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dc.contributor.authorGonzález-Sánchez, Marta
dc.contributor.authorBartolome, Fernando
dc.contributor.authorAntequera, Desireé 
dc.contributor.authorPuertas-Martín, Veronica
dc.contributor.authorGonzález, Pilar
dc.contributor.authorGómez-Grande, Adolfo
dc.contributor.authorLlamas-Velasco, Sara
dc.contributor.authorHerrero-San Martín, Alejandro
dc.contributor.authorPérez-Martínez, David
dc.contributor.authorVillarejo-Galende, Alberto
dc.contributor.authorAtienza, Mercedes
dc.contributor.authorPalomar-Bonet, Miriam
dc.contributor.authorCantero, Jose Luis
dc.contributor.authorPerry, George
dc.contributor.authorOrive, Gorka
dc.contributor.authorIbáñez, Borja 
dc.contributor.authorBueno, Hector 
dc.contributor.authorFuster, Valentin 
dc.contributor.authorCarro, Eva
dc.date.accessioned2020-10-08T11:40:57Z
dc.date.available2020-10-08T11:40:57Z
dc.date.issued2020-07
dc.identifier.citationEBioMedicine. 2020; 57:102834es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/11121
dc.description.abstractEvidences of infectious pathogens in Alzheimer's disease (AD) brains may suggest a deteriorated innate immune system in AD pathophysiology. We previously demonstrated reduced salivary lactoferrin (Lf) levels, one of the major antimicrobial proteins, in AD patients. To assess the clinical utility of salivary Lf for AD diagnosis, we examine the relationship between salivary Lf and cerebral amyloid-β (Aβ) load using amyloid-Positron-Emission Tomography (PET) neuroimaging, in two different cross-sectional cohorts including patients with different neurodegenerative disorders. The diagnostic performance of salivary Lf in the cohort 1 had an area under the curve [AUC] of 0•95 (0•911-0•992) for the differentiation of the prodromal AD/AD group positive for amyloid-PET (PET+) versus healthy group, and 0•97 (0•924-1) versus the frontotemporal dementia (FTD) group. In the cohort 2, salivary Lf had also an excellent diagnostic performance in the health control group versus prodromal AD comparison: AUC 0•93 (0•876-0•989). Salivary Lf detected prodromal AD and AD dementia distinguishing them from FTD with over 87% sensitivity and 91% specificity. Salivary Lf seems to have a very good diagnostic performance to detect AD. Our findings support the possible utility of salivary Lf as a new non-invasive and cost-effective AD biomarker. Instituto de Salud Carlos III (FIS15/00780, FIS18/00118), FEDER, Comunidad de Madrid (S2017/BMD-3700; NEUROMETAB-CM), and CIBERNED (PI2016/01) to E.C.; Spanish Ministry of Economy and Competitiveness (SAF2017-85310-R) to J.L.C., and (PSI2017-85311-P) to M.A.; International Centre on ageing CENIE-POCTEP (0348_CIE_6_E) to M.A.; Instituto de Salud Carlos III (PIE16/00021, PI17/01799), to H.B.es_ES
dc.description.sponsorshipThis study was supported by Dr. Carro grants from Instituto de Salud Carlos III (FIS15/00780, FIS18/00118), FEDER, Comunidad de Madrid (S2017/BMD-3700; NEUROMETAB-CM), and CIBERNED(PI2016/01). This study was also supported by research grants fromthe Spanish Ministry of Economy and Competitiveness (SAF2017-85310-R to Dr. Cantero, PSI2017-85311-P to Dr. Atienza); International Centre on ageing CENIE-POCTEP (0348_CIE_6_E to Dr. Atienza);and CIBERNED (CB06/05/1111 to Dr. Cantero). Dr. Bueno receives research funding from the Instituto de Salud Carlos III, Spain (PIE16/00021, PI17/01799). The H2H-Spain Study was supported in Spain by grant PIE16/00021 from Instituto Carlos III, Ministry of Science, Innovation and Universities, and additional funds from the Centro Nacional de Investigaciones Cardiovasculares (CNIC). The CNIC is supported by the Ministry of Economy, Industry and Competitiveness and the Pro CNIC Foundation, and is a Severo Ochoa Centre of Excellence (SEV-2015-0505).es_ES
dc.language.isoenges_ES
dc.publisherElsevier es_ES
dc.type.hasVersionVoRes_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.titleDecreased salivary lactoferrin levels are specific to Alzheimer's disease.es_ES
dc.typejournal articlees_ES
dc.rights.licenseAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.identifier.pubmedID32586758es_ES
dc.format.volume57es_ES
dc.format.page102834es_ES
dc.identifier.doi10.1016/j.ebiom.2020.102834es_ES
dc.contributor.funderInstituto de Salud Carlos III 
dc.contributor.funderUnión Europea. Fondo Europeo de Desarrollo Regional (FEDER/ERDF) 
dc.contributor.funderComunidad de Madrid (España) 
dc.contributor.funderMinisterio de Economía y Competitividad (España) 
dc.contributor.funderCentro de Investigación Biomedica en Red - CIBER
dc.contributor.funderMinisterio de Ciencia, Innovación y Universidades (España) 
dc.contributor.funderCentro Nacional de Investigaciones Cardiovasculares Carlos III (España) 
dc.contributor.funderFundación ProCNIC 
dc.description.peerreviewedes_ES
dc.identifier.e-issn2352-3964es_ES
dc.relation.publisherversionhttps://doi.org/10.1016/j.ebiom.2020.102834es_ES
dc.identifier.journalEBioMedicinees_ES
dc.repisalud.orgCNICCNIC::Grupos de investigación::Laboratorio Traslacional para la Imagen y Terapia Cardiovasculares_ES
dc.repisalud.orgCNICCNIC::Grupos de investigación::Imagen Cardiovascular y Estudios Poblacionaleses_ES
dc.repisalud.orgCNICCNIC::Grupos de investigación::Investigación Cardiovascular Traslacional Multidisciplinariaes_ES
dc.repisalud.institucionCNICes_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/SEV-2015-0505es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/FIS15/00780es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/FIS18/00118es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/PIE16/00021, PI17/01799es_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/SAF2017-85310-Res_ES
dc.relation.projectIDinfo:eu-repo/grantAgreement/ES/PSI2017-85311-Pes_ES
dc.rights.accessRightsopen accesses_ES


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
Este Item está sujeto a una licencia Creative Commons: Attribution-NonCommercial-NoDerivatives 4.0 Internacional