Literature DB >> 32766456

Depressive symptoms measured using the Edinburgh Postnatal Depression Scale in mothers and partners in the ALSPAC Study: A data note.

Elise Paul1, Rebecca M Pearson1.   

Abstract

Depression is a leading cause of disability and is associated with a number of adverse offspring outcomes when it occurs in parents. Depression is present in men and women at different rates, and recent research suggests that symptom profiles between the sexes may differ. Longitudinal data are needed to answer remaining questions about the long-term course, gender differences, antecedents and outcomes of depression. The Avon Longitudinal Study of Parents and Children (ALSPAC) is a large birth cohort study in England which administered one of the most commonly used depression instruments, the Edinburgh Postnatal Depression Scale (EPDS) at 11 timepoints in mothers and at 10 timepoints in their partners. In addition to repeated measurements of the EPDS, ALSPAC has a wealth of participant data on biological, social, demographic, and lifestyle factors. The purpose of this data note is to introduce potential users of the data to the characteristics of the EPDS in ALSPAC, as well as some key considerations when using the data. Copyright:
© 2020 Paul E and Pearson RM.

Entities:  

Keywords:  ALSPAC; EPDS; depression; gender; intergenerational; longitudinal cohort

Year:  2020        PMID: 32766456      PMCID: PMC7385546          DOI: 10.12688/wellcomeopenres.15925.2

Source DB:  PubMed          Journal:  Wellcome Open Res        ISSN: 2398-502X


Introduction

Depression is one of the common mental disorders and is a leading cause of disability worldwide [1]. Previous research has also shown that individuals suffering from depression are at increased risk of transmitting this and other mental health problems to their offspring [2– 4]. Understanding how depression unfolds over time as well as its risk factors in general population samples is therefore an urgent public health priority. Population wide studies consistently show that depression is more common in women than in men [5]. Depression in the perinatal period has received an increasing amount of research attention. Research indicates that depression in both mothers and fathers in the time before and shortly after the birth of a child is common [6] and is linked with a range of negative offspring outcomes in longitudinal studies [3, 4, 7– 10]. The Avon Longitudinal Study of Parents and Children (ALSPAC) is a birth cohort study of over 20,000 women, partners and their children that started in the early 1990s. Data collection is still ongoing and includes a wealth of repeated measurements of personality characteristics, mental health, biological measurements, lifestyle factors and sociodemographic information. One of these repeated measurements is of depressive symptoms via the Edinburgh Postnatal Depression Scale (EPDS) [11], the most widely used perinatal depression instrument which has been translated into over 60 languages [12]. Because the EPDS was originally developed to measure depression in the perinatal period, somatic depression symptoms (e.g. fatigue or changes in appetite) were omitted. Despite its original intended use, the EPDS is also used to assess depressive symptoms outside of the perinatal period [13– 16] and is administered to fathers as well [4, 17]. Over a dozen published ALSPAC studies have used EPDS data in mothers, partners, or both mothers and partners [8, 16, 18– 28]. One early finding using ALSPAC data is that depressive symptoms were just as common during pregnancy as in the postnatal period [29]. Another ALSPAC study found that adolescents of mothers who had been depressed during and shortly after pregnancy were at significant risk for a diagnosis of depression [10]. More recently it was demonstrated that the prevalence of depression in pregnancy is higher (25%) in the second generation of ALSPAC mothers than in the first (17%) [30]. There are still many unanswered questions regarding depression in mothers and partners. The aim of this data note is to describe the longitudinal data on maternal and partner depression available from ALSPAC to facilitate future research on depression.

Methods

The ALSPAC sample

The Avon Longitudinal Study of parents and Children (ALSPAC) is a longitudinal birth cohort that recruited pregnant women residing in Avon, UK with expected dates of delivery between 1 April 1991 and 31 December 1992. The initial number of pregnancies was 14,541, which resulted in 14,062 live births and 13,988 children alive by the age of 1 year. Further details on the representativeness, cohort profile and recruitment have been published elsewhere [31– 33]. The ALSPAC study website contains details of all data available through a fully searchable data dictionary and variable search tool. Fathers were not initially enrolled in the study directly [34]. Instead, mothers were sent a questionnaire with the option of passing it on to him to complete. Consequently, no information on the number of mothers who invited their partners to participate is available. At least one questionnaire was returned by 75% of the partners of enrolled women. Starting in 2014, study data were collected and managed using REDCap (Research Electronic Data Capture) version 7.4.9 hosted at the University of Bristol [35, 36]. REDCap is a secure, web-based software platform designed to support data capture for research studies.

Ethical approval and consent

Ethical approval for the study was obtained from the ALSPAC Law and Ethics Committee and the local research ethics committees. Full details of the approvals are available from the study website. Written informed consent for the use of data collected via questionnaires and clinics was obtained from participants following the recommendations of the ALSPAC Ethics and Law Committee at the time.

EPDS administration in ALSPAC

The EPDS was administered to ALSPAC mothers and their partners at 11 and 10 timepoints, respectively. Table 1, Table 2 present a complete list of these data collection timepoints which correspond to the focal child’s average age within ALSPAC, as well as the ALSPAC data file and variable names. Nine of the timepoints are the same in both mothers and partners with respect to the focal child’s age: 18 weeks’ gestation, 8 weeks’ post-partum, 8 months, 1 year 9 months, 2 years 9 months, 5 years 1 month, 6 years 1 month, 8 years 1 month, and 11 years 2 months.
Table 1.

Source of Edinburgh Postnatal Depression Scale (EPDS) item-level data, child age at measurement, and mother variable names in ALSPAC.

OccasionChild ageSource File in ALSPACList of Mother EPDS Variable Names in ALSPAC
118 wks. gestationb_4fb360 b361 b362 b363 b364 b365 b366 b367 b368 b369
232 wks. gestationc_8ac590 c591 c592 c593 c594 c595 c596 c597 c598 c599
38 wks. post-partume_4fe380 e381 e382 e383 e384 e385 e386 e387 e388 e389
48 mos. post-partumf_2bf190 f191 f192 f193 f194 f195 f196 f197 f198 f199
51 yr. 9 mos. post-partumg_5cg280 g281 g282 g283 g284 g285 g286 g287 g288 g289
62 yrs. 9 mos. post-partumh_6dh190 h191 h192 h193 h194 h195 h196 h197 h198 h199
75 yrs. 1 mo. post-partumk_r1bk3030 k3031 k3032 k3033 k3034 k3035 k3036 k3037 k3038 k3039
86 yrs. 1 mo. post-partuml_r1bl2010 l2011 l2012 l2013 l2014 l2015 l2016 l2017 l2018 l2019
98 yrs. 1 mo. post-partumn_3an6060 n6061 n6062 n6063 n6064 n6065 n6066 n6067 n6068 n6069
1011 yrs. 2 mos. post-partumr_r1br4010 r4011 r4012 r4013 r4014 r4015 r4016 r4017 r4018 r4019
1118 yrs. post-partumt_2at3240 t3241 t3242 t3243 t3244 t3245 t3246 t3247 t3248 t3249
Table 2.

Source of Edinburgh Postnatal Depression Scale (EPDS) item-level data, child age at measurement, and partner variable names in ALSPAC.

OccasionChild ageSource File in ALSPACList of Partner EPDS Variable Names in ALSPAC
118 wks. gestationpb_4bpb250, pb251, pb252, pb253, pb254, pb255, pb256, pb257, pb258, pb259
28 wks. post-partumpc_3apc092, pc093, pc094, pc095, pc096, pc097, pc098, pc099, pc100, pc101
38 mos. post-partumpd_7bpd190, pd191, pd192, pd193, pd194, pd195, pd196, pd197, pd198, pd199
41 yr. 9 mos. post-partumpe_4ape280, pe281, pe282, pe283, pe284, pe285, pe286, pe287, pe288, pe289
52 yrs. 9 mos. post-partumpf_r1apf4030, pf4031, pf4032, pf4033, pf4034, pf4035, pf4036, pf4037, pf4038, pf4039
65 yrs. 1 mo. post-partumph_1cph3030, ph3031, ph3032, ph3033, ph3034, ph3035, ph3036, ph3037, ph3038, ph3039
76 yrs. 1 mo. post-partumpj_r1apj2010, pj2011, pj2012, pj2013, pj2014, pj2015, pj2016, pj2017, pj2018, pj2019
88 yrs. 1 mo. post-partumpl_r1bpl6060, pl6061, pl6062, pl6063, pl6064, pl6065, pl6066, pl6067, pl6068, pl6069
911 yrs. 2 mos. post-partumpp_r1bpp4010, pp4011, pp4012, pp4013, pp4014, pp4015, pp4016, pp4017, pp4018, pp4019
1021 yrs. post-partumfa_1bfa3240, fa3241, fa3242, fa3243, fa3244, fa3245, fa3246, fa3247, fa3248, fa3249

Description of the population

Due to attrition and other sources of missing data, sample size of mothers with EPDS data at each timepoint varies, from 12,151 at 18 weeks’ gestation to 4,107 at 18 years post-partum. In partners (all of whom were male), sample sizes vary from 9,846 at 18 weeks’ gestation to 1,951 at 21 years post-partum ( Table 3, Table 4). A total of 14,169 mothers have valid EPDS data for at least one timepoint, with 2,854 of these having EPDS data for all 11 timepoints, and 1,476 mothers have data for zero EPDS assessments. In partners, 14,915 have at least one EPDS assessment, with 4,067 having all 10 assessments and 1,476 having zero. As can be seen in Table 5, Table 6, missingness on EPDS data appears to be related to several demographic characteristics.
Table 3.

Descriptive statistics and reliability of the Edinburgh Postnatal Depression Scale (EPDS) in mothers in ALSPAC.

OccasionMean Maternal Age (SD)Mean Child Age (SD)Sample SizeMean EPDS (SD)Above EPDS Threshold (≥13)Above EPDS Threshold (≥10)α
127.76 (4.93)20.85 (5.66) wks. gest.12,1516.99 (4.87)13.91%28.17%0.849
228.64 (4.86)32.65 (1.55) wks. gest.12,1907.09 (5.09)15.23%29.99%0.866
329.05 (4.82)9.93 (3.72) wks. post11,8166.06 (4.79)10.16%21.56%0.857
429.20 (4.77)8.77 (1.49) mos.11,3185.42 (4.70)8.82%17.79%0.867
529.97 (4.75)21.15 (1.18) mos.10,3845.72 (4.80)9.87%19.98%0.868
632.05 (4.73)2.81 (0.12) yrs.9,6676.29 (5.05)12.39%24.11%0.882
734.00 (4.66)5.13 (0.11) yrs.8,9376.05 (5.04)12.38%22.66%0.885
835.08 (4.61)6.17 (0.55) yrs.8,5266.35 (5.15)13.52%25.63%0.889
937.76 (4.58)8.26 (0.26) yrs.7,7626.14 (5.21)12.77%24.05%0.884
1040.32 (4.62)11.28 (0.15) yrs.7,5125.81 (5.29)12.55%22.64%0.888
1148.60 (4.48)18.47 (0.52) yrs.4,1077.47 (5.45)18.24%32.36%0.884
Table 4.

Descriptive statistics and reliability of the Edinburgh Postnatal Depression Scale (EPDS) in partners in ALSPAC.

OccasionMean Partner Age (SD)Mean Child Age (SD)Sample SizeMean EPDS (SD)Above EPDS Threshold (≥13)Above EPDS Threshold (≥10)α
130.40 (5.77)20.23 (3.50) wks. gest.9,8464.23 (3.94)4.08%10.54%0.812
231.08 (5.73)10.28 (4.49) wks. post8,4283.79 (3.85)3.60%9.07%0.825
331.81 (5.53)8.66 (1.59) mos.7,1653.36 (3.70)2.96%7.31%0.823
433.24 (5.02)21.45 (1.22) mos.6,1673.66 (3.82)3.50%8.46%0.840
534.30 (5.62)2.85 (0.17) yrs.5,3873.79 (3.88)3.81%9.17%0.833
636.625.17 (0.11) yrs.4,4963.95 (4.01)4.34%10.36%0.852
737.86 (5.62)6.18 (0.17) yrs.4,4494.46 (4.37)6.32%13.98%0.863
839.948.26 (0.30) yrs.3,9394.27 (4.41)6.12%12.77%0.866
943.24 (5.54)11.28 (0.15) yrs.3,5863.93 (4.35)5.52%11.85%0.859
1053.34 (5.40)20.24 (0.63) yrs.1,9515.85 (4.69)9.17%20.30%0.856
Table 5.

Mother demographic characteristics by number of EPDS measurements in ALSPAC.

No EPDSOne to ten EPDSAll eleven EPDS
Maternal Education at 32 wks. gestation (n = 12,483)
O Level or lower92.86%69.68%47.88%
A Level or Higher7.14%30.32%52.12%
Maternal Social Class at 18 wks. gestation (n = 11,117)
Skilled non-manual or lower71.43%71.85%57.45%
Professional/Managerial/Technical28.57%28.15%42.55%
Mother Parity (n = 13,114)
First Born56.58%43.82%47.80%
Second Born19.74%34.58%36.68%
Third + Born23.68%21.59%15.52%
Maternal Age at child’s birth (n = 14,065)
< 25 Years42.18%27.02%9.74%
25-2934.08%39.06%37.67%
30-3416.20%25.13%38.09%
35+7.54%8.80%14.51%
Table 6.

Partner demographic characteristics by number of EPDS measurements in ALSPAC.

No EPDSOne to nine EPDSAll ten EPDS
Partner Education at 32 wks. gestation (n = 12,001)
O Level or lower30.35%54.65%72.91%
A Level or Higher69.65%45.65%27.09%
Partner Social Class at 32 wks. gestation (n = 10,378)
Professional/Managerial/Technical64.64%39.15%31.73%
Skilled non-manual or lower35.36%60.85%68.27%
Partner Parity at 12 wks. gestation (n = 8,736)
First Born46.78%47.22%46.50%
Second + Born53.22%52.78%53.50%
Partner Age at 18 wks. gestation (n = 9,652)
< 25 Years1.23%13.89%30.95%
25-2925.00%35.22%23.81%
30-3443.17%31.59%33.33%
35+30.60%19.29%11.90%
The EPDS was administered to ALSPAC mothers and their partners at 11 and 10 timepoints, respectively. Table 2, Table 3 present a complete list of these data collection timepoints which correspond to the focal child’s average age within ALSPAC, as well as the ALSPAC data file and variable names. Nine of the timepoints are the same in both mothers and partners with respect to the focal child’s age: 18 weeks’ gestation, 8 weeks’ post-partum, 8 months, 1 year 9 months, 2 years 9 months, 5 years 1 month, 6 years 1 month, 8 years 1 month, and 11 years 2 months. Due to attrition and other sources of missing data, sample size of mothers with EPDS data at each timepoint varies, from 12,151 at 18 weeks’ gestation to 4,107 at 18 years post-partum. In partners, sample sizes vary from 9,846 at 18 weeks’ gestation to 1,951 at 21 years post-partum ( Table 4, Table 5). A total of 14,169 mothers have valid EPDS data for at least one timepoint, with 2,854 of these having EPDS data for all 11 timepoints, and 1,476 mothers have data for zero EPDS assessments. In partners, 14,915 have at least one EPDS assessment, with 4,067 having all 10 assessments and 1,476 having zero. As can be seen in Tables 6- 7, missingness on EPDS data appears to be related to several demographic characteristics.
Table 7.

Edinburgh Postnatal Depression Scale (EPDS) questions.

Responses
1I have been able to laugh and see the funny side of thingsAs much as I always could; Not quite so much now; Definitely not so much now; Not at all
2I have looked forward with enjoyment to thingsAs much as I ever did; Rather less than I used to; Definitely less than I used to; Hardly at all
3I have blamed myself unnecessarily when things went wrongYes, most of the time; Yes, some of the time; Not very often; No never
4I have been anxious or worried for no good reasonNo, not at all; Hardly ever; Yes, sometimes; Yes, often
5I have felt scared or panicky for no very good reasonYes, quite a lot; Yes, sometimes; No, not much; No, not at all
6Things have been getting on top of meYes, most of the time; Yes, sometimes; No, hardly ever; No, not at all
7I have been so unhappy that I have had difficulty sleepingYes, most of the time; Yes, sometimes; Not very often; No, not all
8I have felt sad or miserableYes, most of the time; Yes, quite often; Not very often; No, not at all
9I have been so unhappy that I have been cryingYes, most of the time; Yes, quite often; Only occasionally; No, never
10The thought of harming myself has occurred to meYes, quite often; Sometimes; Hardly ever; Never

The Edinburgh Postnatal Depression Scale (EPDS)

The 10-item Edinburgh Postnatal Depression Scale (EPDS) [11] assesses depressive symptoms during the prior week. Respondents rate the frequency of each symptom on a Likert-type scale with four response options, the exact wording of which varies depending on the item. See Table 7 for a complete item list with corresponding response options. Responses from all ten questions are coded 0–3 and three items (1, 2, and 4) are reverse coded. All ten items are then summed to give a score ranging between 0 and 30, where higher scores indicate more depressive symptoms. The EPDS does not assess or provide information on the duration or intensity of depressive symptoms [12]. A score of 13 or higher on the EPDS is often used to indicate probable depression [11, 37]. Others have used cut-off points of 12 [38, 39] and 10 [17]. For simplicity, we present descriptive statistics using 10 and 13 as cut-offs. Syntax for creating the scores is available upon request.

Characteristics of the EPDS in ALSPAC

The mean number of EPDS depressive symptoms and the prevalence of probable depression using both the 13 and 10 or greater cut-offs for mothers and partners are presented in Table 3, Table 4. In mothers, the greatest prevalence of depression occurs at 18 years post-partum, while the lowest is at 8 months’ post-partum ( Table 3). In partners, the greatest proportion with probable depression occurs at 21 years post-partum, while the lowest proportion is at 8 months’ post-partum ( Table 4). Correlations of depressive symptoms between timepoints within mothers and partners are moderate (0.30 to 0.49) to large (< 0.50) ( Table 8, Table 9), providing initial evidence for predictive validity. Correlations between mother and partner depressive symptoms at the same timepoints are small to moderate (0.228-0.294) ( Table 10). Data users modelling depressive symptoms over time should use statistical methods to account for these correlations. Internal reliability of the EPDS at each timepoint for both mothers and partners in ALSPAC is good ( Table 3, Table 4).
Table 8.

Table of correlations between EPDS scores on all occasions in mothers in ALSPAC.

18 wks. gestation32 wks. gestation8 wks. post-partum8 mos.1 yr. 9 mos.2 yrs. 9 mos.5 yrs. 1 mo.6 yrs. 1 mo.8 yrs. 1 mo.11 yrs. 2 mos.18 yrs.
32 wks. gestation0.643-
8 wks. post-partum0.5290.573-
8 mos.0.5020.5490.614-
1 yr. 9 mos.0.4880.5200.5580.615-
2 yrs. 9 mos.0.4710.4950.5150.5770.619-
5 yrs. 1 mo.0.4360.4600.4590.4990.5400.581-
6 yrs. 1 mo.0.4190.4480.4580.4950.5140.5500.628-
8 yrs. 1 mo.0.4050.4240.4170.4510.5000.5170.5700.579-
11 yrs. 2 mos.0.4020.4070.4140.4370.4770.4920.5140.5130.552-
18 yrs.0.3620.3820.3970.4030.4350.4350.4720.4540.4650.490-
Table 9.

Table of correlations between EPDS scores on all occasions in partners in ALSPAC.

18 wks. gestation8 wks. post- partum8 mos.1 yr. 9 mos.2 yrs. 9 mos.5 yrs. 1 mo.6 yrs. 1 mo.8 yrs. 1 mo.11 yrs. 2 mos.20 yrs.
8 wks. post-partum0.578-
8 mos.0.5550.591-
1 yr. 9 mos.0.5200.5540.584-
2 yrs. 9 mos.0.4720.4930.5260.605-
5 yrs. 1 mo.0.4220.4610.4710.5140.537-
6 yrs. 1 mo.0.4450.4600.4790.4960.4910.631-
8 yrs. 1 mo.0.4070.4190.4410.4550.4620.5130.567-
11 yrs. 2 mos.0.3900.4180.4030.4470.4230.5230.5320.542-
20 yrs.0.3680.3770.3680.3780.3470.4770.4300.4290.493-
Table 10.

Table of correlations between EPDS scores on all nine common occasions in mothers and partners in ALSPAC.

Mother at 18 wks. gestationMother at 8 wks. post- partumMother at 8 mos.Mother at 1 yr. 9 mos.Mother at 2 yrs. 9 mos.Mother at 5 yrs. 1 mo.Mother at 6 yrs. 1 mo.Mother at 8 yrs. 1 mo.Mother at 11 yrs. 2 mos.
Partner at 18 wks. gestation0.2490.1920.1750.1750.1610.1400.1310.1220.118
Partner at 8 wks. post-partum0.1900.2680.2130.1910.1810.1530.1540.1340.124
Partner at 8 mos.0.2180.2210.2800.2200.2020.1820.1800.1500.131
Partner at 1 yr. 9 mos.0.2090.2240.2370.2940.2360.1850.1800.1640.160
Partner at 2 yrs. 9 mos.0.1880.1940.2060.2270.2630.1810.1740.1520.154
Partner at 5 yrs. 1 mo.0.1760.1700.1650.1910.2100.2610.2140.1870.175
Partner at 6 yrs. 1 mo.0.1670.1890.2040.2130.1980.2080.2720.1930.198
Partner at 8 yrs. 1 mo.0.1310.1340.1300.1790.1390.1550.1800.2280.198
Partner at 11 yrs. 2 mos.0.1330.1310.1330.1660.1500.1400.1590.1370.235
As can be seen in Tables 4 and 5, mothers’ depressive symptoms and rates of probable depression are consistently higher than their partners’. This is congruent with other research on gender differences in depression [40]. Figure 1 provides a visual representation of the differences in mothers and partners in the average number of depressive symptoms over time. The mean number of depressive symptoms are also presented in histograms at each timepoint for mothers ( Figure 2) and partners ( Figure 3).
Figure 1.

Mean number of EPDS depressive symptoms in mothers and partners according to average participant age.

Figure 2.

Histograms for the number of Edinburgh Postnatal Depression Scale (EPDS) symptoms in mothers at each of the eleven occasions in ALSPAC.

Figure 3.

Histograms for the number of Edinburgh Postnatal Depression Scale (EPDS) symptoms in partners at each of the ten occasions in ALSPAC.

To help further illustrate these gender differences, Figure 4, Figure 5 present the distribution of the means (on a scale of 0–3) for each specific EPDS item in mothers and partners at all timepoints. In both mothers and partners, a common depressive symptom appears to be unnecessary self-blame. In mothers, being sad/miserable and anxious/worried are common symptoms, while in fathers, anxiety/worry and feeling overwhelmed (“things getting too much”) are common.
Figure 4.

Means (scale of 0–3) of each specific Edinburgh Postnatal Depression Scale (EPDS) symptom at each of the eleven occasions in ALSPAC mothers.

Figure 5.

Means (scale of 0–3) of each specific Edinburgh Postnatal Depression Scale (EPDS) symptom at each of the eleven occasions in ALSPAC partners.

Some researchers have investigated whether the EPDS total score can be disaggregated into meaningful subscales [41]. Using the ALSPAC data, Coates and colleagues [42] identified a three-factor solution to fit maternal EPDS data at 18 and 32 weeks’ gestation and 8 weeks and 8 months post-partum. The three factors were anhedonia (EPDS items 1 and 2), anxiety (EPDS items 3–6), and depression (EPDS items 7-10), similar to what others have found [42, 43]. We examined the fit of these three subscales using EPDS data in ALSPAC ( Figure 6) for mothers and partners at 18 weeks’ gestation and 11 years 2 months post-partum. Model fit statistics indicated generally good fit at both timepoints in both mothers and partners ( Table 11). Correlations between the three subscales within and between parents at 18 weeks’ gestation are presented in Table 12. Associations were strongest within rather than between parents.
Figure 6.

Factor structure of Edinburgh Postnatal Depression Scale (EPDS) symptom sub-scales.

Table 11.

Model fit statistics for EPDS sub-scales in mothers and partners in ALSPAC.

MothersPartners
RMSEA (90% CI)CFITLIRMSEA (95% CI)CFITLI
18 wks. gestation (T1)0.060 (0.057-0.062)0.9660.9520.059 (0.056-0.062)0.9590.943
11 years 2 mos. post-partum (T9 partners T10 for mums)0.076 (0.072-0.079)0.9610.9460.067 (0.063-0.072)0.9610.946

CFI= comparative fit index; TLI= Tucker–Lewis index; RMSEA= root mean square error of approximation.

Table 12.

Correlations between EPDS sub-scales in mothers and partners in ALSPAC at 18 wks. gestation.

Mother AnhedoniaMother AnxietyMother DepressionPartner AnhedoniaPartner AnxietyPartner Depression
Mother Anhedonia-
Mother Anxiety0.428-
Mother Depression0.5090.630-
Partner Anhedonia0.1610.1410.168-
Partner Anxiety0.1410.1970.1850.383-
Partner Depression0.1420.1610.2190.4610.564-
CFI= comparative fit index; TLI= Tucker–Lewis index; RMSEA= root mean square error of approximation.

Related constructs in ALSPAC

Researchers using the EPDS in ALSPAC may want to take advantage of the wealth of information collected on related constructs. In addition to EPDS data in partners at 10 timepoints and in offspring, measures of anxiety, personality, nutrition, IQ, and biological characteristics such as genetic markers are available in ALSPAC. Users of ALSPAC data may consult the searchable database for additional constructs which may be of interest.

ALSPAC publications using the EPDS

Over a dozen peer-reviewed papers that have used the EPDS in ALSPAC have now been published [2, 4, 8, 10, 18, 24, 28, 30, 44– 48]). Interested readers can browse ALSPAC’s catalogue of over 2,000 current and published research papers on the study website.

Considerations for the data

Like all longitudinal studies, missing data due to attrition must be taken into consideration when using ALSPAC data. However, due to the rich nature of information related to missingness in ALSPAC, users will be able to deal with missing data in a competent manner. Table 5, Table 6 list several of the potential characteristics which users can use to account for missing EPDS data. Users should take steps to handle missing data appropriately.

Strengths and limitations of the data

A major strength of the ALSPAC data is the number of participants and that it is a general population sample. Another strength is the number of time points at which the entire EPDS was administered, thus providing identical assessments over time, and that it was administered not only to mothers but also to their partners. ALSPAC is therefore a rich resource for further exploration of questions related to gender differences in the presentation of depression. One possibility for future research with the ALSPAC data is to investigate whether there are gender differences in the depression symptom profiles of men and women [49]. Some research indicates that when men are classified as being depressed by including symptoms such as risk-taking behaviour, anger attacks, and substance abuse, they are just as likely to meet criteria for depression as women [50]. A third advantage is that the offspring of the original cohort are now starting to have their own children, and these mothers, as well as their partners, are also being administered the EPDS. Two generations of EPDS data in mothers and partners are therefore available, enabling researchers to answer important questions about intergenerational depression. The data can also be linked to the wide range of other information already collected on mothers, partners and their children. One limitation of the data is that the EPDS was not designed to measure information on the duration or intensity of depressive symptoms [12]. A further limitation is the lack of consistency in the timing of measurement in mother and partner depressive symptoms in late childhood and adolescence. Both mothers and partners were administered the EPDS at child age 11 years 2 months, but the EPDS was not subsequently given to mothers until child age 18 and to partners at child age 21. The timing of these assessments will therefore somewhat limit questions which can be asked regarding depression in parents of adolescents. Another limitation of the ALSPAC data concerns racial and ethnic diversity. There are insufficient numbers of non-white participants to enable sub-group analyses.

Data availability

Underlying data

ALSPAC data are available through a system of managed open access. The application steps for ALSPAC data access are highlighted below. 1. Please read the ALSPAC access policy which describes the process of accessing the data in detail, and outlines the costs associated with doing so. 2. You may also find it useful to browse the fully searchable research proposals database, which lists all research projects that have been approved since April 2011. 3. Please submit your research proposal for consideration by the ALSPAC Executive Committee. You will receive a response within 10 working days to advise you whether your proposal has been approved. If you have any questions about accessing data, please email alspac-data@bristol.ac.uk. This is a well-written and thorough data note that will be helpful for a researcher who wishes to make use of the rich data on maternal and paternal depression within ALSPAC. Here are a few suggestions: Table 1: Consider adding the scores to the response categories. Description of the population section: I would move tables 6 and 7 to the start of the section. These tables are very relevant to someone who is determining whether or not this dataset can be used to explore their hypothesis. More information about partners may be helpful. E.g., were all partners male? Tables 2 and 3 are very detailed and only relevant to someone who has access to the data set. These do not have to be included here, but may instead be provided as an appendix. Figure 2 and 3 are very detailed and maybe not necessary. These response patterns are to be expected and can be described briefly in the text. I find the unit in Figures 4 and 5 somewhat confusing. How about the number of mothers/ partners who reported each symptom? It is fine to mention that factor analysis has been conducted to explore subscales/ dimensions within the EPDS. ALSPAC given the many waves of assessment provides an excellent opportunity to explore whether these data patterns consist over time, which could be informative but possibly too much to include here. When mentioning the CFA, it may also be relevant to mention Dr. Ted Barker’s work characterizing longitudinal latent classes (LLC) of maternal depression from pregnancy to 33 months (Barker, 2013 [1]) in ALSPAC. He identified three classes of mothers, namely low risk, medium risk, possible clinical depression (10%). It may not be feasible, but it would be helpful to list all previous publications that have used EPDS in ALSPAC. Are sufficient details of methods and materials provided to allow replication by others? Yes Is the rationale for creating the dataset(s) clearly described? Yes Are the datasets clearly presented in a useable and accessible format? Yes Are the protocols appropriate and is the work technically sound? Yes Reviewer Expertise: Effects of early psychosocial experiences (including maternal depression) on early child development I confirm that I have read this submission and believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard. We thank you for taking the time to review our data note. See our responses below. Table 1: Consider adding the scores to the response categories. Description of the population section: I would move tables 6 and 7 to the start of the section. These tables are very relevant to someone who is determining whether or not this dataset can be used to explore their hypothesis. More information about partners may be helpful. E.g., were all partners male? Tables 2 and 3 are very detailed and only relevant to someone who has access to the data set. These do not have to be included here but may instead be provided as an appendix. Figures 2 and 3 are very detailed and maybe not necessary. These response patterns are to be expected and can be described briefly in the text. I find the unit in Figures 4 and 5 somewhat confusing. How about the number of mothers/ partners who reported each symptom? It is fine to mention that factor analysis has been conducted to explore subscales/ dimensions within the EPDS. ALSPAC given the many waves of assessment provides an excellent opportunity to explore whether these data patterns consist over time, which could be informative but possibly too much to include here. We are not sure what you mean here. As in, the mean scores at each time point for each of the item? If so, we believe this would provide readers with an unnecessary amount of information. Tables 6 and 7 are now moved up in the section. All partners were indeed male, and this point has been clarified. We agree with this point, but unfortunately appendices are not possible with Wellcome data notes. We have decided to keep these, as some readers may like to see visual representations of symptom patterns. We agree that this needed clarifying. Rather than dichotomising answers, we present the mean on a 0-3 scale for each item and have clarified this in the text. When mentioning the CFA, it may also be relevant to mention Dr. Ted Barker’s work characterizing longitudinal latent classes (LLC) of maternal depression from pregnancy to 33 months (Barker, 20131) in ALSPAC. He identified three classes of mothers, namely low risk, medium risk, possible clinical depression (10%). It may not be feasible, but it would be helpful to list all previous publications that have used EPDS in ALSPAC. We appreciate this suggestion and citation but feel it would be beyond the scope of this data note to include this. This is an excellent idea. We have cited more previous publications and directed readers to the ALSPAC publications database. The report gives a thorough account of the ALSPAC data and provides potential users with a clear outline of the available data, potential uses, strengths and limitations. The authors might reference the significant background work undertaken to ensure. The EPDS was suitable for use with partners and for use outside the postpartum period (citations below) [1], [2], [3], [4] There are some typographical errors - notable in the abstract. "with' should be "when". Some minor errors in the reference list. Are sufficient details of methods and materials provided to allow replication by others? Yes Is the rationale for creating the dataset(s) clearly described? Yes Are the datasets clearly presented in a useable and accessible format? Yes Are the protocols appropriate and is the work technically sound? Yes Reviewer Expertise: Child Psychology, Developmental Science, Longitidinal research, Life course studies I confirm that I have read this submission and believe that I have an appropriate level of expertise to confirm that it is of an acceptable scientific standard. Thank you very much for taking the time to review our data note. We have taken the typographical errors into account. We thank you for taking the time to review our data note. We have taken your suggestion to add more references on background work using the EPDS outside of the postpartum period. We have also fixed the typographical errors.
  48 in total

1.  Comparative performance of Patient Health Questionnaire-9 and Edinburgh Postnatal Depression Scale for screening antepartum depression.

Authors:  Qiuyue Zhong; Bizu Gelaye; Marta Rondon; Sixto E Sánchez; Pedro J García; Elena Sánchez; Yasmin V Barrios; Gregory E Simon; David C Henderson; Swee May Cripe; Michelle A Williams
Journal:  J Affect Disord       Date:  2014-03-26       Impact factor: 4.839

2.  Association of Maternal and Paternal Depression in the Postnatal Period With Offspring Depression at Age 18 Years.

Authors:  Leticia Gutierrez-Galve; Alan Stein; Lucy Hanington; Jon Heron; Glyn Lewis; Christine O'Farrelly; Paul G Ramchandani
Journal:  JAMA Psychiatry       Date:  2019-03-01       Impact factor: 21.596

3.  Cohort study of depressed mood during pregnancy and after childbirth.

Authors:  J Evans; J Heron; H Francomb; S Oke; J Golding
Journal:  BMJ       Date:  2001-08-04

4.  The experience of symptoms of depression in men vs women: analysis of the National Comorbidity Survey Replication.

Authors:  Lisa A Martin; Harold W Neighbors; Derek M Griffith
Journal:  JAMA Psychiatry       Date:  2013-10       Impact factor: 21.596

5.  Global, regional, and national incidence, prevalence, and years lived with disability for 310 diseases and injuries, 1990-2015: a systematic analysis for the Global Burden of Disease Study 2015.

Authors: 
Journal:  Lancet       Date:  2016-10-08       Impact factor: 79.321

6.  Paternal depression in the postnatal period and child development: mediators and moderators.

Authors:  Leticia Gutierrez-Galve; Alan Stein; Lucy Hanington; Jon Heron; Paul Ramchandani
Journal:  Pediatrics       Date:  2015-01-05       Impact factor: 7.124

7.  Pathways to suicide-related behavior in offspring of mothers with depression: the role of offspring psychopathology.

Authors:  Gemma Hammerton; Stanley Zammit; Liam Mahedy; Rebecca M Pearson; Ruth Sellers; Anita Thapar; Stephan Collishaw
Journal:  J Am Acad Child Adolesc Psychiatry       Date:  2015-02-17       Impact factor: 8.829

8.  Obesity, antenatal depression, diet and gestational weight gain in a population cohort study.

Authors:  Emma Molyneaux; Lucilla Poston; Mizanur Khondoker; Louise M Howard
Journal:  Arch Womens Ment Health       Date:  2016-05-13       Impact factor: 3.633

9.  Mechanisms of Resilience in Children of Mothers Who Self-Report with Depressive Symptoms in the First Postnatal Year.

Authors:  Emily Savage-McGlynn; Maggie Redshaw; Jon Heron; Alan Stein; Maria A Quigley; Jonathan Evans; Paul Ramchandani; Ron Gray
Journal:  PLoS One       Date:  2015-11-30       Impact factor: 3.240

10.  Maternal perinatal mental health and offspring academic achievement at age 16: the mediating role of childhood executive function.

Authors:  Rebecca M Pearson; Marc H Bornstein; Miguel Cordero; Gaia Scerif; Liam Mahedy; Jonathan Evans; Abu Abioye; Alan Stein
Journal:  J Child Psychol Psychiatry       Date:  2015-11-29       Impact factor: 8.982

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  3 in total

1.  Physiological responses to cuddling babies with hypoxic-ischaemic encephalopathy during therapeutic hypothermia: an observational study.

Authors:  David Odd; Satomi Okano; Jenny Ingram; Peter S Blair; Amiel Billietop; Peter J Fleming; Marianne Thoresen; Ela Chakkarapani
Journal:  BMJ Paediatr Open       Date:  2021-12-16

2.  Psychological health of pregnant and postpartum women before and during the COVID-19 Pandemic.

Authors:  Yvonne J Kuipers; Roxanne Bleijenbergh; Laura Van den Branden; Yannic van Gils; Sophie Rimaux; Charlotte Brosens; Astrid Claerbout; Eveline Mestdagh
Journal:  PLoS One       Date:  2022-04-14       Impact factor: 3.752

3.  Relationship Between Postnatal Depression of Mental Health Patients and the Psychological Health of Their Offspring.

Authors:  Fairuz Nazri Abd Rahman; Yun Yaw Wong; Ahmad Qabil Khalib
Journal:  Front Psychiatry       Date:  2022-01-03       Impact factor: 4.157

  3 in total

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