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Chen, Jason A; Chen, Zhongbo; Won, Hyejung; Huang, Alden Y; Lowe, Jennifer K; Wojta, Kevin; Yokoyama, Jennifer S; Bensimon, Gilbert; Leigh, P Nigel; Payan, Christine; Shatunov, Aleksey; Jones, Ashley R; Lewis, Cathryn M; Deloukas, Panagiotis; Amouyel, Philippe; Tzourio, Christophe; Dartigues, Jean-Francois; Ludolph, Albert; Boxer, Adam L; Bronstein, Jeff M; Al-Chalabi, Ammar; Geschwind, Daniel H; Coppola, Giovanni
Molecular neurodegeneration, 08/2018, Letnik: 13, Številka: 1Journal Article
Progressive supranuclear palsy (PSP) is a rare neurodegenerative disease for which the genetic contribution is incompletely understood. We conducted a joint analysis of 5,523,934 imputed SNPs in two newly-genotyped progressive supranuclear palsy cohorts, primarily derived from two clinical trials (Allon davunetide and NNIPPS riluzole trials in PSP) and a previously published genome-wide association study (GWAS), in total comprising 1646 cases and 10,662 controls of European ancestry. We identified 5 associated loci at a genome-wide significance threshold P < 5 × 10 , including replication of 3 loci from previous studies and 2 novel loci at 6p21.1 and 12p12.1 (near RUNX2 and SLCO1A2, respectively). At the 17q21.31 locus, stepwise regression analysis confirmed the presence of multiple independent loci (localized near MAPT and KANSL1). An additional 4 loci were highly suggestive of association (P < 1 × 10 ). We analyzed the genetic correlation with multiple neurodegenerative diseases, and found that PSP had shared polygenic heritability with Parkinson's disease and amyotrophic lateral sclerosis. In total, we identified 6 additional significant or suggestive SNP associations with PSP, and discovered genetic overlap with other neurodegenerative diseases. These findings clarify the pathogenesis and genetic architecture of PSP.
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JCR | SNIP | JCR | SNIP | JCR | SNIP | JCR | SNIP |
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Vir: Osebne bibliografije
in: SICRIS
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