Psychopathology in Adolescent Offspring of Parents With Panic Disorder, Major Depression, or Both: A 10-Year Follow-Up
Publication: American Journal of Psychiatry
Abstract
Objective
The authors examined the specificity and course of psychiatric disorders from early childhood through adolescence in offspring of parents with confirmed panic disorder and major depressive disorder.
Method
The authors examined rates of psychiatric disorders at 10-year-follow-up (mean age, 14 years) in four groups: offspring of referred parents with panic and depression (N=137), offspring of referred parents with panic without depression (N=26), offspring of referred parents with depression without panic (N=48), and offspring of nonreferred parents with neither disorder (N=80). Follow-up assessments relied on structured interviews with the adolescents and their mothers; diagnoses were rated present if endorsed by either.
Results
Parental panic disorder, independently of parental depression, predicted lifetime rates in offspring of multiple anxiety disorders, panic disorder, agoraphobia, social phobia, and obsessive-compulsive disorder. Parental depression independently predicted offspring bipolar, drug use, and disruptive behavior disorders. Parental panic and depression interacted to predict specific phobia and major depressive disorder. Phobias were elevated in all at-risk groups, and depression was elevated in both offspring groups of parents with depression (with or without panic disorder), with the highest rates in the offspring of parents with depression only. Parental depression independently predicted new onset of depression, parental panic disorder independently predicted new onset of social phobia, and the two interacted to predict new onset of specific phobia and generalized anxiety disorder.
Conclusions
At-risk offspring continue to develop new disorders as they progress through adolescence. These results support the need to screen and monitor the offspring of adults presenting for treatment of panic disorder or major depressive disorder.
The high prevalence and morbidity of anxiety and depressive disorders underscores the importance of delineating their risk factors in order to improve early identification and treatment. Studies have found a higher risk for anxiety disorders among children of anxious and depressed parents (1, 2), with children of parents with both panic and depression at especially high risk (1, 3).
Our earlier prospective study of offspring of parents with panic, depression, or no anxiety or mood disorders (4) found that at a mean age of 7 years, parental panic, independently of depression, was associated with a greater risk for offspring panic disorder and agoraphobia, whereas depression was associated with a greater risk for social phobia, depression, and disruptive behavior disorders. At the 5-year follow-up (mean age, 10 years), parental panic predicted a wide range of anxiety disorders in offspring, while parental depression was associated with a greater risk for offspring depression and disruptive behavior disorders (5).
Despite these findings, several important questions remain. First, with only two exceptions (1, 6), previous studies have not prospectively assessed offspring at risk for anxiety over a time span that includes both childhood and adolescence. Increases in adolescent depression and anxiety among offspring at risk might be expected for several reasons. There is an increase in depression and anxiety disorders in the overall population during adolescence (7), particularly after the onset of puberty (8, 9). The developmental emphasis on peer-group acceptance may also contribute to increased vulnerability to depression during this period (10). Second, only one previous study focused on effects of comorbidity in parents with depression (6), and it did not include offspring of parents with anxiety without depression. Research is needed to determine whether the risks for anxiety conferred by parental depression are related to parental comorbid anxiety. Third, whereas previous studies suggest that parental panic confers a greater risk for anxiety disorders and that parental depression increases the risk for mood and disruptive behavior disorders, it is unclear whether the risks conferred by these disorders persist, become more specific, or broaden as offspring enter adolescence. Fourth, it has not been established whether the risks conferred to offspring by parental panic and depression differ on the basis of the sex of the affected parent. Finally, it is important to examine risks for psychosocial impairment in addition to risks for disorders themselves.
To address these questions, we examined specificity and course of risk into adolescence in a 10-year follow-up study. We hypothesized that parental panic would predict a greater risk for anxiety disorders (with the highest risk for panic disorder) and that parental depression would predict a greater risk for mood and disruptive behavior disorders. We examined whether risks conferred to offspring differed by the sex of the diagnosed parent, and we examined trajectories of risk over time to determine whether offspring at risk would have an earlier onset of disorders and would suffer from new disorders in adolescence.
Method
Ascertainment
As previously described (4, 5), we recruited parents receiving treatment for panic disorder and major depressive disorder from clinical referrals and local advertisements. We recruited comparison families in which both parents were free of major anxiety (panic disorder, agoraphobia, social phobia, or obsessive-compulsive disorder [OCD]) or mood disorders through advertisements. We excluded families in which a parent had a psychotic disorder or suicidality and those with a child or parent who was intellectually disabled.
All parents were interviewed with the Structured Clinical Interview for DSM-III-R (11). There were no constraints on comorbid disorders; however, for this analysis, parents with bipolar disorder were excluded. Of the 278 offspring (from 174 families) assessed at baseline (excluding families with parental bipolar disorder), 183 (from 120 families) were reassessed at follow-up. Offspring ages at baseline ranged from 5 to 25 years.
Children were originally classified into four groups on the basis of parental disorder: offspring of parents with panic, offspring of parents with depression, offspring of parents with panic plus depression, and offspring of parents with neither. To maintain accurate classifications, parents were reinterviewed with the Structured Clinical Interview for DSM-IV Axis I Disorders (SCID-IV) at the 5- and 10-year follow-up assessments. Over the course of 10 years, some families changed groups (Table 1). Our follow-up sample comprised 137 children of parents with panic plus depression, 26 children of parents with panic without depression, 48 children of parents with depression without panic, and 80 children of comparison parents. Of the parents with panic or depression, 65 mothers and 20 fathers met criteria for panic disorder, and 82 mothers and 49 fathers had major depression. The hospital institutional review board approved the study protocol. All parents and children over age 14 signed written consent, and younger children assented to study procedures verbally (under age 7) or in writing (ages 7–13).
| Characteristic | Offspring of Parents With Panic Disorder and Major Depressive Disorder (N=137)b | Offspring of Parents With Panic Disorder (N=26) | Offspring of Parents With Major Depressive Disorder (N=48) | Offspring of Comparison Parents (N=80) | ||||
|---|---|---|---|---|---|---|---|---|
| Mean | SD | Mean | SD | Mean | SD | Mean | SD | |
| Age (years) | 15.8 | 6.4 | 14.1 | 3.0 | 12.9 | 3.8 | 14.2 | 3.7 |
| Follow-up duration (years)c | 10.2 | 2.5 | 9.7 | 1.6 | 8.8 | 1.9 | 9.4 | 1.6 |
| Hollingshead Index of Social Position | 2.0 | 0.9 | 1.8 | 0.8 | 2.0 | 0.9 | 1.6 | 0.8 |
| N | % | N | % | N | % | N | % | |
| Gender (male) | 67 | 49 | 15 | 58 | 29 | 60 | 42 | 52 |
| Racial category | ||||||||
| African American | 2 | 1 | 0 | 0 | 1 | 2 | 3 | 4 |
| Caucasian | 128 | 94 | 26 | 100 | 43 | 93 | 75 | 94 |
| Asian American | 1 | 1 | 0 | 0 | 0 | 0 | 1 | 1 |
| Pacific Islander | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| More than one | 4 | 3 | 0 | 0 | 2 | 4 | 1 | 1 |
| Intact familyd | 105 | 77 | 17 | 65 | 34 | 71 | 68 | 85 |
a
There were no significant differences between groups on any variable, although for age the between-group difference approached significance (p=0.06).
b
Using updated parental diagnostic data at wave 3, some offspring were reclassified as follows: three comparison families (seven offspring) became major depressive disorder only families; two comparison families (four offspring) became panic disorder only families; seven major depressive disorder families (15 offspring) and four panic disorder families (11 offspring) became panic disorder plus major depressive disorder families.
c
Calculated only for the subsample originally assessed at wave 1 (N=183).
d
A family was defined as intact if the parents were married or living together and not intact if the parents were living apart.
Assessments
The first assessment (wave 1) was conducted between 1993 and 1998. Wave 2 occurred 5 years later (1999–2004), and wave 3 occurred 10 years later (2004–2010). Baseline diagnostic assessments used the DSM-III-R Schedule for Affective Disorders and Schizophrenia for School-Age Children–Epidemiologic Version, 4th revision (K-SADS-E) (12). Follow-ups used the 5th edition of the K-SADS-E, based on DSM-IV (13), for participants under age 18 and the SCID-IV (14), supplemented with modules from the K-SADS-E to assess childhood diagnoses, for participants age 18 and over. We conducted indirect interviews with mothers for all participants and direct interviews with participants age 12 and over. We diagnosed a disorder if DSM-IV criteria were met in either interview. Interviewers had undergraduate degrees in psychology, were trained to high levels of interrater reliability (kappa values, 0.88–1.0 compared with clinician interviewers), and were supervised by a committee of board-certified psychiatrists and licensed psychologists, who resolved diagnostic uncertainties. All interviewers and diagnostic reviewers were blind to ascertainment status. The kappa values for agreement between diagnostic reviewers (based on 20 interview modules for each diagnosis) ranged from 0.73 (for OCD) to 1.0 (for major depressive disorder), with a median of 0.87.
Lifetime diagnoses were given for participants receiving a diagnosis at any assessment. We defined “multiple anxiety disorders” as meeting criteria for two or more anxiety disorders; “any mood disorder” to index major depressive disorder or mania; and “any disruptive behavior disorder” to indicate attention deficit hyperactivity disorder, oppositional defiant disorder, or conduct disorder.
We assessed overall functioning with the Global Assessment of Functioning Scale (GAF; range: 32–72). We measured overall social functioning by averaging the subscales of the Social Adjustment Inventory for Children and Adolescents (15) (range: 1=not a problem to 4=severe problem). To measure school functioning, we asked about repeated grades, need for academic tutoring, and placement in special classes. We recorded the nature and duration of any treatment the child had received, and we assessed socioeconomic status with the Hollingshead scale (16).
Statistical Analysis
We compared the four groups of offspring on demographic variables, rates of disorders, and functional outcomes. We used logistic regression for binary outcomes, linear regression for continuous outcomes, and ordinal logistic regression for ordinal outcomes. Logistic regression determined which offspring disorders were associated with parental panic and depression (controlling for demographic confounders). We included an interaction of parental panic and depression in these models. If the interaction was not significant, it was removed from the model; if it was significant, we examined the outcome variable in all four groups.
We examined offspring psychiatric disorders using three definitions: onsets of new disorders since the 5-year follow-up, lifetime diagnoses, and current diagnoses (i.e., criteria were met in the month prior to the 10-year assessment). We used clustered standard errors (17) to account for nonindependence of siblings. This method calculates Huber-White standard errors (18) that are robust to within cluster (i.e., family) correlation. Tests were two-tailed with alpha=0.05.
Results
Attrition and Demographic Characteristics
Of the 278 offspring assessed at baseline (excluding families with parental bipolar disorder), 183 (66%) were reassessed at follow-up. Reassessment rates were significantly lower in comparison offspring (61%) and in panic-plus-depression offspring (58%) compared with depression-only offspring (92%) (χ2=9.4, df=3, p=0.02; 85% in panic-only offspring). There were no significant differences between returning and nonreturning offspring on baseline demographic characteristics, lifetime GAF score, or mood or anxiety disorders. Group status and disruptive behavior disorders at baseline interacted to predict loss to follow-up (p<0.01). Nonreturning offspring of depressed parents had significantly higher rates of disruptive behavior disorders at baseline compared with offspring of depressed parents who returned (p<0.01); the other groups did not show this relationship. The four groups did not vary significantly in duration of follow-up.
In addition to the 183 offspring assessed at baseline and follow-up, 108 of their siblings who had been too young to assess in previous waves were assessed for the first time at follow-up, yielding 291 offspring (mean age=14.7 years, SD=5.2). Table 1 summarizes the demographic characteristics of the offspring. Given near-significant group differences in age (p=0.06), all analyses corrected for age.
Psychiatric Disorders in Offspring
New onset of disorders.
Parental depression predicted new onset of depression (odds ratio=5.4, 95% CI=1.4–20.4; z=2.49, p=0.01) independently of parental panic, whereas parental panic independently predicted new onset of social phobia (odds ratio=2.9, 95% CI=1.04–8.2; z=2.03, p=0.04). Specifically, lifetime rates of depression increased between the 5- and 10-year follow-ups from 15% to 32% in the panic-plus-depression offspring (N=85) and from 17% to 45% in the depression-only offspring (N=29). Rates of social phobia increased from 31% to 45% in the panic-plus-depression offspring and from 0% to 20% in the panic-only offspring (N=15).
Significant interaction effects of parental depression and panic were observed for new onsets of specific phobia and generalized anxiety disorder (p values, <0.05). The panic-only and depression-only groups had significantly greater rates of onset of specific phobia relative to the comparison group and the panic-plus-depression group (40% and 29% compared with 2% and 12%, respectively; p values, <0.05). For generalized anxiety disorder, the interaction was accounted for by the significantly lower rate of new onset in the panic-plus-depression group (7%) compared with the panic-only group (27%, p=0.03).
Lifetime disorders.
Figure 1 displays rates of lifetime disorders by offspring group for participants assessed at the 10-year follow-up. Parental panic, independently of parental depression, significantly predicted multiple anxiety disorders, panic disorder, agoraphobia, social phobia, and OCD in offspring (Figure 2). Parental depression, independently of parental panic, significantly predicted offspring bipolar, drug use, and disruptive behavior disorders.
FIGURE 1. Rates of Lifetime Disorders at 10-Year Follow-Up in Offspring of Parents With Panic Disorder or Major Depressive Disorder or Both, and in Offspring of Comparison Parentsa
a Alcohol and drug use disorders and smoking dependence are limited to offspring age 12 and older.
FIGURE 2. Risk for Psychiatric Disorders in Offspring of Parents With Panic Disorder or Major Depressive Disordera
a Odds ratios for each offspring disorder are independent of the presence or absence of the other parental diagnosis (major depressive disorder or panic disorder). Main effects are shown only when the interaction effect is not significant.
*p<0.05. **p<0.01. ***p<0.001.
We observed a significant interaction of parental panic disorder and major depression when predicting specific phobia (p=0.047) and major depression (p=0.03). Rates of specific phobia were elevated in all three high-risk groups relative to the comparison group, but the risk in offspring of parents with panic plus depression was not significantly higher than that for offspring of either disorder alone. Offspring of depressed parents with or without comorbid panic had higher rates of major depression relative to comparison offspring (p<0.001 for both), but offspring of parents with depression alone had significantly higher rates of depression compared with offspring of parents with panic (p=0.007) or panic plus depression (p=0.03).
Risk of lifetime disorders conferred by mothers and by fathers.
We repeated the series of logistic regression analyses predicting offspring lifetime disorders including paternal and maternal panic and depression as separate independent variables. We found that both maternal and paternal panic were associated with higher rates of offspring panic disorder (for mothers, odds ratio=5.81, p=0.011; for fathers, odds ratio=5.01, p=0.012), agoraphobia (for mothers, odds ratio=2.49, p=0.007; for fathers, odds ratio=5.01, p=0.042), and multiple anxiety disorders (for mothers, odds ratio=2.54, p=0.003; for fathers, odds ratio=2.36, p=0.04). Offspring OCD was associated only with paternal panic (odds ratio=5.43, p=0.01) and social phobia only with maternal panic (odds ratio=2.07, p=0.036). Rates of separation anxiety disorder were higher in offspring of mothers with depression (odds ratio=2.20, p=0.031) and fathers with panic (odds ratio=2.48, p=0.039). Offspring depression was predicted by depression in both mothers and fathers (for mothers, odds ratio=2.56, p=0.018; for fathers, odds ratio=2.29, p=0.041), but bipolar and drug use disorders were predicted only by maternal depression (odds ratio=7.18, p=0.010, and odds ratio=2.53, p=0.044, respectively).
Current disorders.
Rates of current disorders at the 10-year follow-up are summarized in Figure S1 in the data supplement that accompanies the online edition of this article. Parental panic significantly predicted agoraphobia (odds ratio=5.7, p=0.005) and social phobia (odds ratio=4.7, p=0.004) independently of parental depression. Parental panic and depression interacted to predict current specific phobia (p=0.049). Specific phobia offspring had elevated rates in all three high-risk groups relative to comparison offspring, with no difference between the three groups.
Figure 3 displays Kaplan-Meier failure functions for anxiety, mood, disruptive behavior, and substance use disorders in offspring, using age at onset reported in the wave when the disorder was first endorsed. For multiple anxiety disorders, associations with parental panic and depression varied with age. For children younger than age 10, panic and depression interacted to predict multiple anxiety disorders (p=0.001), with the risk higher for the panic-only group compared with the panic-plus-depression group (hazard ratio=2.3, 95% CI=1.5–3.6; z=3.88, p<0.001); for children age 10 and older, only parental panic predicted multiple anxiety disorders (hazard ratio=4.1, 95% CI=1.4– 11.8; z=2.58, p=0.01).
Functional and Treatment Outcomes in Offspring
Parental depression, independently of parental panic (Table 2), predicted a 2.4-point lower current GAF score (p=0.004), a 5.0-point lower lifetime GAF score (p<0.001), and a greater risk for hospitalization (odds ratio=5.2, 95% CI=1.2–21.9, p=0.02) and for academic tutoring (odds ratio=2.2, 95% CI=1.1–4.2, p=0.02). Parental panic, independently of parental depression, predicted a 1.8-point lower current GAF score (p=0.03). No significant effects of parental disorder were observed for the Social Adjustment Inventory for Children and Adolescents.
| Characteristic | Offspring of Parents With Panic Disorder and Major Depression (N=137) | Offspring of Parents With Panic Disorder (N=26) | Offspring of Parents With Major Depression (N=48) | Offspring of Comparison Parents (N=80) | Test Statistics | |||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Effect of Parental Panic Disorder | Effect of Parental Major Depression | |||||||||||
| Mean | SD | Mean | SD | Mean | SD | Mean | SD | t | p | t | p | |
| Psychosocial functioning | ||||||||||||
| Social Adjustment Inventory for Children and Adolescents | 1.9 | 0.4 | 1.9 | 0.4 | 1.8 | 0.4 | 1.6 | 0.4 | 1.18a | 0.24 | 0.83a | 0.41 |
| Global Assessment of Functioning | ||||||||||||
| Current | 62.1 | 7.4 | 64.6 | 5.6 | 63.9 | 6.1 | 66.2 | 5.8 | −2.14b | 0.03 | −2.92b | 0.004 |
| Lifetime | 53.9 | 8.7 | 59.2 | 6.0 | 55.5 | 7.6 | 60.3 | 7.6 | −0.56b | 0.58 | −0.16b | <0.0001 |
| N | % | N | % | N | % | N | % | z | p | z | p | |
| School functioning | ||||||||||||
| Repeated grade | 17 | 12 | 1 | 4 | 6 | 12 | 5 | 6 | −045 | 0.65 | 1.61 | 0.11 |
| Needed tutoring | 65 | 48 | 10 | 38 | 28 | 58 | 26 | 32 | −0.90 | 0.37 | 2.38 | 0.02 |
| Placed in special class | 17 | 12 | 1 | 4 | 4 | 8 | 9 | 11 | −0.44 | 0.66 | 0.42 | 0.68 |
| Treatment history | ||||||||||||
| Counseling only | 39 | 28 | 9 | 35 | 14 | 29 | 16 | 20 | 0.64 | 0.52 | 0.41 | 0.68 |
| Pharmacotherapy only | 11 | 8 | 4 | 15 | 4 | 8 | 6 | 8 | 0.57 | 0.57 | −0.68 | 0.50 |
| Counseling and pharmacotherapy | 30 | 22 | 4 | 15 | 7 | 15 | 8 | 10 | 1.33 | 0.18 | 1.12 | 0.26 |
| Psychiatric hospitalization | 11 | 8 | 0 | 0 | 4 | 8 | 2 | 2 | −1.10 | 0.27 | 2.26 | 0.02 |
a
df=81.
b
df=136.
Discussion
This 10-year follow-up study of children at risk for panic and depression showed that parental panic predicted elevated risks for anxiety disorders in offspring and lower global functioning, even after controlling for parental depression. In contrast, parental depression independently predicted greater risks for mood, disruptive behavior, and substance use disorders, more impaired functioning, and greater school dysfunction and psychiatric hospitalization. In addition, high-risk offspring had earlier onset of disorders than comparison offspring, and they remained at risk for onset of new disorders in adolescence, with parental panic conferring risk for new social phobia, and parental depression conferring risk for new major depression.
The finding that parental panic independently predicted offspring panic and agoraphobia confirms our previous findings when the children were 5 years younger (5) and is consistent with family studies documenting specific aggregation of panic and agoraphobia in first-degree relatives of probands with panic (19). Also consistent with the literature are findings that parental panic was associated with risk for multiple anxiety disorders as well as for OCD and social phobia (20). This may be related to the fact that individuals with panic tend to have comorbid anxiety disorders; indeed, the parents with panic in our study had higher rates of generalized anxiety disorder, social phobia, and OCD than comparison parents. These findings underscore the breadth of risk to offspring conferred by parental panic and suggest that anxiety disorders present earlier in childhood are likely to persist into adolescence.
Our finding that parental depression confers an elevated risk for mood disorders in adolescents is consistent with previous studies showing a greater risk for depression in first-degree relatives and offspring of depressed adults (4, 5, 21–23). The elevated risk for bipolar disorder also supports the hypothesis of continuity between unipolar and bipolar mood disorders. That parental depression was associated with a greater risk for disruptive behavior disorder is in line with earlier findings in this sample (5, 24) and others (25); that parental depression was associated with a greater risk for substance use disorders also accords with a growing literature documenting this association (22, 23).
Our finding that parental panic did not increase the risk of offspring depression conflicts with a meta-analysis showing elevated rates of depression in offspring of parents with anxiety (20). Although the reasons for this discrepancy remain unclear, many of the studies included in the meta-analysis did not exclude mood disorders in anxious parents; therefore, elevated depression rates in offspring of anxious parents may be the result of comorbid parental mood disorders. Our findings also contrast with those of the Sequenced Treatment Alternatives to Relieve Depression (STAR*D) study, in which current comorbid panic and agoraphobia in depressed mothers was associated with higher rates of offspring depression compared with maternal depression alone (26). Notably, most mothers in the STAR*D sample had acute depression with high functional impairment; current panic with agoraphobia may have compounded this impairment, leading to a higher risk for depression in offspring. In contrast, our study assessed offspring of parents with lifetime depression and panic, many of whom were not acutely symptomatic. Further studies examining independent effects of parental anxiety versus mood disorders and including probands with a range of acuity are needed to disentangle the risks conferred by both disorders.
At this follow-up, parental depression was not independently associated with a greater risk for anxiety disorders in offspring, with the exception of specific phobia, which increased in prevalence among all offspring groups. This finding is discrepant with a recent family study (27) that found that rates of specific phobia did not differ between offspring of parents with depression only, anxiety only, both, or neither (although rates of specific fears were elevated among offspring of parents with both disorders). However, our findings are consistent with that of Kessler and colleagues (28) suggesting that specific phobia is associated with many subsequent disorders and with Weissman and colleagues’ finding (22) that specific phobia was the only anxiety disorder with an elevated rate among offspring at risk for depression followed into adulthood. Indeed, the rate of comorbid specific phobia among depressed parents in our sample was elevated relative to comparison parents (28% compared with 6%). Other than specific phobia, parental depression was not associated with a greater risk for anxiety in offspring, in contrast to other studies (e.g., references 23, 29, 30). This may be because we covaried parental panic whereas other studies did not. More research is needed to confirm whether elevated risk for anxiety is conferred by parental depression or due to comorbid anxiety in the probands.
The nonsignificant association between parental depression and current (as opposed to lifetime) disorders may be explained by the episodic nature of mood disorders, the tendency for disruptive behavior disorders to resolve by adolescence, and statistical power issues related to the relatively low rates of substance use disorders and mania in the offspring.
A more nuanced picture of the developmental sequence of risk in offspring of parents with depression emerges in the trajectory of risk across the three waves of data. At baseline (mean age, 6.8 years), parental depression independently conferred risks for social phobia and separation anxiety disorder. By 5-year (mean age, 10 years) and 10-year (mean age, 15 years) follow-ups, parental depression conferred risks for mood and disruptive behavior disorders. Similarly, risks for multiple anxiety disorders differed before and after age 10, with parental depression contributing to earlier risk, but only parental panic contributing to later risk. That parental depression confers selective risk for anxiety disorders early in life, but not later on, is consistent with findings that anxiety disorders precede mood disorders in offspring at risk for mood disorders (31).
Although panic disorder in both fathers and mothers appeared to be associated with similar risks for offspring anxiety disorders (particularly panic and agoraphobia), we noted some differences in the risks conferred. Maternal panic disorder was associated with a higher risk for offspring social phobia, while paternal panic was associated with offspring OCD. Whereas both maternal and paternal depression were associated with a greater risk for offspring depression, maternal depression was associated with a broader range of offspring disorders, including bipolar disorder, separation anxiety, and drug use disorders. Future studies should extend these findings by examining factors that contribute to differences between risks conferred by mothers and those conferred by fathers.
Our study’s strengths include its large sample size, systematic assessments in parents and offspring, three collection points spanning early childhood to midadolescence, diagnostic data on fathers as well as mothers, and analyses examining independent effects of parental panic versus depression. Another strength of the study lies in our analysis of the differential effects of maternal versus paternal panic and depression on lifetime rates of psychiatric disorders in offspring.
However, many offspring were still within the age of risk for disorders, which may have led to an underestimate of risks. Although we collected data at three time points, lifetime diagnoses and ages at onset were based on retrospective reports, which may have been subject to biased recall. To minimize bias, we used ages at onset reported in the wave when the disorder was first endorsed, so that individuals did not have to recall onsets over a window greater than 5 years. Our study was limited by the fact that diagnostic information for children under 12 was derived from parent reports. We did not directly interview younger children about their lifetime diagnoses because children under 12 may be limited in their ability to understand questions from diagnostic interviews (32) and to map events in time and have been found to be unreliable in their reports of psychopathology (33, 34). In contrast, maternal reports of psychopathology have shown high reliability (35, 36). It is possible that affected parents overreported their children’s symptoms or that unaffected parents underreported their children’s problems (37). However, we incorporated adolescent self-report for individuals 12 and older, which included most of the offspring in the present wave.
It might be argued that considering a diagnosis as present if endorsed by either the parent or the adolescent may inflate the rate of diagnoses. Because teenagers may not always accurately report their symptoms, or might hesitate to report them, we opted to supplement adolescent reports with parental reports. Agreement about the presence or absence of disorders for the 212 participants for whom we had both mother and adolescent reports ranged from 82% (for specific phobia) to 98% (for OCD and conduct disorder). When we repeated analyses considering diagnoses positive only when both informants agreed, most predictions of child disorders from parental panic and depression remained significant. Future studies could reexamine risks using different approaches to combine discrepant reports.
Although the groups had different rates of attrition, participants did not differ from nonparticipants on baseline demographic characteristics, functional scores, or rates of anxiety or mood disorders. The offspring of depressed parents had lower baseline rates of disruptive behavior disorders; since early disruptive behavior disorders may increase the risk for later substance use or bipolar disorder, this difference may have led to underestimates of psychopathology in depression offspring. The groups also differed in age, with the offspring of depression-only parents being younger than those of parents with depression plus panic, in part because their siblings were younger. However, all findings were controlled for age; moreover, our major analyses focused on predictive effects of parental depression controlling for panic and were not affected by this age difference, since the age difference of offspring of parents with and without depression was not significant. Because proband parents were clinically referred, the generalizability of findings is limited to the offspring of referred patients. However, previously reported findings in this sample were similar to those observed in a nonreferred sample (38). Because of low ethnic and socioeconomic diversity in the sample, the results may not generalize to non-Caucasians and participants from more varied socioeconomic backgrounds. Finally, our analyses did not examine differences by offspring sex.
Despite these limitations, we found distinct patterns of risk conferred by parental panic and depression, with panic conferring risk for panic, agoraphobia, OCD, and social phobia, and depression conferring risk for mood, disruptive behavior, and substance use disorders, and both conferring risk for specific phobia. At-risk youths continued to develop new-onset disorders through adolescence. These results highlight the importance of monitoring offspring of patients with panic disorder and major depressive disorder and referring them for early or preventive intervention.
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Information & Authors
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History
Received: 13 October 2011
Revision received: 13 March 2012
Revision received: 1 June 2012
Accepted: 21 June 2012
Published online: 1 November 2012
Published in print: November 2012
Authors
Funding Information
Drs. Hirshfeld-Becker, Henin, and Micco have received honoraria from Reed Medical Education (a logistics collaborator for the MGH Psychiatry Academy). The education programs conducted by the MGH Psychiatry Academy were supported, in part, through independent medical education grants from pharmaceutical companies, including AstraZeneca, Bristol-Myers Squibb, Forest Laboratories, Janssen, Lilly, McNeil Pediatrics, Pfizer, Pharmacia, the Prechter Foundation, Sanofi-Aventis, Shire, the Stanley Foundation, UCB Pharma, and Wyeth. Dr. Henin also has received honoraria from Shire, Abbott Laboratories, and the American Academy of Child and Adolescent Psychiatry, has been a consultant for Pfizer, Prophase, and Concordant Rater Systems, and receives royalties from Oxford University Press. Dr. Faraone has served as a consultant or adviser to, received research support from, or participated in continuing medical education programs sponsored by Alcobra, Eli Lilly, Janssen, McNeil, NIH, Novartis, Otsuka, Pfizer, and Shire, and he receives royalties from Guilford Press and Oxford University Press. Dr. Biederman has received research support from Elminda, Janssen, McNeil, and Shire; speaking fees from Fundacion Areces (Spain), Fundacion Dr. Manuel Camelo A.C., Medice Pharmaceuticals, and the Spanish Child Psychiatry Association; consulting fees from Shionogi Pharma and Cipher Pharmaceuticals (honoraria were paid to the Department of Psychiatry at Massachusetts General Hospital [MGH]); honoraria from the MGH Psychiatry Academy for a tuition-funded CME course; an honorarium from Cambridge University Press for a chapter publication; and departmental royalties for a rating scale used for ADHD diagnosis (paid by Eli Lilly, Shire, and AstraZeneca to the Department of Psychiatry at MGH). Dr. Rosenbaum serves on the scientific advisory board of Medavante and has equity holdings at Medavante. The other authors report no financial relationships with commercial interests.
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Supported by NIMH grant R01 47077.Metrics & Citations
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