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dc.rights.licenseopenen_US
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorBORDES, Constance
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorSARGURUPREMRAJ, Muralidharan
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorMISHRA, Aniket
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorDEBETTE, Stephanie
dc.date.accessioned2022-03-16T09:05:47Z
dc.date.available2022-03-16T09:05:47Z
dc.date.issued2022-01-05
dc.identifier.issn1759-4766 (Electronic) 1759-4758 (Linking)en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/136475
dc.description.abstractEnCerebral small vessel disease (cSVD) is a leading cause of ischaemic and haemorrhagic stroke and a major contributor to dementia. Covert cSVD, which is detectable with brain MRI but does not manifest as clinical stroke, is highly prevalent in the general population, particularly with increasing age. Advances in technologies and collaborative work have led to substantial progress in the identification of common genetic variants that are associated with cSVD-related stroke (ischaemic and haemorrhagic) and MRI-defined covert cSVD. In this Review, we provide an overview of collaborative studies - mostly genome-wide association studies (GWAS) - that have identified >50 independent genetic loci associated with the risk of cSVD. We describe how these associations have provided novel insights into the biological mechanisms involved in cSVD, revealed patterns of shared genetic variation across cSVD traits, and shed new light on the continuum between rare, monogenic and common, multifactorial cSVD. We consider how GWAS summary statistics have been leveraged for Mendelian randomization studies to explore causal pathways in cSVD and provide genetic evidence for drug effects, and how the combination of findings from GWAS with gene expression resources and drug target databases has enabled identification of putative causal genes and provided proof-of-concept for drug repositioning potential. We also discuss opportunities for polygenic risk prediction, multi-ancestry approaches and integration with other omics data.
dc.description.sponsorshipStopping cognitive decline and dementia by fighting covert cerebral small vessel disease - ANR-18-RHUS-0002en_US
dc.language.isoENen_US
dc.title.enGenetics of common cerebral small vessel disease
dc.typeArticle de revueen_US
dc.identifier.doi10.1038/s41582-021-00592-8en_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
dc.identifier.pubmed34987231en_US
dc.description.sponsorshipEuropeERA-NET for establishing synergies between the Joint Programming on Neurodegenerative Diseases Research and Horizon 2020
dc.description.sponsorshipEuropeStudy on Environmental and GenomeWide predictors of early structural brain Alterations in Young students
dc.description.sponsorshipEuropeCommon mechanisms and pathways in Stroke and Alzheimer's disease.
dc.description.sponsorshipEuropePREvention of STroke in Intracerebral haemorrhaGE survivors with Atrial Fibrillation
bordeaux.journalNature Reviews Neurologyen_US
bordeaux.page84-101en_US
bordeaux.volume18en_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - UMR 1219en_US
bordeaux.issue2en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionINSERMen_US
bordeaux.teamELEANOR_BPHen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.identifier.funderIDAgence Nationale de la Rechercheen_US
hal.identifierhal-03610052
hal.version1
hal.date.transferred2022-03-16T09:05:48Z
hal.exporttrue
dc.rights.ccPas de Licence CCen_US
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