GWAS of cerebrospinal fluid tau levels identifies risk variants for Alzheimer's disease.
Title | GWAS of cerebrospinal fluid tau levels identifies risk variants for Alzheimer's disease. |
Publication Type | Journal Article |
Year of Publication | 2013 |
Authors | Cruchaga, C, Kauwe, JSK, Harari, O, Jin, SChih, Cai, Y, Karch, CM, Benitez, BA, Jeng, AT, Skorupa, T, Carrell, D, Bertelsen, S, Bailey, M, McKean, D, Shulman, JM, De Jager, PL, Chibnik, L, Bennett, DA, Arnold, SE, Harold, D, Sims, R, Gerrish, A, Williams, J, Van Deerlin, VM, Lee, VM-Y, Shaw, LM, Trojanowski, JQ, Haines, JL, Mayeux, R, Pericak-Vance, MA, Farrer, LA, Schellenberg, GD, Peskind, ER, Galasko, D, Fagan, AM, Holtzman, DM, Morris, JC, Goate, AM |
Corporate Authors | GERAD Consortium, Alzheimer’s Disease Neuroimaging Initiative (ADNI), Alzheimer Disease Genetic Consortium (ADGC) |
Journal | Neuron |
Volume | 78 |
Issue | 2 |
Pagination | 256-68 |
Date Published | 2013 Apr 24 |
ISSN | 1097-4199 |
Keywords | Aged, Aged, 80 and over, Alzheimer Disease, Amyloid beta-Peptides, Apolipoproteins E, Case-Control Studies, Chromosomes, Human, Pair 3, Chromosomes, Human, Pair 6, Female, Genome-Wide Association Study, Genotype, Humans, Male, Membrane Glycoproteins, Middle Aged, Muscle Proteins, Peptide Fragments, Phenotype, Phosphorylation, Polymorphism, Single Nucleotide, Receptors, Immunologic, Risk Factors, Serine, tau Proteins, Transcription Factors |
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. |
DOI | 10.1016/j.neuron.2013.02.026 |
Alternate Journal | Neuron |
PubMed ID | 23562540 |
PubMed Central ID | PMC3664945 |
Grant List | P01 AG05131 / AG / NIA NIH HHS / United States K01 AG030514 / AG / NIA NIH HHS / United States MR/K013041/1 / / Medical Research Council / United Kingdom P50 AG05681 / AG / NIA NIH HHS / United States P30 AG010124 / AG / NIA NIH HHS / United States U01 HG006375 / HG / NHGRI NIH HHS / United States K08 AG034290 / AG / NIA NIH HHS / United States P50 AG005131 / AG / NIA NIH HHS / United States U24 AG021886 / AG / NIA NIH HHS / United States K25 AG041906 / AG / NIA NIH HHS / United States U01 AG032984 / AG / NIA NIH HHS / United States R01 AG042611 / AG / NIA NIH HHS / United States R01 AG030146 / AG / NIA NIH HHS / United States U01 AG024904 / AG / NIA NIH HHS / United States U19 AG010483 / AG / NIA NIH HHS / United States G0300429 / / Medical Research Council / United Kingdom U01 AG016976 / AG / NIA NIH HHS / United States P01 AG003991 / AG / NIA NIH HHS / United States P30 AG008051 / AG / NIA NIH HHS / United States P50 AG005681 / AG / NIA NIH HHS / United States P01 AG026276 / AG / NIA NIH HHS / United States R01 AG017917 / AG / NIA NIH HHS / United States P30 NS069329-01 / NS / NINDS NIH HHS / United States P01 AG03991 / AG / NIA NIH HHS / United States G0902227 / / Medical Research Council / United Kingdom P50 AG005136 / AG / NIA NIH HHS / United States AG010124 / AG / NIA NIH HHS / United States P30 AG010161 / AG / NIA NIH HHS / United States P50 AG005138 / AG / NIA NIH HHS / United States AG05136 / AG / NIA NIH HHS / United States P30 AG010129 / AG / NIA NIH HHS / United States R25 DA027995 / DA / NIDA NIH HHS / United States P30 NS069329 / NS / NINDS NIH HHS / United States R01 AG16208 / AG / NIA NIH HHS / United States R01 AG016208 / AG / NIA NIH HHS / United States R01 AG015819 / AG / NIA NIH HHS / United States R01 AG035083 / AG / NIA NIH HHS / United States |