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

被引:5
|
作者
Zhao, Wei [1 ]
Marchani, Elizabeth E. [2 ]
Cheung, Charles Y. K. [1 ]
Steinbart, Ellen J. [3 ,4 ]
Schellenberg, Gerard D. [5 ]
Bird, Thomas D. [2 ,3 ,4 ]
Wijsman, Ellen M. [1 ,2 ,6 ]
机构
[1] Univ Washington, Dept Biostat, Seattle, WA 98195 USA
[2] Univ Washington, Dept Med, Div Med Genet, Seattle, WA 98195 USA
[3] Vet Affairs Puget Sound Hlth Care Syst, Geriatr Res Educ & Clin Ctr, Seattle, WA USA
[4] Univ Washington, Dept Neurol, Seattle, WA 98195 USA
[5] Univ Penn, Dept Pathol & Lab Med, Philadelphia, PA USA
[6] Univ Washington, Dept Genome Sci, Seattle, WA 98195 USA
基金
美国国家卫生研究院;
关键词
linkage analysis; MCMC; oligogenic; dementia; age-censored; NEUROTROPHIC FACTOR BDNF; MONTE-CARLO SEGREGATION; LINKAGE ANALYSIS; APOLIPOPROTEIN-E; GENETIC ASSOCIATION; MULTIPLE IMPUTATION; OF-ONSET; OLIGOGENIC SEGREGATION; IDENTIFIES VARIANTS; WIDE ASSOCIATION;
D O I
10.1002/ajmg.b.32133
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
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. (c) 2013 Wiley Periodicals, Inc.
引用
收藏
页码:201 / 212
页数:12
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