Skip to main content Accessibility help
×
Hostname: page-component-84b7d79bbc-2l2gl Total loading time: 0 Render date: 2024-07-25T21:17:01.999Z Has data issue: false hasContentIssue false

9 - Adult adversity: do early environment and genotype create lasting vulnerabilities for adult social adversity in psychosis?

from Part II - Social factors and the onset of psychosis

Published online by Cambridge University Press:  07 December 2009

Inez Myin-Germeys
Affiliation:
Department of Psychiatry and Neuropsychology, Maastricht University, PO Box 616, (Location DOT10) 6200 MD, Maastricht, The Netherlands
Jim van Os
Affiliation:
Department of Psychiatry and Neuropsychology, Maastricht University, PO Box 616, (Location DOT10) 6200 MD, Maastricht, The Netherlands
Craig Morgan
Affiliation:
Institute of Psychiatry, King's College London
Kwame McKenzie
Affiliation:
University College London
Paul Fearon
Affiliation:
Trinity College, Dublin
Get access

Summary

Introduction

It has long been acknowledged that adult stress is an important factor in the development of psychosis. The vulnerability–stress model (Nuechterlein and Dawson, 1984) has been widely accepted as a heuristically useful framework for the study of the aetiology and clinical course of schizophrenia. According to this model, psychiatric symptoms emerge when a threshold of stressors exceeds the individual's vulnerability level, the latter being a stable within-person characteristic (Zubin et al., 1983). However, despite the apparent agreement that adult stress is a component cause contributing to psychosis, only a limited amount of research is available addressing the question of how stressors impact on vulnerable individuals. The mechanisms underlying the association between life stress and psychosis thus remain unclear.

In this chapter, we will first give an overview of evidence concerning adult adversity and risk of psychosis. In the second part, two possible ways of approaching the question of how the adult environment interacts with the individual to increase the risk of psychosis will be discussed. First, we will ask whether the impact of the adult environment on the risk of psychosis reflects the expression of a lasting vulnerability for adult stress caused by adversity early in life (we will refer to this as behavioural sensitisation). We hypothesise that exposure to early developmental exposures, such as childhood trauma and growing up in an urban environment, increase vulnerability for psychosis by sensitising people to later adverse events.

Type
Chapter
Information
Society and Psychosis , pp. 127 - 142
Publisher: Cambridge University Press
Print publication year: 2008

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Bebbington, P., Wilkins, S., Jones, P.et al. (1993). Life events and psychosis. Initial results from the Camberwell Collaborative Psychosis study. British Journal of Psychiatry, 162, 72–9.CrossRefGoogle Scholar
Bebbington, P., Wilkins, S., Sham, P.et al. (1996). Life events before psychotic episodes: do clinical and social variables affect the relationship? Social Psychiatry and Psychiatric Epidemiology, 31 (3–4), 122–8.Google Scholar
Bergman, A. J., Silverman, J. M., Harvey, P.et al. (2000). Schizotypal symptoms in the relatives of schizophrenia patients: an empirical analysis of the factor structure. Schizophrenia Bulletin, 26 (3), 577–86.Google Scholar
Bilder, R. M., Volavka, J., Lachman, H. M.et al. (2004). The catechol-O-methyltransferase polymorphism: relations to the tonic-phasic dopamine hypothesis and neuropsychiatric phenotypes. Neuropsychopharmacology, 29 (11), 1943–61.Google Scholar
Boydell, J., Os, J., McKenzie, K.et al. (2001). Incidence of schizophrenia in ethnic minorities in London: ecological study into interactions with environment. British Medical Journal, 323 (7325), 1336–8.Google Scholar
Breier, A., Davis, O. R., Buchanan, R. W.et al. (1993). Effects of metabolic perturbation on plasma homovanillic acid in schizophrenia. Relationship to prefrontal cortex volume. Archives of General Psychiatry, 50 (7), 541–50.CrossRefGoogle Scholar
Brown, G. W. and Harris, T. O. (1978). Social Origins of Depression: A Study of Psychiatric Disorder in Women. London: Tavistock.
Cantor-Graae, E. and Selten, J. P. (2005). Schizophrenia and migration: a meta-analysis and review. American Journal of Psychiatry, 162 (1), 12–24.Google Scholar
Carr, V., Halpin, S., Lau, N.et al. (2000). A risk factor screening and assessment protocol for schizophrenia and related psychosis. Australian and New Zealand Journal of Psychiatry, 34 (suppl.), s170–s180.Google Scholar
Caspi, A., McClay, J., Moffitt, T. E.et al. (2002). Role of genotype in the cycle of violence in maltreated children. Science, 297, 851–4.CrossRefGoogle Scholar
Caspi, A., Sugden, K., Moffitt, T. E.et al. (2003). Influence of life stress on depression: moderation by a polymorphism in the 5-HTT gene. Science, 301, 386–9.CrossRefGoogle Scholar
Castine, M. R., Meador-Woodruff, J. H. and Dalack, G. W. (1998). The role of life events in onset and recurrent episodes of schizophrenia and schizoaffective disorder. Journal of Psychiatric Research, 32 (5), 283–8.CrossRefGoogle Scholar
Cotter, D. and Pariante, C. M. (2002). Stress and the progression of the developmental hypothesis of schizophrenia. British Journal of Psychiatry, 181, 363–5.CrossRefGoogle Scholar
Elman, I., Adler, C. M., Malhotra, A. K.et al. (1998). Effect of acute metabolic stress on pituitary-adrenal axis activation in patients with schizophrenia. American Journal of Psychiatry, 155 (7), 979–81.CrossRefGoogle Scholar
Fan, J. B., Zhang, C. S., Gu, N. F.et al. (2005). Catechol-O-methyltransferase gene Val/Met functional polymorphism and risk of schizophrenia: a large-scale association study plus meta-analysis. Biological Psychiatry, 57 (2), 139–44.CrossRefGoogle Scholar
Garner, B., Pariante, C. M., Wood, S. J.et al. (2005). Pituitary volume predicts future transition to psychosis in individuals at ultra-high risk of developing psychosis. Biological Psychiatry, 58 (5), 417–23.CrossRefGoogle Scholar
Glaser, J. P., Os, J., Portegijs, P. J. M.et al. (2006). Childhood trauma and emotional reactivity to daily life stress in adult frequent attenders of the General Practitioner. Journal of Psychosomatic Research, 61 (2), 229–36.CrossRefGoogle Scholar
Glatt, S. J., Faraone, S. V. and Tsuang, M. T. (2003). Association between a functional catechol-O-methyltransferase gene polymorphism and schizophrenia: meta-analysis of case-control and family-based studies. American Journal of Psychiatry, 160 (3), 469–76.CrossRefGoogle 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), 1–24.CrossRefGoogle Scholar
Hanssen, M., Bak, M., Bijl, R.et al. (2005). The incidence and outcome of sub-clinical psychotic experiences in the general population. British Journal of Clinical Psychology, 44 (2), 181–91.CrossRefGoogle Scholar
Henquet, C., Krabbendam, L., Spauwen, J.et al. (2005). Prospective cohort study of cannabis use, predisposition for psychosis, and psychotic symptoms in young people. British Medical Journal, 330, 11.CrossRefGoogle Scholar
Hirsch, S., Bowen, J., Emami, J.et al. (1996). A one year prospective study of the effect of life events and medication in the aetiology of schizophrenic relapse. British Journal of Psychiatry, 168 (1), 49–56.CrossRefGoogle Scholar
Horan, W. P., Ventura, J., Nuechterlein, K. H.et al. (2005). Stressful life events in recent-onset schizophrenia: reduced frequencies and altered subjective appraisals. Schizophrenia Research, 75 (2–3), 363–74.CrossRefGoogle Scholar
Jansen, L. M., Gispen de Wied, C. C., Gademan, P. J.et al. (1998). Blunted cortisol response to a psychosocial stressor in schizophrenia. Schizophrenia Research, 33 (1–2), 87–94.CrossRefGoogle Scholar
Janssen, I., Hanssen, M., Bak, M.et al. (2003). Discrimination and delusional ideation. British Journal of Psychiatry, 182, 71–6.CrossRefGoogle Scholar
Johns, L. C. and Os, J. (2001). The continuity of psychotic experiences in the general population. Clinical Psychology Review, 21 (8), 1125–41.CrossRefGoogle Scholar
Johns, L. C., Cannon, M., Singleton, N.et al. (2004). Prevalence and correlates of self-reported psychotic symptoms in the British population. British Journal of Psychiatry, 185, 298–305.CrossRefGoogle Scholar
Kanner, A. D., Coyne, J. C., Schaefer, C.et al. (1981). Comparison of two modes of stress measurement: daily hassles and uplifts versus major life events. Journal of Behavioral Medicine, 4 (1), 1–39.CrossRefGoogle 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 (1), 13–23.CrossRefGoogle Scholar
Krabbendam, L. and Os, J. (2005). Schizophrenia and urbanicity: a major environmental influence – conditional on genetic risk. Schizophrenia Bulletin, 31 (4), 795–9.CrossRefGoogle Scholar
Laruelle, M. (2000). The role of endogenous sensitization in the pathophysiology of schizophrenia: implications from recent brain imaging studies. Brain Research Review, 31 (2–3), 371–84.Google Scholar
Laruelle, M. and Abi-Dargham, A. (1999). Dopamine as the wind of the psychotic fire: new evidence from brain imaging studies. Journal of Psychopharmacology, 13 (4), 358–71.CrossRefGoogle Scholar
Lieb, R., Isensee, B., Sydow, K.et al. (2000). The Early Developmental Stages of Psychopathology study (EDSP): a methodological update. European Addiction Research, 6 (4), 170–82.CrossRefGoogle Scholar
Malla, A. K., Cortese, L., Shaw, T. S.et al. (1990). Life events and relapse in schizophrenia. Social Psychiatry and Psychiatric Epidemiology, 25, 221–4.Google Scholar
Marcelis, M., Cavalier, E., Gielen, J.et al. (2004). Abnormal response to metabolic stress in schizophrenia: marker of vulnerability or acquired sensitisation? Psychological Medicine, 34, 1103–11.Google Scholar
Mason, O., Startup, M., Halpin, S.et al. (2004). Risk factors for transition to first episode psychosis among individuals with ‘at-risk mental states’. Schizophrenia Research, 71 (2–3), 227–37.CrossRefGoogle Scholar
Mazure, C. M., Quinlan, D. M. and Bowers, M. Jr (1997). Recent life stressors and biological markers in newly admitted psychotic patients. Biological Psychiatry, 41 (8), 865–70.CrossRefGoogle Scholar
Miller, P., Lawrie, S. M., Hodges, A.et al. (2001). Genetic liability, illicit drug use, life stress and psychotic symptoms: preliminary findings from the Edinburgh study of people at high risk for schizophrenia. Social Psychiatry and Psychiatric Epidemiology, 36 (7), 338–42.CrossRefGoogle Scholar
Mitropoulou, V., Goodman, M., Sevy, S.et al. (2004). Effects of acute metabolic stress on the dopaminergic and pituitary-adrenal axis activity in patients with schizotypal personality disorder. Schizophrenia Research, 70 (1), 27–31.CrossRefGoogle Scholar
Moffitt, T. E., Caspi, A. and Rutter, M. (2005). Strategy for investigating interactions between measured genes and measured environments. Archives of General Psychiatry, 62 (5), 473–81.CrossRefGoogle Scholar
Monroe, S. M. (1983). Major and minor life events as predictors of psychological distress: further issues and findings. Journal of Behavioral Medicine, 6 (2), 189–205.Google Scholar
Munafo, M. R., Bowes, L., Clark, T. G.et al. (2005). Lack of association of the COMT (Val158/108Met) gene and schizophrenia: a meta-analysis of case-control studies. Molecular Psychiatry, 10 (8), 765–70.CrossRefGoogle Scholar
Myin-Germeys, I. and Os, J. (2007). Stress-reactivity in psychosis: evidence for an affective pathway to psychosis. Clinical Psychology Review, 17 (4), 409–24.CrossRefGoogle Scholar
Myin-Germeys, I., Os, J., Schwartz, J. E.et al. (2001). Emotional reactivity to daily life stress in psychosis. Archives of General Psychiatry, 58 (12), 1137–44.CrossRefGoogle Scholar
Myin-Germeys, I., Krabbendam, L., Delespaul, P. A. E. G.et al. (2003). Do life events have their effect on psychosis by influencing the emotional reactivity to daily life stress? Psychological Medicine, 33 (2), 327–33.Google Scholar
Myin-Germeys, I., Spauwen, J., Jacobs, N. et al. (2004). The aetiological continuum of psychosis. In Search for the Causes of Schizophrenia, vol. 5, ed. Gattaz, W. F. and Häfner, H.. Berlin: Springer-Verlag, pp. 342–66.CrossRef
Myin-Germeys, I., Delespaul, P. and Os, J. (2005a). Behavioural sensitization to daily life stress in psychosis. Psychological Medicine, 35 (5), 733–41.Google Scholar
Myin-Germeys, I., Marcelis, M., Krabbendam, L.et al. (2005b). Subtle fluctuations in psychotic phenomena as functional states of abnormal dopamine reactivity in individuals at risk. Biological Psychiatry, 58 (2), 105–10.Google Scholar
Norman, R. M. G. and Malla, A. K. (1991). Subjective stress in schizophrenic patients. Social Psychiatry and Psychiatric Epidemiology, 26 (5), 212–16.CrossRefGoogle Scholar
Norman, R. M. G. and Malla, A. K. (1993). Stressful life events and schizophrenia I: a review of the research. British Journal of Psychiatry, 162, 161–6.CrossRefGoogle Scholar
Nuechterlein, K. H. and Dawson, M. E. (1984). A heuristic vulnerability/stress model of schizophrenic episodes. Schizophrenia Bulletin, 10 (2), 300–12.CrossRefGoogle Scholar
Palmatier, M. A., Kang, A. M. and Kidd, K. K. (1999). Global variation in the frequencies of functionally different catechol-O-methyltransferase alleles. Biological Psychiatry, 46 (4), 557–67.CrossRefGoogle Scholar
Pariante, C. M., Vassilopoulou, K., Velakoulis, D.et al. (2004). Pituitary volume in psychosis. British Journal of Psychiatry, 185, 5–10.CrossRefGoogle Scholar
Pariante, C. M., Dazzan, P., Danese, A.et al. (2005). Increased pituitary volume in antipsychotic-free and antipsychotic-treated patients of the ÆSOP first-onset psychosis study. Neuropsychopharmacology, 30 (10), 1923–31.CrossRefGoogle Scholar
Ryan, M. C., Sharifi, N., Condren, R.et al. (2004). Evidence of basal pituitary-adrenal overactivity in first episode, drug naive patients with schizophrenia. Psychoneuroendocrinology, 29 (8), 1065–70.CrossRefGoogle Scholar
Spauwen, J., Krabbendam, L., Lieb, R.et al. (2006a). Impact of psychological trauma on the development of psychotic symptoms: relationship with psychosis proneness. British Journal of Psychiatry, 188, 527–33.Google Scholar
Spauwen, J., Krabbendam, L., Lieb, R.et al. (2006b). Evidence that the outcome of developmental expression of psychosis is worse for adolescents growing up in an urban environment. Psychological Medicine, 36 (3), 407–15.Google Scholar
Os, J. (2004). Does the urban environment cause psychosis? British Journal of Psychiatry, 184, 287–8.Google Scholar
Os, J., Bak, M., Hanssen, M.et al. (2002). Cannabis use and psychosis: a longitudinal population-based study. American Journal of Epidemiology, 156 (4), 319–27.CrossRefGoogle Scholar
Os, J., Hanssen, M., Bak, M.et al. (2003). Do urbanicity and familial liability coparticipate in causing psychosis? American Journal of Psychiatry, 160 (3), 477–82.Google Scholar
Os, J., Pedersen, C. B. and Mortensen, P. B. (2004). Confirmation of synergy between urbanicity and familial liability in the causation of psychosis. American Journal of Psychiatry, 161 (12), 2312–14.CrossRefGoogle Scholar
Os, J., Krabbendam, L., Myin-Germeys, I.et al. (2005). The schizophrenia envirome. Current Opinion in Psychiatry, 18 (2), 141–5.Google Scholar
Winkel, R.Henquet, C.Rosa, A.et al. (in press) Evidence that the COMT Val158Met polymorphism moderates sensitivity to stress: an experience sampling study. American Journal of Medical Genetics B.
Ventura, J., Nuechterlein, K. H., Subotnik, K. L.et al. (2000). Life events can trigger depressive exacerbation in the early course of schizophrenia. Journal of Abnormal Psychology, 109 (1), 139–44.CrossRefGoogle Scholar
Verdoux, H. and Cougnard, A. (2006). Who is at risk? Who is a case? International Clinical Psychopharmacology, 21 (suppl. 2), s17–s19.Google Scholar
Verdoux, H. and Os, J. (2002). Psychotic symptoms in non-clinical populations and the continuum of psychosis. Schizophrenia Research, 54 (1–2), 59–65.CrossRefGoogle Scholar
Walker, E. F. and Diforio, D. (1997). Schizophrenia: a neural diathesis–stress model. Psychological Review, 104 (4), 667–85.CrossRefGoogle Scholar
Wiles, N. J., Zammit, S., Bebbington, P.et al. (2006). Self-reported psychotic symptoms in the general population: results from the longitudinal study of the British National Psychiatric Morbidity Survey. British Journal of Psychiatry, 188, 519–26.CrossRefGoogle Scholar
Wittchen, H. U. and Jacobi, F. (2005). Size and burden of mental disorders in Europe – a critical review and appraisal of 27 studies. European Neuropsychopharmacology, 15 (4), 357–76.CrossRefGoogle Scholar
Zubin, J., Magaziner, J. and Steinhauer, S. R. (1983). The metamorphosis of schizophrenia: from chronicity to vulnerability. Psychological Medicine, 13 (3), 551–71.Google Scholar

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×