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Plant et al
Design
The SLCDS is a prospective longitudinal UK birth cohort study
that was setup in 1986.4,18,2729 All pregnant women who
approached either of two South London National Health Service
antenatal clinics between January 1st 1986 and December 31st
1986 were invited to take part in the SLCDS. One-to-one clinical
interviews were carried out with expectant women at 20 and 36
weeks of pregnancy and 3 and 12 months postpartum, and with
offspring and mothers at 4, 11, 16 and 25 years. Two hundred
and fifty-two women participated in the first assessment visit
at 20 weeks pregnant. Because of time constraints, a 75%
randomised subsample (hereon referred to as the random
sample) were selected for interview at 36 weeks pregnant and 3
months postnatal, with the remaining women completing postal
self-report questionnaires only. The random sample did not differ
statistically in any sociodemographic or clinical characteristics in
comparison with the non-random sample, and is the sample of
interest in this paper.27 Figure 1 depicts the progress of
participation for the random sample from SLCDS onset to 25
Recruited into the study at 20 weeks pregnant
n = 252
6
Completed full interview
at 12 months postnatal
n = 149 (random sample)
6
Completed full interview
at 4 years
n = 131 (random sample)
6
Completed full interview
at 11 years
n = 136 (random sample)
6
Completed full interview
at 16 years
n = 127 (random sample)
6
Contact established
at 25 years
n = 127 (random sample)
6
Participated at 25 years
n = 103 (random sample)
Fig. 1
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Characteristic
Statistic
26.2 (4.8)
12.6
63.1
25.1 (0.7)
52.4
72.8
89.3
8.7
depression in the period between the childs 1st and 16th birthday
was also generated (0 = non-depressed; 1 = depressed).
Offspring child maltreatment
Ethics
Full ethical approval was obtained for all stages of the study. At 25
years from London Camberwell St Giles National Research
Ethics Service Committee (reference number: 11/LO/0812).
Data analysis
Analysis proceeded in three main steps. First, we performed
univariate analyses to assess the relationships between maternal
prenatal depression, offspring childhood factors (i.e. child
maltreatment, maternal depression in offspring childhood),
offspring adulthood depression and other risk variables. Next,
we used hierarchical regression analyses to test for independent
association between maternal depression in pregnancy and
offspring adulthood depression. Finally, mediation analysis was
performed to test whether environmental factors mediated the
association between maternal depression in pregnancy and
offspring adulthood depression.
All statistical analyses were conducted in IBM SPSS Statistics
Version 21 (IBM Ltd., Portsmouth, UK). Log transformations
were applied to improve the normality of the data. For data that
did not benefit from transformation, non-parametric statistical
tests were applied. Mediation analysis was conducted using
PROCESS for SPSS Version 2.041.37 Ordinary least squares
(OLS) regression was used to calculate path estimates and
estimates of the size of the direct and indirect effects. Bootstrap
confidence intervals were generated as an inferential statistical test
of the indirect effect.37 In all analyses the number of bootstrap
samples was set to 10 000 and 95% bias-corrected bootstrap
confidence intervals (CIs) generated.
Results
Descriptives
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Plant et al
Table 2
Group
effect
23.4
51.3
P = 0.004
Maternal characteristics
Age at index pregnancy, M (s.d.)
Ethnicity, % White British
Social class, % middle class
Education, % some qualifications
Marital status in pregnancy, % married
Previous psychiatric history, %b
26.5 (4.8)
79.7
17.2
79.9
73.4
25.4
25.8 (4.9)
74.4
5.1
69.2
51.3
33.3
P = 0.47
P = 0.53
P = 0.12a
P = 0.23
P = 0.02
P = 0.39
4.7 (3.1)
3.7 (5.8)
0.8 (1.5)
29.7
5.6 (3.6)
4.1 (6.8)
1.1 (2.0)
43.6
P = 0.25
P = 0.90
P = 0.19
P = 0.15
3399.1 (432.3)
40.1 (1.5)
3355.4 (582.3)
39.6 (2.0)
P = 0.66
P = 0.27
Childhood factors
Maternal depression 116 years
% exposed
Chronicity of exposure, M (s.d.)c
40.6
0.7 (0.9)
74.4
1.3 (1.0)
P = 0.001
P = 0.002
26.6
0.4 (0.7)
48.7
1.0 (1.3)
P = 0.02
P = 0.007
Offspring characteristics
Gender, % female
Ethnicity, % White British
Education, % some qualifications
IQ, M (s.d.)d
45.3
76.9
92.2
95.8 (16.1)
64.1
66.7
84.6
94.1 (13.8)
P = 0.06
P = 0.27
P = 0.33a
P = 0.56
Note. The independent samples t-test was used for group comparisons comprising continuous parametric data, whilst the MannWhitney test was applied to non-parametric
continuous data. Pearsons chi-square test for independence was used for the analysis of categorical data.
a. Fishers exact test applied because of one contingency table cell showing an expected cell count less than five.
b. n = 102 (well = 63, depressed = 39).
c. n = 100 (62, 38).
d. n = 98 (61, 37).
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Discussion
In the present study we used a 26-year prospective longitudinal
design to demonstrate, for the first time, that exposure to maternal
depression during pregnancy increases offspring vulnerability to
developing clinical depression in adulthood. Moreover, we find
that maternal depression in pregnancy is also associated with
increased vulnerability for child maltreatment in the offspring,
and that this is a mediating mechanism linking exposure to
maternal depression in pregnancy and depression in early
adulthood. When the SLCDS started in 1986, it was the first
UK longitudinal birth cohort to investigate clinical depression
in pregnancy prospectively, and thus it is the only such cohort
today with data available on offspring psychopathology in
adulthood.4,18,2729
0.78
Offspring child
maltreatment
0.65**
Maternal depression
in pregnancy
0.60*
Offspring
adult depression
0.78**
0.46
Maternal depression
during
offspring childhood
Fig. 2 Path estimates for the multiple mediation model of the effect of maternal depression in pregnancy on offspring adulthood
depression mediated by childhood risks.
Note. Estimates are presented as unstandardised B coefficients. All path estimates were calculated whilst controlling for associated covariates. *P50.05, **P50.01.
Table 3 Regression coefficients for the direct and indirect effects of offspring adulthood depression regressed on maternal
depression in pregnancy
Direct effect
Indirect effect
Offspring child maltreatment
B (s.e.)
95% CI
B (s.e.)
95% CI
B (s.e.)
95% CI
0.78 (0.67)
70.55, 2.11
0.39 (0.25)
0.04, 1.05
0.36 (0.29)
70.09, 1.10
Note. n = 100. Boldface type indicates significant effect, i.e. the 95% bootstrap confidence intervals do not cross zero. Regression coefficients presented are unstandardised
B coefficients. All path estimates were calculated whilst controlling for associated covariates. All regression models were significant at the P<0.01 level.
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Plant et al
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Implications
Our study shows that exposure to maternal depression during
pregnancy increases offspring vulnerability for developing
depression in adulthood. We find that child maltreatment is a
putative mediating mechanism in this trajectory. These findings
support the notion that exposure to maternal depression during
pregnancy and exposure to child maltreatment are part of a single
trajectory linking early life insults to risk for adulthood
depression. By intervening during pregnancy, rates of both child
maltreatment and depressive disorders in the young adults could
potentially be reduced. All expectant women could be screened
for depression and those identified offered prioritised access to
psychological therapies as indeed is currently recommended
by the UK guidelines on perinatal mental health.57 Moreover,
our findings will inform the current debate on the use of
antidepressants during pregnancy, by highlighting the adverse
consequences of not treating depression.58
Dominic T. Plant, PhD, Department of Psychological Medicine, Institute of
Psychiatry, Psychology & Neuroscience, Kings College London, UK; Carmine M.
Pariante, MD, FRCPsych, PhD, Department of Psychological Medicine, Institute of
Psychiatry, Psychology & Neuroscience, Kings College London, UK; Deborah Sharp,
MA, FRCGP, PhD, School of Social and Community Medicine, University of Bristol, UK;
Susan Pawlby, MA, PhD, CPsychol, Department of Psychological Medicine, Institute
of Psychiatry, Psychology & Neuroscience, Kings College London, UK.
Correspondence: Dominic Plant, Stress, Psychiatry and Immunology
Laboratory & Perinatal Psychiatry, Department of Psychological Medicine,
Institute of Psychiatry, Psychology & Neuroscience, Kings College London,
2-059 James Black Centre, 125 Coldharbour Lane, London SE5 9NU, UK.
Email: dominic.plant@kcl.ac.uk
First received 24 Aug 2014, final revision 4 Dec 2014, accepted 9 Dec 2014
Funding
The study was supported by the Psychiatry Research Trust, the National Institute for Health
Research (NIHR)/Wellcome Trust Kings Clinical Research Facility, the NIHR Biomedical
Research Centre at South London and Maudsley National Health Service Foundation Trust
and the Institute of Psychiatry, Psychology & Neuroscience, Kings College London and the
Medical Research Council United Kingdom.
Acknowledgements
We thank Ms J. Wertz, Dr T. Chua, Ms H. Allen, Dr A. Mills and Dr G. Schmucker (Kings
College London), and Dr C. Waters and Prof D. Hay (Cardiff University) for their research
contribution to the SLCDS, and we are especially grateful to the families of the SLCDS
who continue to give so generously of their time.
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psychiatry
in the movies
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