Hostname: page-component-6898cfcb55-th4rj Total loading time: 0 Render date: 2026-11-11T09:37:39.105Z Has data issue: false hasContentIssue false
  • English
  • Français

COMT Val158Met moderation of stress-induced psychosis

Published online by Cambridge University Press:  20 July 2007

NICHOLAS C. STEFANIS,
CÉCILE HENQUET,
DIMITRIOS AVRAMOPOULOS,
NIKOLAOS SMYRNIS,
IOANNIS EVDOKIMIDIS,
INEZ MYIN-GERMEYS,
COSTAS N. STEFANIS and
JIM VAN OS
NICHOLAS C. STEFANIS*
Affiliation:
University Mental Health Research Institute, Athens, GreeceEginition Hospital, Department of Psychiatry, National and Kapodistrian University of Athens, GreeceDivision of Psychological Medicine, Institute of Psychiatry, London, UK
CÉCILE HENQUET
Affiliation:
Department of Psychiatry and Neuropsychology, South Limburg Mental Health Research and Teaching Network, EURON, Maastricht University, Maastricht, The Netherlands
DIMITRIOS AVRAMOPOULOS
Affiliation:
University Mental Health Research Institute, Athens, Greece
NIKOLAOS SMYRNIS
Affiliation:
University Mental Health Research Institute, Athens, GreeceEginition Hospital, Department of Psychiatry, National and Kapodistrian University of Athens, Greece
IOANNIS EVDOKIMIDIS
Affiliation:
University Mental Health Research Institute, Athens, Greece
INEZ MYIN-GERMEYS
Affiliation:
Department of Psychiatry and Neuropsychology, South Limburg Mental Health Research and Teaching Network, EURON, Maastricht University, Maastricht, The Netherlands
COSTAS N. STEFANIS
Affiliation:
University Mental Health Research Institute, Athens, Greece
JIM VAN OS
Affiliation:
Division of Psychological Medicine, Institute of Psychiatry, London, UKDepartment of Psychiatry and Neuropsychology, South Limburg Mental Health Research and Teaching Network, EURON, Maastricht University, Maastricht, The Netherlands
*
*Address for correspondence: Dr Nicholas C. Stefanis, Assistant Professor in Psychiatry, Department of Psychiatry, National and Kapodistrian University of Athens, Eginition Hospital, 74 Vas. Sofias Avenue, Athens11528, Greece. (Email: nistefan@med.uoa.gr)
Rights & Permissions [Opens in a new window]

Abstract

Background

Exposure to stressful life events increases the risk of developing a psychotic disorder. Moreover, increased reactivity to stress seems to represent part of the vulnerability for psychosis. This study aimed to investigate whether a functional polymorphism in the catechol-O-methyltransferase (COMT Val158Met) gene moderates the psychosis-inducing effects of stress.

Method

A semi-experimental stress exposure paradigm was used in a sample of 306 genotyped young men (aged 19–24 years), in whom measures of psychotic symptoms were obtained at recruitment in the Greek army (exposed condition) and again after 18 months of military training (unexposed condition).

Results

Stress exposure at army induction was associated with an increased level of psychotic symptoms. In addition, carriers of the COMT Val158Met Val allele were more susceptible to the effect of stress on the psychosis outcome than those with the Met/Met genotype (test for interaction: χ2=5·02, df=1, p=0·025).

Conclusion

The COMT Val158Met genotype may moderate the effect of stress on psychotic symptoms.

Information

Type
Original Article
Information
Psychological Medicine , Volume 37 , Issue 11 , November 2007, pp. 1651 - 1656
Copyright
Copyright © Cambridge University Press 2007

INTRODUCTION

Exposure to stressful life events increases the risk of developing a psychotic disorder in proportion to the intensity of the stressful experiences (Lukoff et al. Reference Lukoff, Snyder, Ventura and Nuechterlein1984; Bebbington et al. Reference Bebbington, Wilkins, Jones, Foerster, Murray, Toone and Lewis1993; Myin-Germeys et al. Reference Myin-Germeys, Krabbendam, Delespaul and Van Os2003). Powerful evidence for the role of stress in the aetiology of psychosis comes from the study of psychosis after semi-experimental stressful conditions such as army induction (Steinberg & Durell, Reference Steinberg and Durell1968). In addition, stresses of urban life (van Os et al. Reference van Os, Hanssen, Bijl and Vollebergh2001), as well as victimization and childhood trauma (Lataster et al. Reference Lataster, van Os, Drukker, Henquet, Feron, Gunther and Myin-Germeys2006), have consistently been found to be associated with increased clinical and subclinical levels of psychosis (Bebbington et al. Reference Bebbington, Wilkins, Jones, Foerster, Murray, Toone and Lewis1993; Read et al. Reference Read, van Os, Morrison and Ross2005). As dopamine is thought to play an important role in mediating stress-related responses (Laruelle, Reference Laruelle2000) and attributing salience to meaningful environmental stimuli (Kapur, Reference Kapur2003), the hypothesis of stress-induced hyperdopaminergic states, resulting in aberrant assignment of salience and development of hallucinatory and delusional experiences, can be put forward. In support of this hypothesis is work showing that patients with an established psychotic disorder display greater psychosis reactivity to small daily stressors compared to healthy controls, as do their first-degree relatives, albeit to a lesser extent (Myin-Germeys et al. Reference Myin-Germeys, Delespaul and van Os2005). Part of the abnormal sensitivity to stress-induced psychosis may thus be due to a familial liability to dysregulation of dopamine neurotransmission. Recently, it was found that a functional polymorphism in the catechol-O-methyltransferase (COMT Val158Met) gene may moderate the psychosis-inducing effect of the dopamine agonist delta-9-tetrahydrocannabinol (Δ-9-THC) (Caspi et al. Reference Caspi, Moffitt, Cannon, McClay, Murray, Harrington, Taylor, Arseneault, Williams, Braithwaite, Poulton and Craig2005; Henquet et al. Reference Henquet, Rosa, Krabbendam, Papiol, Fananas, Drukker, Ramaekers and van Os2006). The COMT gene encodes catechol-O-methyltransferase, which is an enzymatic inactivator of dopamine, in particular in the prefrontal cortex. The functional polymorphism involves a methionine (Met) to valine (Val) substitution at codon 158, which results in two common allelic variants, Val and Met, associated respectively with high versus low enzyme activity (Lotta et al. Reference Lotta, Vidgren, Tilgmann, Ulmanen, Melen, Julkunen and Taskinen1995; Lachman et al. Reference Lachman, Papolos, Saito, Yu, Szumlanski and Weinshilboum1996). In Caucasian populations, this results in a distribution of individuals with the Met/Met (approximately 25%), Val/Met (50%) and Val/Val (25%) genotype. As the COMT Val158Met genotype alone is not associated with overall greater risk for psychotic illness (Fan et al. Reference Fan, Zhang, Gu, Li, Sun, Wang, Feng, St Clair and He2005; Flint & Munafo, Reference Flint and Munafo2007) and reported environmental risk factors for psychosis have weak effect sizes at best, more environmental risk factors may interact with the COMT Val158Met genotype in causing psychosis. Gene–environment interaction occurs when the effect of an environmental stressor on a person's health is conditional upon his or her genotype (Caspi & Moffitt, Reference Caspi and Moffitt2006). In complete gene–environment interaction, the effects of genes and environment are dependent on each other in such a way that exposure to neither, or either one alone, does not result in disease, whereas exposure to both does (van Os et al. Reference van Os, Hanssen, Bak, Bijl and Vollebergh2003). To determine gene–environment interaction, gene–environment correlation (the degree to which exposure to environmental factors may be caused by an individual's genetic vulnerability) needs to be considered as well (Bergeman et al. Reference Bergeman, Plomin, Pedersen and McClearn1991).

In the current study, the interaction between the COMT Val158Met genotype and environmental stress on psychosis outcomes was therefore studied in an observational semi-experimental design. We investigated whether (i) an intense and datable increase in stress (young men at the start of a compulsory army induction programme) was associated with an increase in psychotic symptoms and (ii) whether any increase in psychotic symptoms was moderated by the COMT Val158Met genotype.

METHOD

Subjects

A total of 2243 male recruits, aged 19–24 years, participated in the Athens Study of Psychosis Proneness and Incidence of Schizophrenia (Stefanis et al. Reference Stefanis, Van Os, Avramopoulos, Smyrnis, Evdokimidis, Hantoumi and Stefanis2004), a study of newly recruited conscripts undergoing basic training as part of their compulsory military service in Greece. Subjects were assessed at two measurements in time. The first assessment took place after the first 2 weeks of admission to the military service. A second measurement in a subset of the sample took place at completion of the military training (18 months later). To increase statistical power, high and average schizotypy scores were consecutively oversampled, a priori based on high (above the 90th percentile) or medium (around the 50th percentile) scores on the Schizotypal Personality Questionnaire (SPQ), a self-rated schizotypy scale (Raine, Reference Raine1991), or either high (above the 95th percentile) or medium (around the 50th percentile) scores on the Perceptual Aberration Scale (PAS; Chapman et al. Reference Chapman, Chapman and Raulin1978). Analyses were thus conducted on a risk set of 306 subjects of which 34% scored above the 90th and 27% around the 50th percentile of the SPQ at the first assessment. At both assessments, subjects completed demographic questionnaires and self-rated psychometric evaluations. DNA was extracted from a mouthwash mixture. Genotyping was performed using polymerase chain reaction (PCR) amplification and digestion with the restriction enzyme NiaII and 3% agarose electrophoresis as described by Kirov et al. (Reference Kirov, Murphy, Arranz, Jones, McCandles, Kunugi, Murray, McGuffin, Collier, Owen and Craddock1998). The mean age of these subjects was 20·6 years (s.d.=1·8, range=19–24 years).

The period of induction into compulsory military service compared to the period of conclusion of the training 18 months later was hypothesized to be a proxy measure of stress (Steinberg & Durell, Reference Steinberg and Durell1968; Hatzitaskos et al. Reference Hatzitaskos, Soldatos, Giouzelis, Karvelis and Spilioti1997). Army induction was considered to be associated with increases in stress caused by being away from home for the first time and being exposed to combat scenarios, sleep deprivation and the rules and regime of initiation into the army corps. Several studies have shown increases in stress levels during the first weeks of military training (Clemons, Reference Clemons1996; Larson et al. Reference Larson, Booth-Kewley, Merrill and Stander2001), followed by a subsequent reduction of stress upon leaving the army (Lerew et al. Reference Lerew, Schmidt and Jackson1999; Schmidt et al. Reference Schmidt, Lerew and Joiner2000; Martin et al. Reference Martin, Williamson, Alfonso and Ryan2006). The compulsory aspect of the military training offers a unique natural setting to study genetic differences in stress sensitivity, as the level of environmental exposure to stress was datable, similar for all recruits and not associated with genetic variation (i.e. no evidence of gene–environment correlation). Assessment upon conclusion of military training was hypothesized to be associated with lower levels of stress, as the trainees would be better equipped to face up to the stresses of military life and related assignments. For the current analyses, the level of stress by period (0=low stress condition at conclusion of military training; 1=high stress condition at army induction) served as the environmental exposure.

To capture psychotic symptoms during the first 2 weeks of military training, the self-report Symptom Checklist-90 – Revised (SCL-90-R) was used. The ‘paranoid ideation’ and ‘psychoticism’ subscales were used to assess state-related psychotic symptoms (Henquet et al. Reference Henquet, Krabbendam, Spauwen, Kaplan, Lieb, Wittchen and van Os2005). Mean scores of both subscales were combined into a mean total score (hereafter the SCL-90-R psychosis score; Henquet et al. Reference Henquet, Krabbendam, Spauwen, Kaplan, Lieb, Wittchen and van Os2005). Psychotic symptoms at conclusion of military training were assessed similarly. To investigate whether any moderating effects of the COMT Val158Met genotype on stress sensitivity would specifically result in increased levels of psychosis, or would contribute to variation in psychological distress in general, symptoms of anxiety were also assessed at both measurements, using the SCL-90-R subscale ‘anxiety’ (hereafter the SCL-90-R anxiety score).

Analyses

As each individual had two observations (0, low stress condition at army conclusion; 1, high stress condition at army induction), multilevel random regression analyses were conducted, examining the effects of stress (low versus high stress condition) and the COMT Val158Met genotype (0=Met/Met, 1=Val/Met, 2=Val/Val) on the SCL-90-R psychosis symptom score. The stress×genotype interaction was fitted with genotype as dummy variables with Met/Met as reference category and regressed on the SCL-90-R psychosis symptom score. This allowed estimation of stress effect sizes for each genotype separately. Based on these results, the stress×genotype interaction was post hoc simplified to a stress×Val dominance term as described below (0=no Val alleles, 1=one or two Val alleles). Similarly, main effects of stress and the COMT Val158Met genotype, as well as their interaction, were regressed on the a priori selected SCL-90-R anxiety outcome, to determine whether any interaction between stress and the COMT Val158Met genotype was specific for psychosis. Main effects of the COMT Val158Met genotype on SCL-90-R symptom outcomes were examined in the low stress condition exclusively. Main effects and interactions were a priori adjusted for age and assessed by the Wald test.

RESULTS

The COMT Val158Met genotype distribution in the whole sample was 21% Met/Met, 49% Val/Met and 30% Val/Val and in Hardy–Weinberg equilibrium. Genotype was not associated with age [β=0·24, 95% confidence interval (CI) −0·03 to 0·51, p=0·085], nor with the SCL-90-R psychosis score in the low stress condition (β=−0·01, 95% CI −0·24 to 0·22, p=0·94 and β=−0·11, 95% CI −0·36 to 0·14, p=0·37 for Val/Met and Val/Val respectively) or with the SCL-90-R anxiety score (β=0·09, 95% CI −0·12 to 0·30, p=0·39 and β=0·03, 95% CI −0·20 to 0·26, p=0·80 for Val/Met and Val/Val respectively). The SCL-90-R psychosis score increased significantly with increasing level of stress (β=0·40, 95% CI 0·31−0·49, p<0·001), as did the SCL-90-R anxiety score (β=0·49, 95% CI 0·40−0·57, p<0·001). Carriers of the Val allele were more sensitive to the psychosis-inducing effects of stress than individuals of the Met/Met genotype (interaction for Val/Met: β=0·27, 95% CI 0·02−0·51, χ2=4·42, df=1, p=0·035 and interaction for Val/Val: β=0·26, 95% CI −0·01 to 0·53, χ2=3·50, df=1, p=0·061; Table 1). The effect of stress on the psychosis outcome was similar for the Val/Met and Val/Val genotypes (χ2=0·01, df=1, p=0·94), suggesting Val allele dominance. Thus, the post hoc model using the stress×Val dominance term interaction (0=no Val alleles, 1=one or two Val alleles) displayed significant interaction (Table 1). No interaction effects were observed for the SCL-90-R anxiety score (interaction for Val/Met β=0·20, 95% CI −0·05 to 0·44, χ2=2·52, df=1, p=0·11 and interaction for Val/Val β=0·17, 95% CI −0·10 to 0·43, χ2=1·52, df=1, p=0·22).

Table 1.

Mean SCL-90-R psychosis scores (subscales ‘paranoid ideation’ and ‘psychoticism’) stratified by COMT Val158Met genotype

SCL-90-R, Symptom Checklist-90-Revised; COMT, catechol-O-methyltransferase; Met, methionine; Val, valine; s.d., standard deviation; CI, confidence interval; df, degrees of freedom.

a Regression coefficient indicates change in SCL-90-R psychosis score associated with high stress versus low stress, analyses adjusted for age.

b Stress×COMT Val158Met genotype interaction fitted with Val dominance term (0=no Val alleles, 1=one or two Val alleles), analysis adjusted for age.

DISCUSSION

Exposure to environmental stressful changes associated with induction into compulsory military service was associated with increases in psychotic symptoms as measured with the SCL-90-R. The COMT Val158Met genotype moderated the psychotic response to environmental stress, in that carriers of the Val allele were more sensitive to stress than individuals of the Met/Met genotype. These results suggest that gene–environment interactions, in which the dopamine system may play an important role, partly underlie the complex aetiology of psychotic symptoms.

The finding that psychosis reactivity to stress was greater in the Val/Val and Val/Met subjects compared to Met/Met subjects confirms the hypothesis that lower levels of constant background tonic dopamine, associated with higher COMT enzyme activity in Val carriers, exhibit less control over state-related high-amplitude phasic (subcortical) dopamine release (Grace, Reference Grace1991; Akil et al. Reference Akil, Kolachana, Rothmond, Hyde, Weinberger and Kleinman2003; Bilder et al. Reference Bilder, Volavka, Lachman and Grace2004; Meyer-Lindenberg et al. Reference Meyer-Lindenberg, Kohn, Kolachana, Kippenhan, McInerney-Leo, Nussbaum, Weinberger and Berman2005). It is attractive to further hypothesize that, as a consequence, stress-induced phasic dopamine release may be greater in those who carry the Val allele, given equal levels of environmental exposure. As the mesolimbic (phasic) dopamine system plays an important role in regulating salience to environmental stimuli, a hyperdopaminergic state may facilitate abnormal salience to ambiguous environmental stimuli, leading to erroneous interpretations and subsequent development of psychotic symptoms (Kapur, Reference Kapur2003). This would explain why, at the level of general population, the COMT Val158Met genotype alone does not mediate psychosis risk (Fan et al. Reference Fan, Zhang, Gu, Li, Sun, Wang, Feng, St Clair and He2005), whereas significant increases in psychotic symptoms may be observed by the synergistic action of the COMT Val158Met genotype (alone or in combination with other genetic risk factors) and environmental stimulation of the dopamine system.

Several methodological issues should be considered. We hypothesized that increases in psychotic symptoms at induction compared to symptom level upon conclusion of the military training were attributable to stress (Stefanis et al. Reference Stefanis, Vitoratou, Ntzoufras, Smyrnis, Evdokimidis and Stefanis2006). Other factors, however, such as developmental expression of subclinical psychotic symptoms associated with age, or increases in use of cannabis or other factors known to be associated with entry into military training, may nevertheless have also played a role. Adjustment for age did not change the results. The fact that all subjects were male may limit generalizability of the findings, and replication using female subjects is necessary.

The current findings partly contrast with those from other studies in which an increased sensitivity to stress and anxiety was identified only in carriers of the Met, and not of the Val, allele (Smolka et al. Reference Smolka, Schumann, Wrase, Grusser, Flor, Mann, Braus, Goldman, Buchel and Heinz2005; Drabant et al. Reference Drabant, Hariri, Meyer-Lindenberg, Munoz, Mattay, Kolachana, Egan and Weinberger2006). Other studies, however, have shown that the moderating effects of the COMT Val158Met genotype may be gender specific, and that lower emotional resilience associated with the Met allele may be specific to females (Enoch et al. Reference Enoch, Xu, Ferro, Harris and Goldman2003; Stein et al. Reference Stein, Fallin, Schork and Gelernter2005). In addition, the current analyses did not show that carriers of the Val allele were overall more reactive to stress (i.e. no interaction was observed between the COMT Val158Met genotype and stress for the SCL-90-R anxiety score), but rather that increased stress had a specific psychotogenic effect in carriers of the Val allele. As stated previously by Tunbridge et al. (Reference Tunbridge, Harrison and Weinberger2006), with respect to prefrontal function, the relationship between the COMT Val158Met genotype and stress sensitivity may be more complex than a simple ‘Met-good/Val-bad’, and each allele may be vulnerable to, or benefit from, different environments. The phenotypic expression of the COMT Val158Met polymorphism with respect to psychosis is likely to be similarly diverse, affecting a broad range of behaviours. What this study and other studies suggest is that it is only in interaction with specific environmental factors that the Val allele may have an impact on psychosis outcomes. Carriers of the Val and the Met allele may be equally sensitive to developing psychosis, although by separate pathways and in interaction with different genetic and environmental factors. Replication of the current finding, including more (interacting) single nucleotide polymorphisms within the COMT gene as well as other genes, is required to further investigate the stress response system in relation to psychosis.

ACKNOWLEDGEMENTS

This work was supported by the grant ‘EKBAN 97’ from the General Secretariat of Research and Technology of the Greek Ministry of Development.

DECLARATION OF INTEREST

None.

References

REFERENCES

Akil, M., Kolachana, B. S., Rothmond, D. A., Hyde, T. M., Weinberger, D. R. & Kleinman, J. E. (2003). Catechol-O-methyltransferase genotype and dopamine regulation in the human brain. Journal of Neuroscience 23, 2008–2013.CrossRefGoogle ScholarPubMed
Bebbington, P., Wilkins, S., Jones, P., Foerster, A., Murray, R., Toone, B. & Lewis, S. (1993). Life events and psychosis. Initial results from the Camberwell Collaborative Psychosis Study. British Journal of Psychiatry 162, 72–79.CrossRefGoogle ScholarPubMed
Bergeman, C. S., Plomin, R., Pedersen, N. L. & McClearn, G. E. (1991). Genetic mediation of the relationship between social support and psychological well-being. Psychology and Aging 6, 640–646.CrossRefGoogle ScholarPubMed
Bilder, R. M., Volavka, J., Lachman, H. M. & Grace, A. A. (2004). The catechol-O-methyltransferase polymorphism: relations to the tonic-phasic dopamine hypothesis and neuropsychiatric phenotypes. Neuropsychopharmacology 29, 1943–1961.CrossRefGoogle Scholar
Caspi, A. & Moffitt, T. E. (2006). Gene–environment interactions in psychiatry: joining forces with neuroscience. Nature Reviews. Neuroscience 7, 583–590.Google Scholar
Caspi, A., Moffitt, T. E., Cannon, M., McClay, J., Murray, R., Harrington, H., Taylor, A., Arseneault, L., Williams, B., Braithwaite, A., Poulton, R. & Craig, I. W. (2005). Moderation of the effect of adolescent-onset cannabis use on adult psychosis by a functional polymorphism in the catechol-O-methyltransferase gene: longitudinal evidence of a gene×environment interaction. Biological Psychiatry 57, 1117–1127.CrossRefGoogle Scholar
Chapman, L. J., Chapman, J. P. & Raulin, M. L. (1978). Body-image aberration in schizophrenia. Journal of Abnormal Psychology 87, 399–407.CrossRefGoogle ScholarPubMed
Clemons, E. P. (1996). Monitoring anxiety levels and coping skills among military recruits. Military Medicine 161, 18–21.CrossRefGoogle ScholarPubMed
Drabant, E. M., Hariri, A. R., Meyer-Lindenberg, A., Munoz, K. E., Mattay, V. S., Kolachana, B. S., Egan, M. F. & Weinberger, D. R. (2006). Catechol O-methyltransferase val158met genotype and neural mechanisms related to affective arousal and regulation. Archives of General Psychiatry 63, 1396–1406.Google Scholar
Enoch, M. A., Xu, K., Ferro, E., Harris, C. R. & Goldman, D. (2003). Genetic origins of anxiety in women: a role for a functional catechol-O-methyltransferase polymorphism. Psychiatric Genetics 13, 33–41.CrossRefGoogle ScholarPubMed
Fan, J. B., Zhang, C. S., Gu, N. F., Li, X. W., Sun, W. W., Wang, H. Y., Feng, G. Y., St Clair, D. & He, L. (2005). Catechol-O-methyltransferase gene Val/Met functional polymorphism and risk of schizophrenia: a large-scale association study plus meta-analysis. Biological Psychiatry 57, 139–144.CrossRefGoogle ScholarPubMed
Flint, J. & Munafo, M. R. (2007). The endophenotype concept in psychiatric genetics. Psychological Medicine 37, 163–180.Google Scholar
Grace, A. A. (1991). Phasic versus tonic dopamine release and the modulation of dopamine system responsivity: a hypothesis for the etiology of schizophrenia. Neuroscience 41, 1–24.Google Scholar
Hatzitaskos, P., Soldatos, C., Giouzelis, G., Karvelis, D. & Spilioti, M. (1997). Psychotic symptomatology first appeared in the military environment. Psychiatriki 8, 41–48.Google Scholar
Henquet, C., Krabbendam, L., Spauwen, J., Kaplan, C., Lieb, R., Wittchen, H. U. & van Os, J. (2005). Prospective cohort study of cannabis use, predisposition for psychosis, and psychotic symptoms in young people. British Medical Journal 330, 11–15.CrossRefGoogle ScholarPubMed
Henquet, C., Rosa, A., Krabbendam, L., Papiol, S., Fananas, L., Drukker, M., Ramaekers, J. G. & van Os, J. (2006). An experimental study of catechol-O-methyltransferase val(158)met moderation of delta-9-tetrahydrocannabinol-induced effects on psychosis and cognition. Neuropsychopharmacology 31, 2748–2757.Google Scholar
Kapur, S. (2003). Psychosis as a state of aberrant salience: a framework linking biology, phenomenology, and pharmacology in schizophrenia. American Journal of Psychiatry 160, 13–23.CrossRefGoogle ScholarPubMed
Kirov, G., Murphy, K. C., Arranz, M. J., Jones, I., McCandles, F., Kunugi, H., Murray, R. M., McGuffin, P., Collier, D. A., Owen, M. J. & Craddock, N. (1998). Low activity allele of catechol-O-methyltransferase gene associated with rapid cycling bipolar disorder. Molecular Psychiatry 3, 342–345.CrossRefGoogle ScholarPubMed
Lachman, H. M., Papolos, D. F., Saito, T., Yu, Y. M., Szumlanski, C. L. & Weinshilboum, R. M. (1996). Human catechol-O-methyltransferase pharmacogenetics: description of a functional polymorphism and its potential application to neuropsychiatric disorders. Pharmacogenetics 6, 243–250.CrossRefGoogle ScholarPubMed
Larson, G. E., Booth-Kewley, S., Merrill, L. L. & Stander, V. A. (2001). Physical symptoms as indicators of depression and anxiety. Military Medicine 166, 796–799.CrossRefGoogle ScholarPubMed
Laruelle, M. (2000). The role of endogenous sensitization in the pathophysiology of schizophrenia: implications from recent brain imaging studies. Brain Research. Brain Research Reviews 31, 371–384.Google Scholar
Lataster, T., van Os, J., Drukker, M., Henquet, C., Feron, F., Gunther, N. & Myin-Germeys, I. (2006). Childhood victimisation and developmental expression of non-clinical delusional ideation and hallucinatory experiences: victimisation and non-clinical psychotic experiences. Social Psychiatry and Psychiatric Epidemiology 41, 423–428.CrossRefGoogle ScholarPubMed
Lerew, D. R., Schmidt, N. B. & Jackson, R. J. (1999). Evaluation of psychological risk factors: prospective prediction of psychopathology during basic training. Military Medicine 164, 509–513.CrossRefGoogle ScholarPubMed
Lotta, T., Vidgren, J., Tilgmann, C., Ulmanen, I., Melen, K., Julkunen, I. & Taskinen, J. (1995). Kinetics of human soluble and membrane-bound catechol O-methyltransferase: a revised mechanism and description of the thermolabile variant of the enzyme. Biochemistry 34, 4202–4210.Google Scholar
Lukoff, D., Snyder, K., Ventura, J. & Nuechterlein, K. H. (1984). Life events, familial stress, and coping in the developmental course of schizophrenia. Schizophrenia Bulletin 10, 258–292.CrossRefGoogle ScholarPubMed
Martin, P. D., Williamson, D. A., Alfonso, A. J. & Ryan, D. H. (2006). Psychological adjustment during Army basic training. Military Medicine 171, 157–160.CrossRefGoogle ScholarPubMed
Meyer-Lindenberg, A., Kohn, P. D., Kolachana, B., Kippenhan, S., McInerney-Leo, A., Nussbaum, R., Weinberger, D. R. & Berman, K. F. (2005). Midbrain dopamine and prefrontal function in humans: interaction and modulation by COMT genotype. Nature Neuroscience 8, 594–596.CrossRefGoogle ScholarPubMed
Myin-Germeys, I., Delespaul, P. & van Os, J. (2005). Behavioural sensitization to daily life stress in psychosis. Psychological Medicine 35, 733–741.CrossRefGoogle ScholarPubMed
Myin-Germeys, I., Krabbendam, L., Delespaul, P. A. & Van Os, J. (2003). Do life events have their effect on psychosis by influencing the emotional reactivity to daily life stress? Psychological Medicine 33, 327–333.CrossRefGoogle ScholarPubMed
Raine, A. (1991). The SPQ: a scale for the assessment of schizotypal personality based on DSM-III-R criteria. Schizophrenia Bulletin 17, 555–564.CrossRefGoogle ScholarPubMed
Read, J., van Os, J., Morrison, A. P. & Ross, C. A. (2005). Childhood trauma, psychosis and schizophrenia: a literature review with theoretical and clinical implications. Acta Psychiatrica Scandinavica 112, 330–350.CrossRefGoogle ScholarPubMed
Schmidt, N. B., Lerew, D. R. & Joiner, T. E. Jr. (2000). Prospective evaluation of the etiology of anxiety sensitivity: test of a scar model. Behaviour Research and Therapy 38, 1083–1095.CrossRefGoogle ScholarPubMed
Smolka, M. N., Schumann, G., Wrase, J., Grusser, S. M., Flor, H., Mann, K., Braus, D. F., Goldman, D., Buchel, C. & Heinz, A. (2005). Catechol-O-methyltransferase val158met genotype affects processing of emotional stimuli in the amygdala and prefrontal cortex. Journal of Neuroscience 25, 836–842.CrossRefGoogle ScholarPubMed
Stefanis, N. C., Van Os, J., Avramopoulos, D., Smyrnis, N., Evdokimidis, I., Hantoumi, I. & Stefanis, C. N. (2004). Variation in catechol-O-methyltransferase val158 met genotype associated with schizotypy but not cognition: a population study in 543 young men. Biological Psychiatry 56, 510–515.Google Scholar
Stefanis, N. C., Vitoratou, S., Ntzoufras, I., Smyrnis, N., Evdokimidis, I. & Stefanis, C. N. (2006). Psychometric properties of the Greek version of the Schizotypal Personality Questionnaire (SPQ) in young male obligatory conscripts: a two years test–retest study. Personality and Individual Differences 41, 1275–1286.Google Scholar
Stein, M. B., Fallin, M. D., Schork, N. J. & Gelernter, J. (2005). COMT polymorphisms and anxiety-related personality traits. Neuropsychopharmacology 30, 2092–2102.Google Scholar
Steinberg, H. R. & Durell, J. (1968). A stressful social situation as a precipitant of schizophrenic symptoms: an epidemiological study. British Journal of Psychiatry 114, 1097–1105.CrossRefGoogle ScholarPubMed
Tunbridge, E. M., Harrison, P. J. & Weinberger, D. R. (2006). Catechol-O-methyltransferase, cognition, and psychosis: Val158Met and beyond. Biological Psychiatry 60, 141–151.Google Scholar
van Os, J., Hanssen, M., Bak, M., Bijl, R. V. & Vollebergh, W. (2003). Do urbanicity and familial liability coparticipate in causing psychosis? American Journal of Psychiatry 160, 477–482.Google Scholar
van Os, J., Hanssen, M., Bijl, R. V. & Vollebergh, W. (2001). Prevalence of psychotic disorder and community level of psychotic symptoms: an urban–rural comparison. Archives of General Psychiatry 58, 663–668.CrossRefGoogle ScholarPubMed
Figure 0

Table 1.Mean SCL-90-R psychosis scores (subscales ‘paranoid ideation’ and ‘psychoticism’) stratified by COMT Val158Met genotype