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Catechol‐ O ‐methyltransferase and the clinical features of psychosis
Author(s) -
McClay J.L.,
Fanous A.,
van den Oord E.J.C.G.,
Webb B.T.,
Walsh D.,
O'Neill F.A.,
Kendler K.S.,
Chen X.
Publication year - 2006
Publication title -
american journal of medical genetics part b: neuropsychiatric genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.393
H-Index - 126
eISSN - 1552-485X
pISSN - 1552-4841
DOI - 10.1002/ajmg.b.30401
Subject(s) - catechol o methyl transferase , psychosis , psychology , schizophrenia (object oriented programming) , allele , mania , clinical psychology , psychiatry , genetics , bipolar disorder , cognition , biology , gene
A functional polymorphism (Val‐158‐Met) at the Catechol‐ O ‐methyltransferase ( COMT ) locus has been identified as a potential etiological factor in schizophrenia. Yet the association has not been convincingly replicated across independent samples. We hypothesized that phenotypic heterogeneity might be diluting the COMT effect. To clarify the putative association, we performed an exploratory analysis to test for association between COMT and five psychosis symptom scales. These were derived through factor analysis of the Operational Criteria Checklist for Psychiatric Illness. Our sample was the Irish Study of High Density Schizophrenia Families, a large collection consisting of 268 multiplex families. This sample has previously shown a small but significant effect of the COMT Val allele in conferring risk for schizophrenia. We tested for preferential transmission of COMT alleles from parent to affected offspring (n = 749) for each of the five factor‐derived scales (negative symptoms, delusions, hallucinations, mania, and depression). Significant overtransmission of the Val allele was found for mania ( P < 0.05) and depression ( P = 0.01) scales. Examination of odds ratios (ORs) revealed a heterogeneous effect of COMT , whereby it had no effect on Negative Symptoms, but largest impact on Depression (OR = 1.4). These results suggest a modest affective vulnerability conferred by this allele in psychosis, but will require replication. © 2006 Wiley‐Liss, Inc.