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dc.contributor.authorRábano, Alberto
dc.contributor.authorGuerrero Márquez, Carmen
dc.contributor.authorJuste, Ramón A
dc.contributor.authorGeijo, María V
dc.contributor.authorCalero, Miguel 
dc.date.accessioned2021-04-19T15:23:50Z
dc.date.available2021-04-19T15:23:50Z
dc.date.issued2021-03-10
dc.identifier.citationBiomolecules . 2021 Mar 10;11(3):413.es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/12685
dc.description.abstractHuman prion and non-prion neurodegenerative diseases share pathogenic mechanisms and neuropathological features. The lesion profile of a particular entity results from specific involvement of vulnerable neuron populations and connectivity circuits by a pathogenic protein isoform with strain-like properties. The lesion profile of the medial temporal lobe (MTL) was studied in postmortem tissue of 143 patients with human prion disease (HPD) including sporadic, genetic, and acquired forms. Most cases (90%) were classified according to PrPres type and/or PRNP codon 129 status, in addition to a full neuropathological profile. Mixed histotypes represented 29.4% of total sporadic Creutzfeldt-Jakob disease (sCJD) cases. An intensity score of involvement including spongiosis and astrogliosis was determined for the amygdala, presubiculum, subiculum, entorhinal cortex, CA1 to CA4 sectors of the hippocampal cortex, and dentate gyrus. Connectivity hubs within the MTL presented the highest scores. Diverse lesion profiles were obtained for different types and subtypes of HPD. Impact of mixed PrPres types on the MTL lesion profile was higher for sCJDMV2K cases than in other histotypes. Differences between MTL profiles was globally consistent with current evidence on specific strains in HPD. These results may be relevant for the analysis of possible strain effects in focal non-prion neurodegenerative conditions limited to the MTL.es_ES
dc.language.isoenges_ES
dc.publisherMultidisciplinary Digital Publishing Institute (MDPI) es_ES
dc.type.hasVersionVoRes_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectHuman prion diseaseses_ES
dc.subjectMedial temporal lobees_ES
dc.subjectNeurodegenerative diseaseses_ES
dc.subjectPrion strainses_ES
dc.titleMedial Temporal Lobe Involvement in Human Prion Diseases: Implications for the Study of Focal Non Prion Neurodegenerative Pathology.es_ES
dc.typejournal articlees_ES
dc.rights.licenseAtribución 4.0 Internacional*
dc.identifier.pubmedID33802224es_ES
dc.format.volume11es_ES
dc.format.number3es_ES
dc.identifier.doi10.3390/biom11030413es_ES
dc.description.peerreviewedes_ES
dc.identifier.e-issn2218-273Xes_ES
dc.relation.publisherversionhttps://doi.org/10.3390/biom11030413es_ES
dc.identifier.journalBiomoleculeses_ES
dc.repisalud.centroISCIII::Servicios Centraleses_ES
dc.repisalud.institucionISCIIIes_ES
dc.rights.accessRightsopen accesses_ES


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Atribución 4.0 Internacional
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