Differences of Clinical Characteristics and Phenotypes between Prepubertal- and Adolescent-Onset Bipolar Disorders

Misun Song; Huh Yoon; Inchul Choi; Sungdo David Hong; Yoo Sook Joung

doi:10.3346/jkms.2010.25.6.912

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Song, Yoon, Choi, Hong, and Joung: Differences of Clinical Characteristics and Phenotypes between Prepubertal- and Adolescent-Onset Bipolar Disorders

Original Article

Psychiatry & Psychology

Journal of Korean Medical Science

Journal of Korean Medical Science 2010; 25(6): 912-917.

Published online: 24 May 2010

DOI: https://doi.org/10.3346/jkms.2010.25.6.912

Differences of Clinical Characteristics and Phenotypes between Prepubertal- and Adolescent-Onset Bipolar Disorders

Misun Song, Huh Yoon, Inchul Choi, Sungdo David Hong, Yoo Sook Joung

Department of Psychiatry, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

Address for Correspondence: Yoo Sook Joung, M.D. Department of Psychiatry, Samsung Medical Center, Sungkyunkwan University School of Medicine, 81 Irwondong-gil, Gangnam-gu, Seoul 135-710, Korea. Tel: +82.2-3410-3589, Fax: +82.2-3410-0050, yschoung@skku.edu

Received 4 September 2009 Accepted 12 December 2009

(open-access):

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

The aim of this study is to describe the clinical characteristics of prepubertal- and adolescent-onset bipolar disorder (BD) and to identify any clinical differences between patients with prepubertal- and adolescent-onset BD. We analyzed the clinical records of 53 inpatients with BD. These patients were divided into prepubertal-onset and adolescent-onset groups. We also divided the subjects into narrow, intermediate, and broad phenotypes according to the definitions proposed by Leibenluft and colleagues. Of the total sample, 16 patients (30.2%) were in the prepubertal-onset group and 37 (69.8%) were in the adolescent-onset group. Patients with prepubertal-onset BD were more likely to display an insidious clinical presentation, atypical features, and comorbid psychopathology. And the majority of the subjects, especially in the prepubertal-onset group, were classified under the intermediate and broad phenotypes. These results suggest that the clinical presentation of BD with prepubertal-onset is different from that of adolescent-onset BD. It is inferred that a significant number of patients with prepubertal- and adolescent-onset BD do not meet DSM-IV criteria for mania or hypomania from the results of this study.

Keywords: Clinical Characteristics, Prepubertal, Adolescent, Bipolar Disorder

INTRODUCTION

In recent decades, there has been a dramatic increase in recognition of prepubertal- and adolescent-onset bipolar disorder (BD). As there is no clear consensus among experts regarding the clinical presentation of BD, diagnostic symptom criteria, or clinical course in adolescents and children, the diagnosis and treatment of BD in prepubertal and adolescent youth remains a controversial issue. Some investigators have reported that the phenomenology of adolescent mania is similar to that of adult mania (1, 2), while other researchers have reported that adolescent patients display a significantly higher rate of mixed episodes and a significantly lower rate of psychotic features than adult patients (3). The clinical presentation of BD in prepubertal groups has been debated, as well. Previous studies suggest that the presentation of prepubertal BD is atypical when judged by adult standards and that prepubertal BD is different from that of adolescent BD. The atypical features of prepubertal BD, which have been proposed by researchers, are a mixed presentation rather than the classic euphoric, grandiose presentation with an insidious onset and a chronic course (4-7). A research roundtable meeting was convened to discuss the controversial areas in the diagnosis of prepubertal BD at the National Institute of Mental Health (NIMH), Bethesda, MD, USA on April 27, 2000. Experienced clinicians and researchers with expertise on prepubertal BD agreed that the diagnosis of BD in prepubertal populations is possible with currently available psychiatric assessment instruments. Further, in addition to the phenotypes that fit the Diagnostic Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV) (8) criteria for bipolar I disorder, there exists other phenotypes that do not meet the DSM-IV criteria (9). Leibenluft et al. (10) introduced a framework for the classification of juvenile bipolar spectrum disorders into narrow, intermediate, and broad phenotypes. The phenotypic system is based on the DSM-IV episode and duration criteria, as well as the presence or absence of the classic manic symptoms of elevated mood and grandiosity.

Although BD is more common in children than has been acknowledged previously, prepubertal BD remains difficult to diagnose (11-13). Previous studies about the clinical course of early onset BD have reported that children with BD tend to show a chronic course, severe functional impairment, and other psychiatric complications (14-17). Therefore, it is important to identify the age-specific manifestations of BD and to define the diagnostic possibilities for prepubertal and adolescent groups with BD. Early detection and intervention could improve treatments and clinical outcomes during these important life stages.

The aim of our study is to describe the clinical characteristics of prepubertal- and adolescent-onset BD, and to identify any clinical differences between prepubertal- and adolescent-onset groups.

MATERIALS AND METHODS

Subjects and data

We implemented a retrospective study design. Specifically, all of the patients who had been hospitalized and diagnosed with BD between January 2004 and January 2009 at the Child and Adolescent Psychiatry Service Unit at Samsung Medical Center, Seoul, Republic of Korea were included in the analysis. A total of 53 subjects were identified and diagnosed with bipolar I disorder, bipolar II disorder, or BD NOS based on the DMS-IV diagnostic criteria by experienced child and adolescent psychiatrists. The subjects were divided into two age groups on the basis of recommendations published by a number of authors (7, 18, 19): the prepubertal-onset group (who displayed mood episodes beginning before age 13) and the adolescent-onset group (who displayed mood episodes beginning at or above age 13). We analyzed a range of clinical variables drawn from the medical records of the psychiatrists in charge of the patients. These variables included the age at onset of symptoms of BD, the age at diagnosis, the symptoms in the clinical course, family history, and psychiatric comorbidities. The symptoms at onset, which the subjects had shown dominantly in the initial phase, fell into four categories: irritability and aggressive behavior, depressive symptoms, manic symptoms, and mood swings and fluctuations. The symptoms at the time of hospitalization were divided into four categories based on the DSM-IV episode criteria: mania, hypomania, mixed symptoms, and depression. The treatment before and after the diagnosis of BD were also examined. We reviewed psychological evaluations, including the Korean Educational Development Institute-Wechsler Intelligence Scale for children-III (KEDI-WISC-III) and the Korean Child Behavior Checklist (K-CBCL) (20).

This study was conducted with the approval of the Institutional Review Board at the Samsung Medical Center (IRB file NO 2008.09.068). Informed consent was exempted.

Classification of subjects into phenotypes

All subjects were classified into narrow, intermediate, and broad phenotypes according to the definitions proposed by Leibenluft et al. The narrow phenotype was assigned to those who met the full DSM-IV diagnostic criteria for mania or hypomania and who also had the hallmark symptoms of elevated mood or grandiosity. The intermediate phenotypes included two subcategories: those individuals with hallmark symptoms of a short duration and those with episodic irritable mania or hypomania that meets the duration criteria, but without elation. The broad phenotype consisted of non-episodic symptoms of severe irritability and hyperarousal, however, this phenotype does not include the hallmark symptoms of elated mood or grandiosity (10).

Statistical analysis

Data were analyzed using SPSS 16.0 R Software for Windows. We used the chi-square test and the Mann-Whitney test to evaluate the differences in clinical variables between the groups. The statistical significance level was defined as P<0.05.

RESULTS

Subject characteristics

We assigned 16 patients (30.2%) to the prepubertal-onset group and 37 (69.8%) to the adolescent-onset group. Table 1 shows the mean age at the onset of symptoms of BD, the mean age at initial diagnosis, and the mean age at hospitalization of our sample. The duration between the onset of symptoms and the diagnosis of BD in the prepubertal-onset group was significantly longer than that in the adolescent-onset group (Table 1). There were significant gender differences between the groups, and the majority of the prepubertal-onset group was male. Specifically, 13 (81.2%) of the prepubertal group were male and 18 (48.6%) of the adolescent group were male (P=0.03).

Clinical characteristics

In the prepubertal group, the initial phase of BD was a categorized as a tendency to exhibit irritability and aggressive behavior, while the adolescent group tended to express depressive symptoms. Many of the subjects in the prepubertal and adolescent groups had presented with a mixed episode at the time of admission. There were no differences between the groups with respect to family history of BD or major depressive disorder. In the prepubertal-onset group, the rate of comorbidity was higher than that of the adolescent-onset group and attention-deficit/hyperactivity disorder was the most prevalent comorbid disorder (Table 2).

There were no differences between groups in intelligence scores as assessed by the KEDI-WISC-III. The mean full scale IQ scores for the prepubertal and adolescent groups were 99.36 (SD=25.46) and 90.30 (SD=18.33), respectively. No meaningful differences were detected between the groups in K-CBCL scores. In both groups, all of the K-CBCL clinical subscales other than the somatization subscale were greater than 60, which tends to be predictive of clinically significant psychopathology (Table 3) (21).

Classification of subjects into phenotypes

In the prepubertal-onset group, only three (18.8%) met the DSM-IV criteria for mania or hypomania, and these three were classified into the narrow phenotype. In the adolescent-onset group, 12 (32.4%) met the DSM-IV criteria for mania or hypomania, and they were classified into the narrow phenotype (Table 4).

Treatment before and after diagnosis of bipolar disorder

Four subjects (25.0%) from the prepubertal-onset group had been taking methylphenidate and 13 (35.1%) from the adolescent-onset group had been taking antidepressants prior to the diagnosis of BD. After the diagnosis of BD, the most prevalent prescription in the adolescent-onset group was a mood stabilizer with antipsychotics. There was tendency toward monotherapy with either mood stabilizers or antipsychotics in the prepubertal-onset group (Table 5).

DISCUSSION

These results suggest that prepubertal-onset BD patients tend to show an insidious clinical presentation, atypical features, and more comorbid psychopathology than BD patients with adolescent-onset. We infer that a significant number of patients with prepubertal- and adolescent-onset BD do not meet DSM-IV criteria for mania or hypomania from the results of this study.

Many seriously disturbed children with affective dysregulation and high levels of agitation and aggression present diagnostic and therapeutic challenges to clinicians. Recent research suggests that children with chronic, continuous, severe irritability or prolonged anger outbursts are often diagnosed with BD (22). In our study, the prepubertal sample displayed symptoms, such as marked irritability and aggressive behavior in the year or years prior to receiving a diagnosis of BD. Additionally, the duration between the onset and diagnosis of BD in the prepubertal-onset group was longer than that of the adolescent-onset group. This delay in diagnosis at early ages may be due to the fact that the initial presentation of the prepubertal BD is often not mood symptoms, but rather behavioral problems. Another possible reason for the delayed diagnosis of BD at early ages may be a high frequency of comorbidity. In this study, we found that many patients with prepubertal-onset BD had comorbid externalizing disorders, such as attention-deficit hyperactivity disorder (ADHD) (43.8%), as well as oppositional defiant disorder and conduct disorder (30.8%). Systemic studies show that rates of ADHD range from 60% to 90% in pediatric patients with BD (7, 18). Clinical reports have estimated the rates of conduct disorder in manic children and adolescents with BD to range from 17% to 69% (17, 23). Thus, it may be that the combination of mood changes and disruptive behavior are a specific marker of BD syndrome in young patients (24).

Until now, there have been few studies that have applied the proposed phenotypes of juvenile BD (10) to clinical subjects. When we applied this criteria to the patients examined in this study, the majority of the subjects, especially in the prepubertal-onset group, were classified under the intermediate and broad phenotypes, which did not meet the DSM-IV criteria for either mania or hypomania. The results of the present study correspond with a previous study that reported only approximately 50% of child and adolescent bipolar patients met DSM-IV criteria (4). In this study, 37% of the prepubertal group and 32% of the adolescent group was classified as the broad phenotype. Since the broad phenotype consists of non-episodic symptoms of severe irritability without elated mood or grandiosity, it is easy to confuse the broad phenotype with childhood externalizing disorders. This phenotypic system can help clinicians develop a more clear phenotypic description of prepubertal and adolescent BD and to re-evaluate young patients who do not meet the DSM-IV criteria for mania, but who do have mood symptoms, behavioral changes, and functional impairment. Longitudinal studies that examine the clinical course of the broad phenotype are warranted in order to find out whether this categorization represents a homogenous subgroup of bipolar spectrum disorder.

Early detection of BD and recognition of comorbid disorders is very important for determining the appropriate types and sequences of treatments. In our study, four (25.0%) of the prepubertal-onset group had been taking methylphenidate, and 13 (35.1%) of the adolescent-onset group had been taking antidepressants prior to the diagnosis of BD. Stimulant use to target ADHD symptoms in bipolar patients can be problematic because of its potential to precipitate or exacerbate mood-related symptoms (25). Additionally, previous work has suggested that there is concern that antidepressants can worsen the clinical course of bipolar illness (26).

The CBCL is one of the best-studied, empirically derived, checklists available to examine childhood psychopathology (27). Recently it has been shown that the CBCL is useful in distinguishing BD from ADHD. Additionally, children with BD typically have high scaled scores in the Aggression, Attention Problems, Delinquency, Thought Problems, and Anxious/Depressed subscales of the CBCL (28, 29). Although we failed to find any differences in K-CBCL subscales between groups, the results of this study support the previous studies. It is important to consider a diagnosis of BD when assessing children with high scores on these CBCL subscales even when they do not fit any of DSM-IV diagnostic criteria.

This retrospective study has some limitations, such as the lack of structured or semi-structured interviews for diagnosis. In this study, however, we evaluated the clinical features of the subjects intensively in the inpatient clinic for a month or months. A minimum of two psychiatrists and a psychologist participated in the diagnosis of the subjects. Additionally, it is known that clinical assessment and structured interview are highly consistent with each other (30). We divided the subjects into prepubertal- and adolescent onset BD according to the age. In order to define the prepubertal phase, it is required to examine the secondary sex characteristics of the subjects. The biological marker, such as Tanner stage could be used in the following study. In the results of research examining the clinical presentation of BD, it has been demonstrated that it is ideal to evaluate patients with BD who do not have any other psychiatric disorders. Nonetheless, the examination of pure bipolar patients in prepubertal and adolescent populations is complicated due to the high rates of comorbidity common among individuals with BD. Further research must be conducted to separate the effects of comorbid psychiatric disorders on the clinical course of BD in young patients.

BD in prepubertal and adolescent populations is a serious, recurrent, and debilitating psychiatric concern. Too often BD is not considered as a possible diagnosis in children, and delayed diagnosis may have negative effects on the clinical course and prognosis for children. Alternative diagnostic criteria and assessment instruments for prepubertal and adolescent BD need to be developed.

Figures and Tables

Table 1

Clinical variables in prepubertal and adolescent-onset bipolar disorder

^*by Mann Whitney test.

Table 2

Clinical characteristics in prepubertal and adolescent-onset bipolar disorder

^*by chi-square test.

BD, Bipolar affective disorder; MD, Major depression; ADHD, Attention-deficit/hyperactivity disorder; ODD, Oppositional defiant disorder; CD, Conduct disorder; PDD, Pervasive developmental disorder; PDDNOS, Pervasive developmental disorder, not otherwise specified; MR, Mental retardation; BIF, Borderline interllectual functioning.

Table 3

Comparison of T Scores for CBCL Subscales in prepubertal and adolescent-onset bipolar disorder

^*by the Mann Whitney test. Value are given in mean±SD.

CBCL, Child Behavior Checklist.

Table 4

Classification of subjects into phenotypes depending on research criteria^*

^*Criteria from Defining Clinical Phenotype of Juvenile Mania by Ellen Leibenluft.

Table 5

Treatment before and after diagnosis of bipolar disorder

Antipsychotics include aripiprazole, risperidone and quetiapine, Mood stabilizer include lithium and divalproex, Antidepressant include fluoxetine, paroxetine and escitalopram.

^*by chi-square test, ^†by Fisher's exact test.

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