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dc.rights.licenseopenen_US
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorLINARD DE GUERTECHIN, Morgane
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorLETENNEUR, Luc
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorGARRIGUE, I.
hal.structure.identifierMicrobiologie Fondamentale et Pathogénicité [MFP]
dc.contributor.authorDOIZE, A.
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorDARTIGUES, Jean-Francois
ORCID: 0000-0001-9482-5529
IDREF: 058586105
hal.structure.identifierBordeaux population health [BPH]
hal.structure.identifierCIC Bordeaux
dc.contributor.authorHELMER, Catherine
dc.date.accessioned2023-06-01T15:16:32Z
dc.date.available2023-06-01T15:16:32Z
dc.date.issued2020
dc.identifier.issn1552-5260en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/182403
dc.description.abstractEnIntroduction: Numerous results suggest the implication of infectious agents in the onset of Alzheimer's disease (AD).Methods: In the Bordeaux‐3C prospective cohort, we assessed the impact of herpes simplex virus type 1 (HSV‐1) infection on the incidence of AD according to apolipoprotein E (APOE) status, a genetic susceptibility factor. Cox models were performed to estimate the 10‐year risk of AD associated with anti‐HSV antibodies in 1037 participants according to APOE4 status.Results: Among APOE4 carriers, subjects for whom the frequency of HSV‐1 reactivation is supposed to be high, that is, immunoglobulin M (IgM) positive or elevated levels of IgG, had an increased risk of AD with adjusted hazard ratios (HRs) of 3.68 (1.08–12.55) and 3.28 (1.19–9.03), respectively. No significant association was found in APOE4‐negative subjects.Discussion: These results, in accordance with a solid pathophysiological rationale, suggest a role for HSV‐1 in AD development among subjects with a genetic susceptibility factor, the APOE4 allele.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subject.enAlzheimer’s disease
dc.subject.enAPOE4
dc.subject.endementia
dc.subject.engenetic susceptibility
dc.subject.enherpes virus
dc.subject.enprevention
dc.subject.enAlzheimer’s disease
dc.title.enInteraction between APOE4 and herpes simplex virus type 1 in Alzheimer's disease
dc.typeArticle de revueen_US
dc.identifier.doi10.1002/alz.12008en_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
dc.subject.halSciences du Vivant [q-bio]/Neurosciences [q-bio.NC]/Neurobiologieen_US
dc.subject.halSciences du Vivant [q-bio]/Médecine humaine et pathologie/Maladies infectieusesen_US
dc.subject.halSciences du Vivant [q-bio]/Génétique/Génétique humaineen_US
bordeaux.journalAlzheimer's & Dementia : the Journal of the Alzheimer's Associationen_US
bordeaux.page200-208en_US
bordeaux.volume16en_US
bordeaux.hal.laboratoriesMFP (Laboratoire Microbiologie Fondamentale et Pathogénicité) - UMR 5234en_US
bordeaux.issue1en_US
bordeaux.institutionCNRSen_US
bordeaux.institutionUniversité de Bordeaux
bordeaux.institutionINSERM
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcehal
hal.identifierhal-03130438
hal.version1
hal.exportfalse
workflow.import.sourcehal
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Alzheimer's%20&%20Dementia%20:%20the%20Journal%20of%20the%20Alzheimer's%20Association&rft.date=2020&rft.volume=16&rft.issue=1&rft.spage=200-208&rft.epage=200-208&rft.eissn=1552-5260&rft.issn=1552-5260&rft.au=LINARD%20DE%20GUERTECHIN,%20Morgane&LETENNEUR,%20Luc&GARRIGUE,%20I.&DOIZE,%20A.&DARTIGUES,%20Jean-Francois&rft.genre=article


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