GWAS of cerebrospinal fluid tau levels identifies novel risk variants for Alzheimer’s disease

• Published in: Neuron (Cambridge, Mass.) Vol. 78; no. 2; pp. 256 - 268
• Main Authors: Cruchaga, Carlos, Kauwe, John S.K., Harari, Oscar, Jin, Sheng Chih, Cai, Yefei, Karch, Celeste M., Benitez, Bruno, Jeng, Amanda T., Skorupa, Tara, Carrell, David, Bertelsen, Sarah, Bailey, Matthew, McKean, David, Shulman, Joshua M., De Jager, Philip L., Chibnik, Lori, Bennett, David A., Arnold, Steve E., Harold, Denise, Sims, Rebecca, Gerrish, Amy, Williams, Julie, Van Deerlin, Vivianna M., Lee, Virginia M.-Y., Shaw, Leslie M., Trojanowski, John Q., Haines, Jonathan L., Mayeux, Richard, Pericak-Vance, Margaret A., Farrer, Lindsay A., Schellenberg, Gerard D., Peskind, Elaine R., Galasko, Douglas, Fagan, Anne M., Holtzman, David M., Morris, John C., Goate, Alison M.
• Format: Journal Article
• Language: English
• Published: 04.04.2013
• ISSN: 0896-6273; 1097-4199
• DOI: 10.1016/j.neuron.2013.02.026

Cerebrospinal fluid (CSF) tau, tau phosphorylated at threonine 181 (ptau) and Aβ 42 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 novel 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 datasets 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.