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dc.contributor.authorMolina, Vicente
dc.contributor.authorFernández-Linsenbarth, Inés
dc.contributor.authorQueipo-de-Llano, María
dc.contributor.authorJiménez-Aparicio, María Teresa
dc.contributor.authorVallecillo-Adame, Carmen
dc.contributor.authorAremy-Gonzaga, Abril
dc.contributor.authorde-Andrés-Lobo, Celia
dc.contributor.authorRecio-Barbero, María
dc.contributor.authorDíez, Álvaro
dc.contributor.authorBeño-Ruiz-de-la-Sierra, Rosa M.
dc.contributor.authorMartín-Gómez, Carmen
dc.contributor.authorSanz-Fuentenebro, Javier
dc.date.accessioned2024-02-28T19:05:34Z
dc.date.available2024-02-28T19:05:34Z
dc.date.issued2022
dc.identifier.citationEuropean Archives of Psychiatry and Clinical Neuroscience 273(6):1379-1386es
dc.identifier.issn0940-1334es
dc.identifier.urihttps://uvadoc.uva.es/handle/10324/66439
dc.description.abstractAiming at discerning potential biotypes within the psychotic syndrome, we have recently reported the possible existence of two clusters or biotypes across schizophrenia and bipolar disorder characterized by their cognitive performance using the Brief Assessment of Cognition in Schizophrenia (BACS) instrument and validated with independent biological and clinical indexes (Fernández-Linsenbarth et al. in Schizophr Res 229:102–111, 2021). In this previous work, the group with larger cognitive deficits (N = 93, including 69 chronic schizophrenia, 17 first episodes (FE) of schizophrenia and 7 bipolar disorder patients) showed smaller thalamus and hippocampus volume and hyper-synchronic electroencephalogram than the group with milder deficits (N = 105, including 58 chronic schizophrenia, 25 FE and 22 bipolar disorder patients). We predicted that if these biotypes indeed corresponded to different cognitive and biological substrates, their adaptation to real life would be different. To this end, in the present work we have followed up the patients’ population included in that work at 1st and 3rd years after the date of inclusion in the 2021 study and we report on the statistical comparisons of each clinical and real-life outcomes between them. The first cluster, with larger cognitive deficits and more severe biological alterations, showed during that period a decreased capacity for job tenure (1st and 3rd years), more admissions to a psychiatric ward (1st year) and a higher likelihood for quitting psychiatric follow-up (3rd year). Patients in the second cluster, with moderate cognitive deficits, were less compliant with prescribed treatment at the 3rd year. The differences in real-life outcomes may give additional external validity to that yielded by biological measurements to the described biotypes based on neurocognition.es
dc.format.mimetypeapplication/pdfes
dc.language.isospaes
dc.publisherSpringeres
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.titleReal-life outcomes in biotypes of psychotic disorders based on neurocognitive performancees
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.doi10.1007/s00406-022-01518-1es
dc.identifier.publicationfirstpage1379es
dc.identifier.publicationissue6es
dc.identifier.publicationlastpage1386es
dc.identifier.publicationtitleEuropean Archives of Psychiatry and Clinical Neurosciencees
dc.identifier.publicationvolume273es
dc.peerreviewedSIes
dc.identifier.essn1433-8491es
dc.type.hasVersioninfo:eu-repo/semantics/draftes


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