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Eighteen-year trajectories of depressive symptoms in mothers with a lifetime eating disorder: findings from the ALSPAC cohort

Published online by Cambridge University Press:  14 May 2019

Yu Wei Chua
Affiliation:
PhD candidate in Education, Laboratory for Innovation in Autism, University of Strathclyde, UK
Gemma Lewis
Affiliation:
Research Associate in Psychiatric Epidemiology, Division of Psychiatry, University College London, UK
Abigail Easter
Affiliation:
Senior Postdoctoral Research Fellow, Centre for Implementation Science, Institute of Psychiatry, Psychology and Neuroscience, King's College London, UK
Glyn Lewis
Affiliation:
Professor of Epidemiological Psychiatry, Division of Psychiatry, University College London, UK
Francesca Solmi*
Affiliation:
Sir Henry Wellcome Post-doctoral Fellow, Division of Psychiatry, University College LondonUK
*
Correspondence: Francesca Solmi, UCL Division of Psychiatry, 6th Floor, Wing B, Maple House, 149 Tottenham Court Road, London N1T 7NF, UK. Email: francesca.solmi@ucl.ac.uk
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Abstract

Background

Two longitudinal studies have shown that depressive symptoms in women with eating disorders might improve in the antenatal and early postnatal periods. No study has followed up women beyond 8 months postnatal.

Aims

To investigate long-term trajectories of depressive symptoms in mothers with lifetime self-reported eating disorders.

Method

Using data from the Avon Longitudinal Study of Parents and Children and multilevel growth curves we modelled trajectories of depressive symptoms from the 18th week of pregnancy to 18 years postnatal in women with lifetime self-reported anorexia nervosa, bulimia nervosa or both anorexia and bulimia nervosa. As sensitivity analyses we also investigated these trajectories using quintiles of a continuous measure of body image in pregnancy.

Results

Of the 9276 women in our main sample, 126 (1.4%) reported a lifetime diagnosis of anorexia nervosa, 153 (1.6%) of bulimia nervosa and 60 (0.6%) of both anorexia and bulimia nervosa. Women with lifetime eating disorders had greater depressive symptoms scores than women with no eating disorders, before and after adjustment for confounders (anorexia nervosa: 2.10, 95% CI 1.36–2.83; bulimia nervosa: 2.28, 95% CI: 1.61–2.94, both anorexia and bulimia nervosa: 2.86, 95% CI 1.81–3.90). We also observed a dose–response association between greater body image and eating concerns in pregnancy and more severe trajectories of depressive symptoms, even after adjusting for lifetime eating disorders which also remained independently associated with greater depressive symptoms.

Conclusions

Women with eating disorders experience persistently greater depressive symptoms across the life-course. More training for practitioners and midwives on how to recognise eating disorders in pregnancy could help to identify depressive symptoms and reduce the long-term burden of disease resulting from this comorbidity.

Information

Type
Papers
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
Copyright © The Royal College of Psychiatrists 2019
Figure 0

Table 1 Participants characteristics

Figure 1

Table 2 Results of multilevel models D and E showing the association between maternal lifetime eating disorder and trajectories of depressive symptoms in the complete case participants (n = 9276)a

Figure 2

Fig. 1 Predicted trajectories of depressive symptoms derived from model E by self-reported lifetime eating disorder.

EPDS, Edinburgh Postnatal Depression Scale; ALSPAC, Avon Longitudinal Study of Parents and Children.
Figure 3

Table 3 Results of multilevel models D and E showing the association between quintiles of maternal body image and eating concerns in pregnancy and trajectories of depressive symptoms in complete case participants (n = 8722)a

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