- Research Article
- Open Access
Substance abuse and personality disorder comorbidity in adolescent outpatients: are girls more severely ill than boys?
Child and Adolescent Psychiatry and Mental Health volume 10, Article number: 8 (2016)
Substance use disorders (SUDs) constitute a major health problem and are associated with an extensive psychiatric comorbidity. Personality disorders (PDs) and SUDs commonly co-occur. Comorbid PD is characterized by more severe addiction problems and by an unfavorable clinical outcome. The present study investigated the prevalence of SUDs, PDs and common Axis I disorders in a sample of adolescent outpatients. We also investigated the association between PDs and SUDs, and how this association was influenced by adjustment for other Axis I disorders, age and gender.
The sample consisted of 153 adolescents, aged 14–17 years, who were referred to a non-specialized mental health outpatient clinic with a defined catchment area. SUDs and other Axis I conditions were assessed using the mini international neuropsychiatric interview. PDs were assessed using the structured interview for DSM-IV personality.
18.3 % of the adolescents screened positive for a SUD, with no significant gender difference. There was a highly significant association between number of PD symptoms and having one or more SUDs; this relationship was practically unchanged by adjustment for gender, age and presence of Axis I disorders. For boys, no significant associations between SUDs and specific PDs, conduct disorder (CD) or attention deficit hyperactivity disorder (ADHD) were found. For girls, there were significant associations between SUD and BPD, negativistic PD, more than one PD, CD and ADHD.
We found no significant gender difference in the prevalence of SUD in a sample of adolescents referred to a general mental health outpatient clinic. The association between number of PD symptoms and having one or more SUDs was practically unchanged by adjustment for gender, age and presence of one or more Axis I disorders, which suggested that having an increased number of PD symptoms in itself may constitute a risk factor for developing SUDs in adolescence. The association in girls between SUDs and PDs, CD and ADHD raises the question if adolescent girls suffering from these conditions may be especially at risk for developing SUDs. In clinical settings, they should therefore be monitored with particular diligence with regard to their use of psychoactive substances.
Trial registration The regional committee for medical research ethics for eastern Norway approved the study protocol in October 2004 (REK: 11395). Address correspondence and reprint requests to: Hans Ole Korsgaard, The Nic Waal Institute, Lovisenberg Diakonale Hospital, P.O. Box 2970 Nydalen, N-0440 Oslo, Norway; E-mail firstname.lastname@example.org
Personality disorders (PDs) are defined as enduring and maladaptive patterns of experiencing, coping, and relating to others. In DSM-IV, as well as DSM-5, PD categories may be applied to adolescents when the individual’s particular maladaptive personality traits appear to be pervasive, persistent, and unlikely to be limited to a particular developmental state or an episode of an Axis I disorder. With the exception of antisocial PD (ASPD), any PD can be diagnosed in a person under 18 years of age, as long as the diagnostic features have been present for at least 1 year [1, 2].
PDs are common conditions, with prevalences of about 13 % in the general adult population, up to 40 % in adult outpatient samples, and up to 71 % in inpatient samples when diagnosed with comprehensive semi-structured interviews . In adolescents, prevalences range from 6 to 17 % in community samples, and in clinical samples from 41 to 64 % . Pathological personality traits emerge at an early age and are related to health-risk behaviors in adolescence as well as young adulthood [5–7], but PD diagnoses may be less stable than previously assumed . Maladaptive personality trait constellations, however, seem to be more stable in their structure than PD diagnoses. They may change in severity or expression over time; still they often lead to persistent functional impairment and reduced quality of life, even if the diagnostic threshold for a specific PD is no longer reached [9, 10].
Borderline PD is the single most studied PD, and is generally considered as the prototypical cluster B disorder. BPD may be more prevalent than previously recognized, with a lifetime prevalence of up to 2.7 % in the general adult population . A large population study found BPD equally prevalent among men and women, and frequently associated with considerable mental and physical disability, especially among women . There is an increasing awareness of developmental antecedents and adolescent presentation of BPD [13–15], with several studies pointing out prognostic advantages of early identification and timely treatment of PDs [16, 17]. It has recently been shown that the diagnosis of BPD is as reliable and valid in adolescents as it is in adults, and that adolescents with BPD can benefit from early intervention .
Substance use disorders (SUDs) constitute a major health problem, with estimated prevalence rates of 3.4 % for alcohol dependence and 0.3–1.8 % for cannabis dependence in the general European population . It has generally been assumed that boys use more drugs and alcohol than girls. However, recent findings seem to contradict this long-held assumption; Johnson and colleagues found that male–female differences in adolescent marijuana use have decreased since 1999 , and another study reports that the differences in drinking patterns of adolescent boys and girls narrowed between 2002 and 2012 . Drug abuse is associated with an extensive psychiatric comorbidity and carries an increased risk of premature death, especially in male users of opiates or barbiturates . Estimated lifetime prevalences of SUDs in adolescents and young adults range from 4.6  to 17.7 % . In adolescents, SUDs are of considerable importance in the etiology and prognosis of psychiatric disorders such as mood disorders, conduct disorder (CD), attention-deficit hyperactivity disorder (ADHD), and anxiety disorders . In adults, generalized anxiety disorder (GAD) and SUDs are highly comorbid, and GAD–SUD comorbidity is associated with a host of poor psychosocial outcomes, including higher rates of hospitalization, disability, functional impairment, and inferior GAD and SUD treatment outcomes .
Adolescents with SUDs tend to have higher rates of comorbid psychiatric disorders and are more likely to report a history of trauma and physical and/or sexual abuse than adolescents without a SUD [27, 28]. In addition, psychiatric disorders in adolescents often predate the SUD. Once the SUD develops, the psychiatric disorder may be further exacerbated  and associated with substantial functional impairment . In older adolescence and emerging adulthood, young drug users with comorbid affective disorders have greater mental health and substance use morbidity than those with substance use problems alone . A study of adolescent SUD inpatients found that 40.5 % of the participants fulfilled criteria for at least one comorbid present Axis I disorder, with high prevalences of mood, anxiety, and somatoform disorders. The 37 female participants showed a significantly higher risk for lifetime comorbid disorders; the gender difference was especially pronounced for anxiety and somatoform disorders .
ADHD has been shown to be a significant risk factor for developing SUDs . It is frequently present in SUD populations, with prevalence estimates varying between 14 and 23 %. In general, patients with this type of comorbidity represent a more severe subgroup of SUD patients with more additional comorbidity and a more disadvantageous prognosis than SUD patients without ADHD . It has been suggested that girls with ADHD might be at slightly higher risk than boys for substance abuse . CD is a risk factor of similar magnitude as ADHD, and of equal importance in both genders .
PDs and SUDs commonly co-occur, with many studies finding a particularly frequent association between SUDs and BPD or ASPD [25, 36–38]. Comorbid PD seems to be more prevalent in drug use disorder (DUD) than in alcohol use disorder (AUD) . Comorbid PD is characterized by more severe addiction problems and by an unfavorable clinical outcome . Prevalence rates of PDs in patients with SUD range from 24 to 90 %, depending on the sample characteristics and setting [11, 40–42]. A Norwegian study of first-admission SUD patients aged 16 years and older, found that 46 % of the patients had at least one PD. In this sample, cluster C disorders were as prevalent as cluster B disorders; SUD patients with PDs were younger at the onset of their first SUD and at admission; they used more illicit drugs; had more anxiety disorders; had more severe depressive symptoms; were more distressed and more impaired in their social functioning . Comorbid SUD can be diagnosed in approximately every second patient suffering from a PD .
Some studies have reported gender differences in adolescents and young adults; Foster and colleagues found AUD to be a more severe disorder in women than in men. Despite lower mean levels of overall risk exposure, women were characterized by higher levels of adolescent risk factors and a greater magnitude of AUD consequences. Furthermore, internalizing symptoms appeared to be a gender-specific risk factor for AUD in women . Roberts and colleagues found a tendency in females with SUDs to have higher rates of comorbid disorders, as did older youths . Thus, the question of possible gender differences in SUD prevalence, comorbidity and prognosis has not yet been fully answered.
The objective of the present study, performed on a clinical sample of consecutively referred adolescent outpatients, was to
Investigate the prevalences of alcohol and substance abuse and common Axis I disorders, including possible gender differences.
Investigate the association between PDs and alcohol and other substance abuse. We also wanted to assess the influence of adjusting for other Axis I disorders, age and gender on this association.
The present study used a sample of adolescents aged 14–17 years who were referred to a mental health outpatient clinic for children and adolescents in Oslo (The Nic Waal Institute, Lovisenberg Diakonale Hospital). The catchment area of the clinic comprises 25.000 children and adolescents from 0 to 17 years of age, and consists of four city districts with a population of mixed socioeconomic status, representing all social classes including immigrant workers and well-educated middle and upper class families. Study inclusion took place from February 2005 to April 2007. All referred patients in the study’s age group were asked to participate. Exclusion criteria were the need for immediate hospitalization or other urgent therapeutic measures, clinically assessed mental retardation, lack of fluency in the Norwegian language, and absence of the evaluator at the time of referral .
Axis I disorders
Axis I disorders, including SUDs, were assessed using a Norwegian translation of the mini international neuropsychiatric interview version 5.0.0 (MINI) [49, 50]. The MINI has not been validated for adolescents, but has previously been used in studies on adolescents  and was chosen for its excellent feasibility .
In the assessment of ADHD a primary screening was first performed, using the six-item adult ADHD Self-Report Scale Screener version 1.1 (ASRS Screener) in a Norwegian version . The ASRS Screener is reliable and valid in adult clinical settings, with excellent specificity . It has repeatedly been shown to be in strong concordance with clinician diagnoses . The ASRS Screener has not been validated for use in adolescents, but the full 18-item ASRS symptom checklist, from which it is derived, has been found to be reliable and valid in adolescents .
If the primary screening with the ASRS Screener was positive, the Mini International Neuropsychiatric Interview-PLUS (MINI-PLUS) section W (ADHD in children/adolescents) was used as a diagnostic test instrument  for a final diagnosis of ADHD.
The Structured Interview for DSM-IV (SIDP-IV)  in a Norwegian version was used to assess PDs. The SIDP-IV is a comprehensive semi-structured diagnostic interview for DSM-IV PD (Axis II) diagnoses, which has been used in numerous studies in different countries, including Norway [57–59]. The SIDP-IV has been extensively used in research on PDs in adolescence [51, 60, 61]. The SIDP-IV covers 14 DSM-IV Axis II diagnoses as well as CD as a separate axis I disorder. The Axis II diagnoses comprise the ten standard DSM-IV PDs (paranoid, schizoid, schizotypal, borderline, histrionic, narcissistic, antisocial, obsessive–compulsive, dependent, and avoidant PD), the three provisional DSM-IV PDs (self-defeating, depressive, and negativistic PD), and mixed PD.
All questions address the typical or habitual behavior of the subjects during the last 5 years. Each diagnostic criterion is rated on a four point scale: “0” = criterion not present; “1” = subthreshold level of the trait present; “2” = criterion being present for most of the last 5 years; and “3” = criterion strongly present. Scores “2” and “3” indicate the presence of a criterion according to DSM-IV . In the following text, we will be using the term “PD symptoms” when a diagnostic criterion meets a score of 1, 2 or 3. “PD” is used when a sufficient number of diagnostic criteria for a specific DSM-IV diagnosis are fulfilled, as measured with the SIDP-IV.
In accordance with diagnostic practice applied in other studies on PDs in adolescence, the DSM-IV age criterion for ASPD was waived . Due to the participants’ age, we also waived the 5 year symptom duration criterion. Instead we used 2 years symptom duration as criterion. This is in accordance with the criterion used in previous studies assessing adolescent personality pathology [4, 45].
Procedures and assessment
All patients were assessed immediately upon referral by the first author, who was a male specialist in psychiatry and child and adolescent psychiatry, with 21 years of clinical experience. He was trained in evaluation with SIDP-IV by the second author, who was an experienced rater, who had previously evaluated patients and reported from comparable studies in adults [59, 62]. Twenty ratings were discussed and found to be in accordance with the rating of the experienced evaluator. Axis I conditions were also assessed by the first author, who had been trained by the translator of the Norwegian version of the MINI.
After completion of the initial assessment, the patients were assigned to further clinical evaluation and treatment by clinicians other than the first author in the outpatient clinic.
Descriptive statistics were calculated for the relevant mental health status variables and expressed in mean [with standard deviation (SD) in parentheses] and frequency (percentages in parentheses) as appropriate. Prevalences of PDs, SUDs and other Axis I conditions with 95 % Blaker confidence intervals  were estimated for the total sample and for each gender separately, with testing for gender differences by exact Chi square tests. SUD was classified as none, one [either AUD or cannabis use disorder (CUD)] and two (both AUD and CUD). The association of SUD with number of PD symptoms, unadjusted and adjusted for gender, age and presence of Axis I disorders was investigated by proportional odds ordinal logistic regression. Differences in unadjusted and adjusted odds ratios were, if necessary, investigated by a bootstrap BCa 95 % confidence intervals based on 10,000 bootstrap replicates , with a difference considered as significant if 0 was outside the interval. Data were analysed using the IBM SPSS version 20.0 software, with Blaker confidence intervals and bootstrapping using the R (The R Foundation for Statistical Computing, Vienna, Austria) packages BlakerCI and boot.
The study was approved by the regional committee for medical research ethics for eastern Norway (REK: 11395) and by The Norwegian Data Inspectorate. Informed written consent was obtained from all patients, and for patients younger than 16 years consent was additionally obtained from their parents.
In the study inclusion period a total of 264 adolescents (59.4 % female) were referred to The Nic Waal Institute. Sixty-three patients did not meet the inclusion criteria; they were excluded due to inadequate fluency in the Norwegian language (N = 6, 9.5 %), mental retardation (N = 15, 23.8 %), need of immediate hospitalization (N = 19, 30.2 %), and absence of the evaluator at the time of referral (N = 23, 36.5 %). This left 201 adolescents eligible for inclusion in the study. The attrition was 48 (23.9 %); lack of consent from parents (N = 5, 10.4 %), referral retracted prior to interview (N = 6, 12.5 %), lack of consent from the adolescent (N = 7, 14.6 %), did not show up for appointment (N = 11, 22.9 %), and consent retracted during interview (N = 19, 39.6 %) .
A total of 153 adolescents (61.4 % girls, mean age 16.0 years; SD = 1.1, range 14.1–18.0 years) were finally included in the study. There were no missing data in any items within the ASRS Screener, MINI, MINI-PLUS section W, or SIDP-IV.
Of the adolescents, 18.3 % (N = 28, 95 % CI 12.6–25.3 %) were diagnosed with a SUD using the MINI, with no significant gender difference in prevalence (Table 1). Apart from alcohol, cannabis was the only drug in the sample that qualified for either an abuse or a dependency diagnosis. When analysed separately for alcohol and cannabis problems in each gender, boys had slightly more alcohol-related problems, whereas girls had slightly more cannabis-related problems; the differences were not significant (alcohol; χ2 = 0.027, p = 1.000, cannabis χ2 = 0.055, p = 1.000). The female/male ratio of SUDs was 1.16 (95 % CI = 0.49–2.72, p = 0.73).
Two thirds (63.4 %, N = 97) of the adolescents met the criteria for at least one Axis I disorder (68.1 %, N = 64 girls; 56.0 %, N = 33 boys). Anxiety disorders; simple phobias, GAD, panic disorder, agoraphobia, social phobia and post-traumatic stress disorder (33.3 %, N = 51, 95 % CI 26.0–41.1 %) and mood disorders; dysthymia and major depressive episode (32.7 %, N = 50, 95 % CI 25.3–40.5 %) were most frequent, followed by SUD (18.3 %, N = 28, 95 % CI 12.6–25.3 %), CD (17.6 %, N = 27, 95 % CI 12.2–24.4 %), obsessive–compulsive disorder (9,2 %, N = 14, 95 % CI 5.3–14.8 %) and psychotic disorders (1.3 %, N = 2, 95 % CI 0.2–4.6 %). There were significant gender differences in anxiety (p = 0.022) and mood (p = 0.033) disorders (Table 1).
Of the adolescents, 21.6 % (N = 33) had at least one PD, 7.2 % (N = 11) had more than one PD, and 4.6 % (N = 7) had both ADHD and a PD. The prevalence of PDs was generally higher in the referred girls. Girls showed significant associations between SUD and BPD (p = 0.024), negativistic PD (p = 0.035), more than one PD (p = 0.020) as well as between SUD and CD (p = 0.001) and ADHD (p < 0.001) (Table 2).
Figure 1 illustrates the association between PD symptoms and SUD and other frequent Axis I disorders. As can be seen, girls had more symptoms than boys in all reported Axis I conditions; the difference was significant for anxiety disorders (p = 0.022) and mood disorders (p = 0.033). Substance disorders (p = 0.831) and CD (p = 0.585) did not yield significant gender differences.
There was a significant positive association between the number of PD symptoms and SUD (OR per five points difference in the number of PD symptoms 1.16, 95 % CI 1.06–1.26, p = 0.001). The association was still significant after adjustment for gender, age and presence of one or more Axis I disorders (OR 1.15, 95 % CI 1.04–1.27, p = 0.005). There were no significant deviations from the proportional odds assumption in these analyses (p ≥ 0.466). No bootstrap procedure for comparing the unadjusted and adjusted ORs was performed due to the almost total overlap between the confidence intervals.
The present study investigated the prevalence of SUDs and common Axis I disorders in an unselected sample of adolescents. The participants were all referred to a non-specialized mental health outpatient clinic with a defined catchment area. We also investigated the association between PD symptoms and SUDs, as well as how this relationship was influenced by adjustment for other Axis I disorders, age and gender.
Our finding of 18.3 % of the adolescents having AUD or CUD seems not to be incongruent with previous findings, considering that studies of non-referred adolescents have found SUD prevalence rates of 4.6 %  to 17.7 % , and the prevalence rate in adolescent and young adult inpatients has been reported to be up to 54 % for DUD and 87 % for AUD when first admitted to hospital treatment . As was to be expected, the participants in the present study had a higher prevalence of SUDs than has been found in studies of community samples and primary care patients but a lower prevalence than that seen in participants in studies of more severely ill patients.
An earlier study of adolescents has reported significantly higher risk for lifetime comorbid disorders in women, with an especially pronounced gender difference for anxiety and somatoform disorders . In the present study, however, significant gender differences in anxiety and mood disorders were found only in the adolescents that did not have SUDs.
It has been suggested that girls with ADHD might be at slightly higher risk than boys for substance abuse . In accordance with this, the present study found significantly more ADHD as well as CD in girls than in boys with SUDs.
Recent findings have contradicted the assumption that boys generally use more drugs and alcohol than girls [20, 21]. Our findings of non-significant differences between genders in SUD prevalence are in accordance with this trend. Other recent studies have reported AUD to be a more severe disorder in adolescents and young adults, with higher levels of adolescent risk factors and a greater magnitude of AUD consequences in women , as well as a tendency in females with SUDs to have higher rates of comorbid disorders . The cross-sectional nature of the present study makes it impossible to infer causal relationships, but our findings do support the assumption of a more extensive psychiatric comorbidity in female adolescent SUD patients.
The main finding of the present study is a highly significant association between number of PD symptoms and the presence of one or more SUDs (p = 0.001), with almost totally overlapping confidence intervals after adjustment for gender, age and presence of one or more Axis I disorders (p = 0.005). This finding implies that having an increased number of PD symptoms in itself is a unique risk factor for the later development of a SUD.
Strengths and limitations
The study was performed at a single general service mental health outpatient clinic, receiving adolescents from a geographically defined urban area with a varied socioeconomic and ethnic population. Still, the results from the present study may not be generalizable to other outpatient populations. The participants were included in a limited time span, and we cannot exclude the possibility of prevalence fluctuations over time.
The attrition (23.9 %, N = 48) and the relatively small sample size also constitute limitations. In particular, the sample size limits the degrees of freedom available, so that analysis of single PDs in some cases may be statistically underpowered. Therefore, we have mainly focused on the total number of PD symptoms rather than on specific PDs. This might constitute a limitation. However, in light of current epidemiological knowledge about PDs, the differentiation between having or not having a PD is clearly more relevant than the differentiation between specific PDs. It should also be pointed out that specific PD diagnoses merely reflect the presence of an arbitrarily stipulated number of PD symptoms; there is no indication whatsoever of the existence of categorical breaking points at a given number of PD symptoms. On the contrary, recent literature supports the notion of PDs as dimensional entities with arbitrarily defined diagnostic cut-off points deciding whether or not a patient is above the diagnostic threshold for a specific disorder [4, 65].
The gender distribution of our sample was close to identical to the gender distribution of all referred adolescents in the study inclusion period, and reflects the fact that in adolescence, as opposed to middle and late childhood, more girls than boys are referred to Norwegian mental health outpatient clinics.
Each patient was diagnosed individually with well-documented and semi-structured test instruments by a single, experienced clinician and rater. Due to the fact that just one person performed all assessment work, there was no missing data. The evaluator was trained in rating with SIDP-IV and MINI by experienced evaluators and researchers on PD and Axis I diagnoses. Notwithstanding, the use of a single evaluator constitutes a possible limitation; it may have strengthened the internal validity, but might have been a threat to the external validity of the diagnoses.
The present study comprised 153 adolescents referred to a non-specialized mental health outpatient clinic. Of these adolescents, 18.3 % screened positive for AUD or CUD, with no significant gender difference in prevalence. The female/male ratio of SUDs was 1.13 (95 % CI = 1.10–1.17). More than two-thirds of the adolescents met the criteria for at least one Axis I disorder, with significant gender differences in anxiety (p = 0.022) and mood (p = 0.033) disorders; 21.6 % of the patients had at least one PD and 7.2 % had more than one PD. The prevalence of PDs was generally higher in the referred girls. For boys, no significant associations between SUDs and specific PDs or Axis I disorders could be ascertained. For girls, there were significant associations between SUD and BPD, negativistic PD, more than one PD, CD and ADHD.
There was a highly significant association between number of PD symptoms and the presence of one or more SUDs. This association was practically unchanged when adjusted for gender, age and having one or more Axis I disorders, suggesting that having an increased number of PD symptoms in itself may constitute a unique risk factor for developing SUDs in adolescence. These findings are in accordance with earlier reports of increased co-occurrence of PDs and SUDs in adolescence [36–38].
However, the girls in the study were overall more severely ill than the boys; girls with SUDs differed even more so, with significant associations between SUDs and BPD (p = 0.024), negativistic PD (p = 0.035), more than one PD (p = 0.020), as well as between SUDs and CD (p = 0.001) and ADHD (p < 0.001). This indicates that adolescent girls suffering from these disorders may be especially at risk for developing SUDs. In clinical practice, it might therefore be suggested that girls presenting with BPD, negativistic PD, more than one PD, ADHD, or CD should be monitored with particular diligence with regard to their use of psychoactive substances.
attention deficit hyperactivity disorder
antisocial personality disorder
alcohol use disorder
borderline personality disorder
Cannabis use disorder
drug use disorder
generalized anxiety disorder
oppositional defiant disorder
substance use disorder
American Psychiatric Association. Diagnostic and statistical manual of mental disorders, 4th ed, text revision. Washington: American Psychiatric Association; 2000.
American Psychiatric Association. Diagnostic and statistical manual of mental disorders—DSM-5. 5th ed. Washington: AMerican Psychiatric Association; 2013.
Zimmerman M, Chelminski I, Young D. The frequency of personality disorders in psychiatric patients. Psychiatr Clin North Am. 2008;31(3):405–20.
Kongerslev M, Chanen A, Simonsen E. Personality Disorder in Childhood and Adolescence comes of Age: a Review of the Current Evidence and Prospects for Future Research. Scand J Child Adolesc Psychiatr Psychol. 2015;3(1):31–48.
Caspi A. The child is father of the man: personality continuities from childhood to adulthood. J Pers Soc Psychol. 2000;78(1):158–72.
Caspi A, Begg D, Dickson N, Harrington H, Langley J, Moffitt TE, Silva PA. Personality differences predict health-risk behaviors in young adulthood: evidence from a longitudinal study. J Pers Soc Psychol. 1997;73(5):1052–63.
Caspi A, Harrington H, Milne B, Amell JW, Theodore RF, Moffitt TE. Children’s behavioral styles at age 3 are linked to their adult personality traits at age 26. J Pers. 2003;71(4):495–513.
Newton-Howes G, Clark LA, Chanen A. Personality disorder across the life course. Lancet. 2015;385(9969):727–34.
Grilo CM, Sanislow CA, Gunderson JG, Pagano ME, Yen S, Zanarini MC, Shea MT, Skodol AE, Stout RL, Morey LC, et al. Two-year stability and change of schizotypal, borderline, avoidant, and obsessive-compulsive personality disorders. J Consult Clin Psychol. 2004;72(5):767–75.
Skodol AE. Longitudinal course and outcome of personality disorders. Psychiatr Clin North Am. 2008;31(3):495–503.
Trull TJ, Jahng S, Tomko RL, Wood PK, Sher KJ. Revised NESARC personality disorder diagnoses: gender, prevalence, and comorbidity with substance dependence disorders. J Pers Disord. 2010;24(4):412–26.
Grant BF, Chou SP, Goldstein RB, Huang B, Stinson FS, Saha TD, Smith SM, Dawson DA, Pulay AJ, Pickering RP, et al. Prevalence, correlates, disability, and comorbidity of DSM-IV borderline personality disorder: results from the wave 2 national epidemiologic survey on alcohol and related conditions. J Clin Psychiatry. 2008;69(4):533–45.
Singh MK, Ketter T, Chang KD. Distinguishing bipolar disorder from other psychiatric disorders in children. Curr Psychiatry Rep. 2014;16(12):516.
Helgeland MI, Torgersen S. Developmental antecedents of borderline personality disorder. Compr Psychiatry. 2004;45(2):138–47.
Chanen AM, Kaess M. Developmental pathways to borderline personality disorder. Curr Psychiatry Rep. 2012;14(1):45–53.
Helgeland MI. Prediction of severe psychopathology from adolescence to adulthood. Oslo: University of Oslo; 2004.
Shiner RL. The development of personality disorders: perspectives from normal personality development in childhood and adolescence. Dev Psychopathol. 2009;21(3):715–34.
Kaess M, Brunner R, Chanen A. Borderline personality disorder in adolescence. Pediatrics. 2014;134(4):782–93.
Wittchen HU, Jacobi F, Rehm J, Gustavsson A, Svensson M, Jonsson B, Olesen J, Allgulander C, Alonso J, Faravelli C, et al. The size and burden of mental disorders and other disorders of the brain in Europe 2010. Eur Neuropsychopharmacol. 2011;21(9):655–79.
Johnson RM, Fairman B, Gilreath T, Xuan Z, Rothman EF, Parnham T, Furr-Holden CD. Past 15-year trends in adolescent marijuana use: differences by race/ethnicity and sex. Drug Alcohol Depend. 2015;155:8–15.
White A, Castle IJP, Chen CM, Shirley M, Roach D, Hingson R. Converging patterns of alcohol use and related outcomes among females and males in the United States, 2002 to 2012. Alcohol Clin Exp Res. 2015;39(9):1712–26.
Nyhlen A, Fridell M, Backstrom M, Hesse M, Krantz P. Substance abuse and psychiatric co-morbidity as predictors of premature mortality in Swedish drug abusers: a prospective longitudinal study 1970–2006. BMC Psychiatry. 2011;11:122.
Wittchen HU, Nelson CB, Lachner G. Prevalence of mental disorders and psychosocial impairments in adolescents and young adults. Psychol Med. 1998;28(1):109–26.
Essau CA. Comorbidity of substance use disorders among community-based and high-risk adolescents. Psychiatry Res. 2011;185(1–2):176–84.
van West D, Vermeiren R. Dual disorders in adolescent populations. In: Dom G, Moggi F, editors. Co-occurring addictive and psychiatric disorders. Berlin Heidelberg: Springer; 2015. pp. 335–47.
Magidson JF, Liu SM, Lejuez CW, Blanco C. Comparison of the course of substance use disorders among individuals with and without generalized anxiety disorder in a nationally representative sample. J Psychiatr Res. 2012;46(5):659–66.
Bukstein OG, Brent DA, Kaminer Y. Comorbidity of substance abuse and other psychiatric disorders in adolescents. Am J Psychiatry. 1989;146(9):1131–41.
Lieb R. Epidemiological perspectives on comorbidity between substance use disorders and other mental disorders. In: Dom G, Moggi F, editors. Co-occurring addictive and psychiatric disorders. Berlin Heidelberg: Springer; 2015. pp. 3–12.
Deas D. Adolescent substance abuse and psychiatric comorbidities. J Clin Psychiatry. 2006;67(Suppl 7):18–23.
Roberts RE, Roberts CR, Xing Y. Comorbidity of substance use disorders and other psychiatric disorders among adolescents: evidence from an epidemiologic survey. Drug Alcohol Depend. 2007;88(Supplement 1):S4–13.
Lubman DI, Allen NB, Rogers N, Cementon E, Bonomo Y. The impact of co-occurring mood and anxiety disorders among substance-abusing youth. J Affect Disord. 2007;103(1–3):105–12.
Langenbach T, Sponlein A, Overfeld E, Wiltfang G, Quecke N, Scherbaum N, Melchers P, Hebebrand J. Axis I comorbidity in adolescent inpatients referred for treatment of substance use disorders. Child Adolesc Psychiatry Ment Health. 2010;4:25.
Biederman J, Wilens T, Mick E, Milberger S, Spencer TJ, Faraone SV. Psychoactive substance use disorders in adults with attention deficit hyperactivity disorder (ADHD): effects of ADHD and psychiatric comorbidity. Am J Psychiatry. 1995;152(11):1652–8.
van Emmerik-van Oortmerssen K, Konstenius M, Schoevers R. ADHD and Addiction. In: Dom G, Moggi F, editors. Co-occurring addictive and psychiatric disorders. Berlin Heidelberg: Springer; 2015. pp. 179–91.
Disney ER, Elkins IJ, McGue M, Iacono WG. Effects of ADHD, conduct disorder, and gender on substance use and abuse in adolescence. Am J Psychiatry. 1999;156(10):1515–21.
Walter M. Personality disorder and addiction. In: Dom G, Moggi F, editors. Co-occurring addictive and psychiatric disorders. Berlin Heidelberg: Springer; 2015. pp. 137–48.
Langas AM, Malt UF, Opjordsmoen S. In-depth study of personality disorders in first-admission patients with substance use disorders. BMC Psychiatry. 2012;12:180.
Wapp M, van de Glind G, van Emmerik-van Oortmerssen K, Dom G, Verspreet S, Carpentier PJ, Ramos-Quiroga JA, Skutle A, Bu ET, Franck J, et al. Risk factors for borderline personality disorder in treatment seeking patients with a substance use disorder: an international multicenter study. Eur Addict Res. 2015;21(4):188–94.
Arnevik EP, Wilberg TMDP, Urnes ØMD, Johansen MMD, Monsen JTP, Karterud SMDP. Psychotherapy for personality disorders: 18 months’ follow-up of the Ullevål personality project. J Personal Disord. 2010;24(2):188–203.
Skodol AE, Oldham JM, Gallaher PE. Axis II comorbidity of substance use disorders among patients referred for treatment of personality disorders. Am J Psychiatry. 1999;156(5):733–8.
Verheul R. Co-morbidity of personality disorders in individuals with substance use disorders. Eur Psychiatry. 2001;16(5):274–82.
Gibbie TM, Hides LM, Cotton SM, Lubman DI, Aitken C, Hellard M. The relationship between personality disorders and mental health, substance use severity and quality of life among injecting drug users. Med J Aust. 2011;195(3):S16–21.
Foster KT, Hicks BM, Iacono WG, McGue M. Gender differences in the structure of risk for alcohol use disorder in adolescence and young adulthood. Psychol Med. 2015. FirstView:1–12.
Korsgaard HO, Torgersen S, Wentzel-Larsen T, Ulberg R. Personality Disorders and Quality of Life in Adolescent Outpatients. Scand J Child Adolesc Psychiatr Psychol. 2015;3(3):180–9.
Chanen AM, Jackson HJ, McGorry PD, Allot KA, Clarkson V, Yuen HP. Two-year stability of personality disorder in older adolescent outpatients. J Personal Disord. 2004;18(6):526–41.
Feenstra DJ, Busschbach JJV, Verheul R, Hutsebaut J. Prevalence and comorbidity of Axis I and Axis II disorders among treatment refractory adolescents admitted for specialized psychotherapy. J Personal Disord. 2011;25(6):842–50.
Feenstra DJ, Hutsebaut J, Laurenssen EM, Verheul R, Busschbach JJ, Soeteman DI. The burden of disease among adolescents with personality pathology: quality of life and costs. J Pers Disord. 2012;26(4):593–604.
Kongerslev M, Moran P, Bo S, Simonsen E. Screening for personality disorder in incarcerated adolescent boys: preliminary validation of an adolescent version of the standardised assessment of personality—abbreviated scale (SAPAS-AV). BMC Psychiatry. 2012;12:94.
Sheehan D, Lecrubier Y, Sheehan K, Janavs J, Weiller E, Keskiner A, Schinka J, Knapp E, Sheehan M, Dunbar G. The validity of the mini international neuropsychiatric interview (MINI) according to the SCID-P and its reliability. European Psychiatry. 1997;12(5):232–41.
Sheehan DV, Lecrubier Y, Sheehan K, Amorim P, Janavs J, Weiller E, Hergueta T, Baker R, Dunbar GC. The mini-international neuropsychiatric interview (M.I.N.I): the development and validation of a structured diagnostic psychiatric interview for DSM-IV and ICD-10. J Clin Psychiatry. 1998;59(Suppl 20):22–33.
Chabrol H, Chouicha K, Montovany A, Callahan S, Duconge E, Sztulman H. Personality disorders in a nonclinical sample of adolescents. Encephale. 2002;28(6 Pt 1):520–4.
Adler LA, Spencer T, Faraone SV, Kessler RC, Howes MJ, Biederman J, Secnik K. Validity of pilot adult ADHD self- report scale (ASRS) to rate adult ADHD symptoms. Ann Clin Psychiatry. 2006;18(3):145–8.
Kessler RC, Adler L, Ames M, Demler O, Faraone S, Hiripi E, Howes MJ, Jin R, Secnik K, Spencer T, et al. The world health organization adult ADHD self-report scale (ASRS): a short screening scale for use in the general population. Psychol Med. 2005;35(2):245–56.
Kessler RC, Adler LA, Gruber MJ, Sarawate CA, Spencer T, Van Brunt DL. Validity of the world health organization adult ADHD self-report scale (ASRS) screener in a representative sample of health plan members. Int J Methods Psychiatr Res. 2007;16(2):52–65.
Adler LA, Shaw DM, Spencer TJ, Newcorn JH, Hammerness P, Sitt DJ, Minerly C, Davidow JV, Faraone SV. Preliminary examination of the reliability and concurrent validity of the attention-deficit/hyperactivity disorder self-report scale v1.1 symptom checklist to rate symptoms of attention-deficit/hyperactivity disorder in adolescents. J Child Adolesc Psychopharmacol. 2012;22(3):238–44.
Pfohl BBNZM. Structured interview for DSM-IV personality (SIDP-IV). Washington: American Psychiatric Press; 1997.
Roysamb E, Kendler KS, Tambs K, Orstavik RE, Neale MC, Aggen SH, Torgersen S, Reichborn-Kjennerud T. The joint structure of DSM-IV Axis I and Axis II disorders. J Abnorm Psychol. 2011;120(1):198–209.
Helgeland MI, Kjelsberg E, Torgersen S. Continuities between emotional and disruptive behavior disorders in adolescence and personality disorders in adulthood. Am J Psychiatry. 2005;162(10):1941–7.
Torgersen S, Kringlen E, Cramer V. The prevalence of personality disorders in a community sample. Arch Gen Psychiatry. 2001;58(6):590–6.
Speranza M, Revah-Levy A, Cortese S, Falissard B, Pham-Scottez A, Corcos M. ADHD in adolescents with borderline personality disorder. BMC Psychiatry. 2011;11:158.
Loas G, Speranza M, Pham-Scottez A, Perez-Diaz F, Corcos M. Alexithymia in adolescents with borderline personality disorder. J Psychosom Res. 2012;72(2):147–52.
Torgersen S. Prevalence, sociodemographics, and functional impairment. In: Oldham, JMS AE, Bender DS, editors. Essentials of personality disorders. Arlington: American Psychiatric Publishing, Inc.; 2009. pp. 417.
Blaker H. Confidence curves and improved exact confidence intervals for discrete distributions. Canadian J Stat La Revue Canadienne de Statistique. 2000;28(4):783–98.
Efron B, Tibshirani R. An introduction to the bootstrap. Boca Raton: CRC Press LLC; 1993.
Tyrer P, Reed GM, Crawford MJ. Classification, assessment, prevalence, and effect of personality disorder. Lancet. 2015;385(9969):717–26.
All authors have contributed to the background, design, and drafting of the manuscript. HOK did all the assessment work. HOK and TWL performed the statistical analysis. All authors read and approved the final manuscript.
This study has been supported by Grants from the south-eastern Norway Regional Health Authority, the Centre for Child and Adolescent Mental Health, eastern and southern Norway, and Lovisenberg Diakonale Hospital.
The authors declare that they have no competing interests.
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Korsgaard, H.O., Torgersen, S., Wentzel-Larsen, T. et al. Substance abuse and personality disorder comorbidity in adolescent outpatients: are girls more severely ill than boys?. Child Adolesc Psychiatry Ment Health 10, 8 (2016) doi:10.1186/s13034-016-0096-5
- Alcohol use disorder
- Axis I
- Conduct disorder
- Personality disorder
- Substance use disorder