DNA methylation variability in Alzheimer's disease

被引:29
作者
Huo, Zhiguang [1 ]
Zhu, Yun [2 ]
Yu, Lei [3 ]
Yang, Jingyun [3 ]
De Jager, Philip [4 ]
Bennett, David A. [3 ]
Zhao, Jinying [2 ]
机构
[1] Univ Florida, Dept Biostat, Gainesville, FL 32610 USA
[2] Univ Florida, Dept Epidemiol, Gainesville, FL 32610 USA
[3] Rush Univ, Med Ctr, Rush Alzheimers Dis Ctr, Chicago, IL 60612 USA
[4] Columbia Univ, Coll Phys & Surg, Dept Neurol, New York, NY 10027 USA
基金
美国国家卫生研究院;
关键词
DNA methylation variability; Alzheimer's disease; Amyloid-beta plaques; PHF-tau tangles; Postmortem brain; PFC; ROSMAP; AMYLOID-BETA; ASSOCIATION; INSIGHTS; PACKAGE; MEMORY; GENES; MODEL; FAF1; ANK1;
D O I
10.1016/j.neurobiolaging.2018.12.003
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
DNA methylation plays a critical role in brain aging and Alzheimer's disease (AD). While prior studies have largely focused on testing mean DNA methylation, DNA methylation instability (quantified by DNA methylation variability) may also affect disease susceptibility. Using DNA methylation data collected by the Religious Orders Study and the Rush Memory and Aging Project, we identified 249 and 115 variably methylated probes (VMPs) associated with amyloid-beta and neurofibrillary tangles, respectively. These VMPs clustered into 133 and 14 regions, respectively. Notably, we found that most of these VMPs did not overlap with differentially methylated probes, indicating that VMPs and differentially methylated probes may capture different sets of genes associated with AD pathology. Overall, our results demonstrated that DNA methylation instability affects AD neuropathology and highlights the importance of testing methylation variability in epigenetic research. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:35 / 44
页数:10
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