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SCHRES-06872; No of Pages 6

Schizophrenia Research xxx (2016) xxx–xxx

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Schizophrenia Research

journal homepage: www.elsevier.com/locate/schres

Hallucinations in adolescents and risk for mental disorders and suicidal


behaviour in adulthood: Prospective evidence from the MUSP birth
cohort study
Melissa Connell a, Kim Betts b, John J. McGrath c,d, Rosa Alati b,g, Jake Najman b,f, Alexandra Clavarino b,h,
Abdullah Mamun b, Gail Williams b, James G. Scott a,d,e,⁎
a
The University of Queensland Centre for Clinical Research, Herston, QLD 4029, Australia
b
School of Public Health, University of Queensland, Herston, QLD 4029, Australia
c
Queensland Brain Institute, University of Queensland, St Lucia, QLD 4076, Australia
d
Queensland Centre for Mental Health Research, The Park Centre for Mental Health, Wacol, QLD 4076, Australia
e
Royal Brisbane and Women's Hospital, Herston, QLD 4029, Australia
f
School of Social Science, University of Queensland, St Lucia. QLD 4076, Australia
g
Centre for Youth Substance Abuse Research, University of Queensland, Royal Brisbane and Women's Hospital, Herston, QLD 4006, Australia
h
School of Pharmacy, The University of Queensland, 20 Cornwall Street, Woolloongabba, 4102, Queensland, Australia

a r t i c l e i n f o a b s t r a c t

Article history: Background: Hallucinations, once equated with serious mental disorders, are common in adolescents. Given the
Received 16 February 2016 high prevalence of hallucinations, it is important to determine if they are associated with adverse mental health
Received in revised form 7 May 2016 outcomes in adulthood. This study compared the mental health outcomes of participants (aged 30–33 years) in
Accepted 9 June 2016 the Mater-University of Queensland Study of Pregnancy (MUSP) who reported hallucinations at (a) 14 years only
Available online xxxx
and (b) 14 and 21 years versus cohort members without hallucinations.
Method: Participants (n = 333) were aged between 30 and 33 years and (a) reported hallucinations on the Youth
Keywords:
Hallucinations
Self-Report Questionnaire at 14 and/or the Young Adult Self-Report Questionnaire at 21 years and (b) controls
Birth cohort (n = 321) who did not report hallucinations. Lifetime diagnoses of mental disorders were ascertained by the
Mental disorders Structured Clinical Interview for DSM Disorders (DSM IV-TR) administered by clinical psychologists. Suicidal be-
Psychotic disorders haviour was measured by self report.
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
Hallucinations, cardinal symptoms of psychotic disorders, also occur et al., 2000; Welham et al., 2009) and other psychopathology (Dhossche
in other mental disorders and in otherwise well individuals. For exam- et al., 2002; Fisher et al., 2013; Kelleher et al., 2012b). However, these
ple, a large community-based study reported the lifetime prevalence studies have their limitations and the utility of hallucinations as a pre-
of hallucinations as 5.2% (McGrath et al., 2015) whilst studies of adoles- dictor of future mental health disorders is in debate.
cents have found a higher 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
⁎ Corresponding author at: The University of Queensland Centre for Clinical Research,
on the Dunedin birth cohort assessed diagnostic outcomes of partici-
Herston, QLD 4029, Australia. pants who experienced psychotic symptoms measured at 11 years
E-mail address: james.scott@health.qld.gov.au (J.G. Scott). (based on the Diagnostic Interview 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 The current study examined a broad range of mental health out-
child psychiatrists and identified as having psychotic symptoms had a comes in adulthood for those who reported experiencing hallucinations
16-fold greater risk of adult schizophreniform disorder (odds ratio at (i) 14 years and (ii) both 14 and 21 years. Based on previous findings
[OR], 16.4; 95% confidence interval [CI], 3.9–67.8) at 26 years (Poulton (van Os et al., 2009), it was hypothesised that those experiencing hallu-
et al., 2000). In a subsequent study of the same cohort, outcomes were cinations at 14 years would be at increased risk of adult psychotic and
extended to 38 years, where it was found that hallucinations were asso- non-psychotic disorders as well as suicidality. Additionally, those ado-
ciated with an increased likelihood of schizophrenia (relative risk [RR], lescents who experienced hallucinations at both 14 and 21 years
7.24; 95% CI, 2.17–24.13) and posttraumatic stress disorder (RR, 3.03; would have the highest risk of psychotic and non-psychotic disorder
95% CI, 1.33–6.89) (Fisher et al., 2013), suggesting childhood psychotic and suicidality at 30–33 years.
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 time points over an 8- 2. Method
year period. They found that those who reported hallucinations and
other psychotic experiences at only one time did not have an increased 2.1. Participants
risk of subsequent psychosis (compared with those who never halluci-
nated). However, adolescents with hallucinations at all three time Participants were from the Mater-University of Queensland Study of
points had 10 times the odds of future psychosis (OR, 9.9; 95% CI, 2.5– Pregnancy (MUSP), a prospective birth cohort study of mothers and
39.8) (Dominguez et al., 2011). their offspring who received antenatal care at the Mater Misericordiae
Two studies have reported the diagnostic outcomes of adolescents Mothers' Hospital, a major public hospital in Brisbane, Australia, be-
who experienced auditory or visual hallucinations measured by the tween 1981 and 1984. Baseline data were collected on 7223 mothers
Youth Self-Report (Dhossche et al., 2002; Welham et al., 2009). Welham and their singleton live-birth offspring who have since been prospec-
and colleagues reported that participants of the Mater Hospital Univer- tively followed-up over thirty years. Further information describing
sity of Queensland Study of Pregnancy (MUSP) who experienced hallu- the MUSP cohort study can be found elsewhere (Najman et al., 2005).
cinations at 14 years were at increased risk of non-affective psychosis at At the 14- and 21-year data collections, the Youth Self-Report
age 21 (OR, 5.09; 95% CI, 2.18–11.8 [males]; 2.27; 1.01–5.12 [females]) (Achenbach, 1991) and the Young Adult Self-Report (Achenbach,
(Welham et al., 2009). However, this study did not examine non-psy- 1997) were used to identify those offspring experiencing auditory and
chotic disorders as an outcome. By contrast, Dhossche and colleagues visual hallucinations (Fig. 1). Only participants who provided data at
assessed both psychotic and non-psychotic outcomes in adulthood of both 14- and 21-year follow-ups were eligible for recruitment. In
hallucinations in a community sample of adolescents (Dhossche et al., total, 3535 participants completed the hallucination questions at both
2002). Those reporting hallucinations were at increased risk of a depres- time points, of which 822 (23.3%) endorsed experiencing auditory or vi-
sive disorder (OR, 3.0; 95% CI, 1.1–8.8) or substance use disorder (OR, sual hallucinations at 14 and/or 21 years. This group consisted of 455
7.8; 95% CI, 2.5–24.6) at 8-year follow-up but none had transitioned to participants (12.9%) with hallucinations only at 14 years old, 227
psychotic disorder. (6.4%) with hallucinations only at 21 years old and 140 (4%) with hallu-
Collectively, these studies suggest children and adolescents who hal- cinations at both 14 and 21 years old.
lucinate 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 2.2. Sampling protocol
psychotic and non-psychotic outcomes, and only one (Dominguez et
al., 2011) examined hallucinations in adolescents at more than one The target sample included all 822 MUSP participants who endorsed
time point showing that persistence of hallucinations was important experiencing hallucinations at ages 14 and/or 21 and 490 randomly se-
in predicting future psychosis. There is a need for studies that examine lected MUSP participants who did not report hallucinations at either
a range of outcomes associated with hallucinations, which are mea- time point. The intended ratio of participants endorsing hallucinations
sured at more than one time point, and that follow participants into to those not endorsing hallucinations (roughly 2:1), was chosen to
adulthood after they have transitioned through the period of highest oversample individuals who were at a potentially greater risk of having
risk for psychosis (Dhossche et al., 2002; Welham et al., 2009). a psychotic disorder by age 30. Four hundred and forty-five (54%) of
Another outcome associated with hallucinations in adolescents and those who had experienced hallucinations (56.7% male, M age = 31.6,
adults is suicidality. A cross-sectional study of a large representative SD = 0.88) and 321 (65%) of those who had not experienced hallucina-
sample of adults showed those respondents with psychotic experiences tions were interviewed (42.2% male, M age = 31.1, SD = 0.95). This re-
(PE) were more likely to report current suicidal ideation (OR, 5.24; 95% sulted in a total sample of 766 participants. The current study restricted
CI, 2.85–9.62) and suicide attempts (OR, 9.48; 95% CI, 3.98–22.62) cases to (a) 250 (54.9%) participants who reported hallucinations at age
(DeVylder et al., 2015a). Prospective studies have also reported that 14 alone and (b) 83 (59.2%) participants who reported hallucinations at
PE in adolescents elevate the risk for suicidal behaviours at follow-up. age 14 and age 21. One hundred and twelve cohort members reported
A prospective cohort study of school-based adolescents with baseline hallucinations at 21 years only but were not included in the present
psychopathology and psychotic symptoms found 14% had reported a study as it could not be determined if they had already developed a psy-
suicide attempt by 3 months (OR, 17.91; 95% CI, 3.61–88.82) and 34% chotic disorder prior to this age (we intend to follow these individuals in
reported a suicide attempt by 12 months (OR, 32.67; 95% CI, 10.42– future studies). Methods to assess potential bias resulting from the re-
102.41) (Kelleher et al., 2013). Another longitudinal cohort study of ad- sponse rates are outlined below.
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., 2015). However, persistent psychotic experi- 2.3. Interview procedure
ences (i.e. those present at both baseline and one year follow-up) and
those PE accompanied by psychological distress were associated with Interviews were conducted face to face when possible, and phone
increased odds of suicide attempts (OR, 4.63: 95% CI, 1.21–17.72 and interviews were used when participants were unable to attend the
12.81; 4.02–40.88, respectively). Both studies have follow-up times lim- study location. Interviews involved completion of self-report question-
ited to 12 months and did not report associations with adult suicidal naires and participation in a semi-structured interview. Interviewers
behaviour. were ‘blind’ to age 14 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

Fig. 1. Sampling procedure used in participant selection.

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 To avoid the limitations of single item measures of suicidality, suicid-
Axis I diagnoses and covers key diagnostic groups including mood disor- al ideation, suicide plans and suicide attempts over the person's lifetime
ders, psychotic disorders, anxiety disorders, substance use disorders, were measured using three items which asked if the person had ever se-
somatoform disorders, eating disorders and adjustment disorders riously thought about committing suicide, had they ever made a plan
(First et al., 2002). It requires administration by a clinician or trained and had they ever had an attempt.
mental health professional familiar with DSM classification and diagno-
sis. It assesses both lifetime and current diagnoses and can be used to 2.6. Outcome variables
provide symptom ratings as either absent, 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-
computerized program designed in collaboration with the SCID authors noses from the SCID, including any DSM-IV mood (i.e. major depressive
and found to improve accuracy and reliability of administration. Inter- disorder, bipolar disorders and substance-induced mood disorders),
views were administered by clinical psychologists and clinical psychol- anxiety (i.e. panic disorder, agoraphobia, posttraumatic stress disorder,
ogy registrars with experience and training in interviewing those with generalized anxiety disorder, obsessive compulsive disorder, social pho-
psychotic disorders. Raters undertook training in administration of the bia and specific phobia), psychotic (i.e. schizophrenia, schizoaffective
SCID and were required to meet criteria of 95% diagnostic agreement disorder, psychotic disorder NOS, substance induced psychotic disorder
with SCID training interviews before interviewing the MUSP partici- and brief psychotic disorder), substance use (i.e. disorders of abuse and
pants. Interviewers were required to participate in regular group meet- dependence including alcohol, cannabis, cocaine, opiate, hallucinogen,
ings with J.S. and M.C. in which ratings were reviewed and complex amphetamine, sedative and polysubstance dependence) and eating dis-
presentations discussed. All interviews were audio recorded and ran- order (i.e. anorexia nervosa, bulimia nervosa and eating disorder NOS).
dom audits were undertaken by M.C. to ensure adherence to the proto- A secondary analysis was also conducted based on selected mental dis-
col and accuracy of ratings made. orders (major depressive disorder [MDD], social phobia, specific phobia,

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
4 M. Connell et al. / Schizophrenia Research xxx (2016) xxx–xxx

posttraumatic stress disorder [PTSD], generalized anxiety disorder Table 2


[GAD], panic disorder, obsessive compulsive disorder [OCD], alcohol Multivariable associations between hallucinations at age 14 only and hallucinations at
both 14 and 21 with DSM-IV mental disorder categories, adjusted for potential
abuse and/or dependence [combined as alcohol use disorder], cannabis confoundersa [expressed in OR with 95% confidence intervals (CI)] (n = 650).
abuse and/or dependence [combined as cannabis use disorder] and
polysubstance dependence disorders). Suicidality was measured using Hallucinations

three categorical variables of suicidal thoughts, suicidal plans and suicide None Age 14 only Ages 14 and 21
attempts. Disorder category OR (95% CI) OR (95% CI) OR (95% CI)
Mood 1.00 1.04 (0.74–1.48) 1.47 (0.89–2.43)
2.7. Predictor variables Anxiety 1.00 0.92 (0.63–1.33) 1.52 (0.91–2.54)
Psychotic 1.00 1.09 (0.16–7.60) 8.84 (1.61–48.43)
Substance use 1.00 1.08 (0.71–1.62) 2.34 (1.36–4.07)
Hallucinations were measured at age 14 using the YSR (Achenbach, Eating 1.00 1.23 (0.35–4.30) 3.60 (0.99–13.07)
1991) and at age 21 using the YASR. (Achenbach, 1997) Hallucinations a
Adjusted confounding factors were age, sex, maternal education at baseline and sub-
were assessed at 14 and 21 years with the YSR/YASR questionnaires
stance use at 14 years.
which included two questions: (i) “I hear sounds or voices which
other people think aren't there”; (ii) “I see things that other people
think aren't there”. Respondents answered with very true or often true, 3. Results
somewhat or sometimes true, or not true, which were then reclassified
into three discrete hallucinations categories: (1) did not experience hal- After adjusting for age, sex, maternal education at baseline and sub-
lucinations, (2) experienced hallucinations sometimes or often at age stance use at 14 years, hallucinations at 14 years only were not associat-
14, (3) experienced hallucinations sometimes or often at ages 14 and ed with any groups of mental disorder in adulthood (Table 2). Those
21.The reliability of self-report measures for assessing hallucinations participants who reported hallucinations at both 14 and 21 years had
in adolescents has been established (Kelleher et al., 2011). Of all psy- increased odds of being diagnosed with a psychotic disorder (OR,
chotic experiences, self-report assessment of hearing voices or sounds 8.84; 95% CI, 1.61–48.43) or substance use disorder (OR, 2.34; 95% CI,
that others don't hear was found to be the strongest predictor of a clin- 1.36–4.07) at 30–33 years (See Tables 1 and 2).
ically verifiable history of auditory hallucinations (positive predictive Pertaining to specific mental disorders, there were no associations
value [PPV] = 71.4% and negative predictive value [NPV] = 90.4%), with hallucinations at 14 years. Those with hallucinations at 14 and
with visual hallucinations also showing moderately successful predic- 21 years had increased risk of alcohol use disorder (OR, 2.41; 95% CI,
tive power (PPV = 81.8% and NPV = 80%) (Kelleher et al., 2011). Hallu- 1.35–4.30), cannabis use disorder (OR, 2.71; 95% CI, 1.36–5.41), panic
cination items from the YSR have been used in previous longitudinal disorder (OR, 3.30; 95% CI, 1.35–8.08), polysubstance dependence (OR,
studies (Dhossche et al., 2002; Welham et al., 2009). 3.83; 95% CI, 1.13–13.04) and specific phobia (OR, 2.43; 95% CI, 1.11–
5.29) (Supplementary Table 1). There was no association between hal-
2.8. Statistical analyses lucinations at both 14 and 21 years and major depressive disorder, gen-
eralized anxiety disorder, obsessive compulsive disorder, posttraumatic
Chi-square tests were used to examine the associations between the stress disorder and social phobia.
different categories of hallucinations with the major groups of mental Those reporting hallucinations in both adolescence and young adult-
disorders at age 30. Univariate and multivariate logistic regressions hood were more likely to report lifetime suicidal ideas and behaviours
were then used to examine the associations between hallucinations ad- at 30–33 years. Suicide attempts were almost three times more likely
justed for potential covariates with the mental disorder groups and with to occur in those who had hallucinations at 14 years only (OR, 2.63;
suicidal behaviour. Covariates used in the adjusted models were partic- 95% CI, 1.04–6.63) and seven-fold more likely in those with hallucina-
ipant age, sex, substance use at age 14 and maternal education at base- tions at both follow-ups (OR, 7.11; 95% CI, 2.68–18.83) (Table 3).
line. Secondary analyses were then conducted examining the Lastly, the attrition analyses showed that among participants who
associations between hallucinations with specific mental disorders. reported hallucinations, those included in the sample were more likely
The final sample in all analyses consisted of 650 participants with values to be female and their mothers were more likely to have completed ter-
for all variables of interest. tiary education (Supplementary Table 2). Among participants who did
report hallucinations, those included in the study were more likely to
2.9. Response rates analyses be female, have a higher family income and an older maternal age at
birth.
Two separate attrition analyses were conducted using multivariate
logistic regression to compare differences among baseline measures 4. Discussion
(i.e., pre-pregnancy) between (1) MUSP participants who reported hal-
lucinations at 14 and/or 21 years of age who participated in the current Adolescents who reported experiencing hallucinations at both 14
study versus those who did not participate and (2) MUSP participants and 21 years were at increased risk of both adult psychopathology and
who did not report hallucinations at 14 or 21 years of age (controls) lifetime suicidal ideas and behaviours. Those who reported experienc-
and participated in the current study versus those who did not partici- ing hallucinations at 14 years only did not have an increased risk of
pate These analyses were further limited to participants with all data mental disorders in the main analysis although they were more likely
on baseline variables of interest. to have attempted suicide. Together, these findings suggest that

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

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 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

None Age 14 only Ages 14 and 21

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.

adolescents whose hallucinations remit before adulthood are at no on the assumption that these experiences are forerunners of psychosis.
greater risk of future mental disorders than individuals who do not ex- However, previous studies have shown that hallucinations in adoles-
perience hallucinations. However, those who experience hallucinations cents are associated with serious psychopathology in the short term,
in adolescence and adulthood are more likely to develop a mental disor- in particular, increased risk of suicidal behaviours (Kelleher et al.,
der in adulthood. 2013; Martin et al., 2015) which are also linked to distress and affective
Those with hallucinations present at 14 and 21 years had an almost dysregulation (Yen et al., 2013). Interventions aimed at improving dis-
nine-fold risk of developing a psychotic disorder and a three-fold risk of tress tolerance and affect regulation may ameliorate psychopathological
a substance use disorder. When examining for specific diagnostic out- processes which perpetuate these difficulties and result in mental disor-
comes, hallucinations experienced in both adolescence and adulthood der diagnoses in adulthood (Taylor et al., 2014). Adolescents and their
were associated with a wide range of non-psychotic illness as assessed families can be reassured that most who experience hallucinations
by clinicians including alcohol and cannabis use disorders, panic disor- will not develop psychosis or other mental disorders later in life.
der, polysubstance dependence and specific phobia.
This study supports and extends previous research. Dominguez and 4.2. Limitations
colleagues (Dominguez et al., 2011) previously reported that hallucina-
tions that were present on more than one follow-up were associated The use of lifetime assessments of mental disorders and suicidality
with later psychotic disorders. Other studies have shown that hallucina- made it difficult to confidently ascribe the temporal sequence of the
tions in adolescents are associated with both psychotic and non-psy- onset of the disorders assessed at age 30, and it is feasible that onset
chotic disorders (Fisher et al., 2013). There is now consistent evidence may have preceded the assessments at 14 and 21 years. However, it
of an association between hallucinations and suicidal behaviour would be unlikely that a clinical psychotic disorder would be present
(DeVylder et al., 2015b; Kelleher et al., 2013; Link et al., 2015; Martin prior to 14 years and there is a tendency for respondents to favour re-
et al., 2015). The risk of suicidal ideation and plans and of suicide at- cent experiences in reports of lifetime symptoms and behaviours
tempt was greater in those who had hallucinations at both 14 and (Kelleher et al., 2012c). There are additional confounding factors
21 years compared with those who reported hallucinations at 14 years which may have been associated with outcomes that were not mea-
only. Persistent hallucinations in adolescents have been shown to be as- sured such as experiences of trauma and adversity. Amongst MUSP par-
sociated with suicidality in a study where the follow-up was limited to ticipants experiencing hallucinations at age 14 and/or 21, the response
12 months (Martin et al., 2015). This study is consistent with the find- rate was 54% which may have impacted the generalisability of our find-
ings of Fisher and colleagues (Fisher et al., 2013) who reported psychot- ings. However, the attrition analysis found that aside from gender and
ic experiences in childhood were associated with suicide attempts at maternal education, those included in the sample did not differ by base-
38 years. line variables, and also did not differ by the severity of the reported hal-
These findings demonstrate that hallucinations occurring at more lucinations. However, those with mental disorders in adulthood are
than one point in time are predictive of a range of adult mental disor- more likely to drop out of the MUSP study, thus our estimates may be
ders (Kelleher et al., 2012b). The relationship found with anxiety and conservative.
substance use disorders suggests that hallucinations in adolescents Finally, whilst a strength of this study was the measurement of hal-
may be indicative of a shared vulnerability for broader psychopatholo- lucinations at two time points encompassing the transition from adoles-
gy. It may be that affective dysregulation is the core deficit that under- cence to young adulthood, these were seven years apart, which
lies both the experience of hallucinations in adolescents and the risk precludes assumptions as to whether the hallucinations were persistent
of developing a mental disorder in adulthood. Affective dysregulation or recurrent. Furthermore, there was no information regarding the fre-
is a key feature of affective, anxiety, suicidality (Cisler et al., 2010) and quency or emotional valence of the content of the hallucinations, two
substance use (Cheetham et al., 2010) difficulties and has been pro- characteristics reported of hallucinations in need of treatment
posed as forming a reciprocal relationship with reality distortion (Van (Daalman et al., 2011; Johns et al., 2014). Ideally, more measurements
Rossum et al., 2011; Wigman et al., 2012). Further research is needed of hallucinations at closer time points would better inform the course
to establish whether psychosis and affective dysregulation are part of of hallucinations in adolescents and their associated adult outcomes.
the same continuum or constitute separate but interacting continua
(Taylor et al., 2014; van Os, 2014). 5. Conclusions

4.1. Clinical implications Hallucinations in adolescents are common. When mental health out-
comes were assessed by clinicians using a standardised diagnostic clin-
In this study, hallucinations that are experienced in early adoles- ical instrument, those experiencing hallucinations at both 14 and
cence and remit were found not to be associated with increased risk 21 years had increased odds of adult mental disorders and suicidal be-
for adult psychopathology. However, those whose hallucinations were haviours. In most adolescents, the hallucinations resolved and were
present in both adolescence and young adulthood had an increased not associated with increased odds of adult psychopathology.
risk of mental disorders and suicidal ideation and behaviours at
30 years. It is important to take into account the natural history of hal- Conflict of interest
lucinations in young people to avoid unnecessary interventions based All authors declare no conflicts of interest.

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
6 M. Connell et al. / Schizophrenia Research xxx (2016) xxx–xxx

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 experiences: an 8-year cohort study. Schizophr. Bull. 37 (1), 84–93.
This study was funded by the National Health and Medical Research First, M.B., Spitzer, R.L., Gibbon, M., Williams, J.B.W., 2002. Structured Clinical Interview
Council (NHMRC #1046216). JGS is supported by a National Health and for DSM-IV-TR Axis I Disorders, Research Version, Non-patient Edition (SCID-I/NP)
Revision: January 2010 ed. Biometrics Research. New York State Psychiatric Institute,
Medical Research Council Practitioner Fellowship Grant #1105807. New York.
AAM was funded by the NHMRC CDF Level 2 (ID 1026598). John Fisher, H.L., Caspi, A., Poulton, R., Meier, M.H., Houts, R., Harrington, H., Arseneault, L.,
McGrath received John Cade Fellowship #1056929 from the National Moffitt, 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.
Health and Medical Research Council. Johns, L.C., Kompus, K., Connell, M., Humpston, C., Lincoln, T.M., Longden, E., Preti, A.,
Alderson-Day, B., Badcock, J.C., Cella, M., Fernyhough, C., McCarthy-Jones, S., Peters,
Funders' roles 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),
S255–S264.
The sponsors of the study (the NHMRC) had no role in the design Kelleher, I., Harley, M., Murtagh, A., Cannon, M., 2011. Are screening instruments valid for
and conduct of the study; collection, management, analysis and inter- psychotic-like experiences? A validation study of screening questions for psychotic-
pretation of the data; and preparation, review or approval of the 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
manuscript. of psychotic symptoms in childhood and adolescence: a systematic review and meta-
analysis of population-based studies. Psychol. Med. 42 (9), 1–7.
Contributors' statement Kelleher, I., Keeley, H., Corcoran, P., Lynch, F., Fitzpatrick, C., Devlin, N., Molloy, C., Roddy,
S., Clarke, M.C., Harley, M., Arseneault, L., Wasserman, C., Carli, V., Sarchiapone, M.,
Hoven, C., Wasserman, D., Cannon, M., 2012b. Clinicopathological significance of psy-
JGS and JMM planned the study. MC and JGS supervised the data col- chotic experiences in non-psychotic young people: evidence from four population-
lection. JGS, MC and KB planned the statistical analysis which was con- based studies. Br. J. Psychiatry 201 (1), 26–32.
Kelleher, I., Lynch, F., Harley, M., Molloy, C., Roddy, S., Fitzpatrick, C., Cannon, M., 2012c.
ducted by KB. MC and JGS wrote the initial drafts of the manuscript. All Psychotic symptoms in Adolescence Index Risk for Suicidal Behavior: findings from
authors were involved in later revisions and all authors approved the 2 population-based case-control clinical interview studies. Arch. Gen. Psychiatry 69
final manuscript. (12), 1277–1283.
Kelleher, I., Corcoran, P., Keeley, H., Johanna, T.W.W., Devlin, N., Ramsay, H., Wasserman,
C., Carli, V., Sarchiapone, M., Hoven, C., Wasserman, D., Cannon, M., 2013. Psychotic
Access to data symptoms and 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
MC, JS and KB had full access to the data used in the study and take
attempts among adults with psychotic experiences: data from the Collaborative Psy-
responsibility for the integrity of the data and the accuracy of the data chiatric Epidemiology Surveys. JAMA Psychiatry 72 (3), 219–225.
analysis. Martin, G., Thomas, H., Andrews, T., Hasking, P., Scott, J.G., 2015. Psychotic experiences
and psychological distress predict contemporaneous and future non-suicidal self-in-
jury and suicide attempts in a sample of Australian school-based adolescents.
Acknowledgements
Psychol. Med. 45 (2), 429–437.
The authors thank the MUSP team, MUSP participants, the Mater Misericordiae Hos-
McGrath, J.J., Saha, S., Al-Hamzawi, A., et al., 2015. Psychotic experiences in the general
pital, and the Schools of Social Science, Population Health and Medicine (University of
population: a cross-national analysis based on 31 261 respondents from 18 countries.
Queensland). JAMA Psychiatry.
Najman, J.M., Bor, W., O'Callaghan, M., Williams, G.M., Aird, R., Shuttlewood, G., 2005. Co-
Appendix A. Supplementary data hort profile: the Mater-University of Queensland Study of Pregnancy (MUSP). Int.
J. Epidemiol. 34 (5), 992–997.
Poulton, R., Caspi, A., Moffitt, T.E., Cannon, M., Murray, R., Harrington, H., 2000. Children's
Supplementary data to this article can be found online at http://dx. Self-Reported Psychotic Symptoms and Adult Schizophreniform Disorder: a 15-year
doi.org/10.1016/j.schres.2016.06.009. longitudinal study. Arch. Gen. Psychiatry 57 (11), 1053–1058.
Taylor, H.E., Stewart, S.L.K., Dunn, G., Parker, S., Bentall, R.P., Birchwood, M., Morrison, A.P.,
2014. Psychopathology and affect dysregulation across the continuum of psychosis: a
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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

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