Publication:
Visual memory dysfunction as a neurocognitive endophenotype in bipolar disorder patients and their unaffected relatives. Evidence from a 5-year follow-up Valencia study.

dc.contributor.authorCorrea-Ghisays, Patricia
dc.contributor.authorSánchez-Ortí, Joan Vicent
dc.contributor.authorAyesa-Arriola, Rosa
dc.contributor.authorSetién-Suero, Esther
dc.contributor.authorBalanzá-Martínez, Vicent
dc.contributor.authorSelva-Vera, Gabriel
dc.contributor.authorRuiz-Ruiz, Juan Carlos
dc.contributor.authorVila-Francés, Joan
dc.contributor.authorMartinez-Aran, Anabel
dc.contributor.authorVivas-Lalinde, Juliana
dc.contributor.authorConforte-Molina, Candela
dc.contributor.authorSan-Martín, Constanza
dc.contributor.authorMartínez-Pérez, Carlos
dc.contributor.authorFuentes-Durá, Inmaculada
dc.contributor.authorCrespo-Facorro, Benedicto
dc.contributor.authorTabarés-Seisdedos, Rafael
dc.date.accessioned2023-01-25T13:36:39Z
dc.date.available2023-01-25T13:36:39Z
dc.date.issued2019-07-02
dc.description.abstractScarce research has focused on Visual Memory (VM) deficits as a possible neurocognitive endophenotype of bipolar disorder (BD). The main aim of this longitudinal, family study with healthy controls was to explore whether VM dysfunction represents a neurocognitive endophenotype of BD. Assessment of VM by Rey-Osterrieth Complex Figure Test (ROCF) was carried out on a sample of 317 subjects, including 140 patients with BD, 60 unaffected first-degree relatives (BD-Rel), and 117 genetically-unrelated healthy controls (HC), on three occasions over a 5-year period (T1, T2, and T3). BD-Rel group scores were analyzed only at T1 and T2. Performance of BD patients was significantly worse than the HC group (p  Important attrition in BD-Rel group over time was detected, which precluded analysis at T3. BD patients show significant deficits in VM that remain stable over time, even after controlling sociodemographic and clinical variables. Unaffected relatives also show stable deficits in VM. Accordingly, the deficit in VM could be considered a potential endophenotype of BD, which in turn may be useful as a predictor of the evolution of the disease. Further studies are needed to confirm these findings.
dc.identifier.doi10.1016/j.jad.2019.06.059
dc.identifier.essn1573-2517
dc.identifier.pmid31299402
dc.identifier.urihttp://hdl.handle.net/10668/14238
dc.journal.titleJournal of affective disorders
dc.journal.titleabbreviationJ Affect Disord
dc.language.isoen
dc.organizationHospital Universitario Virgen del Rocío
dc.page.number31-37
dc.pubmedtypeJournal Article
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.subjectBipolar disorder
dc.subjectEndophenotype
dc.subjectFamily study
dc.subjectLongitudinal study
dc.subjectNeurocognition
dc.subjectVisual memory
dc.subject.meshAdolescent
dc.subject.meshAdult
dc.subject.meshAged
dc.subject.meshBipolar Disorder
dc.subject.meshCognition
dc.subject.meshEndophenotypes
dc.subject.meshFemale
dc.subject.meshFollow-Up Studies
dc.subject.meshHealth Status
dc.subject.meshHumans
dc.subject.meshLongitudinal Studies
dc.subject.meshMale
dc.subject.meshMemory Disorders
dc.subject.meshMiddle Aged
dc.subject.meshNeuropsychological Tests
dc.subject.meshYoung Adult
dc.titleVisual memory dysfunction as a neurocognitive endophenotype in bipolar disorder patients and their unaffected relatives. Evidence from a 5-year follow-up Valencia study.
dc.typeresearch article
dc.volume.number257
dspace.entity.typePublication

Files