Naj Adam C, Schellenberg Gerard D
Department of Biostatistics and Epidemiology/Center for Clinical Epidemiology and Biostatistics, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania.
Department of Pathology and Laboratory Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania.
Am J Med Genet B Neuropsychiatr Genet. 2017 Jan;174(1):5-26. doi: 10.1002/ajmg.b.32499.
Alzheimer's disease (AD) (MIM: 104300) is a highly heritable disease with great complexity in its genetic contributors, and represents the most common form of dementia. With the gradual aging of the world's population, leading to increased prevalence of AD, and the substantial cost of care for those afflicted, identifying the genetic causes of disease represents a critical effort in identifying therapeutic targets. Here we provide a comprehensive review of genomic studies of AD, from the earliest linkage studies identifying monogenic contributors to early-onset forms of AD to the genome-wide and rare variant association studies of recent years that are being used to characterize the mosaic of genetic contributors to late-onset AD (LOAD), and which have identified approximately ∼20 genes with common variants contributing to LOAD risk. In addition, we explore studies employing alternative approaches to identify genetic contributors to AD, including studies of AD-related phenotypes and multi-variant association studies such as pathway analyses. Finally, we introduce studies of next-generation sequencing, which have recently helped identify multiple low-frequency and rare variant contributors to AD, and discuss on-going efforts with next-generation sequencing studies to develop statistically well- powered and comprehensive genomic studies of AD. Through this review, we help uncover the many insights the genetics of AD have provided into the pathways and pathophysiology of AD. © 2016 Wiley Periodicals, Inc.
阿尔茨海默病(AD)(MIM:104300)是一种具有高度遗传性的疾病,其遗传因素极为复杂,是痴呆最常见的形式。随着全球人口逐渐老龄化,导致AD患病率上升,以及对患者护理的巨大成本,确定疾病的遗传原因是确定治疗靶点的关键努力。在这里,我们全面综述了AD的基因组研究,从最早识别早发型AD单基因因素的连锁研究,到近年来用于描述晚发型AD(LOAD)遗传因素全貌的全基因组和罕见变异关联研究,这些研究已确定约20个具有常见变异的基因与LOAD风险相关。此外,我们探讨了采用替代方法识别AD遗传因素的研究,包括AD相关表型的研究以及多变量关联研究,如通路分析。最后,我们介绍了新一代测序研究,这些研究最近有助于识别AD的多个低频和罕见变异因素,并讨论了新一代测序研究正在进行的努力,以开展统计学上有力且全面的AD基因组研究。通过本综述,我们有助于揭示AD遗传学在AD通路和病理生理学方面提供的诸多见解。© 2016威利期刊公司