Cognitive alexithymia is associated with the degree of risk for psychosis

PLoS One. 2015 Jun 1;10(6):e0124803. doi: 10.1371/journal.pone.0124803. eCollection 2015.

Abstract

Alexithymia is a personality construct denoting emotion processing problems. It has been suggested to encompass two dimensions: a cognitive and affective dimension. The cognitive dimension is characterized by difficulties in identifying, verbalizing and analyzing emotions, while the affective dimension reflects the level of emotional arousal and imagination. Alexithymia has been previously proposed as a risk factor for developing psychosis. More specifically, the two alexithymia dimensions might be differentially related to the vulnerability for psychosis. Therefore, we examined the two dimensions of alexithymia, measured with the BVAQ in 94 siblings of patients with schizophrenia, 52 subjects at ultra-high risk (UHR) for developing psychosis, 38 patients with schizophrenia and 109 healthy controls. The results revealed that siblings and patients had higher levels of cognitive alexithymia compared to controls. In addition, subjects at UHR for psychosis had even higher levels of cognitive alexithymia compared to the siblings. The levels of affective alexithymia in siblings and patients were equal to controls. However, UHR individuals had significantly lower levels of affective alexithymia (i.e. higher levels of emotional arousal and fantasizing) compared to controls. Alexithymia was further related to subclinical levels of negative and depressive symptoms. These findings indicate that alexithymia varies parametrically with the degree of risk for psychosis. More specifically, a type-II alexithymia pattern, with high levels of cognitive alexithymia and normal or low levels of affective alexithymia, might be a vulnerability factor for psychosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Affective Symptoms / complications*
  • Female
  • Humans
  • Male
  • Psychotic Disorders / etiology*
  • Risk Factors
  • Schizophrenia / etiology
  • Young Adult

Grants and funding

AA is supported in part by a Vici grant from the Dutch organization for scientific research (NWO, grant number: 435-11-004). LK is supported in part by a Vici grant from NWO (grant number 435-11-006). The GROUP project is supported by a grant from The Netherlands organization for health research and development (ZonMw), within the Mental Health program (project number 10.000.1002). ZonMw is a non-profit organisation working for the Ministry of Health, Welfare and Sport (VWS) and the NWO. The authors would like to thank Paula M. Gromann, Roeline Nieboer, Esther M. Opmeer and Edith J. Liemburg for their assistance in collecting the data.