The Dutch Bipolar Offspring Study: 12-Year Follow-Up
Publication: American Journal of Psychiatry
Abstract
Objective
Offspring of bipolar parents have a genetically increased risk of developing mood disorders. In a longitudinal study, the authors followed a bipolar offspring cohort from adolescence into adulthood to determine the onset, prevalence, and early course of mood disorders and other psychopathology.
Method
The Dutch bipolar offspring cohort is a fixed cohort initiated in 1997 (N=140; age range at baseline, 12–21 years). Bipolar offspring were psychiatrically evaluated at baseline and at 1-, 5-, and 12-year follow-ups. Of the original sample, 77% (N=108) were followed for the full 12 years.
Results
Overall, 72% of the bipolar offspring developed a lifetime DSM-IV axis I disorder, 54% a mood disorder, and 13% bipolar spectrum disorders. Only 3% met DSM-IV criteria for bipolar I disorder. In 88% of the offspring with a bipolar spectrum disorder, the illness started with a depressive episode. In total, 24% of offspring with a unipolar mood disorder developed a bipolar spectrum disorder over time. Mood disorders were often recurrent (31%), were complex (comorbidity rate, 67%), and started before age 25.
Conclusions
Even after 12 years of follow-up, from adolescence into adulthood, bipolar I disorder was rare among bipolar offspring. Nevertheless, the risk of developing severe and recurrent mood disorders and other psychopathology was high. Future follow-up of this and other adult bipolar offspring cohorts is essential to determine whether recurrent mood disorders in bipolar offspring reflect the early stages of bipolar disorder.
Given that bipolar disorder is strongly genetically determined, children of patients with bipolar disorder (bipolar offspring) constitute an at-risk population that can provide us with better insight into the development and early course of bipolar disorder. In 1997, Lapalme et al. (1) showed in a meta-analysis (N=2,973) that bipolar offspring have 2.7 times the risk of developing a mental disorder and 4 times the risk of developing a mood disorder compared with children of healthy parents. More recently, two review articles on bipolar offspring reported elevated but varying prevalence rates of bipolar disorder (ranging from 3% to 27%), mood disorders (ranging from 5% to 67%), and non-mood disorders (ranging from 5% to 52%) (2, 3). However, these studies could not fully address the development and early course of bipolar disorder and other mood disorders because they used either a cross-sectional design or a longitudinal design without follow-up into adulthood (1–12). We report here on one of the largest prospective bipolar offspring studies with a follow-up into adulthood: the 12-year follow-up of the Dutch bipolar offspring cohort (7, 10, 12).
To date, only four bipolar offspring cohort studies have prospectively followed bipolar offspring for more than a decade. The first, a U.S. study conducted by Meyer et al. (13), has had the longest follow-up to date, although it has a small sample. The study started in 1979 with 76 mothers with a mood disorder, including 25 mothers with bipolar I or II disorder with 48 bipolar offspring (ages 1.5–7 years at baseline), and 45 healthy community subjects. At the young adult follow-up assessment 23 years later, 19% of the 32 bipolar offspring who were still in the study had developed bipolar disorder; of these, 6% were diagnosed with bipolar I disorder and 13% with bipolar II disorder. The second study is the bipolar offspring cohort from the Amish population followed by Egeland et al. for 16 years (14, 15). This sample included 115 bipolar offspring (ranging from age 13 to beyond age 30) from 15 families with a parent with bipolar I disorder and focused on prodromal symptoms of bipolar I disorder. After 16 years of follow-up, 7% of offspring had developed bipolar I disorder. In addition, bipolar offspring more often showed potentially prodromal characteristics compared with offspring of healthy families (39.2% and 5.9%, respectively). The third study is that of Duffy et al. in Canada (16), started in 1995 with 36 children (ages 10–25 years) from 23 families (with bipolar I and II disorders). Over the past 15 years, Duffy et al. expanded their cohort to 220 children (ages 8–25 years) with a maximum follow-up of 15 years. At a mean age of almost 25 years, 71.4% of the bipolar offspring had received a DSM-IV axis I diagnosis: 55% had developed a mood disorder, including 16.3% with a bipolar spectrum disorder (2.7% bipolar I disorder, 5.9% bipolar II disorder, 5.5% bipolar disorder not otherwise specified, and 1.8% schizoaffective disorder, bipolar type) (3, 16, 17). Despite different methods, the main finding of these studies is the same: low rates of bipolar I diagnoses compared with other mood disorders and psychopathology in general.
The fourth study, which we present here, is the Dutch bipolar offspring cohort, a fixed sample of 140 bipolar offspring from 86 families (with bipolar I and II disorders) followed from adolescence into adulthood to a mean age of 28 years (7, 10, 12). At the 5-year follow-up (mean age, 21 years), we found lifetime prevalence rates of 40% for any mood disorder, 10% for bipolar disorder (3.9% for bipolar I disorder and 6.1% for bipolar II disorder), and 59% for psychopathology in general. Furthermore, in all participants with bipolar disorder, the illness started with a depressive episode. Based on survival analysis, we predicted a further increase in bipolar disorder and unipolar depression in the coming years as the cohort further matured into adulthood (7). In the present study, we sought to provide a thorough description of the onset and early developmental trajectories of mood disorders and other psychopathology in bipolar offspring.
Method
Population and Procedure
The study design and recruitment procedure of the Dutch bipolar offspring cohort have been described in detail by Wals et al. (12). In short, 140 offspring (ages 12–21 years) from 86 families were recruited in the years 1997–1999. Participants were recruited through the Dutch Association for Manic Depressives and Relatives (62 families; 102 children) and through outpatient clinics in nine psychiatric hospitals (24 families; 38 children). All bipolar parents were outpatients at the time of recruitment. DSM-IV diagnoses of bipolar I and II disorders were confirmed by face-to-face interviews using the International Diagnostic Checklist (18) and further confirmed by the clinical diagnosis of the treating psychiatrist (12). Lifetime diagnoses of the biological coparent were assessed using the Family History Research Diagnostic Criteria method (19). At the second assessment (at 1 year), 132 offspring were reassessed (10), and at the third (at 5 years), 129 offspring (7). At the latest assessment (at 12 years), 108 offspring from the original cohort agreed to participate once again, resulting in a 12-year retention rate of 77.1%. The demographic characteristics of the study population and the dropouts are summarized in Table 1. The Medical Ethics Committee of the University Medical Center Utrecht approved the study. Written informed consent was obtained from both the offspring and their parents.
| Participants in 12-Year Follow-Up | Dropouts | |||
|---|---|---|---|---|
| N | % | N | % | |
| Bipolar offspring | 108 | 77.1 | 32 | 22.9 |
| Male | 58 | 53.7 | 14 | 43.8 |
| Female | 50 | 46.3 | 18 | 56.3 |
| Mean | SD | Mean | SD | |
| Age at baseline | 16.5 | 2.00 | 16.5 | 2.80 |
| N | % | N | % | |
| Any lifetime disorder at 5 years | 64 | 59.3 | 16 | 50 |
| Family compositionb | ||||
| Bipolar parent | 70 | 23 | ||
| Bipolar mother | 41 | 58.6 | 15 | 65.2 |
| Bipolar father | 29 | 41.4 | 8 | 34.8 |
| Bipolar I disorder | 52 | 74.3 | 18 | 78.3 |
| Bipolar II disorder | 18 | 25.7 | 5 | 21.7 |
| Nonbipolar probandc | 72 | 24 | ||
| Bipolar disorder | — | — | 1 | 4.2 |
| Unipolar mood disorder | 11 | 15.3 | 4 | 16.7 |
| Psychosis | 1 | 1.4 | — | — |
| Substance use disorder | 2 | 2.8 | 2 | 8.3 |
| No diagnosis | 58 | 54.2 | 17 | 70.8 |
| Married | 45 | 62.5 | 17 | 70.8 |
| Divorced | 27 | 37.5 | 7 | 29.2 |
| Mean | SD | Mean | SD | |
| Parents’ socioeconomic statusd at baseline | 4.97 | 2.08 | 4.87 | 2.44 |
a
There were no significant differences on any variable between offspring who participated in the 12-year assessment and those who dropped out of the study before that time.
b
A total of 16 complete families left the study; seven families have left the study partly.
c
Three bipolar parents have children from a previous marriage participating; therefore, 89 nonbipolar parents are presented here.
d
Socioeconomic status was measured on scale from 1 to 9, as described in Wals et al. (12).
Instruments
Over the past 12 years, the psychiatric interviews were administered by four of the authors (E.M., M.H., M.W., and C.R.) and six intensively trained interviewers with graduate degrees in psychology. Subsequently, all outcomes were evaluated with psychiatrists certified in child and adolescent as well as adult psychiatry (C.R. and M.H.) to reach consensus on final diagnoses. At baseline and at 1 year, DSM-IV diagnoses were obtained by a face-to-face interview with both the child and the parent using the Schedule for Affective Disorders and Schizophrenia for School-Age Children–Present and Lifetime Version (K-SADS-PL) (20). In cases of disagreement between child and parent about the presence of a symptom, greater weight was given to parents’ reports of observed behavior and children’s reports of subjective experiences (20). We also screened for pervasive developmental disorders (12). After offspring reached age 18, the K-SADS-PL was replaced by the Structured Clinical Interview for DSM-IV Axis I Disorders (SCID) (21). As discussed previously (7), the two interviews share many similarities; however, there are some important differences to note: the K-SADS-PL uses more informants, compared with only one informant in the SCID, and the SCID does not include all DSM-IV diagnoses. Therefore, the questionnaires for attention deficit hyperactivity disorder (ADHD), oppositional defiant disorder, conduct disorder, and tic disorders originating from the K-SADS-PL were applied as well.
Lifetime DSM-IV diagnoses at 12 years are based on the four psychiatric interviews that took place over the 12 years of follow-up. Each psychiatric assessment evaluated current and past symptoms during the interim period. For all diagnoses, the age at onset and the duration of the episode were established. For depression not otherwise specified, we included only minor depressive disorder and recurrent brief depressive disorder. Also, because of the perceived uncertainty of the bipolar disorder not otherwise specified diagnosis (22), we decided not to specifically assess for this diagnosis in our studies.
Statistical Analysis
We first assessed the numbers and percentages of offspring with bipolar spectrum disorders, any other mood disorder, and other non-mood disorders, including age at onset. Next, we performed two standard Kaplan-Meier survival analyses. Kaplan-Meier survival analyses provide an estimation of the probability of remaining well at a given point in time. In the first analysis, the age at onset for offspring with a lifetime mood disorder was recorded as event; offspring without a lifetime mood disorder at the end of the follow-up period were recorded as censored. For the second survival analysis, the interval between the first mood episode and the first manic or hypomanic episode was recorded as event; offspring without a bipolar spectrum disorder at the end of the follow-up period were recorded as censored.
Results
A total of 108 offspring (58 of them male; mean age, 28.0 years [SD=2.82]) participated in the 12-year assessment. Table 2 presents the prevalence of lifetime psychopathology at baseline and at 12 years. Over the 12 years of follow-up, the prevalence of mood disorders doubled, with the result that now more than half of the cohort is positive for a lifetime mood disorder, including 13% with lifetime bipolar spectrum disorders. None of the bipolar offspring developed a primary psychotic disorder without affective symptoms. Overall, more than 70% of the cohort met the criteria for at least one lifetime DSM-IV axis I disorder.
| Lifetime Diagnosis at Baseline | Lifetime Diagnosis at 12 Years | Current Diagnosis at 12 Yearsa | ||||
|---|---|---|---|---|---|---|
| Psychopathology | N | % | N | % | N | % |
| Any mood disorder | 38 | 27 | 58 | 54 | 22 | 20 |
| Major depressive disorder | 8 | 6 | 18 | 17 | 6 | 6 |
| Dysthymic disorder | 8 | 6 | 9 | 8 | 2 | 2 |
| Depressive disorder not otherwise specified | 15 | 11 | 22 | 20 | 0 | 0 |
| Bipolar spectrum disorders | 6 | 0 | 14 | 13 | 14 | 13 |
| Bipolar I or II disorder | 4 | 3 | 12 | 11 | 12 | 11 |
| Schizoaffective disorder | — | — | 1 | 1 | 1 | 1 |
| Cyclothymia | 2 | 1 | 1 | 1 | 1 | 1 |
| Adjustment disorder, mood | 1 | 1 | 4 | 4 | 0 | 0 |
| Psychosis | — | — | — | — | — | — |
| Anxiety disorders | 15 | 11 | 27 | 25 | 9 | 8 |
| Disruptive behavioral disorders | 8 | 6 | 8 | 7 | 2 | 2 |
| Attention deficit hyperactivity disorder | 7 | 5 | 5 | 5 | 3 | 3 |
| Substance use disorder | 9 | 6 | 25 | 23 | 8 | 7 |
| Other disordersb | 22 | 16 | 25 | 23 | 5 | 5 |
| Any disorder | 61 | 44 | 78 | 72 | 49 | 45 |
a
Current diagnosis is defined as psychopathology in the past month. A current diagnosis of bipolar disorder does not imply a current episode.
b
Includes enuresis, encopresis, pervasive developmental disorder, tic disorder, body dysmorphic disorder, and eating disorders.
Table 3 summarizes the clinical characteristics of the 17 participants from 15 families who developed a bipolar spectrum disorder during the 12-year follow-up period. Twelve (80%) of the 15 bipolar parents had bipolar I disorder, which is not statistically different from the distribution in the overall group of parents (74%). In 88% of offspring with a bipolar spectrum disorder, the illness began with a depressive episode; in two offspring, the illness started with cyclothymia. The mean age at onset of the first mood episode was 14.6 years (SD=4.65, range=8.6–23.7), and onset of the first manic or hypomanic episode followed on average 5.3 years later (SD=4.10, range=0–13.6; see also Figure 1A). We found no significant difference between age at hypomania onset (median=17.3 years) and age at mania onset (median=20.2). Five participants (29%) had their first depressive episode before age 12 (i.e., prepubertal onset). None of the participants had a prepubertal hypomanic or manic episode. Two participants were diagnosed with ADHD. Nine participants (53%) had a comorbid anxiety disorder; in four of them, the anxiety disorder was present before the onset of their first mood episode or was diagnosed around the same time. All 17 offspring with a bipolar spectrum disorder received psychiatric treatment (pharmacologic, 71%; counseling, 100%) currently or in the past; six offspring had been hospitalized at least once. With regard to pharmacological treatment, only one participant switched into hypomania after starting treatment with an antidepressant. One participant received a stimulant because of comorbid ADHD (before the onset of bipolar II disorder). For more detail on the characteristics of this group, see Table S1 in the data supplement that accompanies the online edition of this article.
| Gender | Type of Bipolar Disorder | Index Mood Episode | Age at Index Mood Episode | Age at First Manic/Hypomanic Episode | Age at Onset of Comorbid Anxiety Disorder | Age at Onset of Comorbid Substance Abuse | Hospitalizationa |
|---|---|---|---|---|---|---|---|
| Female | Bipolar II | Major depression | 13 | 19 | — | — | — |
| Female | Bipolar II | Depression not otherwise specified | 8 | 16 | 16 | — | — |
| Male | Bipolar II | Dysthymia | 10 | 16 | 10 | — | — |
| Female | Bipolar II | Major depression | 20 | 21b | 25 | — | — |
| Female | Bipolar II | Depression not otherwise specified | 19 | 24b | 21 | — | — |
| Female | Bipolar II | Depression not otherwise specified | 16 | 25 | — | — | — |
| Male | Bipolar I | Major depression | 17 | 17 | 22 | — | MM |
| Male | Cyclothymia | Cyclothymia | 22 | 22 | — | — | — |
| Male | Bipolar II | Depression not otherwise specified | 23 | 31 | 25 | 19 | — |
| Male | Bipolar I | Major depression | 10 | 18 | — | 16 | M |
| Male | Bipolar I | Major depression | 15 | 15 | — | — | M |
| Female | Bipolar II | Dysthymia | 11 | 16 | 11 | — | — |
| Female | Schizoaffective disorder, bipolar type | Depression not otherwise specified | 12 | 13 | — | — | MM |
| Male | Bipolar II | Cyclothymia | 12 | 16 | 22 | — | — |
| Male | Bipolar I | Depression not otherwise specified | 15 | 16 | — | — | M |
| Male | Bipolar II | Dysthymia | 8 | 20b,c | — | — | D |
| Male | Bipolar II | Dysthymia | 11 | 25b | 2 | 18 | — |
a
Episode at first hospitalization: D=depression; M=mania; MM=mixed mania.
b
Use of antidepressants before onset of first hypomanic episode.
c
Use of stimulants before onset of first manic/hypomanic episode.
FIGURE 1. Survival Function of the Development of First Mood Disorders in the Dutch Bipolar Offspring Cohorta
a In panel A, the survival function is based on offspring developing their first manic or hypomanic episode (N=17), and censored cases are those who left the study with a lifetime unipolar mood disorder but without developing bipolar disorder (either as a dropout [N=7] or at the end of the study [N=44]). In panel B, the survival function is based on offspring who developed their first mood episode (N=68), and censored cases are those who left the study without a lifetime mood disorder (either as a dropout [N=22] or at the end of the study [N=50]).
Apart from being at risk for bipolar spectrum disorders, bipolar offspring are at substantial risk for developing mood disorders in general. More than half of the cohort (54%) developed a lifetime mood disorder by a mean age of 28 years. The average age at onset of the first mood episode was 17.2 years (SD=5.33, range=6.8–28.4). Of the 58 bipolar offspring with a lifetime mood disorder, 14 (24%) developed a bipolar spectrum disorder during follow-up, and 19 (33%) had a recurrent unipolar depression; taken together, 33 (31%) of the bipolar offspring had a recurrent mood disorder. Among participants with a lifetime mood disorder (N=58), the lifetime prevalence of psychopathology is much more complex: 67% had a comorbid lifetime disorder, including 34% with an anxiety disorder, 19% with a substance use disorder, 7% with a disruptive behavior disorder, 3% with ADHD, and 34% with other disorders (as defined in Table 2). Comorbid disorders were present in 64% of offspring with bipolar spectrum disorders and in 68% of those with unipolar mood disorders. Overall, 71% of participants with a lifetime mood disorder contacted mental health care services at some time between the 5-year and 12-year follow-up assessments, and 33% had received pharmacological treatment. To provide a better insight into the developmental course toward the onset of mood disorders, the transition over the four assessments is depicted in Figure 2.
FIGURE 2. Transition to Mood Disorders in the Dutch Bipolar Offspring Cohort (N=140)a
a Numbers in gray circles indicate the number of offspring in this category who left the study; a participant who left the study with a lifetime diagnosis at baseline, at 1 year, or at 5 years would remain in this category at follow-up and would be added to the gray circle. The mean age at baseline was 16.1 years (range=12–21); at the 1-year follow-up, 17.4 years (range=13–23); at the 5-year follow-up, 20.8 years (range=16–26); and at the 12-year follow-up, 28.0 years (range=22–32).
b Other disorders include any DSM-IV axis I disorder other than bipolar, unipolar mood, or anxiety disorders.
Because the prevalence of first-onset mood disorders increased significantly over the 12-year follow-up period, we performed a Kaplan-Meier survival analysis to check whether a further increase in first-onset mood disorders can be expected in the future (see Figure 1B). In contrast to the 5-year assessment, the slope of the Kaplan-Meier survival function appears now to level out after age 25. In total, only four of 52 offspring over the age of 25 have developed a first-onset mood disorder (data not shown).
Discussion
Our aim in this study was to provide data on the onset and developmental trajectories of mood disorders and other psychopathology in bipolar offspring. In summary, at a mean age of 28 years, more than half of the Dutch bipolar offspring cohort had developed a mood disorder, including 13% with bipolar spectrum disorders (3% with bipolar I disorder; 8% with bipolar II disorder; 1% with schizoaffective disorder, bipolar type; and 1% with cyclothymia) and 41% with a unipolar depressive disorder (major depressive disorder; dysthymia; depressive disorder not otherwise specified; or adjustment disorder, mood). None of the bipolar offspring developed a psychotic disorder without affective symptoms. In almost all participants with bipolar spectrum disorders, the illness started with a depressive episode. Among offspring with lifetime unipolar depression, 24% had a manic or hypomanic episode during follow-up, on average 5.1 years after their first unipolar mood episode. None of the offspring had a prepubertal onset of mania or hypomania. The risk of developing a first mood episode was highest up to age 25; only four participants developed a first mood episode after this age. Finally, we found that unipolar mood disorders in bipolar offspring were often recurrent (33% of the cases) and were prone to be complex (68% with comorbid disorders), and that 71% offspring with unipolar mood disorders received treatment from mental health services. Overall, 72% of the cohort developed a lifetime DSM-IV axis I disorder in 12 years of follow-up.
Our study has some limitations. First, it is not a population-based study: participants were recruited through the Dutch Association for Manic Depressives and Relatives and bipolar outpatient clinics across the country, suggesting a selection of better informed and treatment-seeking bipolar parents. Second, we had no control group of children of parents without bipolar disorder; however, we could compare our results with data from a comparable age group in the Netherlands Mental Health Survey and Incidence Study (NEMESIS-2) (23–25), a recently published Dutch population study. In that study, 1,123 participants in the age range of 25–34 years were psychiatrically evaluated using the Composite International Diagnostic Interview 3.0 (26). Lifetime prevalence was 46.5% for any psychiatric disorder and 19.5% for any mood disorder, including 2.4% for bipolar disorder (without further specification). Although the diagnostic instruments were not identical, data from NEMESIS-2 confirm that the lifetime prevalence of mood disorders, bipolar disorders, and psychiatric disorders in general are considerably higher in our bipolar offspring cohort than in the Dutch general population. A third limitation is that at baseline, offspring were already between 12 and 21 years old; therefore, data on prepubertal and early adolescent disorders or episodes may be affected by a recall bias. In additional analyses (see Table S2 in the online data supplement), we divided our cohort into an early adolescence group (ages 12–16) and a late adolescence group (ages 16–21) at baseline and examined whether data on prevalence rates of psychopathology (per category) at baseline and at 12 years and age at onset of the first mood episode were affected by recall bias. We found no evidence for different rates of psychopathology. However, as depicted in Figure 1B, the age at baseline likely affected the age at onset of mood disorders as reported by offspring and their parents. This supports the notion that diagnoses of internalizing disorders may be more affected by recall bias, since these diagnoses are mainly based on information from offspring (27). Fourth, not specifically assessing for bipolar disorder not otherwise specified in this study may have affected our findings. However, of the four prospective studies of bipolar offspring that we mentioned earlier, only the Canadian study (28) used the bipolar disorder not otherwise specified diagnosis, and the lifetime prevalence of bipolar spectrum disorders was also comparable to the three other studies. Despite limitations, the strengths of this study are the long follow-up period and the high retention rate (77%) of 108 bipolar offspring from adolescence into adulthood.
With regard to both age distribution and psychopathology outcome, our results compare best to those of the prospective Canadian bipolar offspring study from Duffy et al. (3, 17). Cumulatively, their sample consists of 220 offspring with a mean age of 24.6 years (range=8–30) and a mean follow-up of 9.2 years (SD=4.16, range=1–15); 21.4% have been followed for the full 15 years (28, 29; A. Duffy et al., personal communication, Feb. 2012). Despite some methodological differences, the prevalence rates in their study and ours are remarkably similar: bipolar spectrum disorders, 16.3% and 13%, respectively; mood disorders, 55% and 54%, respectively; and any axis I disorder, 71.4% and 72%, respectively. Moreover, in both studies, bipolar spectrum disorders began in the majority of the bipolar offspring with a depressive episode (86% and 88%, respectively) (28). These similarities in prevalence rates appear to be at least partly the result of using the same assessment methods and including bipolar families with comparable socioeconomic status. In addition, the Dutch and Canadian health care systems provide easily accessible basic mental health care. Therefore, no sample selection occurred as a result of study participation in exchange for receiving mental health care.
Apart from these convergent findings, there are also some divergent findings worth mentioning between this and other bipolar offspring studies. Compared with the Duffy et al. study (28), the onset of comorbid anxiety disorders in bipolar spectrum disorders was much later in our study (mean age, 10 years and 17 years, respectively). As described earlier, age at baseline may significantly affect age at onset. Duffy et al. recruited younger offspring and may therefore have detected (mild) anxiety disorders at an earlier stage. In general, we observed much higher rates of comorbid anxiety in bipolar spectrum disorders (28% compared with 52%). Also, whereas some bipolar offspring studies have reported elevated rates of ADHD and disruptive disorders (4–6, 11), we observed close to normal rates of ADHD and disruptive disorders, as did Duffy et al. (3). Again, age at intake may be involved. We may have missed some of these diagnoses because of the age-dependent decline of ADHD symptoms, especially since symptoms of hyperactivity and impulsivity are less overt during adolescence (30). Another possible factor could be the parental characteristics of these cohorts: all studies reporting high rates of ADHD and disruptive disorders in bipolar offspring also show high rates of ADHD in the parental cohort (4–6, 11). Furthermore, we found prevalence rates of substance use disorders close to those in the Dutch general population (23% and 25%, respectively) (24). A possible explanation lies in the recruitment bias of our participating families. Most of these families (and their offspring) are members of the patient association, often aware of and well informed about the risks of substance use. Also, the relatively high socioeconomic status of our cohort may explain the low prevalence of substance use disorders (31).
In the end, one of the most remarkable findings of this and the three other longitudinal studies of bipolar offspring with a follow-up into adulthood (3, 11, 14) is that although the prevalence of mood disorders and other psychopathology in this population is high, the prevalence of bipolar I disorder is low compared with other forms of bipolar disorder. At the same time, the lifetime prevalence rate of recurrent mood disorders in our cohort was 31%. This finding points to the discussion of Kraepelin’s broad concept of manic-depressive illness, which included all recurrent mood disorders (32). It is tempting to speculate that the genetic vulnerability comprises mainly the risk for mood instability and recurrences rather than the risk of developing full-blown mania. On the other hand, the long delay between the first unipolar mood episode and the onset of the first manic or hypomanic episode as found in this study may also suggest that the recurrent unipolar mood disorders in our cohort rather reflect the early stages of future bipolar disorder. These findings are in concordance with findings from a prospective study in adults by Angst et al. (33), and this possibility is also proposed in several theoretical staging models (34, 35). Apart from the meaning of recurrent depression in the concept of bipolar disorder, clinically it is important to realize that the depressive course in bipolar spectrum disorders is especially associated with a high burden of illness (36). Furthermore, it is worth mentioning that although there is emerging evidence for shared genetic susceptibility and etiology between bipolar disorder and schizophrenia (37), none of the bipolar offspring—in either the Dutch or the Canadian study—developed a primary psychotic disorder (3).
In conclusion, after a 12-year follow-up of a large fixed bipolar offspring cohort, we found, like the three other existing prospective bipolar offspring studies, low rates of bipolar I disorders in adult bipolar offspring. Nevertheless, in all bipolar offspring studies, high rates of psychopathology and (recurrent) mood disorders have been observed (1–3, 9, 13, 15, 17). Therefore, early intervention appears indicated to enhance normal development and prevent the onset of mood disorders in bipolar offspring. Future follow-up of this and the other adult bipolar offspring cohorts is essential to determine whether recurrent mood disorders in bipolar offspring reflect the early stages of bipolar disorder.
Acknowledgments
The authors acknowledge Sanne Kemner for her assistance in implementation of the study's 12-year assessment.
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Information & Authors
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Received: 28 March 2012
Revision received: 25 July 2012
Revision received: 4 September 2012
Accepted: 5 October 2012
Published online: 1 May 2013
Published in print: May 2013
Authors
Funding Information
Dr. Nolen has received grants from AstraZeneca, Eli Lilly, GlaxoSmithKline, and Wyeth and has received speaking fees from AstraZeneca, Pfizer, Servier, and Wyeth. Dr. Nolen has served on advisory boards for AstraZeneca and Servier. Dr. Hillegers has received speaking fees from Benecke, AstraZeneca, and Lundbeck. The other authors report no financial relationships with commercial interests.
Supplementary Material
Supported by grant 22963 from the 7FP of the European Commission and grant 9120818 from the Netherlands Organization for Scientific Research (NWO). Previous waves of this study were supported by the Stanley Medical Research Institute and NWO.Metrics & Citations
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