Familiality of Psychiatric Disorders and Risk of Postpartum Psychiatric Episodes: A Population-Based Cohort Study
Publication: American Journal of Psychiatry
Abstract
Objective:
Postpartum psychiatric disorders are common and morbid complications of pregnancy. The authors sought to evaluate how family history of psychiatric disorders is associated with postpartum psychiatric disorders in proband mothers with and without a prior psychiatric history by assessing degree of relationship, type of disorder, and sex of family members.
Method:
The authors linked Danish birth and psychiatric treatment registers to evaluate familial risk of postpartum psychiatric episodes in a national population-based cohort. Probands were first-time mothers who were born in Denmark in 1970 or later and who gave birth after age 15 and before Dec. 31, 2012 (N=362,462). The primary exposure was a diagnosed psychiatric disorder in a relative. Cox regression models were used to estimate the hazard ratio of postpartum psychiatric disorders in proband mothers.
Results:
The relative risk of psychiatric disorders in the postpartum period was elevated when first-degree family members had a psychiatric disorder (hazard ratio=1.45, 95% CI=1.28–1.65) and highest when proband mothers had a first-degree family member with bipolar disorder (hazard ratio=2.86, 95% CI=1.88–4.35). Associations were stronger among proband mothers with no previous psychiatric history. There were no notable differences by sex of the family member.
Conclusions:
Family history of psychiatric disorders, especially bipolar disorder, is an important risk factor for postpartum psychiatric disorders. To assist in identification of women at risk for postpartum psychiatric disorders, questions related to female and male first-degree relatives with bipolar disorder are of the highest importance and should be added to routine clinical screening guidelines to improve prediction of risk.
The postpartum period is a vulnerable time for onset of psychiatric disorders, as it is one of the few identified periods of heightened risk throughout the life course (1–3). A prior history of a psychiatric disorder either within or outside the perinatal period increases the risk of experiencing a postpartum psychiatric disorder (3–8). Although personal psychiatric history is a highly predictive risk factor for postpartum psychiatric disorders, predicting who will experience a new-onset psychiatric disorder in the postpartum period remains a significant challenge.
Family psychiatric history is a strong and consistent risk factor for psychiatric disorders outside the perinatal period (9, 10). Perinatal mood disorders may be more heritable than other mood disorders; the heritability for perinatal depression is estimated to be 44% (11), compared with 37% for major depressive disorder (12, 13). Heritability of other types of perinatal psychiatric disorders is unknown. A family history of a postpartum mood disorder in a mother or sister doubles or triples the risk of experiencing a postpartum mood disorder (14–16), and postpartum psychosis in a mother or sister increases the risk of postpartum psychosis fivefold (14). A family history of nonpostpartum mood disorders is also associated with postpartum mood disorders, especially for bipolar disorder and the most severe postpartum episodes, such as postpartum psychosis (14, 16–19). Studies of postpartum psychosis, however, have been conducted primarily in high-risk populations of women and their families with previously diagnosed psychiatric disorders. Much less is known about how familiality of psychiatric disorders outside the perinatal period influences postpartum psychiatric disorders for the broader spectrum of psychiatric disorders, particularly in women without a personal psychiatric history. The few existing population-based studies examining the association between family history of nonpostpartum mood disorders and postpartum mood disorders have not investigated specific types of psychiatric disorders among different degrees of familial relationships (3, 20).
Previous work has not explored whether the familial associations of postpartum psychiatric disorders are related to a specific female vulnerability (e.g., mother to daughter). Because previous studies of familiality of postpartum psychiatric disorders have primarily evaluated the relationship between postpartum mood disorders in proband mothers and postpartum mood disorders in first-degree relatives, most have exclusively evaluated pairs of female relatives (e.g., mother–daughter or sister–sister pairs) (11, 14–16, 21, 22). Among studies that included both male and female relatives with psychiatric disorders outside the perinatal period, none have evaluated the difference in recurrence risk among female relatives compared with male relatives (11, 17). Understanding the degree to which familial history of psychiatric disorders predicts risk for postpartum psychiatric disorders would substantially aid our ability to identify women at greatest risk for postpartum psychiatric disorders and intervene early.
We aimed to address this gap in the literature by evaluating how family history of psychiatric disorders influences risk for postpartum psychiatric episodes. We wanted to evaluate whether familial risk of postpartum psychiatric disorders differs by degree of relationship and sex of the family members in women both with and without a prior personal psychiatric history. To address these aims, we conducted a population-based study of recurrence risk (the likelihood that a trait in one family member will occur in another family member) (23–25), a study design frequently applied in psychiatric genetics (10, 14, 16, 25, 26). Recurrence risk studies typically evaluate the same disorder in family members (e.g., postpartum depression in both a proband mother and her sister). In our study, we sought to determine the unique familial contributions of psychiatric disorders outside the perinatal period to psychiatric events within the postpartum period; thus, we considered the recurrent event (a psychiatric diagnosis within the postpartum period) to be different from the familial event (a psychiatric diagnosis at any time point). We refer here to this specific type of recurrence risk as “familial risk.”
Method
Study Population
We conducted a population-based cohort study within the Danish Civil Registration System (27). A unique personal identifier for every person living in Denmark allows comprehensive linkages with multiple health-related national registers as well as linkages to family members. Proband mothers were selected from among all women born in Denmark from 1970 onward with nonmissing links to both parents (N=1,336,419). Proband mothers were all first-time mothers who gave live birth when at least 15 years of age and before the end of follow-up on Dec. 31, 2012. A total of 362,462 proband mothers were included in our study (Figure 1).
Identification of Postpartum Psychiatric Episodes
Our outcome of interest was a psychiatric episode diagnosis during the postpartum period in proband mothers. Information on psychiatric episodes was obtained from the Psychiatric Central Register (28), which contains information on inpatient treatment since 1969 and outpatient treatment since 1995. Outpatient diagnoses come from specialty psychiatric clinics and do not include diagnoses from primary care settings. Diagnoses are recorded using ICD codes (ICD-8 before 1994 and ICD-10 1994 and later). We defined a postpartum psychiatric disorder as a treated psychiatric episode (ICD-8 codes 290–315; ICD-10 codes F00–F99), excluding organic mental disorders (ICD-8 codes 290.09, 290.10, 290.11, 290.18, 290.19, 292.x9, 293.x9, 294.x9, and 309.x9; ICD-10 codes F00–F09), substance abuse (ICD-8 codes 291.x9, 294.39, 303.x9, 303.20, 303.28, 303.90, and 304.x9; ICD-10 codes F10–F19), and mental retardation (ICD-8 codes 310–315; ICD-10 codes F70–F79), which have been well validated in these registries (28, 29). For our primary analysis, we considered the postpartum period to be 0 to 6 months after childbirth. Previous work in our data has indicated increasing vulnerability for depressive episodes up to 6 months after childbirth (2), and we wanted to ensure that we accounted for a potential delay between symptom onset and recorded diagnosis. In sensitivity analyses, we also examined two other periods separately: 0 to 3 months postpartum, a more narrowly defined and possibly more etiologically similar phenotype (30–32); and 0 to 12 months postpartum, an increasingly applied clinical definition for the postpartum period (30, 33, 34).
Identification of Relatives of Proband Mothers and Family History of Psychiatric Episodes
To identify relatives, proband mothers were linked to their parents by unique identifier, and subsequent family relationships were identified through these linkages. The degree of relationship of family members was defined as follows: first-degree relatives included mother, father, and full sibling; second-degree relatives included grandparents, half siblings, uncles, and aunts; third-degree relatives included cousins. Because the Danish Civil Registration System (27) was established in 1968, we were unable to identify all people born before that time; thus, second- and third-degree relationships are less complete.
Among the proband mothers included in our study population, we considered the association between a postpartum psychiatric disorder and any psychiatric disorder in our categorized relatives. Furthermore, we investigated specifically five hierarchical diagnostic groups of psychiatric disorders in the relatives: 1) schizophrenia and related disorders (highest in hierarchy; ICD-10 codes F20–F29); 2) bipolar disorder (ICD-10 codes F30–F31); 3) unipolar disorder (ICD-10 codes F32–F33); 4) other mood disorders, excluding bipolar and unipolar disorders (ICD-10 codes F34–F39); and 5) other psychiatric disorders (lowest in hierarchy; ICD-10 codes F40–F69 and F80–F99). This hierarchical system is built into the ICD diagnostic system and accounts for individuals with more than one recorded diagnosis.
Statistical Analysis
We started follow-up at the date of childbirth for each proband mother and followed her until a postpartum psychiatric episode, 6 months postpartum (3 or 12 months in sensitivity analyses), death, emigration, or Dec. 31, 2012, whichever came first. We restricted proband mothers to first-time mothers for several reasons: history of postpartum depression increases risk in subsequent pregnancies; previous birth outcome may influence later reproductive behavior; and environmental factors during the postpartum period are different after first and subsequent births. To ensure that detection of a psychiatric diagnosis in a relative occurred before the postpartum psychiatric diagnosis and was not dependent on the proband mother’s age at childbirth, we assessed whether the relatives had a diagnosis of a psychiatric disorder on or before the proband mother’s 15th birthday, going back to 1970. We adjusted for calendar year and the proband mother’s age at childbirth.
We evaluated the association by determining familial risk, a register-based estimate of the risk of experiencing a postpartum psychiatric disorder when a relative of a proband mother had a psychiatric disorder. We further examined the association of postpartum psychiatric disorders with each of the five hierarchical psychiatric disorders. We used Cox regression analysis to calculate hazard ratios. Given that postpartum psychiatric disorders among proband mothers with a psychiatric history prior to childbirth may be a distinct psychiatric phenotype, we separately examined the associations in proband mothers with and without previous psychiatric history.
To estimate whether the associations between family history of psychiatric disorders and postpartum psychiatric disorders were due to a genetic contribution or shared environmental factors, we repeated the analyses by first-, second-, and third-degree relatives and sex of the relatives with a psychiatric disorder. If an increased risk is due to familial factors attributable to nongenetic factors shared by nuclear families, we would expect to see excess risk only among first-degree relatives. Conversely, if the increased risk is due, at least in part, to a genetic contribution, we would expect to see excess risk among both close and distant relatives in line with their coefficient of relationship.
Statistical analyses were performed using Stata, version 13.1 (www.stata.com).
Results
The final population-based cohort consisted of 362,462 proband mothers who gave birth to their first child in Denmark between 1985 and 2012. The mean age of proband mothers was 27.0 years (SD=4.3) at time of delivery. Of these mothers, 2,603 (0.7%) experienced a psychiatric disorder within 6 months postpartum and 4,085 (1.1%) within 12 months postpartum (Table 1).
| Probands With No Prior Psychiatric History (N=339,112) | Probands With Prior Psychiatric History (N=23,350) | |||||||
|---|---|---|---|---|---|---|---|---|
| Characteristic | Postpartum Episode Within 6 Months (N=1,585) | Postpartum Episode Within 12 Months (N=2,421) | Postpartum Episode Within 6 Months (N=1,018) | Postpartum Episode Within 12 Months (N=1,664) | ||||
| Mean | SD | Mean | SD | Mean | SD | Mean | SD | |
| Age at first childbirth (years) | 27.0 | 4.3 | 26.5 | 4.6 | 26.7 | 4.7 | 26.3 | 4.7 |
| N | % | N | % | N | % | N | % | |
| Birth year of proband mother | ||||||||
| 1985–1994 | 35 | 2.2 | 73 | 3.0 | 12 | 1.2 | 16 | 1.0 |
| 1995–1999 | 254 | 16.0 | 391 | 16.2 | 99 | 9.7 | 151 | 9.1 |
| 2000–2004 | 392 | 24.7 | 619 | 25.6 | 203 | 19.9 | 343 | 20.6 |
| 2005–2009 | 588 | 37.1 | 902 | 37.3 | 438 | 43.0 | 709 | 42.6 |
| 2010–2012 | 316 | 19.9 | 436 | 18.0 | 266 | 26.1 | 445 | 26.7 |
| Familial psychiatric history | ||||||||
| Any psychiatric diagnosis | ||||||||
| Mother | 70 | 4.4 | 109 | 4.5 | 84 | 8.3 | 145 | 8.7 |
| Father | 57 | 3.6 | 85 | 3.5 | 51 | 5.0 | 88 | 5.3 |
| First-degree relative | 132 | 8.3 | 203 | 8.4 | 141 | 13.9 | 244 | 14.7 |
| Second-degree relative | 173 | 10.9 | 281 | 11.6 | 163 | 16.0 | 294 | 17.7 |
| Third-degree relative | 47 | 3.0 | 76 | 3.1 | 49 | 4.8 | 97 | 5.8 |
| Schizophrenia | ||||||||
| First-degree relative | 43 | 2.7 | 60 | 2.5 | 46 | 4.5 | 65 | 3.9 |
| Second-degree relative | 58 | 3.7 | 91 | 3.8 | 45 | 4.4 | 78 | 4.7 |
| Third-degree relative | 8 | 0.5 | 11 | 0.5 | 7 | 0.7 | 11 | 0.7 |
| Bipolar disorder | ||||||||
| First-degree relative | 13 | 0.8 | 18 | 0.7 | 9 | 0.9 | 14 | 0.8 |
| Second-degree relative | 7 | 0.4 | 13 | 0.5 | 8 | 0.8 | 10 | 0.6 |
| Third-degree relative | 0 | 0 | <4b | 0 | 0 | 0 | 0 | |
| Unipolar disorder | ||||||||
| First-degree relative | 50 | 3.2 | 81 | 3.3 | 46 | 4.5 | 83 | 5.0 |
| Second-degree relative | 73 | 4.6 | 118 | 4.9 | 66 | 6.5 | 125 | 7.5 |
| Third-degree relative | <4b | 5 | 0.2 | 6 | 0.6 | 12 | 0.7 | |
| Other mood disorder | ||||||||
| First-degree relative | 9 | 0.6 | 12 | 0.5 | 4 | 0.4 | 14 | 0.8 |
| Second-degree relative | 4 | 0.3 | 14 | 0.6 | 6 | 0.6 | 11 | 0.7 |
| Third-degree relative | 0 | 0 | 0 | 0 | 0 | 0 | <4b | |
| Other psychiatric disorder | ||||||||
| First-degree relative | 21 | 1.3 | 41 | 1.7 | 43 | 4.2 | 81 | 4.9 |
| Second-degree relative | 57 | 3.6 | 103 | 4.3 | 68 | 6.7 | 125 | 7.5 |
| Third-degree relative | 37 | 2.3 | 62 | 2.6 | 40 | 3.9 | 81 | 4.9 |
a
Total proband mothers (N=362,462).
b
Number of observations less than four cannot be presented due to possible identification of personal information.
As described, we evaluated familial risk, a register-based estimate of the risk of experiencing a postpartum psychiatric disorder when a relative of a proband mother had a psychiatric disorder. Results are presented for familial risk of postpartum psychiatric episodes within 6 months postpartum, but results were similar for the 0- to 3-month and 0- to 12-month periods postpartum (see Tables S1 and S2 in the data supplement that accompanies the online edition of this article). Overall, the hazard of experiencing a psychiatric disorder within the first 6 months postpartum was higher among proband mothers with a first-degree relative who had experienced any psychiatric disorder compared with proband mothers whose relatives did not experience any psychiatric disorder (hazard ratio=1.45, 95% CI=1.28–1.65). The hazard ratio of experiencing a postpartum psychiatric episode was highest when proband mothers had a first-degree relative with bipolar disorder (hazard ratio=2.86, 95% CI=1.88–4.35). Familial risk was also elevated for those who had a first-degree relative with schizophrenia (hazard ratio=1.58, 95% CI=1.27–1.95), unipolar disorder (hazard ratio=1.52, 95% CI=1.24–1.87), or other mood disorder (hazard ratio=1.78, 95% CI=1.03–3.06), but not other psychiatric disorders (hazard ratio=0.90, 95% CI=0.70–1.16). The point estimates tended to be larger for proband mothers with no previous psychiatric history (Table 2, Figure 2). We found that prior psychiatric history was a strong risk factor for postpartum psychiatric disorders (hazard ratio=8.66, 95% CI=7.97–9.40 for postpartum disorders in women with a prior psychiatric history compared with women with no psychiatric history, adjusted for psychiatric disorders in first-, second-, and third-degree relatives).
| Relationship to Proband New Mother | Relatives With Any Psychiatric Versus No Psychiatric Disorder | Relatives With Schizophrenia Versus No Schizophrenia | Relatives With Bipolar Disorder Versus No Bipolar Disorder | Relatives With Unipolar Disorder Versus No Unipolar Disorder | Relatives With Other Mood Disorders Versus No Other Mood Disorder | Relatives With Other Psychiatric Disorders Versus No Other Psychiatric Disorder | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Hazard Ratio | 95% CI | Hazard Ratio | 95% CI | Hazard Ratio | 95% CI | Hazard Ratio | 95% CI | Hazard Ratio | 95% CI | Hazard Ratio | 95% CI | |
| All proband mothersa | ||||||||||||
| Mother | 1.50 | 1.27–1.77 | 1.58 | 1.19–2.10 | 2.43 | 1.34–4.39 | 1.58 | 1.21–2.05 | 1.82 | 0.81–4.05 | 1.02 | 0.71–1.46 |
| Father | 1.54 | 1.27–1.87 | 1.66 | 1.20–2.30 | 3.47 | 1.87–6.46 | 1.52 | 1.10–2.10 | 1.87 | 0.89–3.92 | 0.92 | 0.56–1.51 |
| Any first-degree relative | 1.45 | 1.28–1.65 | 1.58 | 1.27–1.95 | 2.86 | 1.88–4.35 | 1.52 | 1.24–1.87 | 1.78 | 1.03–3.06 | 0.90 | 0.70–1.16 |
| Any second-degree relative | 1.16 | 1.02–1.31 | 1.09 | 0.89–1.33 | 1.11 | 0.67–1.84 | 1.15 | 0.97–1.37 | 1.01 | 0.54–1.88 | 1.16 | 0.96–1.41 |
| Any third-degree relative | 1.27 | 1.03–1.58 | 2.15 | 1.29–3.58 | — | — | 1.39 | 0.72–2.68 | — | — | 1.16 | 0.92–1.47 |
| Proband mothers with no prior psychiatric historyb | ||||||||||||
| Mother | 1.78 | 1.40–2.27 | 1.96 | 1.31–2.93 | 3.53 | 1.68–7.42 | 1.56 | 1.04–2.34 | 3.33 | 1.27–8.88 | 1.19 | 0.65–2.16 |
| Father | 1.92 | 1.47–2.51 | 1.54 | 0.93–2.57 | 3.99 | 1.79–8.89 | 2.20 | 1.48–3.27 | 3.10 | 1.29–7.47 | 1.01 | 0.45–2.26 |
| Any first-degree relative | 1.76 | 1.47–2.11 | 1.82 | 1.34–2.47 | 3.61 | 2.09–6.23 | 1.85 | 1.39–2.45 | 3.10 | 1.61–5.97 | 0.90 | 0.58–1.40 |
| Any second-degree relative | 1.35 | 1.14–1.60 | 1.35 | 1.04–1.76 | 0.98 | 0.47–2.07 | 1.30 | 1.02–1.66 | 0.92 | 0.34–2.46 | 1.38 | 1.04–1.82 |
| Any third-degree relative | 1.46 | 1.08–1.98 | 2.68 | 1.33–5.39 | — | — | 1.10 | 0.35–3.43 | — | — | 1.31 | 0.94–1.84 |
| Proband mothers with prior psychiatric historyb | ||||||||||||
| Mother | 1.35 | 1.08–1.69 | 1.32 | 0.88–1.97 | 1.56 | 0.58–4.17 | 1.59 | 1.13–2.23 | 0.94 | 0.24–3.78 | 1.05 | 0.68–1.64 |
| Father | 1.28 | 0.97–1.70 | 1.74 | 1.14–2.65 | 2.79 | 1.04–7.45 | 0.97 | 0.56–1.67 | 0.90 | 0.22–3.60 | 0.96 | 0.51–1.80 |
| Any first-degree relative | 1.27 | 1.06–1.52 | 1.39 | 1.03–1.86 | 2.17 | 1.13–4.18 | 1.28 | 0.95–1.73 | 0.89 | 0.33–2.36 | 0.99 | 0.72–1.36 |
| Any second-degree relative | 1.03 | 0.86–1.24 | 0.88 | 0.65–1.19 | 1.28 | 0.64–2.57 | 1.05 | 0.81–1.36 | 1.12 | 0.50–2.50 | 1.11 | 0.85–1.44 |
| Any third-degree relative | 1.21 | 0.90–1.64 | 1.91 | 0.90–4.03 | — | — | 1.76 | 0.78–3.95 | — | — | 1.13 | 0.81–1.57 |
a
Adjusted for calendar year at delivery and age at delivery and stratified by prior psychiatric history of the proband mothers.
b
Adjusted for calendar year at delivery and age at delivery.
FIGURE 2. Familial Risk of Psychiatric Episodes Within 6 Months Postpartum in Proband Mothers With and Without a Personal Psychiatric History, by Type of Disorder and Sex in Relativesa
a Error bars indicate 95% confidence intervals.
Familial risk of postpartum psychiatric disorders was elevated when first-degree relatives had experienced psychiatric disorders, as described above, and slightly elevated for familial psychiatric disorders among more distant relatives (for any psychiatric disorder, second-degree relatives: hazard ratio=1.16, 95% CI=1.02–1.31; third-degree relatives: hazard ratio=1.27, 95% CI=1.03–1.58). More distant relatives share both a reduced coefficient of relationship (see Figure S1 in the online data supplement ) and reduced shared family environment.
The familial risk of postpartum disorders in proband mothers whose mothers had psychiatric disorders (hazard ratio=1.50, 95% CI=1.27–1.77 for mothers) was similar to that of proband mothers whose fathers had psychiatric disorders (hazard ratio=1.54, 95% CI=1.27–1.87 for fathers). This pattern persisted for all five diagnostic groups of psychiatric disorders (Table 2). Likewise, when we assessed familial risk separately in female and male relatives more generally, we did not observe differences by sex for either any psychiatric disorder or specific diagnostic groups of psychiatric disorders for any degree of relationship (Table 3, Figure 2).
| Relationship to Proband New Mother | Relatives With Any Psychiatric Disorder Versus No Psychiatric Disorder | Relatives With Schizophrenia Versus No Schizophrenia | Relatives With Bipolar Disorder Versus No Bipolar Disorder | Relatives With Unipolar Disorder Versus No Unipolar Disorder | Relatives With Other Mood Disorders Versus No Other Mood Disorder | Relatives With Other Psychiatric Disorders Versus No Other Psychiatric Disorder | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Hazard Ratio | 95% CI | Hazard Ratio | 95% CI | Hazard Ratio | 95% CI | Hazard Ratio | 95% CI | Hazard Ratio | 95% CI | Hazard Ratio | 95% CI | |
| All proband mothersa | ||||||||||||
| Any first-degree relative | 1.45 | 1.28–1.65 | 1.58 | 1.27–1.95 | 2.86 | 1.88–4.35 | 1.52 | 1.24–1.87 | 1.78 | 1.03–3.06 | 0.90 | 0.70–1.16 |
| Female relative | 1.36 | 1.16–1.59 | 1.48 | 1.13–1.95 | 2.48 | 1.40–4.37 | 1.51 | 1.17–1.95 | 1.68 | 0.75–3.74 | 0.92 | 0.70–1.22 |
| Male relative | 1.32 | 1.11–1.57 | 1.52 | 1.12–2.06 | 3.45 | 1.91–6.23 | 1.45 | 1.07–1.98 | 1.73 | 0.83–3.64 | 0.84 | 0.60–1.16 |
| Proband mothers with no prior psychiatric historyb | ||||||||||||
| Any first-degree relative | 1.76 | 1.47–2.11 | 1.82 | 1.34–2.47 | 3.61 | 2.09–6.23 | 1.85 | 1.39–2.45 | 3.10 | 1.61–5.97 | 0.90 | 0.58–1.40 |
| Female relative | 1.61 | 1.27–2.02 | 2.02 | 1.40–2.91 | 3.30 | 1.57–6.93 | 1.60 | 1.09–2.36 | 3.07 | 1.15–8.18 | 0.95 | 0.58–1.54 |
| Male relative | 1.72 | 1.35–2.19 | 1.60 | 1.02–2.51 | 3.66 | 1.64–8.16 | 2.28 | 1.57–3.32 | 2.91 | 1.21–7.00 | 0.81 | 0.46–1.44 |
| Proband mothers with prior psychiatric historyb | ||||||||||||
| Any first-degree relative | 1.27 | 1.06–1.52 | 1.39 | 1.03–1.86 | 2.17 | 1.13–4.18 | 1.28 | 0.95–1.73 | 0.89 | 0.33–2.36 | 0.99 | 0.72–1.36 |
| Female relative | 1.24 | 1.01–1.53 | 1.12 | 0.75–1.68 | 1.84 | 0.76–4.42 | 1.45 | 1.03–2.05 | 0.87 | 0.22–3.50 | 1.01 | 0.71–1.43 |
| Male relative | 1.09 | 0.85–1.41 | 1.45 | 0.96–2.19 | 3.14 | 1.30–7.56 | 0.83 | 0.48–1.44 | 0.83 | 0.21–3.34 | 0.93 | 0.62–1.40 |
a
Hazard ratios are adjusted for calendar year at delivery and age at delivery and stratified by prior psychiatric history of the proband mothers.
b
Hazard ratios are adjusted for calendar year at delivery and age at delivery.
Discussion
We used linked Danish birth and psychiatric registry data to determine familial risk of postpartum psychiatric disorders associated with family history of psychiatric disorders within five hierarchical diagnostic groups. To our knowledge, this study is the first to use a large population-based cohort to investigate familial risk of postpartum psychiatric disorders with psychiatric disorders outside the perinatal period. Our analysis of first-ever postpartum psychiatric disorders provides evidence of the importance of psychiatric disorders in family members, even among women with no personal history of mental illness.
To our knowledge, this is the first study to address whether familial risk of postpartum psychiatric disorders differs by sex of the family member. Since only women can experience a postpartum psychiatric disorder, previous studies of recurrence risk of postpartum psychiatric disorders have exclusively studied female relative pairs (e.g., mother–daughter, sisters) (11, 14–16, 21, 22). However, both males and females experience nonpostpartum psychiatric disorders, and it is unknown whether family history of nonpostpartum psychiatric disorders experienced by male or female relatives differentially influences risk of postpartum psychiatric disorders. Studies of other psychiatric conditions (35) and small studies of mood disorders in selected populations (36, 37) have shown some evidence of greater female heritability or transmission, but larger population-based studies of psychiatric disorders have not found sex differences (10, 38). Consistent with this, we found that although postpartum psychiatric disorders are uniquely female events, a history of psychiatric disorders in male relatives was just as influential as a history of psychiatric disorders in female relatives. Thus, when assessing risk for postpartum episodes, clinicians should inquire about family history of psychiatric disorders broadly and not limit discussion to postpartum psychiatric disorders or psychiatric disorders in female relatives.
We found that familial risk for postpartum psychiatric disorders was higher for family history of bipolar disorder compared with family history of psychiatric disorders, which had previously only been identified for the most severe postpartum psychiatric episodes (14, 17) or among women with a personal history of mood disorders (14–17). Outside the perinatal period, familial risk for bipolar disorder is greater than that of unipolar depression (for bipolar disorder [10], risk ratio=6.4–7.9; for unipolar depression [12], risk ratio=2.8). We found similar patterns in our study of psychiatric disorders within the postpartum period; familial risk was higher with a family history of bipolar disorder than for a family history of unipolar depression (for postpartum episodes with bipolar depression, hazard ratio=2.86, 95% CI=1.88–4.35; for postpartum episodes with unipolar depression, hazard ratio=1.52, 95% CI=1.24–1.87). Our estimates, particularly for familial risk of postpartum disorders with familial bipolar disorder, were similar to previous estimates for postpartum mood disorders overall (risk ratio=2.3–3.9) (14–16). It should be noted that previous recurrence risk studies of postpartum psychiatric disorders have all been conducted in cohorts of women with a prior psychiatric history, whereas we evaluated familial risk separately in women with and without a prior psychiatric history. The link between bipolar disorder and postpartum psychosis is well established (6, 39–42), and recent work in these same data showed that onset of symptoms closer to the time of delivery was associated with a higher risk of conversion to bipolar disorder (18). These findings, together with our findings in the present study demonstrating that family history of bipolar disorder is more strongly associated with any postpartum psychiatric disorder and not only the most severe episodes, provide evidence for a genetic vulnerability or other etiologically similar mechanisms linking bipolar disorder and psychiatric episodes specifically in the postpartum period, which is supported by the literature (6, 14, 17, 39–42).
Our analysis of a large population-based cohort provides the ability to investigate several types of psychiatric events and makes our results more generalizable to the broader population. Most previous studies of familiality of postpartum psychiatric disorders have been conducted in small cohorts or cohorts of high-risk women recruited specifically to study recurrent major depressive disorder and bipolar disorder. This study specifically captured psychiatric disorders in the postpartum period among proband mothers with and without a prior psychiatric history. Previous studies typically have not distinguished between incident episodes and those that may reflect an ongoing psychiatric disorder that recurs during the postpartum period. Differentiating between new-onset episodes and recurrent episodes can have important implications for both screening and treatment. We also considered timing of onset of postpartum psychiatric episodes and separately analyzed three different periods: 0 to 3 months postpartum, 0 to 6 months postpartum, and 0 to 12 months postpartum. There is evidence that the etiology of postpartum psychiatric disorders may differ by timing of symptom onset (2, 31, 32, 43) and that the first few weeks after childbirth may be the most biologically vulnerable period (30, 31). However, because our data provide information about timing of diagnosis or treatment but not about the onset of symptoms, there is likely a potential lag between onset of symptoms and when a mother seeks care. This is an intrinsic limitation in nearly all studies of postpartum psychiatric disorders, and we sought to address this limitation by analyzing the 0- to 6-month period. We also selected 0 to 12 months postpartum as a clinically relevant period (30, 33, 34). External environmental factors change during the first year postpartum, which may influence each time period differently. Despite the potential for differences, we found that the way family psychiatric history affects postpartum psychiatric disorders is similar across all three periods.
Use of registry data improves generalizability to broader populations, but there are also limitations to the data available in the registers. Our data included inpatient hospital admissions and outpatient psychiatric clinic records but not records from general practitioners. Rates of postpartum psychiatric disorders were lower compared with typically reported rates because cases were of patients who obtained psychiatric care in a specialty clinic or hospital, which captured the most severe psychiatric episodes but not patients seeking care from their primary care provider. Therefore, these results are most generalizable to development of severe postpartum psychiatric disorders and potentially not for postpartum psychiatric disorders overall. Additionally, because outpatient diagnoses were not included in the registers until 1995, psychiatric diagnoses prior to 1995 include only the most severe inpatient hospitalizations. To account for the secular trends, we adjusted for calendar year of delivery and age of the proband mother at first delivery in the models. Moreover, to assess how this differentially defined exposure might influence our results, we repeated our analyses in a restricted cohort of mothers who had children born after 1995. A similar trend was observed in this subanalysis, although the interval estimates became wider and less precise because of small numbers of cases. We also acknowledge that our results are only generalizable to primiparous women. Finally, proband mothers were included only if they could be linked to their parents in the registry data. The inability to identify many of the grandparents makes our groupings of second- and third-degree relatives incomplete. Despite our large sample size, there were not enough pairs of sisters or mothers and daughters in whom both experienced incident psychiatric disorders in the postpartum period following the birth of their first child to address the recurrence risk of only postpartum psychiatric disorders. Our sample size also limited our ability to subdivide our outcome into specific types of psychiatric disorders, as we did for our exposure. We also did not see an expected pattern of familial risk aligned with the coefficient of relationship and our study was underpowered to evaluate familial risk by type of disorder for third-degree relatives, both likely because of incomplete identification of third-degree relatives.
Predicting who will experience a postpartum psychiatric disorder is a challenge but also of great importance. The results of this study provide compelling evidence that assessment of risk for postpartum psychiatric illness, with a particular focus on history of bipolar disorder, should include inquiring about family history of psychiatric disorders in any male or female first-degree relative. Thus, inquiring about family history in fathers and brothers is as important as obtaining a history of postpartum psychiatric disorders in mothers and sisters. Furthermore, as expected, we found personal psychiatric history to be a stronger independent predictor of postpartum psychiatric disorders than family history. However, we found associations of family history of psychiatric disorders to be stronger among women without a personal psychiatric history, indicating that family history may be particularly helpful in a risk assessment tool for new-onset postpartum psychiatric episodes among women with no record of psychiatric disorders. Previously, a woman who has a brother with bipolar disorder but no personal history of mental illness would not necessarily be identified as being at higher risk for experiencing a postpartum psychiatric disorder. However, this research provides evidence that such characteristics may identify novel risk groups to which clinicians could direct additional screening efforts, earlier education about symptoms, or earlier referral to mental health resources. Few clinical practice guidelines include family history, but those that do suggest planning the timing of pregnancies in periods of stable mood (44) and increasing surveillance for symptoms of postpartum psychosis in the first 2 weeks after childbirth (45), which should also be considered for these novel risk groups.
Clinical practice guidelines in the United States have recently been updated to reflect a growing emphasis on the importance of perinatal mental health screening, but the current guidelines of the U.S. Preventive Services Task Force (46) and the American College of Obstetricians and Gynecologists (33) do not include family history as a consideration for postpartum psychiatric disorders. This is in contrast to other women’s health conditions, such as breast cancer, in which family history of breast cancer in a first-degree relative is described extensively as an important screening consideration, despite the magnitude of familial risk being similar to that of postpartum psychiatric disorders (47). Therefore, obtaining a family history of psychiatric disorders is highly valuable information that should be acknowledged as an important factor in identifying at-risk women and operationalized in clinical practice to improve prediction of risk for postpartum psychiatric illness.
Footnote
Drs. Meltzer-Brody and Munk-Olsen are joint senior authors.
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References
1.
Munk-Olsen T, Maegbaek ML, Johannsen BM, et al: Perinatal psychiatric episodes: a population-based study on treatment incidence and prevalence. Transl Psychiatry 2016; 6:e919
2.
Munk-Olsen T, Laursen TM, Pedersen CB, et al: New parents and mental disorders: a population-based register study. JAMA 2006; 296:2582–2589
3.
Meltzer-Brody S, Maegbaek ML, Medland SE, et al: Obstetrical, pregnancy, and socio-economic predictors for new-onset severe postpartum psychiatric disorders in primiparous women. Psychol Med 2017; 47:1427–1441
4.
O’Hara MW, Wisner KL: Perinatal mental illness: definition, description, and aetiology. Best Pract Res Clin Obstet Gynaecol 2014; 28:3–12
5.
Howard LM, Molyneaux E, Dennis CL, et al: Non-psychotic mental disorders in the perinatal period. Lancet 2014; 384:1775–1788
6.
Di Florio A, Forty L, Gordon-Smith K, et al: Perinatal episodes across the mood disorder spectrum. JAMA Psychiatry 2013; 70:168–175
7.
Viguera AC, Tondo L, Koukopoulos AE, et al: Episodes of mood disorders in 2,252 pregnancies and postpartum periods. Am J Psychiatry 2011; 168:1179–1185
8.
Rasmussen MH, Strøm M, Wohlfahrt J, et al: Risk, treatment duration, and recurrence risk of postpartum affective disorder in women with no prior psychiatric history: a population-based cohort study. PLoS Med 2017; 14:e1002392
9.
Craddock N, Forty L: Genetics of affective (mood) disorders. Eur J Hum Genet 2006; 14:660–668
10.
Lichtenstein P, Yip BH, Björk C, et al: Common genetic influences for schizophrenia and bipolar disorder: a population-based study of 2 million nuclear families. Lancet 2009; 373:234–239
11.
Viktorin A, Meltzer-Brody S, Kuja-Halkola R, et al: Heritability of perinatal depression and genetic overlap with nonperinatal depression. Am J Psychiatry 2016; 173:158–165
12.
Sullivan PF, Neale MC, Kendler KS: Genetic epidemiology of major depression: review and meta-analysis. Am J Psychiatry 2000; 157:1552–1562
13.
Wray NR, Gottesman II: Using summary data from the Danish national registers to estimate heritabilities for schizophrenia, bipolar disorder, and major depressive disorder. Front Genet 2012; 3:118
14.
Jones I, Craddock N: Familiality of the puerperal trigger in bipolar disorder: results of a family study. Am J Psychiatry 2001; 158:913–917
15.
Murphy-Eberenz K, Zandi PP, March D, et al: Is perinatal depression familial? J Affect Disord 2006; 90:49–55
16.
Payne JL, MacKinnon DF, Mondimore FM, et al: Familial aggregation of postpartum mood symptoms in bipolar disorder pedigrees. Bipolar Disord 2008; 10:38–44
17.
Jones I, Craddock N: Do puerperal psychotic episodes identify a more familial subtype of bipolar disorder? Results of a family history study. Psychiatr Genet 2002; 12:177–180
18.
Munk-Olsen T, Laursen TM, Meltzer-Brody S, et al: Psychiatric disorders with postpartum onset: possible early manifestations of bipolar affective disorders. Arch Gen Psychiatry 2012; 69:428–434
19.
Chaudron LH, Pies RW: The relationship between postpartum psychosis and bipolar disorder: a review. J Clin Psychiatry 2003; 64:1284–1292
20.
Dennis C-L, Ross LE: The clinical utility of maternal self-reported personal and familial psychiatric history in identifying women at risk for postpartum depression. Acta Obstet Gynecol Scand 2006; 85:1179–1185
21.
Forty L, Jones L, Macgregor S, et al: Familiality of postpartum depression in unipolar disorder: results of a family study. Am J Psychiatry 2006; 163:1549–1553
22.
Treloar SA, Martin NG, Bucholz KK, et al: Genetic influences on post-natal depressive symptoms: findings from an Australian twin sample. Psychol Med 1999; 29:645–654
23.
PDQ Cancer Genetics Editorial Board, National Cancer Institute: Recurrence risk, in NCI Dictionary of Genetics Terms, 2015. www.cancer.gov/publications/dictionaries/genetics-dictionary?CdrID=460213
24.
Wessel J: Recurrence risk ratio, in Encyclopedia of Behavioral Medicine. New York, Springer, 2013, pp 1633–1633
25.
Smoller JW, Finn CT: Family, twin, and adoption studies of bipolar disorder. Am J Med Genet C Semin Med Genet 2003; 123C:48–58
26.
Lichtenstein P, Björk C, Hultman CM, et al: Recurrence risks for schizophrenia in a Swedish national cohort. Psychol Med 2006; 36:1417–1425
27.
Pedersen CB: The Danish Civil Registration System. Scand J Public Health 2011; 39(suppl):22–25
28.
Mors O, Perto GP, Mortensen PB: The Danish Psychiatric Central Research Register. Scand J Public Health 2011; 39(suppl):54–57
29.
Kessing L: Validity of diagnoses and other clinical register data in patients with affective disorder. Eur Psychiatry 1998; 13:392–398
30.
Gavin NI, Gaynes BN, Lohr KN, et al: Perinatal depression: a systematic review of prevalence and incidence. Obstet Gynecol 2005; 106:1071–1083
31.
Kendell RE, Chalmers JC, Platz C: Epidemiology of puerperal psychoses. Br J Psychiatry 1987; 150:662–673
32.
Munk-Olsen T, Laursen TM, Mendelson T, et al: Risks and predictors of readmission for a mental disorder during the postpartum period. Arch Gen Psychiatry 2009; 66:189–195
33.
American College of Obstetricians and Gynecologists Committee on Obstetric Practice: Committee opinion no 630: Screening for perinatal depression. Obstet Gynecol 2015; 125:1268–1271
34.
Stuart-Parrigon K, Stuart S: Perinatal depression: an update and overview. Curr Psychiatry Rep 2014; 16:468
35.
Duncan LE, Ratanatharathorn A, Aiello AE, et al: Largest GWAS of PTSD (N=20 070) yields genetic overlap with schizophrenia and sex differences in heritability. Mol Psychiatry (Epub ahead of print, Apr 25, 2017)
36.
Currier D, Mann MJ, Oquendo MA, et al: Sex differences in the familial transmission of mood disorders. J Affect Disord 2006; 95:51–60
37.
Jansson M, Gatz M, Berg S, et al: Gender differences in heritability of depressive symptoms in the elderly. Psychol Med 2004; 34:471–479
38.
Fernandez-Pujals AM, Adams MJ, Thomson P, et al: Epidemiology and heritability of major depressive disorder, stratified by age of onset, sex, and illness course in Generation Scotland: Scottish Family Health Study (GS: SFHS). PLoS One 2015; 10:e0142197
39.
Jones I, Chandra PS, Dazzan P, et al: Bipolar disorder, affective psychosis, and schizophrenia in pregnancy and the post-partum period. Lancet 2014; 384:1789–1799
40.
Wesseloo R, Kamperman AM, Munk-Olsen T, et al: Risk of postpartum relapse in bipolar disorder and postpartum psychosis: a systematic review and meta-analysis. Am J Psychiatry 2016; 173:117–127
41.
Reich T, Winokur G: Postpartum psychoses in patients with manic depressive disease. J Nerv Ment Dis 1970; 151:60–68
42.
Dean C, Williams RJ, Brockington IF: Is puerperal psychosis the same as bipolar manic-depressive disorder? A family study. Psychol Med 1989; 19:637–647
43.
Postpartum Depression: Action Towards Causes and Treatment (PACT) Consortium: Heterogeneity of postpartum depression: a latent class analysis. Lancet Psychiatry 2015; 2:59–67
44.
Best Practice Guidelines for Mental Health Disorders in the Perinatal Period. Vancouver, BC Reproductive Mental Health Program and Perinatal Services BC, 2014
45.
Howard LM, Megnin-Viggars O, Symington I, et al: Antenatal and postnatal mental health: summary of updated NICE guidance. BMJ 2014; 349:g7394
46.
Siu AL, Bibbins-Domingo K, Grossman DC, et al: Screening for depression in adults: US Preventive Services Task Force recommendation statement. JAMA 2016; 315:380–387
47.
Siu AL: Screening for breast cancer: US Preventive Services Task Force recommendation statement. Ann Intern Med 2016; 164:279–296
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Received: 2 November 2017
Revision received: 15 December 2017
Accepted: 8 January 2018
Published online: 7 May 2018
Published in print: August 01, 2018
Keywords
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Funding Information
Australian National Health and Medical Research Council: 1078901, 1087889
Lundbeckfonden10.13039/501100003554: R155-2014-1724
Supported by NIMH grant 1R01MH104468 (principal investigator, Dr. Meltzer-Brody; co-investigators, Dr. Munk-Olsen, Dr. Miller, Dr. Sullivan, Ms. Maegbaek, and Dr. Liu).Dr. Wray has received funding from the Australian National Health and Medical Research Council (grants 1078901 and 1087889). Dr. Sullivan has received grant support from Lundbeck and has served on advisory boards or as a consultant or speaker for Element Genomics, Lundbeck, Pfizer, and Roche. Dr. Meltzer-Brody has received research grant support from Janssen and Sage Therapeutics. Dr. Munk-Olsen is supported by the Lundbeck Foundation Initiative for Integrative Psychiatric Research (iPSYCH) (grant R155-2014-1724). The other authors report no financial relationships with commercial interests.Metrics & Citations
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