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dc.contributor.authorLopera Restrepo, Francisco Javier-
dc.contributor.authorRíos Romenets, Silvia-
dc.contributor.authorGiraldo Chica, Margarita María-
dc.contributor.authorAcosta Baena, Natalia-
dc.contributor.authorTobón Quintero, Carlos Andrés-
dc.contributor.authorRamos Pérez, Claudia Patricia-
dc.contributor.authorLangbaum, Jessica B.-
dc.contributor.authorTariot, Pierre N.-
dc.contributor.authorThomas, Ronald-
dc.contributor.authorHendrix, Suzanne-
dc.contributor.authorSchneider, Lon S.-
dc.contributor.authorEspinosa, Alejandro-
dc.contributor.authorCho, William-
dc.contributor.authorWard, Michael-
dc.contributor.authorClayton, David-
dc.contributor.authorFriesenhahn, Michael-
dc.contributor.authorMackey, Howard-
dc.contributor.authorHonigberg, Lee-
dc.contributor.authorSanabria Bohórquez, Sandra-
dc.contributor.authorChen, Kewei-
dc.contributor.authorWalsh, Trisha-
dc.contributor.authorLanglois, Carolyn-
dc.contributor.authorReiman, Eric M.-
dc.date.accessioned2024-06-03T14:58:00Z-
dc.date.available2024-06-03T14:58:00Z-
dc.date.issued2018-
dc.identifier.issn1552-5260-
dc.identifier.urihttps://hdl.handle.net/10495/39586-
dc.description.abstractABSTRACT: Introduction: Autosomal-dominant Alzheimer's disease (ADAD) represents a crucial population for identifying prevention strategies that might modify disease course for cognitively unimpaired individuals at high imminent risk for developing symptoms due to Alzheimer's disease (AD), that is, who have "preclinical" AD. Crenezumab is an antiamyloid monoclonal antibody that binds monomeric and aggregated forms of amyloid β, with highest affinity for oligomers; it is in development for early stages of sporadic AD and for ADAD. Methods: This is a prospective, randomized, double-blind, placebo-controlled phase 2 study of the efficacy of crenezumab versus placebo in asymptomatic PSEN1 E280A mutation carriers from family kindreds with ADAD in Colombia. Participants were randomized to receive either crenezumab or placebo for 260 weeks. The study was designed to enroll a planned total of 300 participants, including 200 preclinical mutation carriers (approximately 100 treatment, 100 placebo) and an additional control group of mutation noncarriers from the same family kindreds included to mask mutation carrier status (100 placebo only). The primary outcome is change in the Alzheimer's Prevention Initiative ADAD Composite Cognitive Test Score from baseline to week 260. Secondary outcomes include time to progression to mild cognitive impairment due to AD or dementia due to AD; changes in dementia severity, memory, and overall neurocognitive functioning; and changes in amyloid-positron emission tomography, fluorodeoxyglucose-positron emission tomography, magnetic resonance imaging volumes, and cerebrospinal fluid levels of β amyloid, tau, and p-tau. Safety and tolerability are assessed. Results: Two hundred fifty-two participants were enrolled between December 2013 and February 2017. Discussion: We describe the first large-scale, potentially label-enabling clinical trial of a preclinical treatment for ADAD. Results from this trial will inform on the efficacy of crenezumab for delaying onset of, slowing decline in, or preventing cognitive impairment in individuals with preclinical ADAD and will foster an improved understanding of AD biomarkers and their relationship to clinical outcomes. Keywords: Alzheimer's Prevention Initiative; Autosomal-dominant Alzheimer's disease; Crenezumab; Preclinical Alzheimer's disease; Prevention.spa
dc.format.extent11 páginasspa
dc.format.mimetypeapplication/pdfspa
dc.language.isoengspa
dc.publisherElsevierspa
dc.type.hasversioninfo:eu-repo/semantics/publishedVersionspa
dc.rightsinfo:eu-repo/semantics/openAccessspa
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/2.5/co/*
dc.titleThe Alzheimer’s Prevention Initiative Autosomal-Dominant Alzheimer’s Disease Trial: A study of crenezumab versus placebo in preclinical PSEN1 E280A mutation carriers to evaluate efficacy and safety in the treatment of autosomal-dominant Alzheimer’s disease, including a placebo-treated noncarrier cohortspa
dc.typeinfo:eu-repo/semantics/articlespa
dc.publisher.groupGrupo de Neurociencias de Antioquiaspa
dc.publisher.groupGrupo Neuropsicología y Conductaspa
dc.identifier.doi10.1016/j.trci.2018.02.003-
dc.contributor.corporatenameAlzheimer's Prevention Initiativespa
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85spa
dc.rights.accessrightshttp://purl.org/coar/access_right/c_abf2spa
dc.identifier.eissn1552-5279-
oaire.citationtitleAlzheimer's & Dementia : The Journal of the Alzheimer's Associationspa
oaire.citationstartpage150spa
oaire.citationendpage160spa
oaire.citationvolume4spa
dc.rights.creativecommonshttps://creativecommons.org/licenses/by-nc-nd/4.0/spa
oaire.fundernameUniversidad de Antioquia. Vicerrectoría de investigación. Comité para el Desarrollo de la Investigación - CODIspa
oaire.fundernameColombia. Ministerio de Ciencia, Tecnología e Innovación - Minicienciasspa
oaire.fundernameNational Institute on Agingspa
dc.publisher.placeNueva York, Estados Unidosspa
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1spa
dc.type.redcolhttps://purl.org/redcol/resource_type/ARTspa
dc.type.localArtículo de investigaciónspa
dc.subject.decsEnfermedad de Alzheimer-
dc.subject.decsAlzheimer Disease-
dc.subject.decsEnsayo Clínico-
dc.subject.decsClinical Trial-
dc.subject.decsEnfermedad de Alzheimer - prevención y control-
dc.subject.decsAlzheimer Disease - prevention and control-
dc.description.researchgroupidCOL0007551spa
dc.description.researchgroupidCOL0010744spa
oaire.awardnumber2017 408-20543spa
oaire.awardnumber1115-65741185408-20512, 1115-54531651spa
oaire.awardnumber(1RFAG041705-01A1, 1UF1AG046150, R01 AG055444, P30 AG19610)spa
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D000544-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D016430-
dc.relation.ispartofjournalabbrevAlzheimers Dement.spa
oaire.funderidentifier.rorRoR:03bp5hc83-
oaire.funderidentifier.rorRoR:03fd5ne08-
oaire.funderidentifier.ror049v75w11-
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