Catechol-O-Methyltransferase Val super(158)Met Polymorphism and Antisaccade Eye Movements in Schizophrenia

The catechol-O-methyltransferase (COMT) enzyme catabolizes dopamine. The val super(158)met single nucleotide polymorphism (rs4680) in the COMT gene has received considerable attention as a candidate gene for schizophrenia as well as for frontally mediated cognitive functions. Antisaccade performance...

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Veröffentlicht in:Schizophrenia bulletin 2010-01, Vol.36 (1), p.157-164
Hauptverfasser: Haraldsson, Haraldur Magnus, Ettinger, Ulrich, Magnusdottir, Brynja B, Sigmundsson, Thordur, Sigurdsson, Engilbert, Ingason, Andres, Petursson, Hannes
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container_end_page 164
container_issue 1
container_start_page 157
container_title Schizophrenia bulletin
container_volume 36
creator Haraldsson, Haraldur Magnus
Ettinger, Ulrich
Magnusdottir, Brynja B
Sigmundsson, Thordur
Sigurdsson, Engilbert
Ingason, Andres
Petursson, Hannes
description The catechol-O-methyltransferase (COMT) enzyme catabolizes dopamine. The val super(158)met single nucleotide polymorphism (rs4680) in the COMT gene has received considerable attention as a candidate gene for schizophrenia as well as for frontally mediated cognitive functions. Antisaccade performance is a good measure of frontal lobe integrity. Deficits on the task are considered a trait marker for schizophrenia. The aim of this study was to investigate the association of COMT val super(158)met polymorphism with antisaccade eye movements in schizophrenia patients and healthy controls. Schizophrenia patients (N = 105) and healthy controls (N = 95) underwent infrared oculographic assessment of antisaccades. Subjects were genotyped for COMT val super(158)met and divided into 3 groups according to genotype (val/val, val/met, and met/met). Patients displayed significantly more reflexive errors, longer and more variable latency, and lower amplitude gain than controls (all P < 0.02). A greater number of val super(158) alleles was associated with shorter (P = 0.045) and less variable (P = 0.028) antisaccade latency and, nonsignificantly, with lower reflexive error rate (P = 0.056). None of these variables showed a group-by-genotype interaction (P > 0.1). There were no significant associations of genotype with measures of amplitude gain or spatial error (P > 0.2). The results suggest that COMT val super(158) carrier status is associated with better performance on the antisaccade task. Possible explanations of this finding are discussed.
doi_str_mv 10.1093/schbul/sbn064
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title Catechol-O-Methyltransferase Val super(158)Met Polymorphism and Antisaccade Eye Movements in Schizophrenia
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