Fractionation of Verbal Memory Impairment in Schizophrenia and Schizophreniform Psychosis

Author:

Wood Stephen J.12,Tarnawski Aleks U.3,Proffitt Tina M.4,Brewer Warrick J.4,Savage Greg R.5,Anderson Vicki6,McGorry Patrick D.4,Wood Stephen J.12,Tarnawski Aleks U.3,Proffitt Tina M.4,Brewer Warrick J.4,Savage Greg R.5,Anderson Vicki6,McGorry Patrick D.4,Velakoulis Dennis7,Pantelis Christos7

Affiliation:

1. Melbourne Neuropsychiatry Centre, c/– National Neuroscience Facility, 161 Barry Street, Carlton, Vic. 3053, Melbourne, Victoria, Australia

2. Brain Research Institute, Melbourne, Victoria, Australia

3. Melbourne Neuropsychiatry Centre, Department of Psychiatry, University of Melbourne and Murdoch Children's Research Institute, Melbourne, Victoria, Australia

4. ORYGEN Research Centre, Department of Psychiatry, University of Melbourne, Victoria, Australia

5. Melbourne Neuropsychiatry Centre, Department of Psychiatry, University of Melbourne, Melbourne, Victoria and Macquarie Centre for Cognitive Science (MACCS), Macquarie University, Sydney, New South Wales, Australia

6. Department of Psychology, Royal Children's Hospital, Melbourne, Victoria, Australia

7. Melbourne Neuropsychiatry Centre, Department of Psychiatry, University of Melbourne, Melbourne, Victoria, Australia

Abstract

Objectives: The characterization, aetiology, and course of verbal memory deficits in schizophrenia remain ill defined. The impact of antipsychotic medications is also unclear. The purpose of the present paper was to investigate verbal memory performance in established schizophrenia (SZ) and first-episode schizophreniform psychosis (FE). Method: Performances of 32 SZ and 33 FE patients were compared to those of 47 healthy volunteers on measures of verbal working memory, verbal associative learning and story recall. Results: Story recall deficits, but not deficits in working memory or paired associate learning, were demonstrated by both patient groups. Patients treated with typical neuroleptics had more impairment in associative learning with arbitrary word pairings than those treated with atypicals, regardless of patient group. Conclusions: The results are consistent with the notion that some neuropsychological impairment is present at the time of psychosis onset and that this impairment is non-progressive. However, deficits may be specific to subclasses of memory function.

Publisher

SAGE Publications

Subject

Psychiatry and Mental health,General Medicine

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