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- Document type:
- Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.; Article
- Author(s):
- Hoglinger, GU; Melhem, NM; Dickson, DW; Sleiman, PM; Wang, LS; Klei, L; Rademakers, R; de Silva, R; Litvan, I; Riley, DE; van Swieten, JC; Heutink, P; Wszolek, ZK; Uitti, RJ; Vandrovcova, J; Hurtig, HI; Gross, RG; Maetzler, W; Goldwurm, S; Tolosa, E; Borroni, B; Pastor, P; Cantwell, LB; Han, MR; Dillman, A; van der Brug, MP; Gibbs, JR; Cookson, MR; Hernandez, DG; Singleton, AB; Farrer, MJ; Yu, CE; Golbe, LI; Revesz, T; Hardy, J; Lees, AJ; Devlin, B; Hakonarson, H; Müller, U; Schellenberg, GD
- Title:
- Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy.
- Abstract:
- Progressive supranuclear palsy (PSP) is a movement disorder with prominent tau neuropathology. Brain diseases with abnormal tau deposits are called tauopathies, the most common of which is Alzheimer's disease. Environmental causes of tauopathies include repetitive head trauma associated with some sports. To identify common genetic variation contributing to risk for tauopathies, we carried out a genome-wide association study of 1,114 individuals with PSP (cases) and 3,247 controls (stage 1) followed by a second stage in which we genotyped 1,051 cases and 3,560 controls for the stage 1 SNPs that yielded P <= 10(-3). We found significant previously unidentified signals (P < 5 × 10(-8)) associated with PSP risk at STX6, EIF2AK3 and MOBP. We confirmed two independent variants in MAPT affecting risk for PSP, one of which influences MAPT brain expression. The genes implicated encode proteins for vesicle-membrane fusion at the Golgi-endosomal interface, for the endoplasmic reticulum unfolded protein response and for a myelin structural component.
- Journal title abbreviation:
- Nat Genet
- Year:
- 2011
- Journal volume:
- 43
- Journal issue:
- 7
- Pages contribution:
- 699-705
- Language:
- eng
- Fulltext / DOI:
- doi:10.1038/ng.859
- Pubmed ID:
- http://view.ncbi.nlm.nih.gov/pubmed/21685912
- Print-ISSN:
- 1061-4036
- TUM Institution:
- Neurologische Klinik und Poliklinik
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