Alzheimer's Disease Risk Genes and Mechanisms of Disease Pathogenesis

被引：946
作者：
Karch, Celeste M.
Goate, Alison M. [1 ]
机构：
[1] Washington Univ, Sch Med, Dept Psychiat, St Louis, MO 63110 USA
来源：
BIOLOGICAL PSYCHIATRY | 2015年 / 77卷 / 01期
关键词：
Alzheimer's Disease; Amyloid Precursor Protein; Cholesterol Metabolism; Endocytosis; Genome-Wide Association Studies; Immune Response; AMYLOID PRECURSOR PROTEIN; GENOME-WIDE ASSOCIATION; CLASSICAL COMPLEMENT PATHWAY; CASSETTE TRANSPORTER A7; FLUID TAU LEVELS; APOLIPOPROTEIN-E; MOUSE MODEL; BETA-PEPTIDE; PLASMA CLUSTERIN; FRONTOTEMPORAL DEMENTIA;
D O I：
10.1016/j.biopsych.2014.05.006
中图分类号：
Q189 [神经科学];
学科分类号：
071006 ;
摘要：
We review the genetic risk factors for late-onset Alzheimer's disease (AD) and their role in AD pathogenesis. More recent advances in understanding of the human genome-technologic advances in methods to analyze millions of polymorphisms in thousands of subjects-have revealed new genes associated with AD risk, including ABCA7, BIN1, CASS4, CD33, CD2AP, CELF1, CLU, CR1, DSG2, EPHA1, FERMT2, HLA-DRB5-DBR1, INPP5D, MS4A, MEF2C, NME8, PICALM, PTK2B, SLC24H4-RIN3, SORL1, and ZCWPW1. Emerging technologies to analyze the entire genome in large data sets have also revealed coding variants that increase AD risk: PLD3 and TREM2. We review the relationship between these AD risk genes and the cellular and neuropathologic features of AD. Understanding the mechanisms underlying the association of these genes with risk for disease will provide the most meaningful targets for therapeutic development to date.
引用
收藏
页码：43 / 51
页数：9
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