Do measures of schizotypal personality provide non-clinical analogues of schizophrenic symptomatology?
Introduction
Contemporary authors generally conceptualise schizophrenia and other psychopathological disorders as extreme forms of disease processes. The quasi-dimensional approach stems from the psychiatric perspective and focuses on illness; specifically, the degrees of expression of a disease (Rado, 1953, Meehl, 1966). The fully dimensional approach incorporates the quasi-dimensional view of continuity, but also extends the continuity to include the healthy personality, which provides the starting point for the model. Thus, advocates of this model propose that the dimension of schizotypy lies on a continuum that begins with normality and proceeds towards the schizophrenia spectrum disorders, with schizophrenia at the upper end (Claridge and Beech, 1995).
A growing body of evidence has emerged to support the fully dimensional (or continuum) model of schizophrenia. Individuals high in schizotypal personality exhibit a range of cognitive and executive deficits (Peters et al., 1994, Park et al., 1995, Tsakanikos and Claridge, 2005) which are also found in schizophrenic patients (Beech et al., 1989, Liddle and Morris, 1991, Park and Holzman, 1992). Furthermore, the heterogeneous positive, negative and disorganised symptom subtypes found in schizophrenia (Liddle, 1987, Arndt et al., 1991) are also found in schizotypal personality (Raine et al., 1991, Chen et al., 1997).
Some authors report the presence of four schizotypal characteristics; namely the traditional positive, negative and disorganised factors and a fourth factor known as Impulsive Nonconformity (ImpNon) (Mason et al., 1995, Vollema and van den Bosch, 1995). However, Pickering (2004) argues that ImpNon is not a true schizotypal factor because it does not reflect cognitions or behaviours found in schizophrenia. Rather, ImpNon is more reminiscent of the impulsive, antisocial, sensation-seeking (ImpASS) traits found in certain personality disorders, such as borderline, schizoid or antisocial personality disorders. High ImpNon scores are not found in the relatives of schizophrenic patients (Claridge et al., 1983) and high ImpNon scores in healthy individuals do not significantly predict increased risk of psychosis (Chapman et al., 1994).
As previously stated, research has shown that schizophrenic-like symptoms are present, in an attenuated form, in the general population. The complex and multi-dimensional nature of schizotypal personality is captured through the use of reliable and valid measures such as the Schizotypal Personality Questionnaire (SPQ) (Raine, 1991) and the Oxford-Liverpool Inventory of Feelings and Experiences (O-LIFE) (Mason et al., 1995). The SPQ is based on DSM-III-R criteria for schizotypal personality disorder, while the O-LIFE is derived from factor-analytic studies of non-clinical measures (Mason et al., 1995, Vollema and van den Bosch, 1995). Schizophrenic symptomatology is assessed using standard clinical measures such as the Scale for the Assessment of Positive Symptoms and Scale for the Assessment of Negative Symptoms (SAPS/SANS) (Andreasen, 1983, Andreasen, 1984) and the Positive and Negative Syndrome Scales (PANSS) (Kay et al., 1987).
Interestingly, there is a striking paucity of research examining schizotypal characteristics in schizophrenic patients. It is generally assumed that non-clinical schizotypal measures are assessing schizophrenia-like traits in healthy individuals, but this assumption does not appear to have been formally tested. The central aim of this study was to compare the scores of schizophrenic patients and healthy controls on the O-LIFE measures of schizotypal personality. If schizotypy is truly a dimensional construct, and non-clinical measures assess schizophrenia-like characteristics, then the difference in schizotypy scores should be quantitative (i.e. higher in patients than controls) rather than qualitative. Another aim was to assess the relationship between SAPS/SANS symptomatology and O-LIFE schizotypal characteristics in schizophrenic patients.
It was hypothesised that the patients would score significantly higher than controls on the three traditional measures of schizotypy (positive, negative and disorganised). However, based on Pickering's (2004) assertion, it was expected that there would be no significant difference in Impulsive Nonconformity scores between the patients and controls. It was also expected that there would be significant positive relationships between scores on the SAPS/SANS and O-LIFE positive, negative and disorganisation scales in the patient group.
Finally, a measure of fluid IQ was included to rule out the possibility that any differences in symptomatology between patients and controls could be due to a cognitive artefact. Tests of fluid IQ are believed to assess a globally integrated (prefrontally mediated) cognitive function (Duncan, 1993, Duncan, 1995), and therefore an examination of this seemed particularly relevant for the current purposes. A more extensive battery of IQ tests was not possible in the time available as the patients were also tested on a battery of executive function tasks; a manuscript reporting the relationships between symptoms and performance on the executive function tests is currently in preparation.
Section snippets
Ethics
Ethical approval for the study was obtained from the South West London Local Research Ethics Committee and from the Psychology Department's Ethics Committee at Goldsmiths College.
Participants
Twenty schizophrenic patients and two groups of healthy controls participated in the study. The patient sample consisted of 18 males and 2 females, and the mean age of the patient group was 34.3 (S.D. = 8.4). Patients were recruited from inpatient wards at Springfield University Hospital and outpatient clinics in the
Power calculation
Prior to the analyses, a power calculation was made using the G-Power programme. When testing the difference in O-LIFE scores between the patients and the controls, to achieve power of 80% for an anticipated large effect size (Cohen's d = 0.8) at alpha = 0.05, with a 1-tailed t-test, 20 participants were required in each group. In each group of 20 participants, the power to detect a correlation of 0.5 (e.g., between O-LIFE scores and symptom ratings in the patients) is also 0.8.
Assessment of SAPS/SANS inter-rater reliability
The correlations
Discussion
The central aims of this study were to compare levels of O-LIFE schizotypal personality in schizophrenic patients and healthy controls, and to examine relationships between SAPS/SANS symptoms and analogous O-LIFE characteristics in the patient group.
Patients reported significantly higher levels of O-LIFE positive and negative schizotypy than fluid IQ-matched controls and age- and gender-matched controls. They also reported significantly higher levels of O-LIFE disorganised schizotypy than age-
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