Psychosomatic Medicine Faster Service from Outside North America
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

This Article
Right arrow Abstract Freely available
Right arrow Figures Only
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Verkerk, G. J.M.
Right arrow Articles by Pop, V. J.M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Verkerk, G. J.M.
Right arrow Articles by Pop, V. J.M.
Related Collections
Right arrow Depression
Right arrow Sexual Medicine: Female
Right arrow Personality
Right arrow Pregnancy
Psychosomatic Medicine 67:632-637 (2005)
© 2005 American Psychosomatic Society


ORIGINAL ARTICLES

Personality Factors as Determinants of Depression in Postpartum Women: A Prospective 1-Year Follow-up Study

Gerda J.M. Verkerk, PhD, Johan Denollet, PhD, Guus L. Van Heck, PhD, Maarten J.M. Van Son, PhD and Victor J.M. Pop, MD, PhD

From the Tilburg University, Department of Psychology and Health, Tilburg, The Netherlands (G.J.M.V., J.D., G.L.V.H., V.J.M.P.); and the Department of Clinical Psychology, Utrecht University, Utrecht, The Netherlands (M.J.M.V.S).

Address correspondence and reprint requests to Gerda Verkerk, PhD, Tilburg University, Department of Psychology and Health, P.O. Box 90153, 5000 LE, Tilburg, The Netherlands. E-mail: g.j.m.verkerk{at}zonnet.nl


    ABSTRACT
 TOP
 ABSTRACT
 INTRODUCTION
 METHOD
 RESULTS
 DISCUSSION
 NOTES
 REFERENCES
 
Objective: Personality has been associated with clinical depression in general. However, few studies have investigated personality in relation to postpartum depression, and these studies reported inconclusive findings. Therefore, the present study focused on neuroticism and introversion in the prediction of postpartum depression.

Method: In a population-based prospective study, women were screened during mid-pregnancy on standard risk factors for depression. In a group of randomly selected women (n = 277), neuroticism and introversion were measured at 32 weeks gestation. Clinical depression (Research Diagnostic Criteria) and depressive symptoms (Edinburgh Postnatal Depression Scale) were measured at 32 weeks gestation and at 3, 6, and 12 months postpartum.

Results: High neuroticism was associated with an increased risk of clinical depression and depressive symptoms during the postpartum period. The combination of high neuroticism and high introversion was the only independent predictor of clinical depression across the first year postpartum (odds ratios: 3.08, 4.64, and 6.83 at 3, 6, and 12 months postpartum, respectively, p < .05–.01), even when controlling for clinical depression during pregnancy. History of depression was the only other independent predictor during the early but not during the late postpartum. Inclusion of personality not only significantly improved the detection of women at increased depression risk but also the identification of women with an extremely low depression risk.

Conclusions: Personality may be an important and stable determinant of postpartum depression. The combination of high neuroticism and high introversion considerably improved the risk estimates for clinical depression across the first year postpartum.

Key Words: personality • prediction • depression • postpartum

Abbreviations: RDC = research diagnostic criteria; EPDS = Edinburgh Postnatal Depression Scale; N = neuroticism; I = introversion; CPI = California Psychological Inventory; DPQ = Dutch Personality Questionnaire; CI = confidence interval.


    INTRODUCTION
 TOP
 ABSTRACT
 INTRODUCTION
 METHOD
 RESULTS
 DISCUSSION
 NOTES
 REFERENCES
 
Nonpsychotic depression is common after childbirth, affecting 10 to 20% of women in the first year postpartum (1–5). A variety of psychosocial factors have been associated with depression in the postpartum period, including history of pathology, psychopathology during pregnancy, poor marital satisfaction, low social support, and stressful life events (6–9). Personality traits like neuroticism and introversion have been associated with depression in nonchildbearing populations (10–14). Neuroticism and introversion-extraversion represent major sources of individual variation in (a) emotionality and (b) sociability and activity level, respectively. A high neuroticism score indicates feelings of tension, emotional liability, and insecurity, and a low score indicates emotional stability. A high introversion score indicates inhibition and shyness in social interactions, and a low score indicates sociability and feelings of competence in social interactions.

However, few studies have examined personality as a determinant of depression after childbirth. Moreover, these studies have produced mixed findings (15–18) attributable to differences in mode (i.e., clinical interview versus self-reported symptoms) and time (i.e., from 6 weeks to 12 months postpartum) of depression assessment (3,16).

Therefore, the present study was designed to address these issues. More specifically, depression was assessed on syndrome (clinical depression) as well as on symptom (self-report) level at three different measurement points in the first year postpartum. In terms of personality, we studied neuroticism and introversion as possible determinants of clinical depression and of depressive symptoms after childbirth.


    METHOD
 TOP
 ABSTRACT
 INTRODUCTION
 METHOD
 RESULTS
 DISCUSSION
 NOTES
 REFERENCES
 
Subjects
The subjects of the present study participated in a longitudinal study of postpartum depression. During mid-pregnancy, women who visited the obstetrician or midwife for antenatal care were invited to complete a screening questionnaire concerning risk factors for depression.

Of 1618 women referred by midwife or obstetrician, 1031 were eligible: Dutch speaking with a term of 20 to 30 weeks pregnancy, living in the vicinity of Tilburg and Eindhoven, having returned a fully completed questionnaire, and having consented to participate in a follow-up study during pregnancy and the postpartum. Screening questionnaires were numbered in correspondence to the order in which they were received, and odd numbers were selected. A group of 339 selected women assessed during pregnancy continued their participation postpartum. Forty-five women (13%) dropped out of the study. Seventeen women had incomplete data and were excluded from the study. Thus, 277 women participated in the present study.

The mean age of these women was 30.8 years (SD = 4.1, range = 19–43); 94% were living with a partner, 1.4% were divorced, and 4.3% were single; 43.8% were primipara and 56.2% multipara. The educational level of this sample was representative for the Dutch population: 1% primary, 76% secondary (general or occupational), and, 23% tertiary (occupational or university) education. The women who dropped out were not different from those who remained in the study in terms of socio-demographic characteristics, personality, or level of depressive symptomatology during mid-pregnancy.

Procedure
At 34 weeks pregnancy, and at 3, 6, and 12 months postpartum, women were visited at home for psychological assessment, including clinical interview and questionnaire components. Personality traits were assessed once, during the interview at 34 weeks pregnancy. Clinical depression and depressive symptoms were measured at all the four assessment points. The study protocol was approved by the Medical Ethical Committees of the St. Joseph Hospital, Veldhoven, and the Two Cities Hospital, Tilburg.

Clinical Diagnosis of Depression
Clinical depression was the primary endpoint in the present study. In accordance with previous research on postpartum depression in The Netherlands (19–22), research diagnostic criteria (RDC) (23) were used for classifying minor/major depressive disorder on the basis of a structured interview implying all relevant criteria. Women were diagnosed with major depression if they fulfilled one core criterion (depressed mood) and at least five of eight additional criteria (loss of appetite/weight, sleep difficulties, fatigue or loss of energy, psychomotor agitation/retardation, loss of interest or pleasure, low self-esteem/inappropriate guilt, difficulty concentrating/indecisiveness, thoughts of suicide) with a duration of at least 2 weeks and significant impairment in functioning. Those women who fulfilled 3 or 4 additional criteria were diagnosed as minor depressed.

Self-Reported Symptoms of Depression
Depressive symptoms were assessed as a secondary endpoint. The Edinburgh Postnatal Depression Scale (EPDS) was used to assess intensity of depressive symptoms (24). The EPDS is a 10-item self-report scale, developed specifically for the assessment of postnatal depressive symptoms. Each item is scored 0 to 3, according to increased severity of symptoms. The EPDS has good psychometric properties (24,25) and has also been validated in The Netherlands (26).

Personality
Two personality traits, neuroticism (N) and introversion (I), were assessed by the Dutch version of the California Psychological Inventory (CPI) (27). This personality scale, which was termed the "Dutch Personality Questionnaire," is a reliable and valid personality measure (28,29). In the present sample, the Cronbach {alpha} for the N-scale was 0.85 and for the I-scale 0.87. The emotional stability scale of the Dutch Personality Questionnaire (DPQ) negatively correlates with the neuroticism scale of the Five Factor Personality Inventory (30,31), and the Eysenck Personality Questionnaire (32), r = –.74, r = –.78, respectively; likewise the DPQ introversion scale correlates negatively with the extraversion- introversion scale of the Five Factor Personality Inventory (r = –.71) and the Eysenck Personality Questionnaire (r = –.70).

In the present study, the two scales of the DPQ were combined in a 36-item self-report questionnaire with a 3-point response scale (agree = 0, ? = 1, disagree = 2). Neuroticism and introversion-extraversion represent major sources of individual variation in (a) emotionality and (b) sociability and activity level, respectively. Claridge and Davis (33) examined these traits not as separate variables with unitary linear effects but as possible moderator variables in a so-called "zone analysis" of neuroticism and introversion (34) where these traits modulate each others’ role in influencing behavior. This more dynamic analysis can reveal relationships between neuroticism and depression by looking at the possibility that introversion might interact in that relationship.

To address this issue, we used a categorical classification of personality. Subjects scoring in the upper thirds were considered to be high on the corresponding personality trait. Hence, a score of ≥13 on the Neuroticism-scale was used to define high-neuroticism (high N; n = 82; 30%), and a score of ≥12 on the Introversion-scale was used to define high-introversion (high I; n = 92; 33%). With regard to the combination of neuroticism and introversion, four personality types could be differentiated: (a) high on both (high N-high I; n = 44; 16%); (b) high-neuroticism and low-introversion (high N-low I; n = 38; 14%); (c) low-neuroticism and high-introversion (low N-high I; n = 48; 17%); and (d) low on both (low N-low I; n = 147; 53%).

Standard Risk Factors for Depression
During the second trimester of pregnancy, women were screened by means of a questionnaire on the following risk factors for depression: (a) a personal history of depression; (b) a family history of depression; and (c) severe depressive symptomatology during the second trimester of pregnancy (8). The first two factors were each assessed by a single item with a two-point response scale (yes versus no) as follows: (a) Did you ever suffer from depression during your life? (b) Did anyone in your family (father, mother, brothers or sisters) suffer from depression? Women with severe depressive symptomatology were identified by using the EPDS > 11 criterion (8,35).

Statistical Analyses
Descriptive statistics were used to analyze the socio-demographic characteristics and the prevalence rates of clinical depression. Logistic regression analyses were used to test whether personality traits were determinants of depression. Differences in prevalence rates of clinical depression among different personality types were explored by {chi}2 analysis. Multiple logistic regression analyses were used to test whether personality types were determinants of depression.

To examine whether personality types were independent determinants of clinical depression, we used multiple logistic regression analysis. This analysis was repeated, excluding women who were diagnosed during pregnancy as clinically depressed, to assess the risk of depression during the postpartum prospectively in women who were initially free from depression during pregnancy. The repeated measures multivariate analysis of variance were used to analyze changes in levels of depressive symptoms as a function of personality traits. In post hoc analyses, t tests were used to explore the differences in mean scores of depression at symptom level as a function of personality traits.


    RESULTS
 TOP
 ABSTRACT
 INTRODUCTION
 METHOD
 RESULTS
 DISCUSSION
 NOTES
 REFERENCES
 
Prevalence of Clinical Depression
The percentage of women depressed at one or more measurement points during the first postpartum year was 18% (n = 50). Point-prevalence rates were 12.6% (n = 35), at 34 weeks pregnancy and 10.8% (n = 30), 8.7% (n = 24), and 7.2% (n = 20) at 3, 6, and 12 months postpartum, respectively.

Personality Traits as Predictors of Clinical Depression
Neuroticism and introversion were significantly associated with an increased risk of clinical depression at each measurement point (Table 1). Both personality factors predicted clinical depression (at one or more assessment points) during the first year postpartum (odds ratio = 4.53; 95% CI = 2.39–8.60; p < .001, odds ratio = 1.95; 95% CI = 1.05–3.64; p = .034, respectively).


View this table:
[in this window]
[in a new window]
 
TABLE 1. Clinical Depression During the First Year Postpartum (N = 277) on a Function of Personality Traits and Types

 

Personality Types as Predictors of Clinical Depression
Prevalence rates of clinical depression of the four combinations of personality traits are presented in Figure 1. Within the group of low N women, there were no significant differences in prevalence rates between women who scored high on introversion (high I) or low on introversion (low I). Hence, pooling of women in one low N group for further analyses was justified. Prevalence rates of depression were significantly higher in the high N-high I women compared with the low N women at 3, 6, and 12 months postpartum. Also, significantly higher prevalence rates were found in the high N-low I women compared with the low N women at 3 and 12 months postpartum but not at 6 months (Figure 1).



View larger version (28K):
[in this window]
[in a new window]
 
Figure 1. Prevalence rates of clinical depression as a function of four personality types. Note: **p < .01, ***p < .001. N = neuroticism, I = introversion. A, low N–low I versus low N-high I: {chi}2 = 0.52, df = 1, p = .469; low N-low or high I versus high N-low I: {chi}2 = 4.14, df = 1, p = .042; low N-low or high I versus high N-high I: {chi}2 = 17.72, df = 1, p < .001. B, low N-low I versus low N-high I: {chi}2 = 0.16, df = 1, p = .685; low N-low or high I versus high N-low I: {chi}2 = 1.64, df = 1, p = .200; low N-low or high I versus high N-high I: {chi}2 = 14.50, df = 1, p < .001. C, low N-low I versus low N-high I: {chi}2 = 0.65, df = 1, p = .418; low N-low or high I versus high N-low I: {chi}2 = 8.69, df = 1, p = .003; low N-low or high I versus high N-high I: {chi}2 = 24.81, df = 1, p < .001.

 

Moreover, of the two high N personality types, high N-high I was the only predictor of clinical depression across the whole first year postpartum (Table 1). Both personality types high N-high I and high N-low I predicted clinical depression (at one or more assessment points) during the first year postpartum (odds ratio = 5.74; 95% CI = 2.70–12.17; p < .001 and odds ratio = 3.37; 95% CI = 1.46–7.78; p < .01, respectively).

Independent Predictors of Clinical Depression
Multiple logistic regression analyses showed that after controlling for other risk factors of depression, high N-high I was the only independent predictor of clinical depression across the first year postpartum (Table 2). A personal history of depression was the only other factor significantly associated to clinical depression but only at 3 months postpartum. Next, these analyses were repeated, excluding women diagnosed as clinically depressed during late pregnancy. This was done to examine the risk factors associated with the onset of clinical depression during the postpartum in women who were not clinically depressed during pregnancy (n = 242). Those women with a personal history of depression were at increased risk for the onset of depression but only during the early postpartum (odds ratio = 3.67; 95% CI = 1.31–10.28; p = .013). Once again, women with a high score on neuroticism and introversion were at increased risk for the onset of depression both during the early and late postpartum period (odds ratio = 4.78; 95% CI = 1.48–15.44; p = .008, odds ratio = 5.65; 95% CI = 1.45–22.01; p = .013, odds ratio = 9.24; 95% CI = 2.17–39.48; p = .003 at 3, 6, and 12 months, respectively).


View this table:
[in this window]
[in a new window]
 
TABLE 2. Independent Predictors of Clinical Depression During the First Year Postpartum (N = 277)

 

History of Depression and Personality as Predictors of Clinical Depression
To examine the combined effect of both independent predictors of postpartum depression, women were stratified by personal history of depression (yes/no) and high-risk personality (high N-high I/other). Prevalence rates of depression were higher in the group of women with both a history of depression and high-risk personality compared with the group of women with a history of depression but no high-risk personality (37.5% versus 18.4%; p = .053, 25% versus 9.2%; p = .045; 20.8% versus 10.5%; p = .191, respectively, at 3, 6, and 12 months postpartum (Figure 2, subgroups 2 and 3). Only at 6 months were differences in prevalence rates between the two groups significant. Hence, addition of high-risk personality to a history of depression increases the risk for clinical depression at 6 months postpartum. Moreover, by not taking personality into account, an important group of women at increased risk (i.e., no history of depression but high-risk personality) would be missed in depression screening. This is especially noteworthy for depression during the late postpartum (Figure 2, subgroup 4). Of the 20 women who were clinically depressed at 12 months postpartum, 25% were women with a high-risk personality but no history of depression.



View larger version (35K):
[in this window]
[in a new window]
 
Figure 2. Prevalence rates of Depression (RDC, A) in Women With or Without a Personal History of Depression (B) in Combination With or Without a High-risk Personality (C). Note: A, RDC = research diagnostic criteria; B, No personal history of depression (self-reported); C, High-risk personality = high-neuroticism in combination with high-introversion.

 

At 3, 6, and 12 months postpartum, women with no history of depression and no high risk personality were significantly less likely to be at risk for clinical depression than women with no history of depression but with a high-risk personality (2.5% versus 15%, p = .007; 4.5% versus 20.0%, p = .007; 1.3% versus 25%, p < .001, respectively; Figure 2, subgroups 1 and 4).

Accordingly, the addition of personality type in risk stratification did not only add to the detection of women at increased risk but also enhanced the identification of a large group of women with an extreme low depression risk.

Personality Traits as Predictors of Depressive Symptoms
On symptom level, repeated measures multivariate analysis of variance showed a main effect of time (F = 4.12 [2, 271], p = .02), i.e., in the total group there was a significant decrease in depressive symptoms. There was a main effect of neuroticism and introversion; (F = 66.27 (1, 272), p < .001; F = 6.612 (1, 272), p = .01, respectively) but no significant personality x time interaction effects, indicating that neuroticism and introversion were stable predictors of the depressive symptom level across the first year postpartum. There was no significant neuroticism x introversion interaction effect. At each measurement, high neuroticism and high introversion were significantly related to higher levels of depressive symptoms (Table 3). Hence, personality was not only a significant predictor of clinical depression but also of self-reported symptoms.


View this table:
[in this window]
[in a new window]
 
TABLE 3. Depressive Symptoms During the First Year Postpartum (N = 277) as a Function of Personality Traits

 


    DISCUSSION
 TOP
 ABSTRACT
 INTRODUCTION
 METHOD
 RESULTS
 DISCUSSION
 NOTES
 REFERENCES
 
Personality was a stable determinant of both clinical depression and depressive symptoms in the first year postpartum. Introversion contributed to the association between neuroticism and depression; i.e., women scoring high on both neuroticism and introversion (high N-high I) were at 4- to 6-fold increased risk for clinical depression. High N-high I was the only independent and stable predictor of clinical depression across the whole first year postpartum. Moreover, high N-high I was clearly a better predictor of clinical depression than history of depression (the other independent predictor) especially on the long-term. Addition of high N-high I to a previous history of depression enhanced the identification of women at increased risk as well as the identification of women with an extreme low depression risk.

These findings are consistent with the emerging role of personality as a vulnerability factor for depression in other populations (10,11,36–38). Individuals high on neuroticism and introversion are at risk for depressive symptoms (39,40), including depressive symptoms in cardiac patients (41). In childbearing women, however, others have reported mixed findings (15–18). One explanation for these inconclusive findings might be the difference between studies in methods of measuring depression at syndrome level by clinical interviews or at symptom level by self-reports (3). Another explanation might be that the association between neuroticism and depression depends on the time of assessment during the postpartum varying from 6 weeks to 12 months across studies (16). We found evidence that personality predicted depression in the postpartum, regardless of mode or time of assessment. Personality also predicted the onset of depression in women who initially were not depressed during pregnancy. Hence, failure to account for personality may lead to inaccurate risk estimates of depression in the postpartum period.

The strengths of this study are its prospective design over a 1-year period and the repeated assessment of depression at syndrome and symptom level. Of course this study has a number of limitations. First, in accordance with previous research on postpartum depression in The Netherlands (19–22), clinical depression was diagnosed according to the Research Diagnostic Criteria (RDC). Therefore, it is difficult to generalize our present findings on clinical depression to the more current DSM-IV or ICD criteria. Second, one might argue that this personality-depression relationship is spurious because depression during pregnancy might have influenced personality assessment. Some investigators have suggested that personality measures might be state-dependent (42,43), but others have found that neither past nor current depression had significant impact on personality assessment (44–47). Not much is known about the use of the DPQ in depressed populations. Therefore, we controlled for depression at the time of personality assessment. Even when women clinically depressed during pregnancy were excluded, the combination of high N-high I still predicted clinical depression at 3, 6, and 12 months postpartum. These findings support the use of the DPQ in the present study, although more information is needed about the validation of the DPQ in pregnant depressed women. Third, this study focuses on the relationship between personality and postpartum depression. Although we controlled for stable predictors of depression in general, we have not taken into account potential powerful risk factors such as concurrent life events, social support, and quality of the marital relationship (3) or other personal and environmental factors that may influence the personality-depression relationship in postpartum women.

The findings of this study have important clinical implications. Personality assessment in the psychosocial screening of women at risk for postpartum depression is not common in obstetrical practice. Inclusion of personality may significantly improve this screening. Our findings also suggest that to improve the recognition of postpartum depression, it is important to screen women for depression during the first months but also during the late postpartum period. Moreover, treatment of postpartum depression should not only be focused on postpartum related issues but also on patient related issues such as personality. To improve the care for women in obstetrics, depression screening and care management interventions (48) are necessary.

High neuroticism in combination with high introversion was a stable predictor of clinical depression across the whole first year postpartum. It is now time that personality be included in the early identification of those women who are at increased risk for depression in the postpartum period.


    NOTES
 TOP
 ABSTRACT
 INTRODUCTION
 METHOD
 RESULTS
 DISCUSSION
 NOTES
 REFERENCES
 

Received for publication June 30, 2004; revision received March 9, 2005.

DOI:10.1097/01.psy.0000170832.14718.98


    REFERENCES
 TOP
 ABSTRACT
 INTRODUCTION
 METHOD
 RESULTS
 DISCUSSION
 NOTES
 REFERENCES
 

  1. Lee D, Yip A, Chiu H, Leung T, Chung T. A psychiatric epidemiological study of postpartum Chinese women. Am J Psychiatry 2001;158:220–6.[Abstract/Free Full Text]
  2. Miller LJ. Postpartum depression. JAMA 2002;287:762–5.[Free Full Text]
  3. O’Hara M, Swain AM. Rates and risks of postpartum depression: a meta-analysis. Int Rev Psychiatry 1996;8:37–54.
  4. Patel V, Rodrigues M, DeSouza N. Gender, poverty, and postnatal depression: a study of mothers in Goa, India. Am J Psychiatry 2002;159:43–7.[Abstract/Free Full Text]
  5. Yonkers KA, Ramin SM, Rush AJ, Navarrete CA, Carmody T, March D, Heartwell SF, Leveno KJ. Onset and persistence of postpartum depression in an inner-city maternal health clinic system. Am J Psychiatry 2001;158:1856–63.[Abstract/Free Full Text]
  6. Da Costa D, Larouche J, Dritsa M, Brender W. Psychosocial correlates of prepartum and postpartum depressed mood. J Affect Disord 2000;59:31–40.[CrossRef][Medline]
  7. Righetti-Veltema M, Conne-Perreard E, Bousquet A, Manzano J. Risk factors and predictive signs of postpartum depression. J Affect Disord 1998;49:167–80.[CrossRef][Medline]
  8. Verkerk GJM, Pop VJM, Van Son MJM, Van Heck GL. Prediction of depression in the postpartum period: a longitudinal follow-up study in high-risk and low-risk women. J Affect Disord 2003;77:159–66.[CrossRef][Medline]
  9. Watson JP, Elliott SA, Rugg AJ, Brough DI. Psychiatric disorder in pregnancy and the first postnatal year. Br J Psychiatry 1984;144:453–62.[Abstract/Free Full Text]
  10. Hirschfeld RM, Klerman GL, Lavori P, Keller MB, Griffith P, Coryell W. Premorbid personality assessments of first onset of major depression. Arch Gen Psychiatry 1989;46:345–50.[Abstract]
  11. Roberts SB, Kendler KS. Neuroticism and self-esteem as indices of the vulnerability to major depression in women. Psychol Med 1999;29:1101–9.[CrossRef][Medline]
  12. Berlanga C, Heinze G, Torres M, Apiquian R, Caballero A. Personality and clinical predictors of recurrence of depression. Psychiatr Serv 1999;50:376–80.[Abstract/Free Full Text]
  13. Mulder RT. Personality pathology and treatment outcome in major depression: a review. Am J Psychiatry 2002;159:359–71.[Abstract/Free Full Text]
  14. Scott J, Williams JM, Brittlebank A, Ferrier IN. The relationship between premorbid neuroticism, cognitive dysfunction and persistence of depression: a 1-year follow-up. J Affect Disord 1995;33:167–72.[CrossRef][Medline]
  15. Areias ME, Kumar R, Barros H, Figueiredo E. Comparative incidence of depression in women and men, during pregnancy and after childbirth. Validation of the Edinburgh Postnatal Depression Scale in Portuguese mothers. Br J Psychiatry 1996;169:30–5.[Abstract/Free Full Text]
  16. Boyce P, Parker G, Barnett B, Cooney M, Smith F. Personality as a vulnerability factor to depression. Br J Psychiatry 1991;159:106–14.[Abstract/Free Full Text]
  17. Matthey S, Barnett B, Ungerer J, Waters B. Paternal and maternal depressed mood during the transition to parenthood. J Affect Disord 2000;60:75–85.[CrossRef][Medline]
  18. Kumar R, Robson KM. A prospective study of emotional disorders in childbearing women. Br J Psychiatry 1984;144:35–47.[Abstract/Free Full Text]
  19. Pop VJ, De Rooy HA, Vader HL, Van der Heide D, Van Son MM, Komproe IH. Microsomal antibodies during gestation in relation to postpartum thyroid dysfunction and depression. Acta Endocrinol 1993;129:26–30.
  20. Pop VJ, Essed GG, de Geus CA, van Son MM, Komproe IH. Prevalence of post partum depression–or is it post-puerperium depression? Acta Obstet Gynecol Scand 1993;72:354–8.[Medline]
  21. Pop VJ, Wijnen HA, Van Montfort M, Essed GG, De Geus CA, Van Son MM, Komproe IH. Blues and depression during the early puerperium: home versus hospital deliveries. Br J Obstet Gynaecol 1995;102:701–06.[Medline]
  22. Kuijpens JL, Vader HL, Drexhage HA, Wiersinga WM, Son MJ van, Pop VJ. Thyroid peroxidase antibodies during gestation are a marker for subsequent depression postpartum. Eur J Endocrinol 2001;145:579–84.[Abstract]
  23. Spitzer RL, Endicott J, Robins E. Research diagnostic criteria: rationale and reliability. Arch Gen Psychiatry 1978;35:773–82.[Abstract]
  24. Cox JL, Holden JM, Sagovsky R. Detection of postnatal depression. Development of the 10-item Edinburgh Postnatal Depression Scale. Br J Psychiatry 1987;150:782–6.[Abstract/Free Full Text]
  25. Cox JL, Murray D, Chapman G. A controlled study of the onset, duration and prevalence of postnatal depression. Br J Psychiatry 1993;163:27–31.[Abstract/Free Full Text]
  26. Pop VJ, Komproe IH, van Son MJ. Characteristics of the Edinburgh Post Natal Depression Scale in The Netherlands. J Affect Disord 1992;26:105–10.[CrossRef][Medline]
  27. Gough H. Manual for the California Psychological Inventory. Palo Alto, CA: Consulting Psychology Press; 1964.
  28. Luteijn F, Starren J, Dijk H. Nederlandse Persoonlijkheids Vragenlijst, Handleiding [Dutch Personality Questionnaire, Manual]. Lisse, The Netherlands: Swets & Zeitlinger; 1985.
  29. Barelds DP, Luteijn F. Measuring personality: a comparison of three personality questionnaires in the Netherlands. Pers Individ Dif 2002;33:499–510.[CrossRef]
  30. Hendriks AAJ. The Construction of the Five-Factor Personality Inventory. Unpublished doctoral dissertation. Groningen, The Netherlands, University of Groningen; 1997.
  31. Hendriks AAJ, Hofstee WKB, De Raad B. Handleiding bij de Five-Factor Personality Inventory (FFPI) [The Five-Factor Personality Inventory: Professional Manual]. Lisse, The Netherlands: Swets & Zeitlinger; 1999.
  32. Sanderman R, Arrindell W, Ranchor AV, Eysenck HJ, Eysenck SBG. Het meten van persoonlijkheidskenmerken met de Eysenck Personality Questionnaire (EPQ) [Measuring Personality Aspects with the Eysenck Personality Questionnaire (EPQ)]. Groningen, The Netherlands, Noordelijk Centrum voor Gezondheidsvraagstukken; 1995.
  33. Claridge G, Davis C. What’s the use of neuroticism? Pers Indiv Diff 2001;31:383–400.[CrossRef]
  34. Eysenck H. The Biological Basis of Personality. Springfield, Charles C Thomas; 1967.
  35. Gerrard J, Holden JM, Elliott SA, McKenzie P, McKenzie J, Cox JL. A trainer’s perspective of an innovative programme teaching health visitors about the detection, treatment and prevention of postnatal depression. J Adv Nurs 1993;18:1825–32.[CrossRef][Medline]
  36. Aben I, Denollet J, Lousberg R, Verhey F, Wojciechowski F, Honig A. Personality and vulnerability to depression in stroke patients: a 1-year prospective follow-up study. Stroke 2002;33:2391–2395.[Abstract/Free Full Text]
  37. Angst J, Clayton P. Premorbid personality of depressive, bipolar, and schizophrenic patients with special reference to suicidal issues. Compr Psychiatry 1986;27:511–32.[CrossRef][Medline]
  38. Ernst C, Schmid G, Angst J. The Zurich Study. XVI. Early antecedents of depression. A longitudinal prospective study on incidence in young adults. Eur Arch Psychiatry Clin Neurosci 1992;242:142–51.[CrossRef][Medline]
  39. Gershuny BS, Sher KJ. The relation between personality and anxiety: findings from a 3-year prospective study. J Abnorm Psychol 1998;107:252–62.[CrossRef][Medline]
  40. McFatter RM. Interactions in predicting mood from extraversion and neuroticism. J Pers Soc Psychol 1994;66:570–8.[CrossRef][Medline]
  41. Denollet J, Vaes J, Brutsaert DL. Inadequate response to treatment in coronary heart disease: adverse effects of type D personality and younger age on 5-year prognosis and quality of life. Circulation 2000;102:630–5.[Abstract/Free Full Text]
  42. Hirschfeld RM, Klerman GL, Clayton PJ, Keller MB. Personality and depression. Empirical findings. Arch Gen Psychiatry 1983;40:993–8.[Abstract]
  43. Kendler KS, Kessler RC, Neale MC, Heath AC, Eaves LJ. The prediction of major depression in women: toward an integrated etiologic model. Am J Psychiatry 1993;150:1139–48.[Abstract/Free Full Text]
  44. Bagby RM, Rector NA, Bindseil K, Dickens SE, Levitan RD, Kennedy SH. Self-report ratings and informants’ ratings of personalities of depressed outpatients. Am J Psychiatry 1998;155:437–8.[Abstract/Free Full Text]
  45. Santor DA, Bagby RM, Joffe RT. Evaluating stability and change in personality and depression. J Pers Soc Psychol 1997;73:1354–62.[CrossRef][Medline]
  46. Shea MT, Leon AC, Mueller TI, Solomon DA, Warshaw MG, Keller MB. Does major depression result in lasting personality change? Am J Psychiatry 1996;153:1404–10.[Abstract/Free Full Text]
  47. Surtees PG, Wainwright NW. Fragile states of mind: neuroticism, vulnerability and the long-term outcome of depression. Br J Psychiatry 1996;169:338–47.[Abstract/Free Full Text]
  48. Hudson Scholle S, Haskett RD, Hanusa BH, Pincus HA, Kupfer DJ. Adressing depression in obstetrics/gynecology practice. Gen Hospital Psychiatry 2003;25:83–90.[CrossRef]




This Article
Right arrow Abstract Freely available
Right arrow Figures Only
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Verkerk, G. J.M.
Right arrow Articles by Pop, V. J.M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Verkerk, G. J.M.
Right arrow Articles by Pop, V. J.M.
Related Collections
Right arrow Depression
Right arrow Sexual Medicine: Female
Right arrow Personality
Right arrow Pregnancy


HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS