Comparison of three computer-administered cognitive tasks as putative endophenotypes of schizophrenia
Received 12 April 2006; received in revised form 1 August 2006; accepted 2 August 2006. published online 27 September 2006.
Abstract
It has been repeatedly demonstrated that individuals with schizotypal personality features (SPF) exhibit similar endophenotypic traits as persons with schizophrenia. Less research has compared the relative sensitivity of different endophenotypes in the same sample of individuals with SPF. Fourteen university students with SPF (mean age 20.5±1.6; 43% male) and 26 controls (mean age 20.3±1.1; 31% male) were defined by the Abbreviated Schizotypal Personality Questionnaire (SPQ-B). All participants reported no known biological relative with schizophrenia. Participants completed three computer-administered cognitive tasks: a 6-min degraded-stimuli A–X Continuous Performance Test (CPT), the Wisconsin Card Sort Test (WCST), and a Span of Apprehension (SOA) task (6- and 12-letter arrays). On the CPT, only omission errors resulted in a statistically significant group difference, U=115.5, p=.05, Cohen's d=0.54 (medium effect size), with the SPF group (mean errors: 3.43±3.28) making more omission errors than controls (mean errors: 1.88±2.66). Notably, 46% of the controls had no omission errors, compared to 14% of the SPF group. The only SPQ-B factor score to show a statistically significant linear relationship with CPT omission errors was the Cognitive–Perceptual factor (rs=.33, p=.04). Group differences on performance indices from the SOA and WCST did not approach statistical significance. Based on performance from the community-identified schizotypes, results suggest that performance on the CPT may represent a more robust endophenotype of schizophrenia, compared to the SOA and WCST.
Department of Psychology, University of Central Florida, Orlando, FL, USA
Corresponding author. Department of Psychology, P.O. Box 161390, University of Central Florida, Orlando, FL 32816-1390, USA. Tel.: +1 407 823 5858; fax: +1 407 823 5862.