Analyses of the National Institute on Aging Late-Onset Alzheimer's Disease Family Study Implication of Additional Loci

作者：Lee Joseph H; Cheng Rong; Graff Radford Neill; Foroud Tatiana; Mayeux Richard^*

来源：Archives of Neurology, 2008, 65(11): 1518-1526.

DOI：10.1001/archneur.65.11.1518

Objective: To identify putative genetic loci related to the risk of late-onset Alzheimer disease (LOAD).
Design: Linkage analysis and family-based and case-control association analyses from a genomewide scan using approximately 6000 single-nucleotide polymorphic markers at an average intermarker distance of 0.65 cM.
Setting: The National Institute on Aging Genetics Initiative for Late-Onset Alzheimer's Disease (NIA-LOAD) was created to expand the resources for studies to identify additional genes contributing to the risk for LOAD.
Participants: We investigated 1902 individuals from 328 families with LOAD and 236 unrelated control subjects.
Main Outcome Measures: Clinical diagnosis of LOAD.
Results: The strongest overall finding was at chromosome 19q13.32, confirming the effect of the apolipoprotein E gene on LOAD risk in the family-based and case-control analyses. However, single-nucleotide polymorphisms at the following loci were also statistically significant in 1 or more of the analyses performed: 7p22.2, 7p21.3, and 16q21 in the linkage analyses; 17q21.31 and 22q11.21 in the family-based association analysis; and 7q31.1 and 22q12.3 in the case-control analysis. Positive associations at 7q31.1 and 20q13.33 were also significant in the meta-analysis results in a publicly available database.
Conclusions: Several additional loci may harbor genetic variants associated with LOAD. This data set provides a wealth of phenotypic and genotypic information for use as a resource in discovery and confirmatory research.

• 出版日期2008-11