Cardiovascular disease contributes to Alzheimer's disease: evidence from large-scale genome-wide association studies

被引:90
作者
Liu, Guiyou [1 ,2 ]
Yao, Lifen [3 ]
Liu, Jiafeng [4 ]
Jiang, Yongshuai [5 ]
Ma, Guoda [1 ]
Chen, Zugen [6 ]
Zhao, Bin [7 ]
Li, Keshen [1 ,7 ]
机构
[1] Guangdong Med Coll, Inst Neurol, Zhanjiang 524001, Guangdong, Peoples R China
[2] Chinese Acad Sci, Genome Anal Lab, Tianjin Inst Ind Biotechnol, Tianjin 300308, Peoples R China
[3] Harbin Med Univ, Affiliated Hosp 1, Dept Neurol, Harbin, Heilongjiang, Peoples R China
[4] First Hosp Harbin, Dept Neurol, Harbin, Heilongjiang, Peoples R China
[5] Harbin Med Univ, Coll Bioinformat Sci & Technol, Harbin, Heilongjiang, Peoples R China
[6] Univ Calif Los Angeles, Dept Human Genet, Los Angeles, CA USA
[7] Guangdong Med Coll, Affiliated Hosp, Key Lab Aging Related Cardiocerebral Dis Guangdon, Zhanjiang, Peoples R China
基金
英国医学研究理事会; 英国惠康基金;
关键词
Alzheimer's disease; Cardiovascular disease; Pathway analysis; Genome-wide association studies; VASCULAR RISK-FACTORS; DILATED CARDIOMYOPATHY; IDENTIFIES VARIANTS; COMMON VARIANTS; HEART-FAILURE; PROGRESSION; MYOCARDITIS; INFECTION; MUTATIONS; SYSTEM;
D O I
10.1016/j.neurobiolaging.2013.10.084
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Alzheimer's disease (AD) is the most common and complex neurodegenerative disease in the elderly individuals. Recently, genome-wide association studies (GWAS) have been used to investigate AD pathogenesis. These GWAS have yielded important new insights into the genetic mechanisms of AD. However, these newly identified AD susceptibility loci exert only very small risk effects and cannot fully explain the underlying AD genetic risk. We hypothesize that combining the findings from different AD GWAS may have greater power than genetic analysis alone. To identify new AD risk factors, we integrated findings from 3 previous large-scale AD GWAS (n = 14,138) using a gene-based meta-analysis and subsequently conducted a pathway analysis using the kyoto encyclopedia of genes and genomes and gene ontology databases. Interestingly, we not only confirmed previous findings, but also highlighted, for the first time, the involvement of cardiovascular disease-related pathways in AD. Our results provided the clues as to the link between these diseases using pathway analysis methods. We believe that these findings will be very useful for future genetic studies of AD. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:786 / 792
页数:7
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