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dc.contributor.authorMattson, Niklas
dc.contributor.authorGroot, Colin
dc.contributor.authorJansen, Willemijn J.
dc.contributor.authorLandau, Susan
dc.contributor.authorVillemagne, Victor
dc.contributor.authorEngelborghs, Sebastiaan
dc.contributor.authorMintun, Mark
dc.contributor.authorLleo, Alberto
dc.contributor.authorMolinuevo, José Luis
dc.contributor.authorJagust, William
dc.contributor.authorFrisoni, Giovanni B.
dc.contributor.authorIvanoiu, Adrian
dc.contributor.authorChételat, Gaël
dc.contributor.authorResende de Oliveira, Catarina
dc.contributor.authorRodrigue, Karen M.
dc.contributor.authorKornhuber, Johannes
dc.contributor.authorWallin, Anders
dc.contributor.authorKlimkowicz-Mrowiec. Aleksandra
dc.contributor.authorRodríguez Rodríguez, Eloy Manuel 
dc.contributor.authorKandimella, Ramesh
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2024-03-26T18:53:31Z
dc.date.available2024-03-26T18:53:31Z
dc.date.issued2018
dc.identifier.issn1552-5260
dc.identifier.issn1552-5279
dc.identifier.urihttps://hdl.handle.net/10902/32467
dc.description.abstractIntroduction: Apolipoprotein E (APOE) ε4 is the major genetic risk factor for Alzheimer's disease (AD), but its prevalence is unclear because earlier studies did not require biomarker evidence of amyloid β (Aβ) pathology. Methods: We included 3451 Aβ+ subjects (853 AD-type dementia, 1810 mild cognitive impairment, and 788 cognitively normal). Generalized estimating equation models were used to assess APOE ε4 prevalence in relation to age, sex, education, and geographical location. Results: The APOE ε4 prevalence was 66% in AD-type dementia, 64% in mild cognitive impairment, and 51% in cognitively normal, and it decreased with advancing age in Aβ+ cognitively normal and Aβ+ mild cognitive impairment (P < .05) but not in Aβ+ AD dementia (P = .66). The prevalence was highest in Northern Europe but did not vary by sex or education. Discussion: The APOE ε4 prevalence in AD was higher than that in previous studies, which did not require presence of Aβ pathology. Furthermore, our results highlight disease heterogeneity related to age and geographical location.es_ES
dc.format.extent12 p.es_ES
dc.language.isoenges_ES
dc.publisherJohn Wiley & Sonses_ES
dc.rights© 2018 the Alzheimer's Association. Published by Elsevier Inc. All rights reserved.es_ES
dc.sourceAlzheimer's & Dementia, 2018, 14(7), 913-924es_ES
dc.subject.otherAPOEes_ES
dc.subject.otherAgees_ES
dc.subject.otherAlzheimer's diseasees_ES
dc.subject.otherAmyloides_ES
dc.subject.otherCSFes_ES
dc.subject.otherEducationes_ES
dc.subject.otherGeographical locationes_ES
dc.subject.otherMild cognitive impairmentes_ES
dc.subject.otherPETes_ES
dc.subject.otherPrevalencees_ES
dc.subject.otherSexes_ES
dc.subject.otherSubjective cognitive declinees_ES
dc.titlePrevalence of the apolipoprotein E ε4 allele in amyloid β positive subjects across the spectrum of Alzheimer’s diseasees_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1016/j.jalz.2018.02.009
dc.type.versionacceptedVersiones_ES


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