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GWAS of Cerebrospinal Fluid Tau Levels Identifies Risk Variants for Alzheimer’s Disease

Authors :
Lori B. Chibnik
Anne M. Fagan
Carlos Cruchaga
Sheng Chih Jin
David McKean
John S. K. Kauwe
John Q. Trojanowski
Steve E. Arnold
Amy Gerrish
Richard Mayeux
Celeste M. Karch
Jonathan L. Haines
John C. Morris
Julie Williams
Oscar Harari
Matthew H. Bailey
Gerard D. Schellenberg
Bruno A. Benitez
Virginia M.-Y. Lee
Denise Harold
Douglas Galasko
Leslie M. Shaw
Holtzman David M
Tara Skorupa
Philip L. De Jager
Sarah Bertelsen
Lindsay A. Farrer
David A. Bennett
David Carrell
Yefei Cai
Alison Goate
Vivianna M. Van Deerlin
Margaret A. Pericak-Vance
Joshua M. Shulman
Rebecca Sims
Elaine R. Peskind
Amanda T. Jeng
Source :
Neuron. 78(2):256-268
Publication Year :
2013
Publisher :
Elsevier BV, 2013.

Abstract

SummaryCerebrospinal fluid (CSF) tau, tau phosphorylated at threonine 181 (ptau), and Aβ42 are established biomarkers for Alzheimer’s disease (AD) and have been used as quantitative traits for genetic analyses. We performed the largest genome-wide association study for cerebrospinal fluid (CSF) tau/ptau levels published to date (n = 1,269), identifying three genome-wide significant loci for CSF tau and ptau: rs9877502 (p = 4.89 × 10−9 for tau) located at 3q28 between GEMC1 and OSTN, rs514716 (p = 1.07 × 10−8 and p = 3.22 × 10−9 for tau and ptau, respectively), located at 9p24.2 within GLIS3 and rs6922617 (p = 3.58 × 10−8 for CSF ptau) at 6p21.1 within the TREM gene cluster, a region recently reported to harbor rare variants that increase AD risk. In independent data sets, rs9877502 showed a strong association with risk for AD, tangle pathology, and global cognitive decline (p = 2.67 × 10−4, 0.039, 4.86 × 10−5, respectively) illustrating how this endophenotype-based approach can be used to identify new AD risk loci.

Details

ISSN :
08966273
Volume :
78
Issue :
2
Database :
OpenAIRE
Journal :
Neuron
Accession number :
edsair.doi.dedup.....96e49a6316e4b97dd2b84bffeadef784
Full Text :
https://doi.org/10.1016/j.neuron.2013.02.026