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GWAS of cerebrospinal fluid tau levels identifies risk variants for Alzheimer's disease.
- Source :
-
Neuron [Neuron] 2013 Apr 24; Vol. 78 (2), pp. 256-68. Date of Electronic Publication: 2013 Apr 04. - Publication Year :
- 2013
-
Abstract
- Cerebrospinal 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.<br /> (Copyright © 2013 Elsevier Inc. All rights reserved.)
- Subjects :
- Aged
Aged, 80 and over
Amyloid beta-Peptides cerebrospinal fluid
Apolipoproteins E genetics
Case-Control Studies
Chromosomes, Human, Pair 3 genetics
Chromosomes, Human, Pair 6 genetics
DNA-Binding Proteins
Female
Genotype
Humans
Male
Membrane Glycoproteins genetics
Middle Aged
Muscle Proteins genetics
Peptide Fragments cerebrospinal fluid
Phenotype
Phosphorylation
Receptors, Immunologic genetics
Repressor Proteins
Risk Factors
Serine metabolism
Trans-Activators
Transcription Factors genetics
Alzheimer Disease cerebrospinal fluid
Alzheimer Disease genetics
Genome-Wide Association Study
Polymorphism, Single Nucleotide genetics
tau Proteins cerebrospinal fluid
Subjects
Details
- Language :
- English
- ISSN :
- 1097-4199
- Volume :
- 78
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Neuron
- Publication Type :
- Academic Journal
- Accession number :
- 23562540
- Full Text :
- https://doi.org/10.1016/j.neuron.2013.02.026