD sample of 119 pedigrees, using age-at-onset as the trait of interest. The analysis approach used allows for a multilocus trait model while at the same time accommodating age censoring, effects of APOE as a known genetic covariate, and full pedigree and marker information. The results provide strong evidence for linkage of loci contributing to age-at-onset to genomic regions on chromosome 6q16.3, and to 19q13.42 in the region of the APOE locus. There was evidence for interaction between APOE and the locus on chromosome 6q and suggestive evidence for linkage to chromosomes 11p13, 15q12-14, and 19p13.12. These results provide the first independent confirmation of an AD age-at-onset locus on chromosome 6 and suggest that further efforts towards identifying the underlying causal locus or loci are warranted.
机译:阿尔茨海默氏病(AD)是一种常见的,遗传复杂且致命的晚期神经退行性疾病。尽管已知有几种基因在早发性AD中起作用,但鉴定迟发性AD(LOAD)的遗传基础一直具有挑战性,只有已知的APOE基因对AD风险和成年年龄都有很高的贡献。 -开始。在这里,我们使用开始年龄作为研究对象,对119个家谱的完整,特征明确的华盛顿大学LOAD样本进行了首次基因组扫描分析。使用的分析方法允许使用多基因座性状模型,同时适应年龄检查,作为已知遗传协变量的APOE的作用以及完整的谱系和标记信息。该结果提供了强有力的证据,证明了发病年龄的基因座与染色体6q16.3上的基因组区域以及APOE基因座区域上的19q13.42相关。有证据表明APOE和6q染色体上的基因座之间存在相互作用,并且暗示了与11p13、15q12-14和19p13.12染色体连锁的证据。这些结果首次确认了第6号染色体上AD发病年龄的基因座,并表明需要进一步努力确定潜在的病因基因座或基因座。

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