Skip to main content
Frontiers in Psychology logoLink to Frontiers in Psychology
. 2015 Nov 23;6:1768. doi: 10.3389/fpsyg.2015.01768

Gender Differences in the Physical and Psychological Manifestation of Childhood Trauma and/or Adversity in People with Psychosis

Shaun Sweeney 1,*, Tracy Air 1, Lana Zannettino 2, Sonal S Shah 3, Cherrie Galletly 1
PMCID: PMC4655246  PMID: 26635676

Abstract

The link between childhood trauma and/or adversity and risk of psychosis is well known. Our aim was to determine the prevalence of childhood trauma and/or adversity in people who have psychotic disorders and to investigate the association between childhood trauma and/or adversity and a range of social and health measures. Participants (n = 391, 42% male) were specifically asked about any experience of childhood trauma and/or adversity. Respondents provided information about education, employment, physical health, and health service utilization. Univariate analyses revealed that childhood trauma and/or adversity was associated with poorer levels of self-reported physical health and social problems. This includes the experience of chronic pain, headaches, arthritis, asthma, and victimization/stigma in men. Participants with a childhood trauma and/or adversity history indicated higher rates of lifetime suicide attempts with women reporting more lifetime depressive symptoms. Multivariate analyses revealed differing profiles in relation to physical and psychological health variable between males and females. Males with the experience of childhood trauma and/or adversity were significantly more likely to report cardiovascular/stroke issues, migraines and anhedonia. Females with the experience of childhood trauma and/or adversity were more likely to report a lifetime history of elevated mood and to be married or in a de facto relationship. There has been very little research into the assessment and treatment of the effects of childhood trauma and/or adversity in adults with psychosis. Childhood trauma and/or adversity may contribute to higher rates of self-reported poor health in men and is associated with increased depression in women. Our findings suggest that interventions to address the effects of past trauma are urgently needed.

Keywords: childhood trauma and/or adversity, psychosis, self-reported health status, gender

Introduction

Psychosis is defined as the presence of hallucinations and delusions and is present in a number of psychiatric disorders including schizophrenia, delusional disorders, schizoaffective disorders, and drug-induced psychosis. These symptoms can result in impaired functioning in work and school, and can affect parenting, self-care, independent living, interpersonal relationships, and leisure time (Mueser and McGurk, 2004). Psychotic disorders are complex illnesses that can have a profound long-term health, psychological and social impact on the individual. Research in the field indicates that complex, interrelated factors can determine the etiology and course of the illness. There is also strong evidence pointing to the relationship between the experiences of trauma and/or adversity and the development of psychosis, including a correlation between trauma and/or adversity in childhood and the development of psychosis (Morgan and Fisher, 2007).

Estimates of the rates of childhood trauma and/or adversity (CTA) worldwide indicate that every year millions of children experience trauma including physical, sexual, emotional abuse, and severe neglect (Krause, 2008). The terminology associated with trauma, adversity, and early life stress is often used interchangeably across numerous social and health contexts. In discussing the different interpretations of trauma and adversity, Brown et al. (1999) provide a definitive definition of trauma and adversity in childhood that encompasses child abuse and neglect. This definition includes the experience of verbal assaults on a child’s sense of worth, bodily assaults that pose risk of injury, sexual contact, failure to provide basic psychological/emotional needs, and a failure to provide basic needs (Bernstein and Fink, 1998; Browne and Winkelman, 2007). CTA is associated with a range of poor health and psychological outcomes, (Spataro et al., 2004) and is associated with the development of psychotic disorders in adulthood (Janssen et al., 2004; Matheson et al., 2013). In particular, the experience(s) of CTA can lead to high levels of anxiety and is associated with hallucinations, psychological withdrawal, depression, and hopelessness (Lysaker and Salyers, 2007). The health and psychosocial outcomes of CTA can vary according to gender, with women being more likely to experience sexual abuse whilst men tend to be subjected to physical abuse and/or bullying (Read et al., 2005). Additionally, in particular cohorts, such as adult women in drug treatment services, as many as 62–81% report CTA (Teets, 1995; Gil-Rivas et al., 1997; Liebschutz et al., 2002).

While research has been conducted into the influence of CTA, particularly child sexual abuse on health, psychological, and social functioning in female populations, CTA in male cohorts has received less attention, primarily due to its seemingly lower prevalence rates and less overt symptomatic presentation(s). There is widespread evidence that psychosis is correlated with poor physical health, lower levels of educational attainment, and poorer socioeconomic outcomes (Lund et al., 2010). People with psychosis can also exhibit higher rates of obesity (Taylor et al., 2012), illness comorbidity (Sim et al., 2004), and substance abuse than in the general population (Addington and Addington, 2007). For those with a history of CTA and who have developed a psychotic disorder, the combination of this serious mental illness along with the challenges of living with the psychological effects of CTA can make health, economic and social functioning extremely difficult (Spataro et al., 2004).

Despite an extensive collection of research into the effects of psychosis on many of the domains of life there has been little exploration of the physical impact of CTA on people living with psychosis. The present study took place in the northern region of Adelaide, South Australia. This is a disadvantaged region with a high proportion of people in receipt of government benefits, high unemployment rates, lower levels of education, and high rates of mental health (Ahern et al., 2006). Within this adverse socioeconomic environment, our aim was to determine the prevalence of CTA in people who have psychotic disorders, and to investigate the associations between CTA and a range of psychiatric, social, and health measures. Given that gender differences in both the nature and adult consequences of CTA were likely, we undertook separate analyses for men and for women.

It was expected that co-existing CTA and psychosis would be associated with a poorer outcome than psychosis alone. Additionally, the role of gender in affecting psychosocial and health outcomes was also explored. We expected participants who experienced CTA to have left school earlier, be more likely to be unemployed, and to have poorer economic functioning. We also expected people subject to CTA to be more likely to abuse drugs and alcohol, self-harm and/or attempt suicide. Given their exposure to abuse and/or violence during childhood, we also considered it likely that they would experience stigma, bullying, and/or violence as adults. We also expected that their physical health (both objective and subjective) would be worse. These assumptions are based on evidence in the CTA literature indicating the correlation between CTA and lower socio-economic status, and poor health compared to non-CTA populations.

Materials and Methods

Participants for the study were randomly selected from people who have been in contact with a mental health service or a non-government organization funded to provide mental health services. The SHIP projected utilized a psychosis screener to identify potential participants. Potential participants were screened for psychosis between April 1st, 2009 and March 31st, 2010. The psychosis screener identified potential SHIP participants who were positive for psychosis on the basis of their contact(s) with mental health services or who recorded ICD-10 diagnosis of psychosis. The psychosis screener identified 1825 adults aged 18–64 years who were residents in the South Australian postcode catchment area. Potential participants needed to have been in contact with public mental health services in the 12 months prior to the survey to be eligible to participate in the SHIP study. The exclusion criteria included severe cognitive impairment, the inability to comprehend English sufficiently to complete the interview without the use of an interpreter. Attempts were made to recruit all of these potential participants. Eight hundred and twenty three were unable to be contacted due to change of personal circumstance (e.g., moved away from the catchment area, changed their phone number, were non-responders to phone/mail contact or did not attend the SHIP interview), 16 were known to have died, 33 did not meet inclusion criteria due to inability to sufficiently communicate in English, 42 did not have capacity to give informed consent, and 507 refused. Potential participants were identified during the SHIP census period and in total 402 participants were interviewed. Comparison of screening data for interviewed participants and those selected for interview but not participating for any reason indicated no systematic selection biases. Both groups were alike in terms of sex (60% of those interviewed were male compared to 62% of those selected but not interviewed) and age group (44% of those interviewed were aged 18–34 years at the time of screening compared with 43% of those not interviewed). The psychosis screening profiles for both groups were similar indicating no marked differences in terms of lifetime symptom profiles based on the screener items.

The SHIP interview schedule consisted of 32 modules and asked participants about psychopathology, substance use, physical health, functioning, disability and quality of life, education, employment, accommodation, and childhood adversity. The social, health, and economic profile information of participants consisted of, but were not limited to: demographic status, socioeconomic and psychosocial status, health and physical functioning, diagnosis, and symptomology. Diagnoses were made using the Diagnostic Interview for Psychosis (DIP; Castle et al., 2006). The DIP contains selected interview questions and probes from the WHO Schedules for Clinical Assessment in Neuropsychiatry (Wing et al., 1990) mapped onto the 90 diagnostic items of the operational criteria checklist for psychotic and affective illness (McGuffin et al., 1991). The DIP measured both lifetime and current illness symptoms for psychosis. A computer algorithm provided the diagnostic classification in accordance with ICD-10, DSM-IV, and other criteria on the basis of the DIP scores. This reduced the subjective bias in the interpretation of symptoms and signs (Shah et al., 2014). No specific analysis was conducted regarding the non-responders to the SHIP research project. Further information regarding the method of the SHIP research project is detailed in Morgan et al. (2012).

Questions regarding the occurrence and nature of CTA were included in the interview. In Australia, all states follow a national framework of guidelines for defining the four types of child abuse (a) sexual abuse, (b) physical abuse, (c) emotional abuse, and (d) neglect. The classification of reported CTA was undertaken in collaboration with staff from the Western Australian Department of Child Protection to ensure conformity to national guidelines. This paper includes only those cases where the CTA is consistent with the standard Australian definitions, took place when the participant was aged 18 years or younger and occurred prior to the onset of psychotic illness.

Ethics Statement

Ethics approval for this research was obtained from the Human Research Ethics Committee of the Queen Elizabeth Hospital (Protocol number: 2009179).

Assessments

The Second Australian Survey of Psychosis 2010 interview schedule was comprised of 32 modules, including the Alcohol Use Disorders Identification Test (Babor et al., 2001), the World Health Organization Schedules for Clinical Assessment in Neuropsychiatry (Kirkpatrick et al., 1989; World Health Organization, 1999). The details for all other measures are described in Morgan et al. (2012).

Childhood Trauma and/or Adversity

Questions about the occurrence and nature of CTA were included in the SHIP interview. CTA was coded on the basis of responses to the question: “Were there any other very distressing or traumatic events in your childhood (not including parental separation or divorce, or loss of a close relative)?”

Statistical Analyses

Statistical analyses were performed using Stata, version 12 (StataCorp, 2011). A two-step model building procedure was used to determine variables associated with CTA. In the first step, we used univariate analyses (chi-squares and t-tests) to examine relationships between CTA and independent variables. In the second step, we used multivariate logistic regressions, including only variables that were significantly associated with CTA status at alpha ≤0.05 in the first step. As the incidence of CTA was much higher in females, the analyses were also stratified by gender to explore gender specific associations. In the final stratified model, only the significant variables were retained, adjusting for possible confounders of health status such as lifetime histories of smoking, heavy alcohol usage and cannabis use.

Given the difference between genders in the numbers reporting CTA, a post hoc power analysis with the program GPower, Version 3.1.9.2 (Faul et al., 2009) was conducted. The analysis implied that statistical power (power = 0.96) was sufficient, rendering it unlikely that significant differences between the groups could have been overlooked.

Results

Of the 391 participants, 59.3% of reported experiencing CTA. CTA was reported more in females than males (χ2 = 19.7, df = 1, p < 0.001). Table 1 depicts the results of the univariate analyses comparing CTA and no CTA participants on socio-demographic data. Participants who had experienced CTA were more likely to be married or living in a de facto relationship (χ2 = 13.2, df = 2, p = 0.001), and had left school earlier (t = –3.22, df = 389, p = 0.001). There was no difference in diagnosis or in rates of current smoking, lifetime history of heavy alcohol use, or cannabis use, between those with and without CTA.

Table 1.

Socio-demographic data for people with psychosis, comparing those who had experienced childhood trauma and/or adversity (CTA) with those who had not.

CTA (n = 232) No CTA (n = 159) Total (n = 391) p
Age and sex
Female (n, %) 118 50.9 45 28.3 163 41.7 <0.001
Age (mean ± SD, years) 39.1 10.2 37.5 11.1 38.4 10.5 0.16
Age left school (mean ± SD, years) 15.8 1.3 16.3 1.2 16.0 1.3 0.001
Marital status (n, %)
Single 106 45.7 102 84.6 208 53.2 0.001
Married/de facto 59 25.4 24 15.1 83 21.2
Currently separated, divorced, widowed 67 28.9 33 20.8 100 25.5
Income (n, %)
Main income source: pension 212 91.8 147 93.0 359 92.3 0.65
Duration of illness (years) 15.3 10.0 13.2 9.4 14.4 9.8 0.043
Employment (n, %)
Paid Employment (past year) 54 23.3 38 23.9 92 23.5 0.89
Voluntary/Unpaid work (past 12 months) 0.34 14.7 20 12.6 54 13.8 0.56

Physical and Psychological Health

Table 2 displays the results for the univariate analyses on physical health. The CTA group generally indicated higher rates of reported lifetime physical health conditions. More of the CTA positive group experienced chronic pain (χ2 = 18.24, df = 1, p = 0.001), headaches/migraines (χ2 = 19.73, df = 1, p = 0.001), arthritis (χ2 = 10.88, df = 1, p = 0.001) and asthma (χ2 = 5.52, df = 1, p = 0.019). In the overall sample, cardiovascular disease and/or stroke was also more common in the CTA positive group (χ2 = 9.80, df = 1, p = 0.002).

Table 2.

Lifetime physical conditions.

CTA (n = 232) No CTA (n = 159) Total (n = 391) p
Lifetime physical conditions (n, %)
Chronic pain 101 43.5 35 22.4 136 35.1 <0.001
Asthma 81 34.9 37 23.7 118 30.4 0.019
Cardiovascular/stroke 54 23.5 17 10.9 71 18.4 0.002
Severe headaches/migraines 89 38.4 27 17.3 116 29.9 <0.001
Arthritis 64 27.6 21 13.5 85 21.9 0.001
Diabetes 56 24.5 39 25.2 95 24.7 0.88
Epilepsy 25 10.8 10 6.5 35 9.0 0.15
Cancer 11 4.7 4 2.6 15 3.9 0.28
Males (n, %)
Chronic pain 41 36.0 25 22.1 66 29.1 0.022
Asthma 33 29.0 24 21.2 57 25.1 0.18
Cardiovascular/stroke 27 23.7 11 9.7 38 16.7 0.005
Severe headaches/migraines 39 34.2 18 15.9 57 25.1 0.001
Arthritis 20 17.5 9 8.0 29 12.8 0.031
Diabetes 26 23.2 24 21.4 50 22.3 0.75
Epilepsy 18 15.8 7 6.2 25 11.0 0.021
Cancer 2 1.8 3 2.7 5 2.2 0.64
Females (n, %)
Chronic pain 60 50.9 10 23.3 70 43.5 0.002
Asthma 48 40.7 13 30.2 61 37.9 0.23
Cardiovascular/stroke 27 23.3 6 14.0 33 20.8 0.20
Severe headaches/migraines 50 42.4 9 20.9 59 36.7 0.012
Arthritis 44 37.3 12 27.9 56 34.8 0.27
Diabetes 30 25.6 15 34.9 45 28.1 0.25
Epilepsy 7 5.9 3 7.1 10 6.3 0.78
Cancer 9 7.6 1 2.3 10 6.2 0.21

More males with a history of CTA than expected reported chronic pain (χ2 = 5.2, df = 1, p = 0.022), cardiovascular disease/stroke (χ2 = 7.9, df = 1, p = 0.005), headaches/migraines (χ2 = 10.0, df = 1, p = 0.001), arthritis (χ2 = 4.7, df = 1, p = 0.031) and epilepsy (χ2 = 5.3, df = 1, p = 0.021). More females with CTA than expected reported chronic pain (χ2 = 9.8, df = 1, p = 0.002) and headaches/migraines (χ2 = 6.2, df = 1, p = 0.012).

Univariate analyses revealed that the CTA positive group experienced different rates of lifetime psychological symptoms than the non-CTA group (Table 3). For example, the CTA group were more likely to report a lifetime history of depressive mood (χ2 = 7.96, df = 1, p = 0.005), anhedonia (χ2 = 14.30, df = 1, p = 0.001), poor concentration (χ2 = 4.67, df = 1, p = 0.031), elevated mood (χ2 = 5.16, df = 1, p = 0.023). However, the non-CTA group were more likely to report a lack of insight (χ2 = 5.68, df = 1, p = 0.017). Males with CTA also were more likely to have experienced anhedonia (χ2 = 8.44, df = 1, p = 0.004) and subjective thought disorder (χ2 = 3.87, df = 1, p = 0.049). Conversely, females with CTA were more likely to have reported depressive mood symptoms (χ2 = 5.59, df = 1, p = 0.018) and elevated mood symptoms (χ2 = 4.30, df = 1, p = 0.038).

Table 3.

Psychological symptoms: lifetime.

CTA (n = 232) No CTA (n = 159) Total (n = 391) p
Lifetime symptoms (n, %)
Delusions 213 91.8 148 93.1 361 92.3 0.64
Hallucinations 194 83.6 135 84.9 329 84.1 0.73
Subjective thought disorder 159 68.5 94 59.1 253 64.7 0.06
Depressed mood 212 91.4 130 81.8 342 87.5 0.005
Anhedonia 203 87.5 115 72.3 318 81.3 <0.001
Suicidal ideation 171 73.7 105 66.0 276 70.6 0.10
Poor concentration 179 77.2 107 67.3 286 73.2 0.031
Irritable Mood 87 37.5 55 34.6 142 36.3 0.56
Elevated Mood 110 47.4 57 35.9 167 42.7 0.023
Lack of insight 47 20.3 49 30.8 96 24.6 0.017
Males (n, %)
Delusions 105 92.1 105 92.1 210 92.1 1.00
Hallucinations 95 83.3 99 86.8 194 85.1 0.46
Subjective thought disorder 83 72.8 69 60.5 152 66.7 0.049
Depressed mood 98 86.0 91 79.8 189 82.9 0.22
Anhedonia 95 83.3 76 66.7 171 75.0 0.004
Suicidal ideation 84 73.7 76 66.7 160 70.2 0.25
Poor concentration 77 67.5 73 64.0 150 65.8 0.58
Irritable mood 35 30.7 36 31.6 71 31.1 0.89
Elevated mood 44 38.6 40 35.1 84 36.8 0.58
Lack of insight 26 22.8 38 33.3 64 28.1 0.08
Females (n, %)
Delusions 108 91.5 43 95.6 151 92.6 0.38
Hallucinations 99 83.9 36 80.0 135 82.8 0.56
Subjective thought disorder 76 64.4 25 55.6 101 62.0 0.30
Depressed mood 114 96.6 39 86.7 153 93.9 0.018
Anhedonia 108 91.5 39 86.7 147 90.2 0.35
Suicidal ideation 87 73.7 29 64.4 116 71.2 0.24
Poor concentration 102 86.4 34 75.6 136 83.4 0.10
Irritable mood 52 44.1 19 42.2 71 43.6 0.83
Elevated mood 66 55.9 17 37.8 83 50.9 0.038
Lack of insight 21 17.8 11 24.4 32 19.6 0.34

Physical and Psychological Health Profile

Table 4 displays the results of the final multivariate logistic regression model for men and women, adjusted for age at interview and socioeconomic status. Most of the physical and psychological health variables that had been significant in the univariate analyses were no longer so in the multivariate models for either gender. However, males who had experienced CTA were more likely to report experiencing a lifetime history of cardiovascular/stroke health issues, migraines and anhedonia. Conversely, females who had experienced CTA were significantly more likely to be in a married/de facto relationship and a lifetime history of elevated mood. The physical health measures were not significantly associated with CTA.

Table 4.

Relationship between CTA and demographics, psychological and physical health profiles in people with psychosis, stratified by sex.

Males
Females
OR 95% CI p OR 95% CI p
Age at interview 0.98 0.9–1.0 0.36 1.04 0.9–1.1 0.29
Marital status
Single, never married Reference group Reference group
Married/de facto 4.89 1.2–19.2 0.02
Currently separated, divorced, widowed 2.05 0.6–7.5 0.28
Lifetime history of smoking 0.41 0.1–2.6 0.34 1.24 0.6–27.3 0.89
Lifetime history of heavy alcohol use 1.43 0.7–3.0 0.34 1.39 0.4–4.4 0.57
Lifetime history of cannabis use 0.93 0.9–1.0 0.07 1.07 0.9–1.2 0.18
Psychological symptoms
Anhedonia 2.70 1.2–5.9 0.012
Elevated Mood 4.11 1.38–12.2 0.01
Physical symptoms
Cardiovascular/Stroke 4.18 1.5–11.8 0.007
Migraines 3.08 1.2–7.1 0.008

Discussion

Considerable research has been conducted into the effect of CTA on health, psychological, and social functioning in female populations. Associations between CTA and physical illnesses, including cardiac, respiratory, and gastrointestinal diseases, has also been reported in general population samples (Goodwin and Stein, 2004). However, CTA in male cohorts has received less consideration, primarily due to its seemingly lower prevalence rates and less overt symptomatic presentation(s). The high rate of the self-reporting of physical illness in male psychosis populations such as ours may be evidence of a CTA history. Most significantly, it may characterize a psychological disorder, one that represents a manifestation of an undisclosed CTA experience(s). Self-reported health risks can potentially compound the already high health, psychological, and social burden associated with psychotic illness for this population. These represent deficits that can exacerbate the psychological burden of the experience(s) of CTA. The SHIP cohort presented with a myriad of physical, psychological, and social challenges that did not translate into multivariate explanatory models. Given that the entire sample was in poor physical and psychological health and were socio-economically marginalized, this should not surprise. Overall, prevalence of CTA was high, with over 60% of participants reporting physical, sexual and/or emotional abuse, and neglect. This is consistent with the association between CTA and adult psychotic disorders (Morgan and Fisher, 2007; Matheson et al., 2013). Participants with a CTA history left school earlier and experienced higher rates of employment. Conversely, unlike general population samples where CTA has been associated with higher rates of substance use (Dube et al., 2003), the CTA cohort in this sample did not replicate this research. Furthermore, the CTA cohort was more likely to be married and have children, suggesting a better capacity to form intimate relationships. Additionally, the self-reported poorer physical health, which was more prominent in men, may reflect somatic expression of emotional distress, or poorer self-care with greater vulnerability to physical illness.

Our study accessed a large representative sample of people with psychotic illness living in a disadvantaged region of urban Adelaide, South Australia. The finding that CTA may influence and potentially compromise health functioning among adults with psychosis is intriguing. Despite this, there has been very little research into the assessment and treatment of the effects of CTA in adults with psychosis. Thus, there are unanswered questions about the role of CTA in the symptoms and outcomes of men with psychosis and this awaits future research. Further research is also needed to determine the extent to which the relationship between CTA and health and psychosocial functioning is moderated by other intervening variables, such as cognitive function, substance abuse, and illness symptomology, in psychosis populations. A significant portion of non-psychosis trauma in the literature links CTA to deficits in areas such as psychological and social functioning (Mulvihill, 2005) as well as health functioning (Norman et al., 2006). Nonetheless, our sample unexpectedly did not replicate this association, either at a univariate or multivariate level of analysis. Our findings suggest that interventions are urgently needed. These challenges highlight the importance of an integrated approach to mental health and community based service provision. Such an approach may help to ensure that people with psychosis and the experience(s) of CTA have their health and social needs met in ways that can enhance their illness recovery. Answers to these questions will help in better understanding the processes surrounding health and psychosocial functioning in psychosis populations and to develop and deliver more effective clinical treatments. The population-level data collected as part of the 2010 SHIP research provide a solid empirical foundation to guide health and social policy development and the provision of mental health services regarding many aspects of psychosis/CTA populations.

Limitations

This study has a number of important limitations. Although we were able to explore the temporal relationship between self-reported physical health and clinical outcomes in adulthood, we were unable to determine severity, frequency, duration and perpetrator of the abuse due to the interview design. Therefore, we may have missed important patterns of association. In addition, we acknowledge that longitudinal studies that collect CTA data prospectively are the optimal design for this type of research.

As our data rely on retrospective self-report, the accuracy may be affected by recall bias. However, a number of studies have demonstrated the validity and reliability of retrospective reports of trauma in psychosis populations. These studies indicated that reports of CTA are stable across time, unaffected by current symptoms, and generally correlate well with other sources of information (Arseneault et al., 2011). Additionally, there is evidence that the retrospective assessment of child abuse tends to underestimate rather than over-report real rates, possibly due to poor memory, denial, or embarrassment. Consequently, our data may underestimate the strength of the relationship between CTA and subsequent outcomes.

Author Contributions

SS was primarily responsible for the conception of the research upon which this paper is based. CG, LZ, and TA assisted in the development of the ideas for the paper and in refining the final manuscript. SS produced the first draft of the manuscript and submitted the final manuscript and completed the literature search and wrote the main body of the manuscript. TA analyzed the data. SSS contributed to acquisition, analysis and interpretation of the national SHIP data; was part of initial discussions on the substance of this paper, and critically contributed to the draft of the revised version. All authors approved the final manuscript.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

This publication is based on data collected in the framework of the 2010 Australian National Survey of High Impact Psychosis. The members of the Survey of High Impact Psychosis Study Group are: V. Morgan (National Project Director), A. Jablensky (Chief Scientific Advisor), A. Waterreus (National Project Coordinator), R. Bush, V. Carr, D. Castle, M. Cohen, C. Galletly, C. Harvey, B. Hocking, A. Mackinnon, P. McGorry, J. McGrath, A. Neil, S. Saw, H. Stain. Ethics approvals for the study were obtained from relevant institutional human research ethics committees.

The Second Australian Survey of Psychosis 2010 acknowledges and thanks the hundreds of mental health professionals who participated in the preparation and conduct of the survey and the many Australians with psychotic disorders who gave their time and whose responses form the basis of this publication.

Footnotes

Funding. The 2010 Australian National Survey of Psychosis was funded by the Australian Government Department of Health and Ageing.

References

  1. Addington J., Addington D. (2007). Patterns, predictors and impact of substance use in early psychosis: a longitudinal study. Acta Psychiatr. Scand. 115 304–309. 10.1111/j.1600-0447.2006.00900.x [DOI] [PubMed] [Google Scholar]
  2. Ahern N. R., Kiehl E. M., Lou Sole M., Byers J. (2006). A review of instruments measuring resilience. Issues Compr. Pediatr. Nurs. 29 103–125. 10.1080/01460860600677643 [DOI] [PubMed] [Google Scholar]
  3. Arseneault L., Cannon M., Fisher H. L., Polanczyk G., Moffitt T. E., Caspi A. (2011). Childhood trauma and children’s emerging psychotic symptoms: a genetically sensitive longitudinal cohort study. Am. J. Psychiatry 168 65–72. 10.1176/appi.ajp.2010.10040567 [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Babor T. F., Higgins-Biddle J. C., Saunders J. B., Monteiro M. G. (2001). The Alcohol Use Disorders Identification Test. Guidelines for Use in Primary Care Vol. 2 Geneva: World Health Organization. [Google Scholar]
  5. Bernstein D. P., Fink L. (1998). Childhood Trauma Questionnaire: A Retrospective Self-Report: Manual. San Diego, CA: Harcourt Brace & Company. [Google Scholar]
  6. Brown J., Cohen P., Johnson J. G., Smailes E. M. (1999). Childhood abuse and neglect: specificity of effects on adolescent and young adult depression and suicidality. J. Am. Acad. Child Adolesc. Psychiatry 38 1490–1496. 10.1097/00004583-199912000-00009 [DOI] [PubMed] [Google Scholar]
  7. Browne C., Winkelman C. (2007). The effect of childhood trauma on later psychological adjustment. J. Interpers. Violence 22 684–697. 10.1177/0886260507300207 [DOI] [PubMed] [Google Scholar]
  8. Castle D. J., Jablensky A., McGrath J. J., Carr V., Morgan V., Waterreus A., et al. (2006). The diagnostic interview for psychoses (DIP): development, reliability and applications. Psychol. Med. 36 69–80. 10.1017/S0033291705005969 [DOI] [PubMed] [Google Scholar]
  9. Dube S. R., Felitti V. J., Dong M., Chapman D. P., Giles W. H., Anda R. F. (2003). Childhood abuse, neglect, and household dysfunction and the risk of illicit drug use: the adverse childhood experiences study. Pediatrics 111 564–572. 10.1542/peds111.3.564 [DOI] [PubMed] [Google Scholar]
  10. Faul F., Erdfelder E., Buchner A., Lang A.-G. (2009). Statistical power analyses using GPower 3.1: tests for correlation and regression analysis. Behav. Res. Methods 41 1149–1160. 10.3758/BRM.41.4.1149 [DOI] [PubMed] [Google Scholar]
  11. Gil-Rivas V., Fiorentine R., Douglas Anglin M., Taylor E. (1997). Sexual and physical abuse: do they compromise drug treatment outcomes? J. Subst. Abuse Treat. 14 351–358. 10.1016/S0740-5472(97)84631-4 [DOI] [PubMed] [Google Scholar]
  12. Goodwin R. D., Stein M. B. (2004). Association between childhood trauma and physical disorders among adults in the United States. Psychol. Med. 34 509–520. 10.1017/S003329170300134X [DOI] [PubMed] [Google Scholar]
  13. Janssen I., Krabbendam L., Bak M., Hanssen M., Vollebergh W., Graaf R. D., et al. (2004). Childhood abuse as a risk factor for psychotic experiences. Acta Psychiatr. Scand. 109 38–45. 10.1046/j.0001-690X.2003.00217.x [DOI] [PubMed] [Google Scholar]
  14. Kirkpatrick B., Buchanan R. W., McKenny P. D., Alphs L. D., Carpenter W. T. (1989). The schedule for the deficit syndrome: an instrument for research in schizophrenia. Psychiatry Res. 30 119–123. 10.1016/0165-1781(89)90153-4 [DOI] [PubMed] [Google Scholar]
  15. Krause N. (2008). Lifetime trauma, prayer, and psychological distress in late life. Int. J. Psychol. Religion 19 55–72. 10.1080/10508610802471112 [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Liebschutz J., Savetsky J. B., Saitz R., Horton N. J., Lloyd-Travaglini C., Samet J. H. (2002). The relationship between sexual and physical abuse and substance abuse consequences. J. Subst. Abuse Treat. 22 121–128. 10.1016/S0740-5472(02)00220-9 [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Lund C., Breen A., Flisher A. J., Kakuma R., Corrigall J., Joska J. A., et al. (2010). Poverty and common mental disorders in low and middle income countries: a systematic review. Soc. Sci. Med. 71 517–528. 10.1016/j.socscimed.2010.04.027 [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Lysaker P., Salyers M. (2007). Anxiety symptoms in schizophrenia spectrum disorders: associations with social function, positive and negative symptoms, hope and trauma history. Acta Psychiatr. Scand. 116 290–298. 10.1111/j.1600-0447.2007.01067.x [DOI] [PubMed] [Google Scholar]
  19. Matheson S., Shepherd A., Pinchbeck R., Laurens K., Carr V. (2013). Childhood adversity in schizophrenia: a systematic meta-analysis. Psychol. Med. 43 225–238. 10.1017/S0033291712000785 [DOI] [PubMed] [Google Scholar]
  20. McGuffin P., Farmer A., Harvey I. (1991). A polydiagnostic application of operational criteria in studies of psychotic illness. Development and reliability of the OPCRIT system. Arch. Gen. Psychiatry 48 764–770. 10.1001/archpsyc.1991.01810320088015 [DOI] [PubMed] [Google Scholar]
  21. Morgan C., Fisher H. (2007). Environment and schizophrenia: environmental factors in schizophrenia: childhood trauma—a critical review. Schizophr. Bull. 33 3–10. 10.1093/schbul/sbl053 [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Morgan V. A., Waterreus A., Jablensky A., Mackinnon A., McGrath J. J., Carr V., et al. (2012). People living with psychotic illness in 2010: the second Australian national survey of psychosis. Aust. N. Z. J. Psychiatry 46 735–752. 10.1177/0004867412449877 [DOI] [PubMed] [Google Scholar]
  23. Mueser K., McGurk S. (2004). Schizophrenia. Lancet 363 2063–2072. 10.1016/S0140-6736(04)16458-1 [DOI] [PubMed] [Google Scholar]
  24. Mulvihill D. (2005). The health impact of childhood trauma: an interdisciplinary review, 1997–2003. Issues Compr. Pediatr. Nurs. 28 115–136. 10.1080/01460860590950890 [DOI] [PubMed] [Google Scholar]
  25. Norman S. B., Means-Christensen A. J., Craske M. G., Sherbourne C. D., Roy-Byrne P. P., Stein M. B. (2006). Associations between psychological trauma and physical illness in primary care. J. Trauma. Stress 19 461–470. 10.1002/jts.20129 [DOI] [PubMed] [Google Scholar]
  26. Read J., van Os J., Morrison A., Ross C. A. (2005). Childhood trauma, psychosis and schizophrenia: a literature review with theoretical and clinical implications. Acta Psychiatr. Scand. 112 330–350. 10.1111/j.1600-0447.2005.00634.x [DOI] [PubMed] [Google Scholar]
  27. Shah S., Mackinnon A., Galletly C., Carr V., McGrath J. J., Stain H. J., et al. (2014). Prevalence and impact of childhood abuse in people with a psychotic illness. Data from the second Australian National Survey of Psychosis. Schizophr. Res. 159 20–26. 10.1016/j.schres.2014.07.011 [DOI] [PubMed] [Google Scholar]
  28. Sim K., Swapna V., Mythily S., Mahendran R., Kua E., McGorry P., et al. (2004). Psychiatric comorbidity in first episode psychosis: the Early Psychosis Intervention Program (EPIP) experience. Acta Psychiatr. Scand. 109 23–29. 10.1111/j.0001-690X.2004.00196.x [DOI] [PubMed] [Google Scholar]
  29. Spataro J., Mullen P. E., Burgess P. M., Wells D. L., Moss S. A. (2004). Impact of child sexual abuse on mental health. Br. J. Psychiatry 184 416–421. 10.1192/bjp.184.5.416 [DOI] [PubMed] [Google Scholar]
  30. StataCorp (2011). Stata Statistical Software: Release 12. College Station, TX: StataCorp LP. [Google Scholar]
  31. Taylor V. H., McIntyre R. S., Remington G., Levitan R. D., Stonehocker B., Sharma A. M. (2012). Beyond pharmacotherapy: understanding the links between obesity and chronic mental illness. Can. J. Psychiatry 57 5–12. [DOI] [PubMed] [Google Scholar]
  32. Teets J. M. (1995). Childhood sexual trauma of chemically dependent women. J. Psychoactive Drugs 27 231–238. 10.1080/02791072.1995.10472468 [DOI] [PubMed] [Google Scholar]
  33. Wing J. K., Babor T., Brugha T., Burke J., Cooper J. E., Giel R., et al. (1990). SCAN. Schedules for clinical assessment in neuropsychiatry. Arch. Gen. Psychiatry 47 589–593. 10.1001/archpsyc.1990.01810180089012 [DOI] [PubMed] [Google Scholar]
  34. World Health Organization (1999). Schedules for Clinical Assessment in Neuropsychiatry. Geneva: World Health Organization. [Google Scholar]

Articles from Frontiers in Psychology are provided here courtesy of Frontiers Media SA

RESOURCES