Department of Biostatistics, University of Washington, Seattle, WA 98195, USA.
Am J Med Genet B Neuropsychiatr Genet. 2013 Mar;162B(2):201-12. doi: 10.1002/ajmg.b.32133. Epub 2013 Jan 25.
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.
阿尔茨海默病(AD)是一种常见的、遗传复杂的、致命的晚年神经退行性疾病。虽然有几个基因已知在早发性 AD 中起作用,但确定晚发性 AD(LOAD)的遗传基础一直具有挑战性,只有 APOE 基因被认为对 AD 风险和发病年龄都有很高的贡献。在这里,我们使用发病年龄作为感兴趣的特征,展示了对 119 个家系的完整、特征良好的华盛顿大学 LOAD 样本的首次全基因组扫描分析。所使用的分析方法允许多基因特征模型,同时适应年龄截尾、APOE 作为已知遗传协变量的影响,以及完整的家系和标记信息。结果提供了强有力的证据,表明与发病年龄相关的基因座与染色体 6q16.3 上的基因组区域以及 APOE 基因座所在的 19q13.42 区域存在连锁。APOE 与染色体 6 上的基因座之间存在相互作用的证据,与染色体 11p13、15q12-14 和 19p13.12 之间存在连锁的暗示证据。这些结果首次独立证实了染色体 6 上存在 AD 发病年龄的基因座,并表明有必要进一步努力确定潜在的因果基因座或多个基因座。