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dc.contributor.authorBlennow, Kaj
dc.contributor.authorDiaz-Lucena, Daniela
dc.contributor.authorZetterberg, Henrik
dc.contributor.authorVillar-Pique, Anna
dc.contributor.authorKarch, Andre
dc.contributor.authorVidal, Enric
dc.contributor.authorHermann, Peter
dc.contributor.authorSchmitz, Matthias
dc.contributor.authorFerrer Abizanda, Isidro
dc.contributor.authorZerr, Inga
dc.contributor.authorLlorens, Franc
dc.contributor.otherProducció Animalca
dc.date.accessioned2020-05-06T10:53:34Z
dc.date.available2020-05-06T10:53:34Z
dc.date.issued2019-05-16
dc.identifier.citationBlennow, Kaj, Daniela Diaz-Lucena, Henrik Zetterberg, Anna Villar-Pique, Andre Karch, Enric Vidal, and Peter Hermann et al. 2019. "CSF Neurogranin As A Neuronal Damage Marker In CJD: A Comparative Study With AD". Journal Of Neurology, Neurosurgery & Psychiatry 90 (8): 846-853. BMJ. doi:10.1136/jnnp-2018-320155.ca
dc.identifier.issn0022-3050ca
dc.identifier.urihttp://hdl.handle.net/20.500.12327/780
dc.description.abstractObjective To investigate whether cerebrospinal fluid (CSF) neurogranin concentrations are altered in sporadic Creutzfeldt-Jakob disease (CJD), comparatively with Alzheimer’s disease (AD), and associated with neuronal degeneration in brain tissue. Methods CSF neurogranin, total tau, neurofilament light (NFL) and 14-3-3 protein were measured in neurological controls (NCs, n=64), AD (n=46) and CJD (n=81). The accuracy of neurogranin discriminating the three diagnostic groups was evaluated. Correlations between neurogranin and neurodegeneration biomarkers, demographic, genetic and clinical data were assessed. Additionally, neurogranin expression in postmortem brain tissue was studied. Results Compared with NC, CSF neurogranin concentrations were increased in CJD (4.75 times of NC; p<0.001, area under curve (AUC), 0.96 (95% CI 0.93 to 0.99) and AD (1.94 times of NC; p<0.01, AUC 0.73, 95% CI 0.62 to 0.82), and were able to differentiate CJD from AD (p<0.001, AUC 0.85, 95% CI 0.78 to 0.92). CSF tau was increased in CJD (41 times of NC) and in AD (3.1 times of NC), both at p<0.001. In CJD, neurogranin positively correlated with tau (r=0.55, p<0.001) and was higher in 14-3-3-positivity (p<0.05), but showed no association with NFL (r=0.08, p=0.46). CJD-MM1/MV1 cases displayed higher neurogranin levels than VV2 cases. Neurogranin was increased at early CJD disease stages and was a good prognostic marker of survival time in CJD. In brain tissue, neurogranin was detected in the cytoplasm, membrane and postsynaptic density fractions of neurons, with reduced levels in AD, and more significantly in CJD, where they correlated with synaptic and axonal markers. Conclusions Neurogranin is a new biomarker of prion pathogenesis with diagnostic and prognostic abilities, which reflects the degree of neuronal damage in brain tissue in a CJD subtype manner.ca
dc.format.extent29ca
dc.language.isoengca
dc.publisherBMJ Publishing Groupca
dc.relation.ispartofJournal of Neurology, Neurosurgery and Psychiatryca
dc.rightsAttribution-NonCommercial 4.0 Internationalca
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/*
dc.titleCSF neurogranin as a neuronal damage marker in CJD: a comparative study with ADca
dc.typeinfo:eu-repo/semantics/articleca
dc.description.versioninfo:eu-repo/semantics/acceptedVersionca
dc.rights.accessLevelinfo:eu-repo/semantics/openAccess
dc.embargo.termscapca
dc.relation.projectIDEC/INTERREG-POCTEFA/EU/ / /ca
dc.relation.projectIDISCIII/Programa Estatal de I+D+I orientada a los retos de la Sociedad/CP16-00041/ES/ /ca
dc.subject.udc619ca
dc.identifier.doihttp://dx.doi.org/10.1136/jnnp-2018-320155ca
dc.contributor.groupSanitat Animalca


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