Alzheimer's disease risk genes and mechanisms of disease pathogenesis - PubMed (original) (raw)
Review
Alzheimer's disease risk genes and mechanisms of disease pathogenesis
Celeste M Karch et al. Biol Psychiatry. 2015.
Abstract
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.
Keywords: Alzheimer’s Disease; Amyloid Precursor Protein; Cholesterol Metabolism; Endocytosis; Genome-Wide Association Studies; Immune Response.
Copyright © 2015 Society of Biological Psychiatry. Published by Elsevier Inc. All rights reserved.
Figures
Figure 1. Rare and common variants contribute to Alzheimer's disease risk
Figure updated and modified from (149).
References
- Hardy J, Selkoe DJ. The amyloid hypothesis of Alzheimer's disease: progress and problems on the road to therapeutics. Science. 2002;297:353–356. -PubMed
Publication types
MeSH terms
Substances
Grants and funding
- 503147/WT_/Wellcome Trust/United Kingdom
- U01 AG032438/AG/NIA NIH HHS/United States
- P50 AG005681/AG/NIA NIH HHS/United States
- G0801418/WT_/Wellcome Trust/United Kingdom
- G0801418/MRC_/Medical Research Council/United Kingdom
- R01 AG035083/AG/NIA NIH HHS/United States
- G0800509/MRC_/Medical Research Council/United Kingdom
- K01 AG046374/AG/NIA NIH HHS/United States
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Molecular Biology Databases
Research Materials
Miscellaneous