Translating genetic risk of Alzheimer's disease into mechanistic insight and drug targets.


Journal

Science (New York, N.Y.)
ISSN: 1095-9203
Titre abrégé: Science
Pays: United States
ID NLM: 0404511

Informations de publication

Date de publication:
02 10 2020
Historique:
entrez: 2 10 2020
pubmed: 3 10 2020
medline: 5 11 2020
Statut: ppublish

Résumé

To provide better prevention and treatment, we need to understand the environmental and genetic risks of Alzheimer's disease (AD). However, the definition of AD has been confounded with dementia in many studies. Thus, overinterpretation of genetic findings with regard to mechanisms and drug targets may explain, in part, controversies in the field. Here, we analyze the different forms of genetic risk of AD and how these can be used to model disease. We stress the importance of studying gene variants in the right cell types and in the right pathological context. The lack of mechanistic understanding of genetic variation has become the major bottleneck in the search for new drug targets for AD.

Identifiants

pubmed: 33004512
pii: 370/6512/61
doi: 10.1126/science.abb8575
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

61-66

Subventions

Organisme : Medical Research Council
ID : MR/L010305/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : G0801418
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/T04604X/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/P005748/1
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/L023784/2
Pays : United Kingdom

Informations de copyright

Copyright © 2020, American Association for the Advancement of Science.

Auteurs

Annerieke Sierksma (A)

VIB Center for Brain & Disease Research, Leuven, Belgium.
Laboratory for the Research of Neurodegenerative Diseases, Department of Neurosciences, Leuven Brain Institute (LBI), KU Leuven (University of Leuven), Leuven, Belgium.

Valentina Escott-Price (V)

Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, UK. escottpricev@cardiff.ac.uk b.strooper@ukdri.ucl.ac.uk.
UK Dementia Research Institute, Cardiff University, Cardiff, UK.

Bart De Strooper (B)

VIB Center for Brain & Disease Research, Leuven, Belgium. escottpricev@cardiff.ac.uk b.strooper@ukdri.ucl.ac.uk.
Laboratory for the Research of Neurodegenerative Diseases, Department of Neurosciences, Leuven Brain Institute (LBI), KU Leuven (University of Leuven), Leuven, Belgium.
UK Dementia Research Institute, University College London, London, UK.

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Classifications MeSH