Original Article

Neuropsychopharmacology (2007) 32, 162–170. doi:10.1038/sj.npp.1301151; published online 28 June 2006

Clinical Research

Impact of Catechol-O-Methyltransferase on Prefrontal Brain Functioning in Schizophrenia Spectrum Disorders

Ann-Christine Ehlis1, Andreas Reif1, Martin J Herrmann1, Klaus-Peter Lesch1 and Andreas J Fallgatter1

1Department of Psychiatry and Psychotherapy, University of Wuerzburg, Wuerzburg, Germany

Correspondence: Dr A-C Ehlis, Laboratory for Psychophysiology and Functional Imaging, Department of Psychiatry and Psychotherapy, University of Wuerzburg, Fuechsleinstrasse 15, Wuerzburg 97080, Germany, Tel: +49 931 201 77410, Fax: +49 931 201 77550, E-mail: Ehlis_A@klinik.uni-wuerzburg.de

Received 28 November 2005; Revised 13 April 2006; Accepted 17 May 2006; Published online 28 June 2006.

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Abstract

The enzyme catechol-O-methyltransferase (COMT) has attracted increasing interest regarding a genetic disposition towards schizophrenias and as a modulator of prefrontal brain function. A common SNP in the COMT gene causes a Val to Met transition at AA158/AA108 (Val158Met), resulting in reduced COMT activity in Met allele carriers. An impact of COMT genotype on cognition has been well established; however, the exact nature of this influence has yet to be elucidated. The aim of this study was to determine whether COMT genotype affects an electrophysiological marker of prefrontal activation and neuropsychological frontal lobe measures in schizophrenia. To this end, 56 acutely psychotic in-patients with schizophrenia spectrum disorders were investigated. Patients with the COMT 1947AA (Met/Met) genotype (n=13) were compared to a carefully matched sample of patients with a G1947A (Val/Met) genotype (n=15); matching criteria included patients' age, handedness, gender distribution, diagnosis, and medication status. A small group of six homozygous Val allele carriers was additionally included to allow an assessment of possible gene-dosage effects. P300 amplitudes and latencies, as well as an electrophysiological marker of prefrontal brain function (NoGo-Anteriorization/NGA) and neuropsychological measures (Stroop Test, Verbal Fluency, Trail Making Test) were regarded. Homozygous Met allele carriers had significantly increased NGA values and fronto-central Nogo amplitudes compared to patients with at least one Val allele. They also tended to perform better in the Stroop task, as compared to the matched group of Val/Met patients. These results indicate that COMT genotype exerts a strong impact on prefrontal functioning and executive control in schizophrenia spectrum disorders.

Keywords:

COMT (catechol-O-methyltransferase), schizophrenia, prefrontal cortex, anterior cingulate cortex (ACC), response control, executive functions

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