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基于基因的分析在 HRC 导入基因组全基因组关联数据中确定了三个新的阿尔茨海默病基因。

Gene-based analysis in HRC imputed genome wide association data identifies three novel genes for Alzheimer's disease.

机构信息

Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University, Cardiff, United Kingdom.

UK Dementia Research Institute at Cardiff University, Cardiff, United Kingdom.

出版信息

PLoS One. 2019 Jul 8;14(7):e0218111. doi: 10.1371/journal.pone.0218111. eCollection 2019.

Abstract

Late onset Alzheimer's disease is the most common form of dementia for which about 30 susceptibility loci have been reported. The aim of the current study is to identify novel genes associated with Alzheimer's disease using the largest up-to-date reference single nucleotide polymorphism (SNP) panel, the most accurate imputation software and a novel gene-based analysis approach which tests for patterns of association within genes, in the powerful genome-wide association dataset of the International Genomics of Alzheimer's Project Consortium, comprising over 7 million genotypes from 17,008 Alzheimer's cases and 37,154 controls. In addition to earlier reported genes, we detected three novel gene-wide significant loci PPARGC1A (p = 2.2 × 10-6), RORA (p = 7.4 × 10-7) and ZNF423 (p = 2.1 × 10-6). PPARGC1A and RORA are involved in circadian rhythm; circadian disturbances are one of the earliest symptoms of Alzheimer's disease. PPARGC1A is additionally linked to energy metabolism and the generation of amyloid beta plaques. RORA is involved in a variety of functions apart from circadian rhythm, such as cholesterol metabolism and inflammation. The ZNF423 gene resides in an Alzheimer's disease-specific protein network and is likely involved with centrosomes and DNA damage repair.

摘要

迟发性阿尔茨海默病是最常见的痴呆症形式,目前已经报道了约 30 个易感基因位点。本研究的目的是利用最大的最新参考单核苷酸多态性(SNP)面板、最准确的 imputation 软件和一种新的基于基因的分析方法,在国际阿尔茨海默病基因组学项目联盟的全基因组关联数据集(包含超过 700 万例基因型,来自 17008 例阿尔茨海默病病例和 37154 例对照)中识别与阿尔茨海默病相关的新基因。除了早期报道的基因,我们还检测到三个新的全基因组显著位点 PPARGC1A(p=2.2×10-6)、RORA(p=7.4×10-7)和 ZNF423(p=2.1×10-6)。PPARGC1A 和 RORA 参与昼夜节律;昼夜节律紊乱是阿尔茨海默病的最早症状之一。PPARGC1A 还与能量代谢和淀粉样β斑块的生成有关。RORA 除了昼夜节律外,还参与多种功能,如胆固醇代谢和炎症。ZNF423 基因位于阿尔茨海默病特异性蛋白质网络中,可能与中心体和 DNA 损伤修复有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b19a/6613773/421aaf14f52b/pone.0218111.g001.jpg

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