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Common variants in alzheimer's disease and risk stratification by polygenic risk scores

Abstract: Genetic discoveries of Alzheimer's disease are the drivers of our understanding, and together with polygenetic risk stratification can contribute towards planning of feasible and efficient preventive and curative clinical trials. We first perform a large genetic association study by merging all available case-control datasets and by-proxy study results (discovery n = 409,435 and validation size n = 58,190). Here, we add six variants associated with Alzheimer's disease risk (near APP, CHRNE, PRKD3/NDUFAF7, PLCG2 and two exonic variants in the SHARPIN gene). Assessment of the polygenic risk score and stratifying by APOE reveal a 4 to 5.5 years difference in median age at onset of Alzheimer's disease patients in APOE ?4 carriers. Because of this study, the underlying mechanisms of APP can be studied to refine the amyloid cascade and the polygenic risk score provides a tool to select individuals at high risk of Alzheimer's disease

Otras publicaciones de la misma revista o congreso con autores/as de la Universidad de Cantabria

 Fuente: Nature Communications, 2021, 12(1), 3417 - (CORRECTION), 2023, 14(1), 716

Editorial: Nature Publishing Group

 Año de publicación: 2021

Nº de páginas: 16

Tipo de publicación: Artículo de Revista

 DOI: 10.1038/s41467-021-22491-8

ISSN: 2041-1723

Autoría

DE ROJAS, ITZIAR

MORENO-GRAU, SONIA

TESI, NICCOLO

GRENIER-BOLEY

ANDRADE, VICTOR

JANSEN, IRIS E.

PEDERSON, NANCY L.

STRINGA, NAJADA

ZETTERGREN, ANNA

HERNÁNDEZ, ISABEL

MONRREAL, LAURA

ANTÚNEZ, CARMEN

ANTONELL, ANA

TANKARD, RICK M.

BIS, JOSHUA C.

SIMS, REBECCA

BELLENGUEZ, CÉLINE

QUINTELA, INÉS

GONZÁLEZ-PEREZ, ANTONIO