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Article history:
Received 16 February 2016
Background: Hallucinations, once equated with serious mental disorders, are common in adolescents. Given the high
Received in revised form 7 May 2016 prevalence of hallucinations, it is important to determine if they are associated with adverse mental health outcomes in
Accepted 9 June 2016 adulthood. This study compared the mental health outcomes of participants (aged 30–33 years) in the Mater-University of
Available online xxxx Queensland Study of Pregnancy (MUSP) who reported hallucinations at (a) 14 years only and (b) 14 and 21 years versus
cohort members without hallucinations.
Keywords: Method: Participants (n = 333) were aged between 30 and 33 years and (a) reported hallucinations on the Youth Self-Report
Hallucinations Birth Questionnaire at 14 and/or the Young Adult Self-Report Questionnaire at 21 years and (b) controls (n = 321) who did not
cohort Mental report hallucinations. Lifetime diagnoses of mental disorders were ascertained by the Structured Clinical Interview for DSM
disorders Psychotic
Disorders (DSM IV-TR) administered by clinical psychologists. Suicidal be- haviour was measured by self report.
disorders Suicide
Results: Hallucinations at 14 years only were not associated with an increased risk of mental disorders in adult- hood.
Hallucinations reported at both 14 and 21 years were associated with lifetime diagnoses of psychotic dis- orders (OR, 8.84;
95% CI: 1.61–48.43 and substance use disorders (OR, 2.34; 95% CI: 1.36–4.07) and also strongly associated with lifetime
suicide attempts (OR, 7.11; 95% CI: 2.68–18.83).
Conclusions: Most adolescents who experience hallucinations do not have an increased rate of mental disorder in adulthood;
however, those with hallucinations that are experienced at more than one point in time are at in- creased risk of suicidal
behaviour and both psychotic and non-psychotic psychopathology.
© 2016 Elsevier B.V. All rights reserved.
1. Introduction
2012a). Studies exploring the outcomes of hallucinations in adolescents have
found an increased risk of subsequent psychotic disorder (Poulton et al., 2000;
Hallucinations, cardinal symptoms of psychotic disorders, also occur in other
Welham et al., 2009) and other psychopathology (Dhossche et al., 2002; Fisher
mental disorders and in otherwise well individuals. For exam- ple, a large
et al., 2013; Kelleher et al., 2012b). However, these studies have their limitations
community-based study reported the lifetime prevalence of hallucinations as
and the utility of hallucinations as a pre- dictor of future mental health disorders
5.2% (McGrath et al., 2015) whilst studies of adoles- cents have found a higher
is in debate.
prevalence of almost 15% (Kelleher et al.,
Five population studies have examined adult mental health out- comes of
children and adolescents who hallucinate. Two studies based on the Dunedin
* Corresponding author at: The University of Queensland Centre for Clinical Research, Herston, birth cohort assessed diagnostic outcomes of partici- pants who experienced
QLD 4029, Australia. psychotic symptoms measured at 11 years (based on the Diagnostic Interview
E-mail address: james.scott@health.qld.gov.au (J.G. Scott).
Schedule for Children) (Fisher et
http://dx.doi.org/10.1016/j.schres.2016.06.009 0920-
9964/© 2016 Elsevier B.V. All rights reserved.
Please cite this article as: Connell, M., et al., Hallucinations in adolescents and risk for mental disorders and suicidal behaviour in adulthood: Prospective evidence
from the MUS..., Schizophr. Res. (2016), http://dx.doi.org/10.1016/j.schres.2016.06.009
2 M. Connell et al. / Schizophrenia Research xxx (2016) xxx–xxx
al., 2013; Poulton et al., 2000). Participants who were interviewed by child
The current study examined a broad range of mental health out- comes in
psychiatrists and identified as having psychotic symptoms had a 16-fold
adulthood for those who reported experiencing hallucinations at (i) 14 years and
greater risk of adult schizophreniform disorder (odds ratio [OR], 16.4; 95%
(ii) both 14 and 21 years. Based on previous findings (van Os et al., 2009), it
confidence interval [CI], 3.9–67.8) at 26 years (Poulton et al., 2000). In a
was hypothesised that those experiencing hallu- cinations at 14 years would be at
subsequent study of the same cohort, outcomes were extended to 38 years,
increased risk of adult psychotic and non-psychotic disorders as well as
where it was found that hallucinations were asso- ciated with an increased
suicidality. Additionally, those ado- lescents who experienced hallucinations at
likelihood of schizophrenia (relative risk [RR], 7.24; 95% CI, 2.17–24.13) and
both 14 and 21 years would have the highest risk of psychotic and non-
posttraumatic stress disorder (RR, 3.03; 95% CI, 1.33–6.89) (Fisher et al.,
psychotic disorder and suicidality at 30–33 years.
2013), suggesting childhood psychotic symptoms may be a useful predictor of
future mental health problems. In a longitudinal study of youth aged 14–17
years, Dominguez and col- leagues measured psychotic experiences at three
2. Method
time points over an 8- year period. They found that those who reported
hallucinations and other psychotic experiences at only one time did not have an
2.1. Participants
increased risk of subsequent psychosis (compared with those who never
halluci- nated). However, adolescents with hallucinations at all three time
points had 10 times the odds of future psychosis (OR, 9.9; 95% CI, 2.5– 39.8) Participants were from the Mater-University of Queensland Study of
(Dominguez et al., 2011). Pregnancy (MUSP), a prospective birth cohort study of mothers and their
Two studies have reported the diagnostic outcomes of adolescents who offspring who received antenatal care at the Mater Misericordiae Mothers'
experienced auditory or visual hallucinations measured by the Youth Self- Hospital, a major public hospital in Brisbane, Australia, be- tween 1981 and
Report (Dhossche et al., 2002; Welham et al., 2009). Welham and colleagues 1984. Baseline data were collected on 7223 mothers and their singleton live-
reported that participants of the Mater Hospital Univer- sity of Queensland Study birth offspring who have since been prospec- tively followed-up over thirty
of Pregnancy (MUSP) who experienced hallu- cinations at 14 years were at years. Further information describing the MUSP cohort study can be found
increased risk of non-affective psychosis at age 21 (OR, 5.09; 95% CI, 2.18–11.8 elsewhere (Najman et al., 2005). At the 14- and 21-year data collections, the
[males]; 2.27; 1.01–5.12 [females]) Youth Self-Report (Achenbach, 1991) and the Young Adult Self-Report
(Welham et al., 2009). However, this study did not examine non-psy- chotic (Achenbach, 1997) were used to identify those offspring experiencing auditory
disorders as an outcome. By contrast, Dhossche and colleagues assessed both and visual hallucinations (Fig. 1). Only participants who provided data at both
psychotic and non-psychotic outcomes in adulthood of hallucinations in a 14- and 21-year follow-ups were eligible for recruitment. In total, 3535
community sample of adolescents (Dhossche et al., 2002). Those reporting participants completed the hallucination questions at both time points, of which
hallucinations were at increased risk of a depres- sive disorder (OR, 3.0; 95% CI, 822 (23.3%) endorsed experiencing auditory or vi- sual hallucinations at 14
1.1–8.8) or substance use disorder (OR, 7.8; 95% CI, 2.5–24.6) at 8-year follow- and/or 21 years. This group consisted of 455 participants (12.9%) with
up but none had transitioned to psychotic disorder. hallucinations only at 14 years old, 227 (6.4%) with hallucinations only at 21
Collectively, these studies suggest children and adolescents who hal- lucinate years old and 140 (4%) with hallu- cinations at both 14 and 21 years old.
are at increased risk of psychotic and non-psychotic disorders in adulthood.
However, all studies assessed diagnostic outcomes using lay interviewers rather
than clinicians, few examined a range of both psychotic and non-psychotic 2.2. Sampling protocol
outcomes, and only one (Dominguez et al., 2011) examined hallucinations in
adolescents at more than one time point showing that persistence of The target sample included all 822 MUSP participants who endorsed
hallucinations was important in predicting future psychosis. There is a need for experiencing hallucinations at ages 14 and/or 21 and 490 randomly se- lected
studies that examine a range of outcomes associated with hallucinations, which MUSP participants who did not report hallucinations at either time point. The
are mea- sured at more than one time point, and that follow participants into intended ratio of participants endorsing hallucinations to those not endorsing
adulthood after they have transitioned through the period of highest risk for hallucinations (roughly 2:1), was chosen to oversample individuals who were at
psychosis (Dhossche et al., 2002; Welham et al., 2009). a potentially greater risk of having a psychotic disorder by age 30. Four
Another outcome associated with hallucinations in adolescents and adults is hundred and forty-five (54%) of those who had experienced hallucinations
suicidality. A cross-sectional study of a large representative sample of adults (56.7% male, M age = 31.6, SD = 0.88) and 321 (65%) of those who had not
showed those respondents with psychotic experiences (PE) were more likely to experienced hallucina- tions were interviewed (42.2% male, M age = 31.1, SD
report current suicidal ideation (OR, 5.24; 95% CI, 2.85–9.62) and suicide = 0.95). This re- sulted in a total sample of 766 participants. The current study
attempts (OR, 9.48; 95% CI, 3.98–22.62) (DeVylder et al., 2015a). restricted cases to (a) 250 (54.9%) participants who reported hallucinations at age
Prospective studies have also reported that PE in adolescents elevate the risk for 14 alone and (b) 83 (59.2%) participants who reported hallucinations at age 14
suicidal behaviours at follow-up. A prospective cohort study of school-based and age 21. One hundred and twelve cohort members reported hallucinations
adolescents with baseline psychopathology and psychotic symptoms found at 21 years only but were not included in the present study as it could not be
14% had reported a suicide attempt by 3 months (OR, 17.91; 95% CI, 3.61– determined if they had already developed a psy- chotic disorder prior to this age
88.82) and 34% (we intend to follow these individuals in future studies). Methods to assess
reported a suicide attempt by 12 months (OR, 32.67; 95% CI, 10.42– 102.41) potential bias resulting from the re- sponse rates are outlined below.
(Kelleher et al., 2013). Another longitudinal cohort study of ad- olescents found
that PE at one time point only without psychological distress was not
associated with an increased risk of suicidality at 12 months (Martin et al., 2.3. Interview procedure
2015). However, persistent psychotic experi- ences (i.e. those present at both
baseline and one year follow-up) and those PE accompanied by psychological Interviews were conducted face to face when possible, and phone
distress were associated with increased odds of suicide attempts (OR, 4.63: interviews were used when participants were unable to attend the study
95% CI, 1.21–17.72 and 12.81; 4.02–40.88, respectively). Both studies have location. Interviews involved completion of self-report question- naires and
follow-up times lim- ited to 12 months and did not report associations with participation in a semi-structured interview. Interviewers were ‘blind’ to age 14
adult suicidal behaviour. and age 21 hallucination group status.
Please cite this article as: Connell, M., et al., Hallucinations in adolescents and risk for mental disorders and suicidal behaviour in adulthood: Prospective evidence
from the MUS..., Schizophr. Res. (2016), http://dx.doi.org/10.1016/j.schres.2016.06.009
M. Connell et al. / Schizophrenia Research xxx (2016) xxx–xxx 3
2.4. Structured clinical interview for DSM-IV Axis I disorders (SCID I) 2.5. Suicidality
The SCID I is a semi-structured interview used for making DSM-IV Axis I To avoid the limitations of single item measures of suicidality, suicid- al
diagnoses and covers key diagnostic groups including mood disor- ders, ideation, suicide plans and suicide attempts over the person's lifetime were
psychotic disorders, anxiety disorders, substance use disorders, somatoform measured using three items which asked if the person had ever se- riously
disorders, eating disorders and adjustment disorders (First et al., 2002). It thought about committing suicide, had they ever made a plan and had they
requires administration by a clinician or trained mental health professional ever had an attempt.
familiar with DSM classification and diagno- sis. It assesses both lifetime and
current diagnoses and can be used to provide symptom ratings as either absent, 2.6. Outcome variables
subthreshold or threshold.
The research version of the SCID was administered using netSCID, a For the main analyses, we used the major categories of Axis 1 diag- noses
computerized program designed in collaboration with the SCID authors and found from the SCID, including any DSM-IV mood (i.e. major depressive disorder,
to improve accuracy and reliability of administration. Inter- views were bipolar disorders and substance-induced mood disorders), anxiety (i.e. panic
administered by clinical psychologists and clinical psychol- ogy registrars with disorder, agoraphobia, posttraumatic stress disorder, generalized anxiety disorder,
experience and training in interviewing those with psychotic disorders. Raters obsessive compulsive disorder, social pho- bia and specific phobia), psychotic
undertook training in administration of the SCID and were required to meet (i.e. schizophrenia, schizoaffective disorder, psychotic disorder NOS, substance
criteria of 95% diagnostic agreement with SCID training interviews before induced psychotic disorder and brief psychotic disorder), substance use (i.e.
interviewing the MUSP partici- pants. Interviewers were required to participate in disorders of abuse and dependence including alcohol, cannabis, cocaine, opiate,
regular group meet- ings with J.S. and M.C. in which ratings were reviewed hallucinogen, amphetamine, sedative and polysubstance dependence) and eating
and complex presentations discussed. All interviews were audio recorded and dis- order (i.e. anorexia nervosa, bulimia nervosa and eating disorder NOS). A
ran- dom audits were undertaken by M.C. to ensure adherence to the proto- col secondary analysis was also conducted based on selected mental dis- orders
and accuracy of ratings made. (major depressive disorder [MDD], social phobia, specific phobia,
4 M. Connell et al. / Schizophrenia Research xxx (2016) xxx–xxx
Table 1
Univariable associations between hallucinations at age 14 only and hallucinations at both 14 and 21 with lifetime DSM-IV mental disorder categories (n = 650).
Hallucinations, %(n)
Disorder category None Age 14 only Ages 14 and 21 Chi-square (df) P value
Mood 42.3 (134) 48.8 (112) 53.0 (44) 3.08 (2) 0.22
Anxiety 33.1 (105) 33.6 (84) 47.0 (39) 5.94 (2) 0.05
Psychotic 0.6 (2) 1.2 (3) 07.2 (6) 17.80 (2) b0.001
Substance use 23.7 (75) 30.0 (75) 44.6 (37) 14.35 (2) 0.001
M. Connell et al. / Schizophrenia Research xxx (2016) xxx–xxx 5
Table 3
Multivariable associations between hallucinations at age 14 only and hallucinations at both 14 and 21 with suicidal behaviours at age 30, Adjusted for potential confoundersa [expressed in OR with 95%
confidence intervals (CI)] (n = 644).
Hallucinations
Suicidal behaviour % yes (n) OR (95% CI) % yes (n) OR (95% CI) % yes (n) OR (95% CI)
Ideation 16.8 (53) 1.00 24.8 (61) 1.44 (0.93–2.23) 39.0 (32) 2.89 (1.66–5.02)
Plans 6.0 (19) 1.00 11.0 (27) 1.30 (0.67–2.52) 20.7 (17) 2.89 (1.37–6.09)
Attempts 2.2 (7) 1.00 7.7 (19) 2.63 (1.04–6.63) 18.3 (15) 7.11 (2.68–18.83)
a
Adjusted confounding factors were age, sex, maternal education at baseline and substance use at 14 years.
Funding/Support Dominguez, M.D.G., Wichers, M., Lieb, R., Wittchen, H.-U., Van Os, J., 2011. Evidence that onset of
clinical psychosis is an outcome of progressively more persistent subclinical psychotic
This study was funded by the National Health and Medical Research Council experiences: an 8-year cohort study. Schizophr. Bull. 37 (1), 84–93.
First, M.B., Spitzer, R.L., Gibbon, M., Williams, J.B.W., 2002. Structured Clinical Interview for DSM-
(NHMRC #1046216). JGS is supported by a National Health and Medical IV-TR Axis I Disorders, Research Version, Non-patient Edition (SCID-I/NP) Revision: January
Research Council Practitioner Fellowship Grant #1105807. AAM was funded 2010 ed. Biometrics Research. New York State Psychiatric Institute, New York.
by the NHMRC CDF Level 2 (ID 1026598). John McGrath received John Cade Fisher, H.L., Caspi, A., Poulton, R., Meier, M.H., Houts, R., Harrington, H., Arseneault, L., Moffitt,
Fellowship #1056929 from the National Health and Medical Research Council. T.E., 2013. Specificity of childhood psychotic symptoms for predicting schizo- phrenia by 38 years of
age: a birth cohort study. Psychol. Med. 43 (10), 2077–2086. Johns, L.C., Kompus, K., Connell, M.,
Humpston, C., Lincoln, T.M., Longden, E., Preti, A., Alderson-Day, B., Badcock, J.C., Cella, M.,
Funders' roles Fernyhough, C., McCarthy-Jones, S., Peters, E., Raballo, A., Scott, J., Siddi, S., Sommer, I.E., Laroi, F.,
2014. Auditory verbal hallucina- tions in persons with and without a need for care. Schizophr. Bull.
40 (Suppl. 4),
The sponsors of the study (the NHMRC) had no role in the design and S255–S264.
conduct of the study; collection, management, analysis and inter- pretation of Kelleher, I., Harley, M., Murtagh, A., Cannon, M., 2011. Are screening instruments valid for psychotic-
the data; and preparation, review or approval of the manuscript. like experiences? A validation study of screening questions for psychotic- like experiences
using in-depth clinical interview. Schizophr. Bull. 37 (2), 362–369.
Kelleher, I., Connor, D., Clarke, M.C., Devlin, N., Harley, M., Cannon, M., 2012a. Prevalence of
Contributors' statement psychotic symptoms in childhood and adolescence: a systematic review and meta- analysis of
population-based studies. Psychol. Med. 42 (9), 1–7.
Kelleher, I., Keeley, H., Corcoran, P., Lynch, F., Fitzpatrick, C., Devlin, N., Molloy, C., Roddy, S.,
JGS and JMM planned the study. MC and JGS supervised the data col- lection. Clarke, M.C., Harley, M., Arseneault, L., Wasserman, C., Carli, V., Sarchiapone, M., Hoven, C.,
JGS, MC and KB planned the statistical analysis which was con- ducted by KB. Wasserman, D., Cannon, M., 2012b. Clinicopathological significance of psy- chotic experiences in
MC and JGS wrote the initial drafts of the manuscript. All authors were involved non-psychotic young people: evidence from four population- based studies. Br. J. Psychiatry 201
(1), 26–32.
in later revisions and all authors approved the final manuscript.
Kelleher, I., Lynch, F., Harley, M., Molloy, C., Roddy, S., Fitzpatrick, C., Cannon, M., 2012c.
Psychotic symptoms in Adolescence Index Risk for Suicidal Behavior: findings from 2
Access to data population-based case-control clinical interview studies. Arch. Gen. Psychiatry 69 (12), 1277–
1283.
Kelleher, I., Corcoran, P., Keeley, H., Johanna, T.W.W., Devlin, N., Ramsay, H., Wasserman, C., Carli,
MC, JS and KB had full access to the data used in the study and take V., Sarchiapone, M., Hoven, C., Wasserman, D., Cannon, M., 2013. Psychotic symptoms and
responsibility for the integrity of the data and the accuracy of the data analysis. population risk for suicide attempt: a prospective cohort study. JAMA Psychiatry 70 (9), 940.
Link, B.G., Lieberman, J.A., Lukens, E.P., DeVylder, J.E., 2015. Suicidal ideation and suicide attempts
among adults with psychotic experiences: data from the Collaborative Psy- chiatric Epidemiology
Acknowledgements
Surveys. JAMA Psychiatry 72 (3), 219–225.
The authors thank the MUSP team, MUSP participants, the Mater Misericordiae Hos- pital, and
Martin, G., Thomas, H., Andrews, T., Hasking, P., Scott, J.G., 2015. Psychotic experiences and
the Schools of Social Science, Population Health and Medicine (University of Queensland).
psychological distress predict contemporaneous and future non-suicidal self-in- jury and suicide
attempts in a sample of Australian school-based adolescents. Psychol. Med. 45 (2), 429–437.
Appendix A. Supplementary data McGrath, J.J., Saha, S., Al-Hamzawi, A., et al., 2015. Psychotic experiences in the general population: a
cross-national analysis based on 31 261 respondents from 18 countries. JAMA Psychiatry.
Najman, J.M., Bor, W., O'Callaghan, M., Williams, G.M., Aird, R., Shuttlewood, G., 2005. Co- hort
Supplementary data to this article can be found online at http://dx. profile: the Mater-University of Queensland Study of Pregnancy (MUSP). Int. J. Epidemiol. 34
doi.org/10.1016/j.schres.2016.06.009. (5), 992–997.
Poulton, R., Caspi, A., Moffitt, T.E., Cannon, M., Murray, R., Harrington, H., 2000. Children's Self-
Reported Psychotic Symptoms and Adult Schizophreniform Disorder: a 15-year longitudinal
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