Web of Science: 7 cites, Scopus: 7 cites, Google Scholar: cites,
The role of schizotypal traits and the OXTR gene in theory of mind in schizophrenia : A family-based study
Giralt López, Maria (Universitat Autònoma de Barcelona. Departament de Psiquiatria i de Medicina Legal)
Miret, S. (Hospital Universitari Santa Maria, Lleida)
Soler, J. (Universitat de Barcelona)
Campanera i Reig, Sílvia (Hospital Universitari Santa Maria, Lleida)
Parellada, M. (Hospital General Universitario Gregorio Marañón)
Fañanás Saura, Lourdes (Universitat de Barcelona)
Fatjó-Vilas, Mar (Universitat de Barcelona)

Data: 2020
Resum: There is consistent evidence that theory of mind (ToM) is impaired in schizophrenia (SZ); however, it remains unclear whether such deficits are trait- or state-dependent. We evaluated ToM in patients with schizophrenia spectrum disorders (SSDs), their healthy first-degree relatives, and controls to test its suitability as an endophenotypic marker. We also studied the modifying effect of markers of clinical and genetic liability to SZ (schizotypy and genetic variability in the oxytocin receptor gene: OXTR) on ToM in healthy individuals. The sample included 38 stable SSD patients, 80 unaffected first-degree relatives, and 81 controls. ToM was assessed using the Hinting Task (HT) and schizotypy via the Schizotypal Personality Questionnaire-Brief (SPQ-B), which generates interpersonal (SPQ-IP), cognitive-perceptual (SPQ-CP), and disorganization (SPQ-D) scores. The polymorphism rs53576 of OXTR was genotyped. Patients presented poorer HT performance than relatives and controls (p = 0. 003 and p < 0. 001). High SPQ-IP and SPQ-CP scores correlated with poorer ToM performance in relatives (p = 0. 010 and p = 0. 030), but not in controls. OXTR was not associated with HT scores, but it showed a modifying effect within controls; high SPQ-CP was related to HT poorer performance conditional to GG genotype (p = 0. 007). ToM deficits were present in patients but not in unaffected relatives or controls. However, our data indicate the usefulness of clinical and genetic liability markers to characterize differences in ToM abilities within healthy individuals. Then, the observed link between ToM and SZ liability suggests the putative role of ToM as an endophenotypic marker. Nevertheless, new analyses in larger samples are needed.
Ajuts: Instituto de Salud Carlos III PI15-01420
Instituto de Salud Carlos III CD16-00264
Agència de Gestió d'Ajuts Universitaris i de Recerca 2017-SGR-1577
Agència de Gestió d'Ajuts Universitaris i de Recerca 2017-SGR-1271
Drets: Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original. Creative Commons
Llengua: Anglès
Document: Article ; recerca ; Versió publicada
Matèria: Family-based study ; OXTR gene ; Schizophrenia ; Schizotypy ; Theory of mind
Publicat a: European psychiatry, Vol. 63 (february 2020) , ISSN 1778-3585

DOI: 10.1192/j.eurpsy.2019.17
PMID: 32093796


8 p, 208.7 KB

El registre apareix a les col·leccions:
Documents de recerca > Documents dels grups de recerca de la UAB > Centres i grups de recerca (producció científica) > Ciències de la salut i biociències > Institut d'Investigació en Ciencies de la Salut Germans Trias i Pujol (IGTP)
Articles > Articles de recerca
Articles > Articles publicats

 Registre creat el 2020-07-13, darrera modificació el 2024-05-24



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