Shared genetic etiology underlying late-onset Alzheimer's disease and posttraumatic stress syndrome

被引:14
作者
Lutz, Michael W. [1 ]
Luo, Sheng [2 ]
Williamson, Douglas E. [3 ,4 ,5 ]
Chiba-Falek, Ornit [1 ,6 ]
机构
[1] Duke Univ, Dept Neurol, Div Translat Brain Sci, Med Ctr, Durham, NC USA
[2] Duke Univ, Med Ctr, Dept Biostat & Bioinformat, Durham, NC USA
[3] Duke Univ, Dept Psychiat & Behav Sci, Med Ctr, Durham, NC USA
[4] Durham VA Med Ctr, Res Serv, Durham, NC USA
[5] Duke Univ, Ctr Appl Genom & Precis Med, Med Ctr, 300 North Duke St, Durham, NC 27701 USA
[6] Duke Univ, Ctr Genom & Computat Biol, Med Ctr, Durham, NC USA
基金
美国国家卫生研究院;
关键词
genetic pleiotropy; inflammation and immune-based pathways and Alzheimer's disease; late-onset Alzheimer's disease; MS4A gene family; posttraumatic stress disorder; PTSD; NEUROPSYCHIATRIC SYMPTOMS; FUNCTIONAL ANNOTATION; COMMON VARIANTS; RISK LOCI; DISORDER; PLEIOTROPY; SUSCEPTIBILITY; EXPRESSION; DEMENTIA; IMMUNITY;
D O I
10.1002/alz.12128
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: Late-onset Alzheimer's disease (LOAD) manifests comorbid neuropsychiatric symptoms and posttraumatic stress disorder (PTSD) is associated with an increased risk for dementia in late life, suggesting the two disorders may share genetic etiologies. Methods: We performed genetic pleiotropy analysis using LOAD and PTSD genome-wide association study (GWAS) datasets from white and African-American populations, followed by functional-genomic analyses. Results: We found an enrichment for LOAD across increasingly stringent levels of significance with the PTSD GWAS association (LOAD vertical bar PTSD) in the discovery and replication cohorts and a modest enrichment for the reverse conditional association (PTSD vertical bar LOAD). LOAD vertical bar PTSD association analysis identified and replicated the MS4A genes region. These genes showed similar expression pattern in brain regions affected in LOAD, and across-brain-tissue analysis identified a significant association for MS4A6A. The African-American samples showed moderate enrichment; however, no false discovery rate-significant associations. Discussion: We demonstrated common genetic signatures for LOAD and PTSD and suggested immune response as a common pathway for these diseases.
引用
收藏
页码:1280 / 1292
页数:13
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