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      Association of Persistent and Severe Postnatal Depression With Child Outcomes

      research-article
      , DPhil 1 , , PhD 2 , , PhD 3 , 4 , 5 , , DPhil 3 , 4 , 5 , , PhD 6 , 7 , , FRCPsych 1 , 8 ,
      JAMA Psychiatry
      American Medical Association

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          Key Points

          Question

          What is the association of differing levels of persistence and severity of postnatal depression with long-term child outcomes?

          Findings

          This observational study of 9848 women with varying levels of postnatal depression and 8287 children found that, compared with children of women with postnatal depression that did not persist, of either moderate or severe intensity, children of women with persistent and severe depression are at an increased risk for behavioral problems by age 3.5 years as well as lower mathematics grades and depression during adolescence. Furthermore, women with persistent postnatal depression are likely to experience significant depressive symptoms until at least 11 years after childbirth.

          Meaning

          Women with persistent and severe postnatal depression should be prioritized for treatment because they are likely to continue to experience high levels of depressive symptoms and because of the high risk of adverse child development.

          Abstract

          Importance

          Maternal postnatal depression (PND) is common and associated with adverse child outcomes. These effects are not inevitable, and it is critical to identify those most at risk. Previous work suggests that the risks of adverse outcomes are increased when PND is severe and persistent, but this has not been systematically studied.

          Objective

          To examine the association between differing levels of persistence and severity of PND and long-term child outcomes.

          Design, Setting, and Participants

          The sample for this observational study comprised participants in the Avon Longitudinal Study of Parents and Children in the United Kingdom. Three thresholds of PND severity—moderate, marked, and severe—were defined using the self-rated Edinburgh Postnatal Depression Scale (EPDS). Depression was defined as persistent when the EPDS score was above the threshold level at both 2 and 8 months after childbirth. For each of these severity and persistence categories, the following were examined: (1) the trajectories of later EPDS scores (6 time points between 21 months and 11 years after childbirth) and (2) child outcomes—behavioral problems at 3.5 years of age, school-leaving mathematics grades at 16 years of age, and depression at 18 years of age. Data analysis was conducted from July 12, 2016, to February 8, 2017.

          Main Outcomes and Measures

          Child behavioral problems at 3.5 years of age using the Rutter total problems scale, school-leaving mathematics grades at 16 years of age extracted from records of external national public examinations, and offspring depression at 18 years of age using the Clinical Interview Schedule–Revised.

          Results

          For the 9848 mothers in the sample, the mean (SD) age at delivery was 28.5 (4.7) years. Of the 8287 children, 4227 (51%) were boys and 4060 (49%) were girls. Compared with women with PND that was not persistent and women who did not score above the EPDS threshold, for all 3 severity levels, women with persistent PND showed elevated depressive symptoms up to 11 years after childbirth. Whether persistent or not, PND doubled the risk of child behavior disturbance. The odds ratio (OR) for child behavioral disturbance for mothers with moderate PND was 2.22 (95% CI, 1.74-2.83), for mothers with marked PND was 1.91 (95% CI, 1.36-2.68), and for mothers with severe PND was 2.39 (95% CI, 1.78-3.22). Persistence of severe PND was particularly important to child development, substantially increasing the risk for behavioral problems at 3.5 years of age (OR, 4.84; 95% CI, 2.94-7.98), lower mathematics grades at 16 years of age (OR, 2.65; 95% CI, 1.26-5.57), and higher prevalence of depression at 18 years of age (OR, 7.44; 95% CI, 2.89-19.11).

          Conclusions and Relevance

          Persistent and severe PND substantially raises the risk for adverse outcome on all child measures. Meeting criteria for depression both early and late in the postnatal year, especially when the mood disturbance is severe, should alert health care professionals to a depression that is likely to be persistent and to be associated with an especially elevated risk of multiple adverse child outcomes. Treatment for this group should be prioritized.

          Abstract

          This study uses data from a longitudinal study to examine the association between chronic and severe postpartum depression in mothers and adverse outcomes in their children.

          Related collections

          Most cited references23

          • Record: found
          • Abstract: found
          • Article: not found

          Detection of postnatal depression. Development of the 10-item Edinburgh Postnatal Depression Scale.

          The development of a 10-item self-report scale (EPDS) to screen for Postnatal Depression in the community is described. After extensive pilot interviews a validation study was carried out on 84 mothers using the Research Diagnostic Criteria for depressive illness obtained from Goldberg's Standardised Psychiatric Interview. The EPDS was found to have satisfactory sensitivity and specificity, and was also sensitive to change in the severity of depression over time. The scale can be completed in about 5 minutes and has a simple method of scoring. The use of the EPDS in the secondary prevention of Postnatal Depression is discussed.
            • Record: found
            • Abstract: found
            • Article: not found

            Prevalence and determinants of common perinatal mental disorders in women in low- and lower-middle-income countries: a systematic review.

            To review the evidence about the prevalence and determinants of non-psychotic common perinatal mental disorders (CPMDs) in World Bank categorized low- and lower-middle-income countries. Major databases were searched systematically for English-language publications on the prevalence of non-psychotic CPMDs and on their risk factors and determinants. All study designs were included. Thirteen papers covering 17 low- and lower-middle-income countries provided findings for pregnant women, and 34, for women who had just given birth. Data on disorders in the antenatal period were available for 9 (8%) countries, and on disorders in the postnatal period, for 17 (15%). Weighted mean prevalence was 15.6% (95% confidence interval, CI: 15.4-15.9) antenatally and 19.8% (19.5-20.0) postnatally. Risk factors were: socioeconomic disadvantage (odds ratio [OR] range: 2.1-13.2); unintended pregnancy (1.6-8.8); being younger (2.1-5.4); being unmarried (3.4-5.8); lacking intimate partner empathy and support (2.0-9.4); having hostile in-laws (2.1-4.4); experiencing intimate partner violence (2.11-6.75); having insufficient emotional and practical support (2.8-6.1); in some settings, giving birth to a female (1.8-2.6), and having a history of mental health problems (5.1-5.6). Protective factors were: having more education (relative risk: 0.5; P = 0.03); having a permanent job (OR: 0.64; 95% CI: 0.4-1.0); being of the ethnic majority (OR: 0.2; 95% CI: 0.1-0.8) and having a kind, trustworthy intimate partner (OR: 0.52; 95% CI: 0.3-0.9). CPMDs are more prevalent in low- and lower-middle-income countries, particularly among poorer women with gender-based risks or a psychiatric history.
              • Record: found
              • Abstract: found
              • Article: found

              Maternal depression during pregnancy and the postnatal period: risks and possible mechanisms for offspring depression at age 18 years.

              Some small studies suggest that maternal postnatal depression is a risk factor for offspring adolescent depression. However, to our knowledge, no large cohort studies have addressed this issue. Furthermore, only 1 small study has examined the association between antenatal depression and later offspring depression. Understanding these associations is important to inform prevention. To investigate the hypothesis that there are independent associations between antenatal and postnatal depression with offspring depression and that the risk pathways are different, such that the risk is moderated by disadvantage (low maternal education) with postnatal depression but not with antenatal depression. Prospective investigation of associations between symptoms of antenatal and postnatal parental depression with offspring depression at age 18 years in a UK community-based birth cohort (Avon Longitudinal Study of Parents and Children) with data from more than 4500 parents and their adolescent offspring. Diagnosis of offspring aged 18 years with major depression using the International Classification of Diseases, 10th Revision. Antenatal depression was an independent risk factor. Offspring were 1.28 times (95% CI, 1.08-1.51; P = .003) more likely to have depression at age 18 years for each standard deviation increase in maternal depression score antenatally, independent of later maternal depression. Postnatal depression was also a risk factor for mothers with low education, with offspring 1.26 times (95% CI, 1.06-1.50; P = .01) more likely to have depression for each standard deviation increase in postnatal depression score. However, for more educated mothers, there was little association (odds ratio, 1.09; 95% CI, 0.88-1.36; P = .42). Analyses found that maternal education moderated the effects of postnatal but not antenatal depression. Paternal depression antenatally was not associated with offspring depression, while postnatally, paternal depression showed a similar pattern to maternal depression. The findings suggest that treating maternal depression antenatally could prevent offspring depression during adulthood and that prioritizing less advantaged mothers postnatally may be most effective.

                Author and article information

                Journal
                JAMA Psychiatry
                JAMA Psychiatry
                JAMA Psychiatry
                JAMA Psychiatry
                American Medical Association
                2168-622X
                2168-6238
                31 January 2018
                March 2018
                31 January 2018
                : 75
                : 3
                : 247-253
                Affiliations
                [1 ]Department of Psychiatry, University of Oxford, Oxford, United Kingdom
                [2 ]School of Social and Community Medicine, University of Bristol, Oakfield House, Bristol, United Kingdom
                [3 ]School of Psychology and Clinical Language Sciences, University of Reading, Reading, United Kingdom
                [4 ]Department of Psychology, Stellenbosch University, Matieland, Stellenbosch, South Africa
                [5 ]Department of Psychology, University of Cape Town, Rondebosch, Cape Town, South Africa
                [6 ]Department of Psychology, University of California, Los Angeles
                [7 ]Department of Psychiatry and Biobehavioral Sciences, University of California, Los Angeles
                [8 ]Medical Research Council/Wits Rural Public Health and Health Transitions Research Unit (Agincourt), School of Public Health, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa
                Author notes
                Article Information
                Accepted for Publication: December 1, 2017.
                Published Online: January 31, 2018. doi:10.1001/jamapsychiatry.2017.4363
                Open Access: This is an open access article distributed under the terms of the CC-BY License. © 2018 Netsi E et al. JAMA Psychiatry.
                Corresponding Author: Alan Stein, FRCPsych, Department of Psychiatry, University of Oxford, Warneford Lane, Oxford OX3 7JX, UK ( alan.stein@ 123456psych.ox.ac.uk ).
                Author Contributions: Dr Pearson had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.
                Study concept and design: All authors.
                Acquisition, analysis, or interpretation of data: All authors.
                Drafting of the manuscript: All authors.
                Critical revision of the manuscript for important intellectual content: All authors.
                Statistical analysis: Netsi, Pearson.
                Administrative, technical, or material support: Netsi, Pearson.
                Study supervision: Stein.
                Conflict of Interest Disclosures: None reported.
                Funding/Support: The UK Medical Research Council, the Wellcome Trust (grant 102215/2/13/2), and the University of Bristol provide core support for the Avon Longitudinal Study of Parents and Children (ALSPAC). This work was supported by grant 090139 from the Wellcome Trust and by the National Institute for Health Research (NIHR) Biomedical Research Centre at the University Hospitals Bristol National Health Service (NHS) Foundation Trust , the University of Bristol, and the NIHR Oxford Health Biomedical Research Centre. Dr Netsi is supported by an Economic and Social Research Council Global Challenges Research Fund Postdoctoral Fellowship (ES/P009794/1).
                Role of the Funder/Sponsor: The funders had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.
                Additional Contributions: We are extremely grateful to all the families who took part in this study; the midwives for their help in recruiting them; and the ALSPAC team, including interviewers, computer and laboratory technicians, clerical workers, research scientists, volunteers, managers, receptionists, and nurses.
                Disclaimer: The views expressed here are those of the authors and do not necessarily reflect those of the NHS, the NIHR, or the Department of Health.
                Article
                yoi170104
                10.1001/jamapsychiatry.2017.4363
                5885957
                29387878
                ddb1b2ea-9ef6-4970-b2de-a54c4b17be2d
                Copyright 2018 Netsi E et al. JAMA Psychiatry.

                This is an open access article distributed under the terms of the CC-BY License.

                History
                : 25 September 2017
                : 1 December 2017
                : 1 December 2017
                Funding
                Funded by: Wellcome Trust
                Funded by: National Institute for Health Research (NIHR) Biomedical Research Centre at the University Hospitals Bristol National Health Service (NHS) Foundation Trust
                Funded by: University of Bristol
                Funded by: NIHR Oxford Health Biomedical Research Centre
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