Data Resource Profile: ECHILD only-children and siblings (ECHILD-oCSib): a national cohort of linked health, education and social care data on mothers and children in England
Main Article Content
Abstract
Introduction
Sibling dynamics play a crucial role in individual development, health and wellbeing. We established a national birth cohort using administrative health, education and social care data in England featuring clusters of mothers and their children (mothers and only-children, MoC; and mothers and siblings, MSib).
Methods
From 13.6 million mother-baby pairs from births between April 1997 and January 2022 captured in Hospital Episode Statistics in England, we identified MoC and MSib clusters by identifying livebirths linked to the same mother. We compared only-children and children with siblings, by ethnicity, sociodemographic variables, and birth characteristics. We calculated birth intervals for children with siblings.
Results
We identified 4,086,648 MoC and 3,957,856 MSib clusters. Compared with only-children, children with siblings were more likely to be Asian, live in more deprived areas, and have younger mothers, but were less likely to be overdue births (>=42 weeks), or to have very low birth weight (< 1500g). Children with siblings were also less likely to have been admitted to special neonatal care after birth compared to only-children. Among the MSib clusters, sibship sizes varied between 2 and 15, with a mean of 2.4 children per mother. The median birth interval was 3.0 years.
Conclusion
This national cohort ECHILD-oCSib of 4.1 million MoC and 4.0 million MSib clusters in England is an important resource for investigating the effects of maternal exposures, sibling dynamics and their interplay on individual development, health and wellbeing. Potential sources of bias should be considered in analyses of these data.
Key features
- We derived a national cohort of 4.1 million clusters of mothers and only-children and 4.0 million clusters of mothers and siblings using administrative health, education and social care data in England.
- Compared with only-children, children with siblings were more likely to be Asian, live in more deprived areas, and have younger mothers, but less likely to be overdue births (>=42 weeks of gestation), or to have very low birth weight (<1500 g).
- Among children with siblings, sibship sizes varied between 2 and 15, with a mean of 2.4 children per mother (median = 2.0). The median birth interval was 3.0 years.
- The cohort is linked to longitudinal administrative data on health, education and social care use, and provides a valuable opportunity to investigate the effects of maternal factors, sibling dynamics, and their interaction on children development, health, education and wellbeing.
- The data can be accessed as part of ECHILD database.
Background
In the UK, approximately 57% of families comprise two or more dependent children, and more than half of the population grows up with sibling(s) [1]. Previous research has revealed notable variation in the development, health and overall wellbeing in various stages of the life course between children with sibling(s) and only-children (i.e., those without sibling(s)). Siblings, through their interactions, contribute to the development of health behaviours, social support systems, personalities, and wellbeing [2]. Analysis of Swedish National Registry data has shown that compared to individuals raised with siblings, only-children have lower stature and fitness levels, and are more likely to be obese in late adolescence and experience higher mortality in later life [3]. Systematic review evidence has highlighted that children with siblings tended to engage in higher levels of physical activity relative to their only-children counterparts [4]. Other studies suggest that only-children and children with siblings differ in adulthood obesity [5, 6], metabolism [7], life satisfaction, violent and altruistic behaviour [8], academic performance and psychological adjustment [9].
Sibship characteristics, encompassing factors such as sibship size, birth order, age difference, and sibling relationship dynamics, also significantly influence individual outcomes of development, education, health and wellbeing [10–15]. For example, a British cohort found that the presence of older siblings was associated with relatively better mental health, while presence of younger siblings was associated with poorer mental health [16]. A Swedish study also showed that almost half of the variation in school attainment was attributable to family-level factors, including sibship size, birth spacing and sibling sex composition [17]. A study of 26 countries similarly found a link between sibship size and individual educational attainment, and observed its variation across regions [18]. Living with a chronically ill sibling was found to increase the risk of mental, behavioural and social problems [19–21].
Numerous sibling cohorts have been established around the world, with a predominant focus on twin pairs, such as the US National Heart, Lung, and Blood Institute Male Veteran Twin Study [22], Swedish Twin Registry [23], Danish Twin Registry [24], Norwegian Twin Registry [25], Chinese National Twin Registry [26], alongside large collaborative consortia, for example, CODATwin study [27]. While twin studies provide distinctive insights in epidemiological research, twin births account for only a small proportion of all births, for instance, 1.5% in the UK [28]. It remains unclear whether the different characteristics of twin and non-twin siblings might undermine the generalisability of findings from twin-based studies to broader sibling population [29–32].
Beyond twin-based approaches, sibling cohorts encompassing a wider spectrum of sibling types offer larger coverage of general population and valuable perspectives. Examples include the California sibling study [33], the Swedish National Registry-based sibling study [34], and the Danish sibling study [35]. These cohorts serve as crucial complements to twin cohorts, yet they often lack comprehensive information on maternal factors. A UK-based sibling cohort integrated data from four birth cohorts, and identified siblings through their residence information [36]. However, this compilation comprised survey cohorts with a modest sample size of 41,000 children, resulting in limited representativeness. Therefore, there is an imperative to establish a large sibling cohort that has comprehensive coverage of population, incorporates multiple data sources on mothers and children, and facilitates extensive follow-up. The establishment of such a sibling cohort presents an important resource for understanding the effects of and the interplay between maternal factors, and sibling-related dynamics in shaping child outcomes.
In this paper, we first provide a comprehensive overview of the background, data sources and methods for establishing a national cohort of clusters of mothers and their child(ren) in England. In this cohort, we have special focus on clusters of mothers and only-children (MoC) and clusters of mothers and siblings (MSib). We describe the basic characteristics of the cohorts in the Results, and discuss the strengths, limitations and their potential use in child research in the Discussion. Lastly, we discuss how to access the data.
Methods
Data sources and participants
We used the Education and Child Health Insights from Linked Data (ECHILD) [37] and ECHILD mother-baby (ECHILD-MB) cohort [38] to establish the MoC and MSib cohorts.
ECHILD is a comprehensive national linkage of administrative health and education databases for children and young people born after 1984 in England. The linkage involved the integration of administrative hospital data from the National Health Service (NHS) Hospital Episode Statistics (HES) [39] and education and children’s social care data from the Department for Education (DfE) National Pupil Database (NPD) [40].
HES includes records of all hospital activities funded by NHS in England, including deliveries, births, inpatient admissions, outpatient appointments, accident and emergency attendances, mortality, demographics and standardised codes for diagnoses and procedures [39].
NPD contains records related to state-funded educations and children’s social care services, incorporating several data modules that are collected by DfE. NPD includes information from different educational settings about pupil’s characteristics, including age, gender, ethnicity, special educational needs and free school meals. Educational outcomes are captured, including absences, exclusions, attainment in national assessments and examination, and participation in post-16 education. NPD also features two social care modules, including Children in Need (for children referred to social care services) and Children Looked after Return (for children in care, referred to as looked after children in the UK) [40].
ECHILD ensures the anonymity of individuals by removing all direct identifiers. The linkage between HES and NPD was performed by NHS England. Briefly, DfE securely transferred identifiers from NPD to NHS England, and NHS England performed deterministic linkage to link direct identifiers to create an anonymized linkage spine connecting the NPD and HES [41, 42]. Table 1 shows the key datasets in ECHILD and other cohorts derived from it.
Data source | Description | Year coverage | Age coverage (years) | Key variables |
HES | ||||
---|---|---|---|---|
Admitted patient care | Diagnoses, operations, operation dates, consultant specialty | 1997-2022 | All | Diagnoses, operations, operation dates, etc. |
Critical care | Critical care start and end dates, number of days of support by organ group, discharge destination | 2006-2022 | Adults | Diagnosis codes, etc. |
Accident and emergency / Emergency Care Services Dataset | Type of attendance, mode of arrival, treatments, duration | 2006-2022 | All | Diagnosis codes, etc. |
Outpatient | Type of appointment, outcome of appointment, medical staff type seeing patient, duration of elective wait | 2002- 2022 | All | Diagnosis codes, etc. |
ONS linked mortality death registration | Month and year of death, underlying cause of death | 1997- 2022 | All | Date of death, cause of death, etc. |
Birth notification | Birth notification | 2001-2022 | Birth | Birth weight, gestational age |
Birth registration | Birth registration | 1996-2022 | Birth | Sex, multiple indicator, parents’ country of birth and occupation |
NPD | ||||
Early Years Census | All 2 to 4-year olds in state-funded early years care and education | 2007-2022 | 2-4 | Age, gender, ethnicity, SEN |
School census pupil level | All pupils in state-maintained educational settings, excluding hospital schools | 2005-2022 | 2-16 | Age; gender; ethnicity; SEN; FSM eligibility; language |
Pupil referral Unit census | All pupils in a PRUs (non-mainstream schools maintained by the state) | 2009-2013 | 2-16 | Age; gender; ethnicity; SEN; FSM eligibility; language |
Alternative provision census | All pupils in non-mainstream, non-maintained educational settings for whom the state are covering tuition costs | 2007-2022 | 2-16 | Age; gender; ethnicity; SEN; FSM eligibility |
Absences | All pupils in state-maintained educational settings, excluding boarding pupils | 2005-2022 | 4-16 | Number of absences; numbers that were authorized and unauthorized |
Exclusions | All pupils in state-maintained educational settings | 2001-2021 | 2-16 | Number of fixed period exclusions; number of permanent exclusions |
Early years foundation stage profile | All children at the end of the Early Years Foundation Stage of education | 2002-2019 | 3-5 | Early years practitioner assessment scores |
KS1 assessment | All children at the end of KS1 | 1997-2022 | 5-7 | Teacher assessments scores |
KS2 assessment | All children at the end of KS2 | 1995-2022 | 7-11 | Teacher assessments scores |
KS3 assessment | All children at the end of KS3 | 1998-2013 | 11-14 | Teacher assessments scores |
KS4 qualification | All pupils in KS4, including those in private schools | 2001-2021 | 14-16 | Entry for and attainment in GCSE and equivalent qualifications |
KS5 qualification | All pupils in KS5, including those in private schools | 2002-2021 | 16-18 | Entry for and attainment in A-level and equivalent qualifications |
National Client caseload information system | All young people aged 16–25 who have an SEN or disability | 2010-2022 | 16-25 | Post-16 activity; not in education, employment or training indicator |
Children in Need Census | Referrals to children’s social care and all children in need | 2008-2022 | 2-16 | Referral date; category of need; start date of child protection plan |
Children Looked After Return | All children who are looked after | 1991-2021 | 2-16 | Placement start and end date; type of placement setting; legal basis for placement |
The ECHILD-MB cohort, nested within ECHILD, specifically focuses on mother-baby pairs. In HES, delivery records and birth records are separately documented for mothers and babies, with no routine process for identifying mother-baby pairs for NHS England. We employed a validated linkage algorithm, encompassing both deterministic and probabilistic linkage methods, using information of demographics, geographic, delivery and birth characteristics to identify these pairs [43]. The algorithm successfully linked 13.6 million out of 14.5 million (overall linkage rate 94.1%) birth records to maternal delivery records between April 1997 and January 2022. External validation of the mother-baby linking status against an independent administrative dataset (Community Service Data Set) covering a subset of the ECHILD-MB cohort demonstrated low levels of linkage error. ECHILD-MB covers 87% of all livebirths in England and is representative of national birth statistics [38]. We excluded stillbirths from the ECHILD-MB cohort before deriving the MoC and MSib cohorts. (Supplementary Table 1).
Statistical analysis
Based on the number of livebirths identified for each mother in HES, we identified clusters of MoC and of MSib to form the ECHILD-MoC cohort and the ECHILD-MSib cohort. In ECHILD-MSib cohort, we integrated information across births from a multiple pregnancy (such as twins, triples, etc.) to impute missing data for gestational age and maternal age. We calculated the sibship size as the total number of livebirths (not deliveries) up to January 2022.
We compared the basic characteristics between the MoC and MSib cohorts, as well as by sibship size in the MSib cohort, including sex, birth weight (g), gestational age (weeks), mother’s ethnic background (White, Asian, Black, Mixed, and Others), maternal age (years), and mother’s Index of Multiple Deprivation (IMD) quintiles (based on residential postcode). Differences between groups were compared using standardized differences and their 95% confidence intervals. When calculating the summary statistics of these characteristics for each group of sibship size, we used individual-level data, instead of cluster-level data. For maternal characteristics (maternal age, ethnic background, IMD), the same mother may be included multiple times if she had two or more children. Based on whether a variable was time varying or not, there were three categories: (1) time-constant variables, such as maternal ethnicity; (2) delivery-specific variables, such as gestational age, maternal age, and maternal IMD; and (3) baby-specific variables, such as birth weight, baby sex, neonatal care admission, and birth status.
In the MSib cohort, we assessed the proportion of boys and of multiple births overall and by sibship size, where the latter was calculated as the number of children who were born in multiple births divided by the total number of children. We also compared the characteristics of children based on their birth order (first born vs. later born children), after removing the records where the first birth was a multiple birth.
We calculated birth interval and inter-pregnancy interval. Birth interval was defined as the time period between a delivery and the next delivery; interpregnancy-interval was defined as the time period between delivery and estimated conception date of the subsequent pregnancy. The conception date was estimated by subtracting gestational age from the derived delivery date. Derived delivery date was estimated from mothers’ delivery records using the same algorithm as used in a previous study [44]. When gestational age was missing (for 17.8% of mother-baby dyads), we used the median value (39.0 weeks). By definition, birth interval and inter-pregnancy interval for the first delivery was zero. We summarised the mean, median and interquartile rage of birth interval and interpregnancy interval, overall and by sibship size.
Results
In the ECHILD-MB cohort, after excluding 29 440 stillbirths, we identified a total of 8 044 504 mothers with at least one livebirth. Among these, 4 086 648 (50.8%) had a single livebirth, constituting the MoC cohort, while the remaining 3 957 856 (49.2%) had more than one livebirth, forming the MSib cohort (Figure 1).
Compared to the only-children, children with siblings exhibited different characteristics. They were more likely to be Asian (12.0% vs. 10.3%) and less likely to have a Mixed ethnicity background (4.4% vs. 5.3%). Children with siblings were also more likely to live in the most deprived quintile (28.5% vs. 24.4%), to have younger mothers (29.0 vs. 30.0 years), less likely to be overdue births (>=42 weeks; 3.2% vs. 3.8%), have higher birth weight (3263.6 vs. 3252.0g), and less likely to have very low birth weight (>1500g; 0.8% vs. 1.0%). They were also less likely to be admitted to special neonatal care following birth (12.5% vs. 13.8%) (Table 2).
Children in MoC cohort | Children in MSib cohort | Total | Standardised mean difference (95%CI) between MoC and MSib children | ||||||
n = 4086648 (30.0%) | Sibship size = 2 n = 5631314 (41.4%) | Sibship size = 3 n = 2465997 (18.1%) | Sibship size = 4 n = 906060 (6.6%) | Sibship size = 5 n = 315990 (2.3%) | Sibship ize ≥ 6 n = 200206 (1.5%) | Children with siblings n = 9519567 (70.0%) | n = 13606215 (100.0%) | ||
Male sex, n(%) | 2079237 (50.9%) | 2880700 (51.2%) | 1271899 (51.6%) | 462069 (51.0%) | 159925 (50.6%) | 101336 (50.7%) | 4875929 (51.2%) | 6955166 (51.1%) | 0.007 (0.005, 0.008) |
Ethnicities | 0.187 (0.186, 0.188) | ||||||||
Asian | 292432 (10.3%) | 426679 (9.8%) | 271574 (14.1%) | 125163 (17.8%) | 42750 (17.5%) | 18483 (11.9%) | 884649 (12.0%) | 1177081 (11.5%) | |
Black | 162520 (5.7%) | 186211 (4.3%) | 121038 (6.3%) | 51879 (7.4%) | 19208 (7.8%) | 11994 (7.7%) | 390330 (5.3%) | 552850 (5.4%) | |
Mixed | 152267 (5.3%) | 193974 (4.5%) | 81867 (4.3%) | 29415 (4.2%) | 10765 (4.4%) | 6736 (4.3%) | 322757 (4.4%) | 475024 (4.6%) | |
White | 2240465 (78.7%) | 3544697 (81.5%) | 1445046 (75.3%) | 496169 (70.6%) | 172096 (70.3%) | 117933 (76.0%) | 5775941 (78.3%) | 8016406 (78.4%) | |
Unknown | 1238964 (30.3%) | 1279753 (22.7%) | 546472 (22.2%) | 203434 (22.5%) | 71171 (22.5%) | 45060 (22.5%) | 2145890 (22.5%) | 3384854 (24.9%) | |
Maternal Index of multiple deprivation categories | 0.105 (0.104, 0.107) | ||||||||
Quintile 1 (most deprived) | 991941 (24.4%) | 1263312 (22.5%) | 788331 (32.1%) | 386088 (42.7%) | 156951 (49.8%) | 106715 (53.4%) | 2701397 (28.5%) | 3693338 (27.3%) | |
Quintile 2 | 882832 (21.8%) | 1158159 (20.6%) | 537191 (21.8%) | 206330 (22.8%) | 72123 (22.9%) | 45002 (22.5%) | 2018805 (21.3%) | 2901637 (21.4%) | |
Quintile 3 | 757712 (18.7%) | 1068541 (19.0%) | 418057 (17%) | 132575 (14.7%) | 40372 (12.8%) | 23626 (11.8%) | 1683171 (17.7%) | 2440883 (18.0%) | |
Quintile 4 | 676437 (16.7%) | 1013771 (18.0%) | 354100 (14.4%) | 94000 (10.4%) | 25316 (8.0%) | 13753 (6.9%) | 1500940 (15.8%) | 2177377 (16.1%) | |
Quintile 5 (least deprived) | 748818 (18.5%) | 1112681 (19.8%) | 361738 (14.7%) | 84757 (9.4%) | 20428 (6.5%) | 10564 (5.3%) | 1590168 (16.7%) | 2338986 (17.3%) | |
Unknown | 28908 (0.7%) | 14850 (0.3%) | 6580 (0.3%) | 2310 (0.3%) | 800 (0.3%) | 546 (0.3%) | 25806 (0.3%) | 54714 (0.4%) | |
Maternal age* (years), mean (SD) | 30.02 (5.99) | 29.65 (5.57) | 28.36 (5.83) | 27.41 (5.95) | 27.12 (6.04) | 27.62 (6.24) | 28.98 (5.77) | 29.28 (5.85) | 0.178 (0.177, 0.179) |
<20 | 158475 (4.6%) | 195488 (4.0%) | 143554 (6.6%) | 72074 (9.0%) | 28733 (10.3%) | 17388 (9.8%) | 457237 (5.5%) | 615712 (5.2%) | 0.186 (0.185, 0.188) |
20-24 | 500232 (14.7%) | 751482 (15.2%) | 461451 (21.2%) | 205399 (25.7%) | 74846 (26.9%) | 44068 (24.8%) | 1537246 (18.4%) | 2037478 (17.3%) | |
25-29 | 880091 (25.8%) | 1379567 (27.9%) | 636632 (29.3%) | 233900 (29.2%) | 79536 (28.5%) | 48962 (27.6%) | 2378597 (28.4%) | 3258688 (27.7%) | |
30-34 | 1053499 (30.9%) | 1625854 (32.9%) | 586956 (27.0%) | 181337 (22.7%) | 59470 (21.3%) | 39666 (22.3%) | 2493283 (29.8%) | 3546782 (30.1%) | |
35-39 | 641648 (18.8%) | 833673 (16.9%) | 291742 (13.4%) | 88494 (11.1%) | 29336 (10.5%) | 21753 (12.2%) | 1264998 (15.1%) | 1906646 (16.2%) | |
40-44 | 168105 (4.9%) | 147212 (3.0%) | 52949 (2.4%) | 17971 (2.2%) | 6392 (2.3%) | 5407 (3.0%) | 229931 (2.7%) | 398036 (3.4%) | |
>=45 | 10516 (0.3%) | 6844 (0.1%) | 2396 (0.1%) | 827 (0.1%) | 365 (0.1%) | 342 (0.2%) | 10774 (0.1%) | 21290 (0.2%) | |
Unknown | 674082 (16.5%) | 691194 (12.3%) | 290317 (11.8%) | 106058 (11.7%) | 37312 (11.8%) | 22620 (11.3%) | 1147501 (12.1%) | 1821583 (13.4%) | |
Gestational age at birth (weeks), median (interquartile range) | 39 (38, 40) | 39 (38, 40) | 39 (38, 40) | 39 (38, 40) | 39 (38, 40) | 39 (38, 40) | 39 (38, 40) | 39 (38, 40) | 0.048 (0.047, 0.050) |
<= 27 | 7478 (0.3%) | 8377 (0.2%) | 4372 (0.2%) | 1909 (0.3%) | 807 (0.3%) | 557 (0.4%) | 16022 (0.2%) | 23500 (0.2%) | 0.045 (0.044, 0.046) |
28-31 | 20029 (0.7%) | 25748 (0.6%) | 13030 (0.7%) | 5577 (0.8%) | 2372 (1.0%) | 1546 (1.0%) | 48273 (0.7%) | 68302 (0.7%) | |
32-36 | 167628 (5.7%) | 245424 (5.9%) | 126643 (6.9%) | 52952 (7.7%) | 20648 (8.6%) | 13714 (9%) | 459381 (6.5%) | 627009 (6.3%) | |
37-41 | 2626033 (89.5%) | 3750281 (89.9%) | 1642561 (89.1%) | 604590 (88.2%) | 209556 (87.1%) | 132190 (86.4%) | 6339178 (89.4%) | 8965211 (89.4%) | |
>= 42 | 112909 (3.8%) | 141071 (3.4%) | 56669 (3.1%) | 20368 (3.0%) | 7184 (3.0%) | 4980 (3.3%) | 230272 (3.2%) | 343181 (3.4%) | |
Unknown | 1152571 (28.2%) | 1460413 (25.9%) | 622722 (25.3%) | 220664 (24.4%) | 75423 (23.9%) | 47219 (23.6%) | 2426441 (25.5%) | 3579012 (26.3%) | |
Birth weight (g), mean (SD) | 3252.05 (517.29) | 3285.34 (513.01) | 3250.85 (530.55) | 3210.49 (538.2) | 3184.06 (546.48) | 3188.425 (547.67) | 3263.6 (522.9) | 3260.23 (521.3) | 0.029 (0.028, 0.031) |
<1500 | 31404 (1.0%) | 35048 (0.8%) | 17400 (0.9%) | 7128 (1.0%) | 2795 (1.1%) | 1854 (1.1%) | 64225 (0.8%) | 95629 (0.9%) | 0.051 (0.050, 0.053) |
1500-1999 | 39101 (1.3%) | 55683 (1.2%) | 29354 (1.5%) | 12563 (1.7%) | 4912 (1.9%) | 3114 (1.9%) | 105626 (1.4%) | 144727 (1.4%) | |
2000-2499 | 145238 (4.6%) | 201403 (4.5%) | 106918 (5.4%) | 45044 (6.1%) | 17256 (6.7%) | 10961 (6.7%) | 381582 (5.0%) | 526820 (4.9%) | |
2500-2999 | 584429 (18.7%) | 766564 (17.2%) | 371834 (18.8%) | 152510 (20.8%) | 56333 (21.9%) | 35107 (21.4%) | 1382348 (18.2%) | 1966777 (18.4%) | |
3000-3499 | 1267376 (40.6%) | 1761738 (39.5%) | 765319 (38.7%) | 283635 (38.7%) | 99107 (38.5%) | 62974 (38.4%) | 2972773 (39.2%) | 4240149 (39.6%) | |
3500-3999 | 952924 (30.5%) | 1460925 (32.7%) | 607548 (30.8%) | 207660 (28.3%) | 69084 (26.8%) | 44974 (27.4%) | 2390191 (31.5%) | 3343115 (31.2%) | |
4000-4499 | 94125 (3.0%) | 162804 (3.6%) | 69041 (3.5%) | 22698 (3.1%) | 7247 (2.8%) | 4643 (2.8%) | 266433 (3.5%) | 360558 (3.4%) | |
4500-4999 | 8229 (0.3%) | 15714 (0.4%) | 7023 (0.4%) | 2181 (0.3%) | 769 (0.3%) | 419 (0.3%) | 26106 (0.3%) | 34335 (0.3%) | |
>= 5000 | 1503 (0.1%) | 2158 (0.1%) | 965 (0.1%) | 301 (0.1%) | 97 (0.1%) | 51 (0.1%) | 3572 (0.1%) | 5075 (0.1%) | |
Unknown | 962319 (23.5%) | 1169277 (20.8%) | 490595 (19.9%) | 172340 (19.0%) | 58390 (18.5%) | 36109 (18.0%) | 1926711 (20.2%) | 2889030 (21.2%) | |
Neonatal care admission | 0.056 (0.055, 0.057) | ||||||||
Normal care | 2342795 (86.2%) | 3331307 (87.6%) | 1488677 (87.7%) | 554409 (87.5%) | 192616 (86.9%) | 123811 (86.9%) | 5690820 (87.5%) | 8033615 (87.1%) | |
Special care | 304313 (11.2%) | 379784 (10.1%) | 164133 (9.7%) | 61142 (9.7%) | 22230 (10.0%) | 14145 (9.9%) | 641434 (9.9%) | 945747 (10.3%) | |
L1 intensive care | 43541 (1.6%) | 58411 (1.5%) | 28114 (1.7%) | 11373 (1.8%) | 4410 (2.0%) | 2921 (2.0%) | 105229 (1.6%) | 148770 (1.6%) | |
L2 intensive care | 28775 (1.1%) | 35327 (0.9%) | 16604 (1.1%) | 6605 (1.0%) | 2449 (1.1%) | 1666 (1.2%) | 62651 (1.0%) | 91426 (1.0%) | |
Unknown | 1367224 (33.5%) | 1826485 (32.4%) | 768469 (31.2%) | 272531 (30.1%) | 94285 (29.8%) | 57663 (28.8%) | 3019433 (31.7%) | 4386657 (32.2%) |
Within the MSib cohort, the number of children in each cluster varied between 2 and 15, with a mean of 2.4 children per mother (median 2.0, mode 2.0, interquartile range 2.0–3.0). Of mothers with two or more children, 71.1% (n = 2 815 657) had two children, 20.8% (n = 821 999) had three children, 5.7% (n = 226 515) had four children, and 2.4% had more than four children.
Among the sibling clusters with two children, 51.4% consisted of one boy and one girl, 23.1% two boys, and 25.5% two girls. Distributions of sex for higher order births are provided in Supplementary Table 2. The percentage of sibling clusters that included one or more pregnancy with multiple births ranged from 2.2% in 2-sibling-clusters to 12.1% in clusters with more than five children (Figure 2).
Compared to the first born children, later born children were more likely to have lower gestational age (39 vs. 40 weeks), higher birth weight (3298 vs. 3259g), and were less likely to be overdue births (2.2% vs. 4.9%) (Table 3).
First born children n = 3898717 (41.7%) | Later born children n = 5457990 (58.3%) | Total n = 9356707 (100.0%) | Standardised mean difference (95%CI) between first born and later born | |
Male sex, n (%) | 2000284 (51.3%) | 2795032 (51.2%) | 4795316 (51.3%) | 0.002 (0.001, 0.003) |
Ethnicities | 0.277 (0.276, 0.278) | |||
Asian | 309237 (11.2%) | 564952 (12.6%) | 874189 (12%) | |
Black | 139507 (5.0%) | 243737 (5.4%) | 383244 (5.3%) | |
Mixed | 112998 (4.1%) | 204251 (4.5%) | 317249 (4.4%) | |
White | 2201216 (79.7%) | 3479318 (77.5%) | 5680534 (78.3%) | |
Unknown | 1135759 (29.1%) | 965732 (17.7%) | 2101491 (22.5%) | |
Index of multiple deprivation categories | 0.081 (0.080, 0.083) | |||
Quintile 1 (most deprived) | 1076228 (27.7%) | 1590426 (29.2%) | 2666654 (28.6%) | |
Quintile 2 | 947472 (24.4%) | 1314712 (24.1%) | 2262184 (24.2%) | |
Quintile 3 | 852241 (21.9%) | 1133733 (20.8%) | 1985974 (21.3%) | |
Quintile 4 | 777559 (20.0%) | 1015838 (18.6%) | 1793397 (19.2%) | |
Quintile 5 (least deprived) | 716799 (18.4%) | 935514 (17.2%) | 1652313 (17.7%) | |
Unknown | 12456 (0.3%) | 11070 (0.2%) | 23526 (0.3%) | |
Maternal age (years), mean (SD) | 26.6 (5.5) | 30.5 (5.4) | 28.9 (5.8) | 0.713 (0.711, 0.714) |
<20 | 388890 (11.6%) | 62925 (1.3%) | 451815 (5.5%) | 0.703 (0.701, 0.704) |
20-24 | 840523 (25.1%) | 678016 (13.9%) | 1518539 (18.5%) | |
25-29 | 1026440 (30.6%) | 1314876 (27.0%) | 2341316 (28.5%) | |
30-34 | 835713 (24.9%) | 1604924 (33.0%) | 2440637 (29.7%) | |
35-39 | 241913 (7.2%) | 990879 (20.4%) | 1232792 (15.0%) | |
40-44 | 18333 (0.5%) | 204016 (4.2%) | 222349 (2.7%) | |
>=45 | 503 (0.1%) | 8623 (0.2%) | 9126 (0.1%) | |
Unknown | 546402 (14.0%) | 593731 (10.9%) | 1140133 (12.2%) | |
Gestational age at birth (weeks), median (interquartile range) | 40 (39, 41) | 39 (38, 40) | 39 (38, 40) | 0.212 (0.210, 0.213) |
< = 27 | 5190 (0.2%) | 8355 (0.2%) | 13545 (0.2%) | 0.155 (0.153, 0.156) |
28-31 | 14777 (0.5%) | 24921 (0.6%) | 39698 (0.6%) | |
32-36 | 145994 (5.1%) | 250682 (6.2%) | 396676 (5.7%) | |
37-41 | 2569704 (89.3%) | 3697705 (90.9%) | 6267409 (90.2%) | |
>= 42 | 141428 (4.9%) | 88267 (2.2%) | 229695 (3.3%) | |
Unknown | 1021624 (26.2%) | 1388060 (25.4%) | 2409684 (25.8%) | |
Birth weight (g), mean(SD) | 3259 (495) | 3298 (512) | 3282 (505) | 0.113 (0.112, 0.114) |
<1500 | 21571 (0.7%) | 29853 (0.7%) | 51424 (0.7%) | 0.108 (0.107, 0.110) |
1500-1999 | 31831 (1.0%) | 51767 (1.2%) | 83598 (1.1%) | |
2000-2499 | 136605 (4.4%) | 194755 (4.5%) | 331360 (4.5%) | |
2500-2999 | 592619 (19.2%) | 739753 (17.0%) | 1332372 (17.9%) | |
3000-3499 | 1273434 (41.3%) | 1682794 (38.7%) | 2956228 (39.7%) | |
3500-3999 | 927067 (30.0%) | 1459805 (33.5%) | 2386872 (32.1%) | |
4000-4499 | 93433 (3.0%) | 172676 (4.0%) | 266109 (3.6%) | |
4500-4999 | 8149 (0.3%) | 17940 (0.4%) | 26089 (0.4%) | |
>= 5000 | 1172 (0.1%) | 2156 (0.1%) | 3328 (0.1%) | |
Unknown | 812836 (20.8%) | 1106491 (20.3%) | 1919327 (20.5%) | |
Neonatal care admission | 0.065 (0.064, 0.067) | |||
Normal care | 2496099 (88.5%) | 3126876 (87.8%) | 5622975 (88.1%) | |
Special care | 263689 (9.3%) | 344525 (9.7%) | 608214 (9.5%) | |
L1 intensive care | 37949 (1.3%) | 56407 (1.6%) | 94356 (1.5%) | |
L2 intensive care | 23162 (0.8%) | 33345 (0.9%) | 56507 (0.9%) | |
Unknown | 1077818 (27.6%) | 1896837 (34.8%) | 2974655 (31.8%) |
The median birth interval was 3.0 (mean 3.7, SD 2.4, mode 1.9) years, and the median interpregnancy-interval was 2.2 (mean 2.9, SD 2.4, mode 1.1) years. The median birth interval decreased as the number of siblings increased, from 3.1 years for clusters with two children to 2.8 for clusters with four children, to 2.0 for clusters with five or more children (Figure 3). Similarly, the median interpregnancy-interval decreased from 2.3 years for clusters with two children to 2.0 years for clusters with four children, to 1.3 years for clusters with five or more children (Supplementary Figure 1).
Discussion
We established a nationwide cohort of 4.1 million MoC clusters and 4.0 million MSib clusters, covering 87% of livebirths in England between April 1997 and January 2021. Through continuous linkage with longitudinal HES and NPD datasets, the cohort provides comprehensive insights into the health, education, and social care service use of each individual, spanning both mothers and the children they gave birth to. The unique combination of this extensive data resource and the well-defined cohort structure renders it valuable for addressing a diverse range of research questions.
First, the mother-baby structure provides a robust framework for investigating intergenerational effects of maternal exposures on children’s outcomes measured in education, health or social care records [37, 42, 45, 46]. Extensive previous research has suggested the significant role of maternal factors in children’s short- and long-term outcomes, spanning from birth through childhood to adolescent and adulthood [47–50]. For example, linked mother-baby HES has been used to examine the effects of a range of pre-pregnancy psychosocial risk factors on birth weight, injury admission and infant mortality [49]. Our data enable the examination of how the conditions and events experienced by mothers prior to and during pregnancy may shape the trajectories of all of their children, with special emphasis on health, education and social care use.
Second, this cohort enables comparison between MoC and MSib clusters, offering insights at both the child and mother levels. At the child level, the cohort facilitates research into whether having siblings is a risk/protective factor, or a potential effect modifier [6–8, 16, 51]. At the mother level, the cohort facilitates research into examining whether the number of children (or parity) a mother has is a potential risk or protective factor for outcomes, or if it serves as a potential effect modifier [52–56]. For example, for children, it has been suggested that having siblings promotes a more healthy weight status, while only-children are at a higher risk of overweight and obesity [6], and of adverse lipid profile [7]. Yu et al. found that sibling additions were associated with cognitive development, but only to first and second born children, but not later born children [51]. Despite the efforts put into this research field, uncertainty remains [51]. For instance, A Dutch study showed that the psychological wellbeing of mothers declines more rapidly than in childless women [53], whereas another study found an inverse association between having more children and risk of suboptimal mental health in White mothers aged 65 years or older [52]. A US study showed that multiparity is associated with poorer cardiovascular health [54], which was similar to a finding in UK Biobank [56], but in contrast to a null association between number of children and cardiovascular risk factors found in NHANES [55].
Third, the MSib cohort will be instrumental in facilitating examination of sibling dynamics and their impact on health, education, and social care involvement. The study of sibling characteristics is essential for gaining insights into the dynamics within family structures and their broader implications on individual development. On one hand, siblings contribute to establishment of social networks and emotional support; while on the other hand, they may dilute the care, support and resources provided by caregivers. A 30-year longitudinal study in the United States suggested the time-dependent nature of family resource-dilution processes; they revealed that having an older sibling is beneficial for sociobehavioral development, but gaining a younger sibling increases behavioural problems for some first-born children [51]. Investigating sibling relationships provides a unique lens through which researchers can comprehend the influence of familial environments on social, emotional, and cognitive development. By exploring siblings dynamics, researchers can inform the design of interventions and support systems that cater to the diverse needs arising from sibling relationships.
Fourth, sibling studies can be implemented within the MSib cohort, disentangling the influence of genetic and environmental confounders, thereby enhancing the potential for establishing causal inferences regarding exposure-outcome associations [57–59]. Conventional epidemiological study designs are prone to unmeasured genetic and environmental confounders, which may distort the association estimates.
In contrast, sibling comparison designs leverage the shared genetic background, lifestyle and environmental factors among siblings, serving to minimise such bias by comparing siblings that are discordant for particular exposures or outcomes [60]. It is acknowledged that new sources of bias, including birth order, age differences, gestational age, and maternal and paternal age at birth, may still be present, necessitating additional adjustments in the analytical approach.
Fifth, the structure of this cohort allows research into interactions between maternal factors and sibling dynamics, thus yielding a more comprehensive picture of how family-level factors influence child outcomes. This holistic approach not only contributes to a more comprehensive understanding of the complexities involved within families but also affords greater precision in drawing meaningful conclusions regarding the multifaceted relationships within family structures and their impact on health, education, and overall well-being. Currently, research evidence in this area is lacking.
Several potential sources of bias warrant careful consideration. Firstly, the siblings identified in our dataset are based on children born to the same mother, and we are not able to distinguish whether they share the same father (full sibling) or have different fathers (half-sibling). Secondly, the identified siblings may not necessarily be the individuals with whom a specific child grew up, as circumstances such as adoption or stepsibling relationships could alter family composition; for similar reasons, the linked mothers may not necessarily be the caregivers. However, these factors are anticipated to be validated in the future through linkage to Unique Property Reference Numbers (UPRN) [61]. Thirdly, the inclusion of an external, independent dataset to corroborate sibling status is recommended for robust validation. Fourthly, HES only captures birth records in NHS hospitals in England between April 1997 and January 2022, therefore, we may miss births before April 1997, or after January 2022, or outside NHS hospitals, or outside England (for example, if a mother immigrated to England with her existing child(ren) born in other countries), which introduces bias in underestimating the number of children a mother actually had. The size of ECHILD-MoC may be overestimated, while the size of ECHILD-MSib may be underestimated as well as the size of sibship. A previous UK study demonstrated that mothers who had out of NHS hospital deliveries were more likely to be older, white, more affluent and multiparous [62], which might imply possibility of selection bias. Fifthly, as the cohort is linked to national datasets with constant updates of data, we expect some mothers to give birth to more babies in the future, thus meaning that some individuals in the MoC cohort may be moved to the MSib cohort, and sizes of sibships in the MSib cohort will increase over time. Sixthly, NHS England apply opt outs for overall 5.4% of English population (1.3% of children aged 0-9 years and 8.5% for those aged 30-39 years). Seventhly, there is missing data in our cohort, as is in other administrative databases. Some variables have higher proportions of missing data than others, such as ethnicity, gestational age, birth weight, neonatal care admission. Data completeness has been significantly increased via data imputation based on mother-baby pairs and sibling status (for some delivery/birth related variables) and mapping across multiple medical records (for ethnicity), however, missingness is still high for some variables. These limitations may contribute to selection and information biases and should be taken into account when interpreting findings based on these data. Vigilance in addressing these potential biases will ensure a more accurate and nuanced understanding of the complex familial dynamics under investigation.
Data access
ECHILD-MoC and ECHILD-MSib data is available to accredited researchers, as part of ECHILD database. ECHILD is accessible via ONS Secure Research Service, a trusted research environment. Researchers wishing to access the ECHILD Database must apply to the ECHILD Data Access Committee. For more information on application process, please contact ich.echild@ucl.ac.uk.
Acknowledgement
We thank NHS England and Department for Education for providing the access to the Hospital Episode Statistics and the National Pupil Database. We thank NHS England for performing the initial data linkages for ECHILD project.
The authors would like to thank the wider ECHILD team including Milagros Ruiz, Ruth Blackburn, Matthew Lilliman, Farzan Ramzan, Tony Stone, Vincent Nguyen and Ania Zylbersztejn for their support with data management, and Linda Wijlaars for contributing to data extraction. We would like to thank the Health Data Research UK Social and Environmental Determinants of Health Research Driver Programme for their input to this work.
Ethics statement
Ethical approval for the ECHILD project was granted by the National Research Ethics Service (17/LO/1494), NHS Health Research Authority Research Ethics Committee (20/EE/0180 and 21/SW/0159) and is overseen by the UCL Great Ormond Street Institute of Child Health’s Joint Research and Development Office (20PE16).
Conflict of interests statement
The authors report no conflicts of interest.
Publication consent
The authors have gained publication consent to publish and openly share the data to accredited researchers via a safe research environment.
Funding statement
This work is supported by ADR UK (Administrative Data Research UK), an Economic and Social Research Council (part of UK Research and Innovation) programme (ES/V000977/1, ES/X000427/1 and ES/X003663/1). RG was supported by NIHR Senior Investigator Award and Health Data Research UK (HDRUK2023.0029), an initiative funded by UK Research and Innovation, Department of Health and Social Care (England) and the devolved administrations, and leading medical research charities.
Data availability statement
ECHILD-MoC and ECHILD-MSib data is available to accredited researchers, as part of ECHILD database. ECHILD is accessible via ONS Secure Research Service, a trusted research environment. Researchers wishing to access the ECHILD Database must apply to the ECHILD Data Access Committee. For more information on application process, please contact mailto:ich.echild@ucl.ac.ukich.echild@ucl.ac.uk.
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