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Interpregnancy intervals and child development at age 5: a population data linkage study

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Objective To investigate the associations between interpregnancy intervals (IPIs) and developmental vulnerability in children’s first year of full-time school (age 5). Design Retrospective cohort study using logistic regression. ORs were estimated for associations with IPIs with adjustment for child, parent and community sociodemographic variables. Setting Western Australia (WA), 2002–2015. Participants 34 574 WA born singletons with a 2009, 2012 or 2015 Australian Early Development Census (AEDC) record. Main outcome measure The AEDC measures child development across five domains; Physical Health and Wellbeing, Social Competence, Emotional Maturity, Language and Cognitive Skills (school-based) and Communication Skills and General Knowledge. Children with scores <10th percentile were classified as developmentally vulnerable on, one or more domains (DV1), or two or more domains (DV2). Results 22.8% and 11.5% of children were classified as DV1 and DV2, respectively. In the adjusted models (relative to the reference category, IPIs of 18–23 months), IPIs of <6 months were associated with an increased risk of children being classified as DV1 (adjusted OR (aOR) 1.17, 95% CI 1.08 to 1.34), DV2 (aOR 1.31, 95% CI 1.10 to 1.54) and an increased risk of developmental vulnerability for the domains of Physical Health and Wellbeing (aOR 1.25, 95% CI 1.06 to 1.48) and Emotional Maturity (aOR 1.36, 95% CI 1.12 to 1.66). All IPIs longer than the reference category were associated with and increased risk of children being classified as DV1 and DV2 (aOR >1.15). IPIs of 60–119 months and ≥120 months, were associated with an increased risk of developmental vulnerability on each of the five AEDC domains, with greater odds for each domain for the longer IPI category. Conclusions IPIs showed independent J-shaped relationships with developmental vulnerability, with short (<6 months) and longer (≥24 months) associated with increased risks of developmental vulnerability.
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DhamraitGK, etal. BMJ Open 2021;11:e045319. doi:10.1136/bmjopen-2020-045319
Open access
Interpregnancy intervals and child
development at age 5: a population data
linkage study
Gursimran Kaur Dhamrait ,1,2 Catherine Louise Taylor ,1,3 Gavin Pereira 1,4,5
To cite: DhamraitGK, TaylorCL,
PereiraG. Interpregnancy
intervals and child development
at age 5: a population data
linkage study. BMJ Open
2021;11:e045319. doi:10.1136/
bmjopen-2020-045319
Prepublication history and
additional materials for this
paper is available online. To
view these les, please visit
the journal online (http:// dx. doi.
org/ 10. 1136/ bmjopen- 2020-
045319).
Received 28 September 2020
Revised 27 January 2021
Accepted 05 March 2021
1Telethon Kids Institute,
University of Western Australia,
Perth, Western Australia,
Australia
2School of Population and Global
Health, University of Western
Australia, Perth, Western
Australia, Australia
3Centre for Child Health
Research, University of Western
Australia, Perth, Western
Australia, Australia
4Curtin School of Population
Health, Curtin University, Perth,
Western Australia, Australia
5Centre for Fertility and Health
(CeFH), Norwegian Institute of
Public Health, Oslo, Norway
Correspondence to
Gursimran Kaur Dhamrait;
gursimran. dhamrait@
telethonkids. org. au
Original research
© Author(s) (or their
employer(s)) 2021. Re- use
permitted under CC BY- NC. No
commercial re- use. See rights
and permissions. Published by
BMJ.
ABSTRACT
Objective To investigate the associations between
interpregnancy intervals (IPIs) and developmental
vulnerability in children’s rst year of full- time school (age
5).
Design Retrospective cohort study using logistic
regression. ORs were estimated for associations with
IPIs with adjustment for child, parent and community
sociodemographic variables.
Setting Western Australia (WA), 2002–2015.
Participants 34 574 WA born singletons with a 2009,
2012 or 2015 Australian Early Development Census (AEDC)
record.
Main outcome measure The AEDC measures child
development across ve domains; Physical Health and
Wellbeing, Social Competence, Emotional Maturity,
Language and Cognitive Skills (school- based) and
Communication Skills and General Knowledge. Children
with scores <10th percentile were classied as
developmentally vulnerable on, one or more domains
(DV1), or two or more domains (DV2).
Results 22.8% and 11.5% of children were classied as
DV1 and DV2, respectively. In the adjusted models (relative
to the reference category, IPIs of 18–23 months), IPIs of
<6 months were associated with an increased risk of
children being classied as DV1 (adjusted OR (aOR) 1.17,
95% CI 1.08 to 1.34), DV2 (aOR 1.31, 95% CI 1.10 to 1.54)
and an increased risk of developmental vulnerability for
the domains of Physical Health and Wellbeing (aOR 1.25,
95% CI 1.06 to 1.48) and Emotional Maturity (aOR 1.36,
95% CI 1.12 to 1.66). All IPIs longer than the reference
category were associated with and increased risk of
children being classied as DV1 and DV2 (aOR >1.15). IPIs
of 60–119 months and ≥120 months, were associated
with an increased risk of developmental vulnerability on
each of the ve AEDC domains, with greater odds for each
domain for the longer IPI category.
Conclusions IPIs showed independent J- shaped
relationships with developmental vulnerability, with short
(<6 months) and longer (≥24 months) associated with
increased risks of developmental vulnerability.
INTRODUCTION
Interpregnancy interval (IPI), the time from
birth to the conception of the next pregnancy,
has been proposed as an important modifi-
able risk factor for adverse birth and perinatal
outcomes.1 The WHO recommends an IPI
of approximately 2–3 years to reduce infant
and child morbidity and mortality and these
recommendations are informed by several
studies which have reported a strong J- shaped
relationship between various adverse birth
outcomes and IPIs, with the lowest risk of
adverse perinatal outcomes observed for IPIs
of 18–23 months.1–5 Both shorter (<6 months)
and longer IPIs (>60 months) have been
reported to be associated with an increased
risk of adverse birth outcomes however, it is
believed that the pathways governing these
outcomes are different. Associations between
short IPIs and adverse birth outcomes have
been interpreted as evidence in support of the
maternal depletion hypothesis, which proposes
that short IPIs lead to insufficient recovery
time from a pregnancy and the subsequent
period of lactation.1 3 6–8 Associations between
longer IPIs and adverse birth outcomes have
been interpreted as support for the physical
regression hypothesis, such that long IPIs result
Strengths and limitations of this study
The study is based on a large population- level and
otherwise healthy sample of singleton Australian
children at the time of their rst year of full- time
school.
The study is the rst to examine associations be-
tween interpregnancy intervals and child devel-
opmental vulnerability in a population of healthy
children in the early childhood period.
Logistic regression analysis with the calculation of
adjusted ORs was performed to explore the asso-
ciations between multiple interpregnancy interval
categories.
Important social risk factors including parenting ex-
perience and/or technique, stability and quality of
housing and availability of learning resources within
the household could not be accounted for.
We did not have information as to whether the preg-
nancies were planned or unplanned and as admin-
istrative records do not include pregnancies ending
before 20 weeks of gestation, we are unable to iden-
tify and account for the effect of miscarriages.
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Open access
in a loss of the beneficial physiological adaptations from
the previous pregnancy thus, resulting in a state which
resembles a primigravida.9
There is a paucity of research investigating the effects
of IPIs on children’s development during the early child-
hood period. Studies investigating the impacts of IPIs on
child development outcomes have typically focused on
neurodevelopmental morbidities and disabilities such as
autism spectrum disorder or attention- deficit/hyperac-
tivity problems.10–13 In terms of school- based outcomes,
studies have more readily examined the impact of adver-
sities associated with suboptimal IPIs such as preterm
birth and low birth weight. The available studies assessing
the relationship between birth spacing and child devel-
opment outcomes, beyond those observed at birth and
in children without diagnosed developmental disabili-
ties, have primarily examined the impact of birth inter-
vals.14–18 To our knowledge, one study has examined
the associations between IPIs and childhood develop-
ment during the early and middle childhood periods
for children without diagnosed developmental disabil-
ities.19 However, the findings of this study reported no
statistically significant associations between IPI duration
and child development outcomes, after adjustment for
a range of sociodemographic factors.19 Furthermore,
existing studies have reported mixed findings for the
associations between birth intervals and school perfor-
mance.16 20 Compared with IPIs, interdelivery intervals
have an inherent bias, as this measure is conflated by
the gestational length of the subsequent pregnancy.21
Thus, IPIs are a measure of sibling spacing that are not
confounded by gestational age. Furthermore, the first
5 years of a child’s life is recognised as a critical time for
identifying and responding to developmental vulner-
ability. Children’s developmental achievements in the
early childhood period lay the foundation for success at
school. School readiness is a multidimensional concept
that includes the child’s physical health and wellbeing,
social and emotional competence, language and cogni-
tive development and communication skills and general
knowledge22 as well as attitudes towards learning and
classroom skills and behaviours.23 This study aimed to
examine the association between IPIs and child develop-
mental vulnerability in the first year of full- time school in
Australia.
METHODS
Data sources
This study used anonymised individual- level data from
the Midwives Notification System (MNS), which is a
statutory record of all births (stillborn and live- born) in
Western Australia (WA) with either a birth weight >400
g and/or a final gestational length of 20 weeks. MNS
variables were cross validated with corresponding records
from WA Birth Registrations. Australian Early Develop-
ment Census (AEDC) records were obtained for all avail-
able years (2009, 2012 and 2015) for all children with WA
birth and perinatal records. WA Register for Develop-
mental Anomalies (WARDA) records were used to iden-
tify children with a diagnosed developmental disability.
Statistical linkage of all records, by matching identifiers
(eg, name, address, date of birth) common to sets of
records,24 was provided by the WA Data Linkage Branch
from the Department of Health WA.
Study population
The study population included all children born in
WA with an AEDC record in either 2009, 2012 or 2015
(n=73 903; figure 1). Children were sequentially excluded
from the study if they, (1) were from a multiple birth
(n=2194 (3.0%)); (2) had a parity equal to zero, that
is, were firstborns (n=29 664 (41.4%)); (3) identified by
their teacher as having ‘special- needs’ based on a diag-
nosed physical and/or intellectual disability (n=1460
(3.5%)); (4) were reported as having any congenital
anomaly in WARDA (n=1828 (4.5%)); (5) had invalid/
Figure 1 Eligible cohort and numbers included for
analyses. AEDC, Australian Early Development Census;
IPIs, Interpregnancy Intervals; WARDA, Western Australian
Register of Developmental Anomalies.
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Open access
incomplete AEDC scores (n=534 (1.4%)); (6) had
missing IPIs (n=3648 (9.5%)); or (7) had missing small
for gestational age data (n=1 (>0.01%)). The final study
sample consisted of 34 574 children.
Patient and public involvement
No patients were involved in the development of the
research question or the outcome measures, or in the
development of the plans for the design or implementa-
tion of the study.
Outcome measure
The AEDC is a national census of early childhood devel-
opment spanning across five developmental domains;
(1) Physical Health and Wellbeing, (2) Social Compe-
tence, (3) Emotional Maturity, (4) Language and Cogni-
tive Skills (school- based) and (5) Communication Skills
and General Knowledge. Based on the Canadian Early
Development Instrument,25 the AEDC is a teacher-
completed instrument collected for all children in the
first year of compulsory schooling, which in WA is pre-
primary (the year level prior to grade 1). The AEDC
is conducted every 3 years, with the first national data
collection conducted in 2009.26 AEDC cut- off scores are
based on the first national AEDC data collection in 2009
and apply to all AEDC data collections.27 Children who
score less than the 10th percentile in a given domain are
classified as ‘developmentally vulnerable.’ A child is clas-
sified as ‘special needs’ if they require special assistance
because of chronic medical, physical or intellectually
disabling condition. Domain scores are not calculated for
those students classified as ‘special needs,’ as these chil-
dren have already been identified as having substantial
developmental needs. Across the 2009, 2012 and 2015
AEDC data collections child participation for the state
of WA ranged between 98.7% and 99.6%.28 We used two
summarised outcome measures; developmentally vulner-
able on one or more AEDC domains (DV1), and devel-
opmentally vulnerable on two or more AEDC domains
(DV2), and assessed developmental vulnerability on each
AEDC domain.
Exposure variables
IPI was derived as the time between the birth of the
older sibling and the estimated start of the pregnancy
(birth date minus gestational age of child, measured in
completed weeks of gestation) of the cohort child. In
line with previous studies,1–4 7 short IPIs were classified
as; <6 months, 6–11 months and 12–17 months, IPIs of
18–23 months formed the reference category and long
IPIs were classified as; 24–59 months, 60–119 months and
120 months.
Adjustment variables
Adjustments were made for pregnancy and birth, child
and sociodemographic characteristics, selected on the
basis of availability and findings of previous studies
(table 1).29–32 We conducted univariate analysis for the
association between the background characteristics and
Table 1 Characteristics of the study cohort
Characteristics
Total
population
n (%)
n=34 574
Children classied as developmentally vulnerable on
one or more AEDC domains (DV1)
7899 (22.8)
Children classied as developmentally vulnerable on
two or more AEDC domains (DV2)
3966 (11.5)
Pregnancy and birth
Interpregnancy interval
(months)
<6 1703 (4.9)
6–11 5226 (15.1)
12–17 6451 (18.7)
18–23* 5311 (15.4)
24–59 11 531 (33.4)
60–119 3517 (10.2)
≥120 835 (2.4)
Maternal smoking status
during pregnancy
No* 28 331 (81.9)
Yes 6243 (18.1)
Mode of delivery Vaginal birth* 21 654 (62.6)
Caesarean birth 10 949 (31.7)
All other 1971 (5.7)
Preterm birth Term* 32 488 (94.0)
Preterm 2086 (6.0)
Small for gestational age No* 32 404 (93.7)
Yes 2170 (6.3)
Parity 1* 20 065 (58.0)
2 9086 (26.3)
≥3 5423 (15.7)
Maternal age at time of
child’s birth (years)
<20 508 (1.5)
20–24 4436 (12.8)
25–29* 8969 (25.9)
30–34 12 210 (35.3)
35–39 7101 (20.5)
≥40 1350 (3.9)
Child
Sex Female* 17 229 (49.8)
Male 17 345 (50.2)
Ethnicity All other* 31 736 (91.8)
Indigenous Australian 2838 (8.2)
Child speaks language
other than English at
home
No 31 296 (90.5)
Yes 3278 (9.5)
Age category at time of
AEDC collection
≥3 years and 10 months
to <5 years and 1 month
5982 (17.3)
≥5 years and 1 month to
<5 years and 10 months
25 626 (74.1)
≥5 years and 10 months 2966 (8.6)
Sociodemographic
Continued
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the likelihood of children being classified as DV1 (online
supplemental table 1).
Pregnancy and birth variables
Maternal smoking status during pregnancy, mode of
delivery, preterm birth, small for gestational age, parity
and maternal age at time of child’s birth were all obtained
from the MNS and Birth Registrations.
Child variables
Sex and ethnicity33 of child were obtained from the MNS
and Birth Registrations. The age of the child at the time
of the AEDC collection (reported as a categorical vari-
able) and language other than English spoken at home
by the child were obtained from the AEDC. The mean
age category for the study population was 5 years and
1 month and <5 years and 4 months. To balance frequen-
cies, the age of children at the time of AEDC completion
was categorised into three groups; (1) 3 years and 10
months to <5 years and 1 month, (2) 5 years and 1 month
to <5 years and 10 months (reference category) and (3)
5 years and 10 months.
Sociodemographic variables
We derived the total number of siblings by calculating
the number of live births each mother had prior to the
year that the cohort child had the AEDC conducted for
them. Siblings of the cohort who died within the neonatal
period were excluded from the calculations. Maternal
marital status at time of child’s birth was obtained from
the MNS and Birth Registrations.
Parental occupational at birth was obtained from Birth
Registrations data and converted to a four- digit standard
code using the Australian and New Zealand Standard
Classification of Occupations. These codes were assigned
a value ranging from 0 to 100 in line with the Australian
Socioeconomic Index 2006 (AUSEI06).34 Low AUSEI06
values represent low- status occupations and high values
represent high- status occupations. Records were assigned
an AUSEI06 value of zero if occupation was reported as
‘unemployed’, ‘stay at home’ parent or ‘pensioner.’ Cases
were classified as missing where parental occupation was
not stated. The AUSEI06 values were categorised into five
groups: [0, 20], (20, 40], (40, 60], (60, 80] and (80, 100].
Remoteness and socioeconomic indices were defined
with the Accessibility and Remoteness Index of Australia
(ARIA)35 and the Index of Relative Socioeconomic Disad-
vantage (IRSD),36 respectively, and were calculated using
the residential address at the time of birth. The ARIA
classifies geographical areas based on access to goods,
services and community resources into five categories
ranging from; 1 (major cities) to 5 (very remote). The
IRSD reflects area- level disadvantage through variables
such as low levels of household income, low educational
attainment and high levels of unemployment. Geograph-
ical areas are given a score from 1 (most disadvantaged)
to 5 (most advantaged).
Characteristics
Total
population
n (%)
n=34 574
Number of siblings 0† 62 (0.2)
1* 13 874 (40.1)
212 374 (35.8)
≥3 8264 (23.9)
Maternal marital status at
time of child’s birth
Married (including de
facto)*
31 776 (91.9)
All other 2561 (7.4)
Missing 237 (0.7)
Maternal occupation
status‡
0–≤20 7828 (22.6)
>20–≤40 5195 (15.0)
>40–≤60 6100 (17.6)
>60–≤80 6405 (18.5)
>80–100* 6635 (19.2)
Missing 2411 (7.0)
Paternal occupation
status‡
0–≤20 5878 (17.0)
>20–≤40 6922 (20.0)
>40–≤60 6422 (18.6)
>60–≤80 5746 (16.6)
>80–100* 7142 (20.7)
Missing 2464 (7.1)
Accessibility and
Remoteness Index of
Australia quintiles§
1* 23 363 (67.6)
2 4140 (12.0)
3 3714 (10.7)
4 1819 (5.3)
5 1008 (2.9)
Missing 530 (1.5)
Index of Relative
Socioeconomic
Disadvantage quintiles¶
1 6255 (18.1)
2 6312 (18.3)
3 6220 (18.0)
4 7381 (21.3)
5* 7766 (22.5)
Missing 640 (1.9)
*Reference group for logistic regression.
†Older sibling died within the neonatal period and therefore each
cohort child has a valid interpregnancy interval but has no additional
siblings born prior to the rst year of school.
‡Maternal and paternal occupation status are classied into ve
categories in line with Australian Socioeconomic Index 2006
(AUSEI06); low AUSEI06 values represent low- status occupations.
§Categorised as nationally dened into ve classes of remoteness;
1=major cities of Australia (least remote) to 5=very remote Australia
(most remote).
¶Categorised as nationally dened quintiles (1=most disadvantaged to
5=least disadvantaged); as quintiles are dened nationally (rather than
within study population), numbers within each category vary from 20%
of total.
AEDC, Australian Early Development Census.
Table 1 Continued
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Multiple imputation
Overall complete covariate information was available
for 86.5% (n=29 911) of the study population. A total
of five covariates had missing data; (1) maternal marital
status at birth, (2) maternal occupation status scale,
(3) paternal occupation status scale, (4) ARIA and (5)
IRSD. All variables used in the analysis had <1.9% missing
data, apart from maternal occupation status (7.0%) and
paternal occupation status (7.1%). Multiple imputation
with chained equations, using 20 imputed data sets, was
applied to minimise bias attributable to missing data,37
and the adjusted analyses presented here were performed
by pooling estimates from these imputed data sets.
Sensitivity analysis
To assess the effect of multiple imputation, we compared
the main results of (1) the study based on the imputed
data (n=34 574) to (2) the results based on the analysis of
the complete cases only (n=29 911; online supplemental
table 2). Although children classified as ‘special needs’
on the AEDC or with a WARDA record lacked outcome
data, it is however, possible that some of the conditions
classified as ‘special needs’ may be related to IPI dura-
tion. Therefore, we also conducted a sensitivity analysis
that assumed a worst- case scenario, whereby all children
with an otherwise complete/valid AEDC record, clas-
sified as either ‘special needs’ on the AEDC or with a
WARDA record were classed as developmentally vulner-
able (online supplemental table 3; n=37 789). Finally, to
assess whether our results were sensitive to IPI categorisa-
tion thresholds, we repeated the analysis by categorising
short IPIs as; <6 months, 6–11 months and 12–17 months,
IPIs of 18–23 months forming the reference category
and long IPIs as; 24–41 months, 42–59 months, 60–119
months and 120 months (online supplemental table 4).
Statistical modelling
Logistic regression models were used to estimate the odds
of a child being classified as DV1, DV2 or developmen-
tally vulnerable on an individual AEDC domain. Adjust-
ment variables were added simultaneously to the models.
ORs and the associated 95% CIs were estimated for IPIs
and adjustment variables. All statistical analyses were
conducted in SAS V.9.4.38
RESULTS
Associations between IPIs and developmental vulnerability
22.8% of children were classified as DV1 and 11.5% were
classified as DV2 (table 1). Both unadjusted and adjusted
IPIs exhibited J- shaped associations with developmental
vulnerability (figure 2). In the adjusted models, IPIs of <6
months were associated with an increased risk of children
being classified as DV1 (adjusted OR (aOR) 1.17, 95% CI
1.08 to 1.34) and DV2 (aOR 1.31, 95% CI 1.10 to 1.54),
relative the reference category. All IPIs longer than the
reference category were associated with an increased risk
of children being classified as DV1; 24–59 months (aOR
1.15, 95% CI 1.05 to 1.25), 60–119 months (aOR 1.43,
95% CI 1.28 to 1.60) and 120 months (aOR 1.84, 95% CI
1.54 to 2.19), and DV2; 24–59 months (aOR 1.19, 95% CI
1.06 to 1.34), 60–119 months (aOR 1.55, 95% CI 1.35 to
1.79) and 120 months (aOR 1.78, 95% CI 1.42 to 2.24).
Figure 2 Unadjusted and adjusted ORs for the association between interpregnancy intervals (IPIs) and developmental
vulnerability on Australian Early Development Census (AEDC) domains. ORs relative to the IPI interval reference category of
18–23 months between IPI and (A) developmental vulnerability on one or more AEDC domains (DV1) and (B) developmental
vulnerability on two or more AEDC domains (DV2). Adjusted for maternal smoking status during pregnancy, mode of delivery,
preterm birth, small for gestational age, parity, mother’s age at time of child’s birth, sex of child, ethnicity, child speaks a
language other than English at home, age of child at time of AEDC completion, number of siblings, mother’s marital status at
time of child’s birth, father’s and mother’s occupational status scale at time of child’s birth, Accessibility and Remoteness Index
of Australia and Index of Relative Socioeconomic Disadvantage category. All data is presented as ORs and 95% CIs; logistic
regression (n=34 574).
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Associations between IPIs and domain-specic
developmental vulnerability
A total of 3691 (10.7%) children were classified as devel-
opmentally vulnerable for the domains of; Physical Health
and Wellbeing, 2794 (8.1%) for Social Competence, 2817
(8.1%) for Emotional Maturity, 3381 (9.8%) for Language
and Cognitive Skills (school- based) and 2856 (8.3%) for
Communication Skills and General Knowledge (table 2).
In the adjusted models, IPIs of <6 months were associated
with an increased risk of developmental vulnerability for
the domains of Physical Health and Wellbeing (aOR 1.25,
95% CI 1.06 to 1.48; table 2) and Emotional Maturity (aOR
1.36, 95% CI 1.12 to 1.66) and IPIs of 6–11 months were asso-
ciated with an increased risk of developmental vulnerability
on the domain of Emotional Maturity (aOR 1.27, 95% CI
1.09 to 1.48), only. IPIs of 60–119 and 120 months were
associated with an increased risk of developmental vulnera-
bility on each of the five AEDC domains, with greater odds
for each domain for the longer IPI category. IPIs of 24–59
months were associated with an increased risk of develop-
mental vulnerability for all AEDC domains, except Phys-
ical Health and Wellbeing, and Communication Skills and
General Knowledge.
Sensitivity analysis
Sensitivity analysis revealed that the overall associations
between IPIs and developmental vulnerability at age 5
were not substantially different between complete cases
and the imputed cases (online supplemental table 2).
DISCUSSION
We found that short IPIs of <6 months and all longer
IPIs (24 months) were associated with increased odds
of developmental vulnerability, compared with an IPI of
18–23 months. These results were obtained from a large
population of >34 000 children and associations were
not fully explained by pregnancy, birth, child and socio-
demographic characteristics. Thus, the results indicate
the potential for the adverse effects of short and longer
IPIs to persist beyond the perinatal period and into early
childhood.
Few studies have examined the associations between
pregnancy spacing and school readiness or academic
performance.16 20 A US study of 5339 children using
data from the National Longitudinal Survey of Youth
1979 (NLSY79) assessed the associations between IPIs
and child cognitive ability and externalising behavioural
symptoms (as assessed by the Behaviour Problem Index)
in early and middle childhood.19 This study reported that
after controlling for the sex of the child and birth order,
short IPIs (12 months) were associated with scores lower
than the mean for performance in the Peabody Picture
Vocabulary Test and the maths, reading and reading
recognition subtests of the Peabody Individual Achieve-
ment Test- Revised (PIAT- R).19 Furthermore, this study
also reported that long IPIs (>36 months) were associated
with scores lower than the mean on the maths component
of the PIAT- R.19 However, after controlling for several
additional factors including, maternal age, ethnicity and
family income this study reported no statistically signif-
icant association between suboptimal IPI duration and
child development outcomes.19 Furthermore, this study
reported no statistically significant associations between
short or long IPIs and externalising behavioural problems
in children.19 Our results also indicate that very short IPIs
(<6 months) and long IPIs (24 months) are associated
with increased odds of developmental vulnerability in the
adjusted models. Likewise, a cohort study of 6915 chil-
dren from South Carolina (USA) concluded that chil-
dren born after short birth intervals (<24 months) were
more likely to fail a school readiness test when compared
with children born with longer birth intervals (24–120
months), after controlling for maternal risk factors
including education level, ethnicity and marital status.16
Our results also indicate that very short IPIs (<6 months)
are associated with increased odds of developmental
vulnerability. However, we also reported that IPIs 24
months were associated with developmental vulnerability.
Differences in findings between these studies and our
study may be attributed to differences in the definition of
the reference categories. The birth interval reference cate-
gory of 24–120 months used in the South Carolina study
would equate to an IPI of roughly 15–111 months (based
on a term pregnancy), while the reference category for the
NLSY79 study was 12–36 months. These reference catego-
ries are wide and overlaps with several of the IPI categories
used in our study, for which the direction of associations
were not consistent.16 Taken together the results of both
US studies and our study provide preliminary evidence to
suggest that short IPIs may be associated with an increased
likelihood of developmental vulnerability in children and
that the effects of the maternal depletion hypothesis may
extend beyond birth outcomes. It is estimated that approxi-
mately half of the pregnancies in Australia are unplanned.39
Decreasing the frequency of suboptimal IPIs may improve
birth outcomes and as a result, may further improve overall
school readiness in the population. However, further
research is needed to establish if this relationship is causal.
Alternatively, a longitudinal study of 1154 French chil-
dren, assessing the relationship between language skills
of children aged between 5 and 6 years of age and the age
gap between their immediately older sibling, reported
that more closely spaced siblings were more likely to
have higher language scores.17 The results of our study
however, reported an increased, although statistically
insignificant odds of developmental vulnerability the
AEDC domains of Language and Cognitive Skills (school-
based) and Communication Skills and General Knowl-
edge. It should be noted that the French study modelled
age gap as a continuous variable and thus this may account
for variations in the findings of the association between
birth spacing and child development outcomes between
this study and our study. Furthermore, the French study
concluded that a larger study would be required to deter-
mine if the negative age- gap effect was genuine.
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Table 2 Unadjusted and adjusted ORs1 for the association between developmental vulnerability for each AEDC domain and interpregnancy interval
AEDC domain and model
Interpregnancy interval (months)
OR (95% CI)†
<6 6–11 12–17 18–23 24–59 60–119 ≥120
Physical health and
Wellbeing (n=3691)‡
Unadjusted 2.01 (1.72 to 2.35)*** 1.12 (0.98 to 1.27) 1.02 (0.90 to 1.15) 1 (referent) 1.13 (1.01 to 1.26)* 1.56 (1.36 to 1.78)*** 1.58 (1.27 to 1.96)***
Adjusted§ 1.25 (1.06 to 1.48)** 0.97 (0.84 to 1.10) 0.98 (0.86 to 1.11) 1 (referent) 1.03 (0.92 to 1.16) 1.35 (1.17 to 1.55)*** 1.44 (1.14 to 1.82)**
Social Competence (n=2794) Unadjusted 1.78 (1.47 to 2.14)*** 1.23 (1.06 to 1.43)** 1.11 (0.96 to 1.28) 1 (referent) 1.29 (1.13 to 1.46)*** 1.68 (1.44 to 1.96)*** 2.10 (1.66 to 2.64)***
Adjusted 1.19 (0.98 to 1.45) 1.11 (0.95 to 1.30) 1.08 (0.93 to 1.25) 1 (referent) 1.20 (1.06 to 1.37)** 1.51 (1.28 to 1.77)*** 2.01 (1.57 to 2.58)***
Emotional Maturity (n=2817) Unadjusted 1.91 (1.58 to 2.30)*** 1.36 (1.17 to 1.58)*** 1.18 (1.02 to 1.37) 1 (referent) 1.31 (1.15 to 1.49)*** 1.71 (1.46 to 1.99)*** 2.04 (1.61 to 2.59)***
Adjusted 1.36 (1.12 to 1.66)** 1.27 (1.09 to 1.48)** 1.16 (1.00 to 1.35) 1 (referent) 1.23 (1.08 to 1.41)** 1.55 (1.32 to 1.83)*** 1.90 (1.47 to 2.45)***
Language and Cognitive
Skills (school- based)
(n=3381)
Unadjusted 2.05 (1.73 to 2.42)*** 1.22 (1.06 to 1.40)** 1.03 (0.90 to 1.18) 1 (referent) 1.35 (1.20 to 1.52)*** 1.92 (1.67 to 2.21)*** 1.82 (1.45 to 2.28)***
Adjusted 1.15 (0.96 to 1.38) 1.01 (0.87 to 1.17) 0.98 (0.85 to 1.13) 1 (referent) 1.25 (1.10 to 1.42)*** 1.71 (1.47 to 1.99)*** 1.87 (1.46 to 2.39)***
Communication Skills and
General Knowledge (n=2856)
Unadjusted 1.94 (1.63 to 2.32)*** 1.19 (1.03 to 1.38)* 1.08 (0.93 to 1.24) 1 (referent) 1.24 (1.10 to 1.41)** 1.55 (1.33 to 1.80)*** 1.51 (1.18 to 1.93)**
Adjusted 1.20 (1.00 to 1.45) 1.02 (0.88 to 1.19) 1.03 (0.89 to 1.19) 1 (referent) 1.14 (1.00 to 1.30) 1.35 (1.15 to 1.58)*** 1.51 (1.16 to 1.98)**
Interpregnancy interval was dened as the time between the birth of the older sibling and the estimated start of the pregnancy (birth date minus gestational age of child, measured in completed weeks
of gestation) of the cohort child.
***p<0.001, **p<0.01, *p<0.05.
†All data are presented as ORs (95% CIs) (total population: n=34 574).
‡Number of children classied as vulnerable for each AEDC domain for each cohort.
§Adjusted for maternal smoking status during pregnancy, mode of delivery, preterm birth, small for gestational age, parity, mother’s age at time of child’s birth, sex of child, ethnicity, child speaks a
language other than English at home, age of child at time of AEDC completion, number of siblings, mother’s marital status at time of child’s birth, father’s and mother’s occupational status scale at time
of child’s birth, Accessibility and Remoteness Index of Australia and Index of Relative Socioeconomic Disadvantage category.
AEDC, Australian Early Development Census.
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Open access
The available studies assessing associations between
birth spacing and academic performance have been
primarily conducted in children older than those assessed
in our study. One of the earliest studies to investigate the
relationship between school performance conducted
in Singapore reported that children born after a birth
interval of 24 months performed better at school, at
age 9 than children born after a birth interval of <24
months.20 Alternatively, a cross- sectional study of Saudi
boys, aged between 9 and 10 years, reported that chil-
dren born after short birth intervals of <17 months were
more likely to be classified as below average on teacher-
assessed school performance in comparison to children
born after long birth intervals (>31 months).14 Again,
differences in findings between these studies and those
of our study may be attributed to the fact that both of
these studies used binary birth interval categories, which
overlap with several of the IPI categories used in our study
and with the current WHO recommendations of an IPI of
approximately 2–3 years.40 Given these mixed results and
the relatively small number of studies on the topic, the
association between IPIs and developmental vulnerability
beyond the perinatal period remains not well- established.
Furthermore, as prior research assessing the associations
between IPIs and child development outcomes has largely
been confined to the perinatal period, further research
is required to assess the relationship between IPIs and
developmental vulnerability in early childhood and to
determine causality.
Limitations
Our study had several limitations. First, important social
risk factors including parenting experience and/or tech-
nique, stability and quality of housing and availability of
learning resources within the household could not be
accounted for due to the nature of administrative data.
Second, we did not have information as to whether the
pregnancies were planned or unplanned and as adminis-
trative records do not include pregnancies ending before
20 weeks of gestations, we are unable to identify and
account for the effect of miscarriages. Third, as the birth-
dates of older siblings were obtained from Birth Registra-
tions and MNS records in the state of WA, we were not
able to calculate IPIs for children with an older sibling
born in another state. Finally, there are a wide range of
reproductive health behaviours and physiological factors
governing the length of IPIs including, fertility levels, the
use of contraception, time- until- conception and breast-
feeding durations,41 which we could not control for as
they are not recorded in administrative data.
Implications of ndings
The behaviours, emotions and physical and cognitive
capacities that develop in the first 5 years of life assist
in the facilitation of learning and are predictive of later
school achievement and behavioural outcomes.25–27 The
cumulative nature of school- based learning means that
children who begin school with poor school readiness
often fail to catch up with their peers and tend to fall
further behind as they progress through schooling.28 In
particular, research has indicated that children classified
as DV1 are more likely to score in the bottom 20% of all
students on the National Assessment Program Literacy
and Numeracy assessments in grades 3, 5 and 7.42 This
study supports the hypothesis that IPIs are a predictor of
developmental vulnerability and poor school readiness.
The concept of optimising birth spacing has been widely
discussed in the literature, and the findings of our study
imply that the adverse impacts of IPIs may extend beyond
birth outcomes. Decreasing the frequency of suboptimal
IPIs may improve birth outcomes and as a result, may
further improve overall child development outcomes in
the population.
CONCLUSIONS
IPIs exhibited independent J- shaped associations with
developmental vulnerability. For our cohort, very short
IPIs of less than 6 months and longer IPIs of 2 years or
longer were associated with increased risk of develop-
mental vulnerability on one or more and two or more
AEDC domains. IPIs of 5 years or longer were associ-
ated with developmental vulnerability on all five AEDC
domains. The results provide empirical support for the
association between long IPIs of 2 years or longer and
developmental vulnerability at age 5. Although further
research is required to establish causality, the results of
this study add to the current body of literature suggesting
the potential for optimising IPIs as a means for improving
child development outcomes.
Acknowledgements We gratefully acknowledge the WA Data Linkage Branch
and Data Custodians who provided data for this study and the people of Western
Australia for the use of their administrative data. This study does not necessarily
reect their views. This study uses data from the Australian Early Development
Census (AEDC). The AEDC is funded by the Australian Government Department of
Education and Training. The ndings and views reported are those of the authors
and should not be attributed to the Department or the Australian Government. We
thank Helen Bailey for assistance in the use of these data and Scott Sims and
Daniel Christensen for statistical advice and support.
Contributors GKD led study conceptualisation and design, conducted the literature
review, performed data manipulation, analysis and interpretation of ndings,
drafted the initial manuscript and reviewed and revised the manuscript critically
for important intellectual content. GP and CLT contributed to conceptualising and
designing the study, interpreting the results and writing the manuscript. All authors
approved the nal manuscript as submitted and agree to be accountable for all
aspects of the work.
Funding This work was supported by the National Health and Medical Research
Grants (grant numbers GNT1173991 and GNT1099655 to GP), the Australian
Research Council Centre of Excellence for Children and Families over the Life
Course (grant number CE140100027 to CLT). GKD was supported by the ARC
Centre of Excellence for Children and Families over the Life Course Scholarship,
the ARC Centre of Excellence for Children and Families over the Life Course Top- Up
Scholarship and the Stan and Jean Perron Top- Up Scholarship. GP was supported
with funding from the National Health and Medical Research Council Project and
Investigator (grant numbers 1099655 and 1173991) and the Research Council of
Norway through its Centres of Excellence funding scheme (grant number 262700).
Competing interests None declared.
Patient consent for publication Not required.
Ethics approval Ethics approval for this study was granted by the Western
Australian Department of Health Human Research Ethics Committee (2016/51)
on March 23, 2021 by guest. Protected by copyright.http://bmjopen.bmj.com/BMJ Open: first published as 10.1136/bmjopen-2020-045319 on 23 March 2021. Downloaded from
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DhamraitGK, etal. BMJ Open 2021;11:e045319. doi:10.1136/bmjopen-2020-045319
Open access
and the University of Western Australia Human Research Ethics Committee
(RA/4/20/4776).
Provenance and peer review Not commissioned; externally peer reviewed.
Data availability statement All data relevant to the study are included in the
article or uploaded as supplementary information. We received data from WA
Department of Health through the Data Linkage Branch. The data are not publicly
available, and privacy and legal restrictions apply to the provision of the data to
third parties.
Supplemental material This content has been supplied by the author(s). It has
not been vetted by BMJ Publishing Group Limited (BMJ) and may not have been
peer- reviewed. Any opinions or recommendations discussed are solely those
of the author(s) and are not endorsed by BMJ. BMJ disclaims all liability and
responsibility arising from any reliance placed on the content. Where the content
includes any translated material, BMJ does not warrant the accuracy and reliability
of the translations (including but not limited to local regulations, clinical guidelines,
terminology, drug names and drug dosages), and is not responsible for any error
and/or omissions arising from translation and adaptation or otherwise.
Open access This is an open access article distributed in accordance with the
Creative Commons Attribution Non Commercial (CC BY- NC 4.0) license, which
permits others to distribute, remix, adapt, build upon this work non- commercially,
and license their derivative works on different terms, provided the original work is
properly cited, appropriate credit is given, any changes made indicated, and the use
is non- commercial. See:http:// creativecommons. org/ licenses/ by- nc/ 4. 0/.
ORCID iDs
Gursimran KaurDhamrait http:// orcid. org/ 0000- 0002- 5191- 211X
Catherine LouiseTaylor http:// orcid. org/ 0000- 0001- 9061- 9162
GavinPereira http:// orcid. org/ 0000- 0003- 3740- 8117
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... In particular, children who face adversities, such as unstable housing, marriage breakdown, and poverty, in their early, formative years are at risk of falling short of their potential (3). Furthermore, sociodemographic factors such as maternal age at birth (4)(5)(6), maternal reproductive history (7), and socioeconomic status (including parental educational and occupational characteristics) (8)(9)(10)(11) can also influence pregnancy and interpregnancy intervals. Thus, it is important to understand and identify how particular influences associated with pregnancy, birth, and childhood impact children's physical, emotional, and educational development (12). ...
... The studies were conducted in very different settings-three in the United States, two in Saudi Arabia, one in Australia, and one in France. Two studies used a cross-sectional design (69,70), four used a retrospective cohort design (8,(71)(72)(73), and one used a case-control design (74). Study sample sizes ranged from 536 to 34,574 children. ...
... Four studies relied on parental self-report (69-71, 73) and three from medical records for birth spacing measures (8,72,74). The categories and reference categories of birth spacing intervals differed across the seven studies. ...
Article
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Objective This study aimed to systematically review the literature on the associations between birth spacing and developmental outcomes in early childhood (3–10 years of age). Studies examining the associations between interpregnancy intervals and child development outcomes during and beyond the perinatal period have not been systematically reviewed. Methods We searched Ovid/MEDLINE, Global Health, PsycINFO, EMBASE, CINAHL Plus, Educational Source, Research Starters, ERIC, Scopus, PubMed, Social Science Research Network database, and ProQuest's Social Sciences Databases for relevant articles published between 1 January 1989 and 25 June 2021. Studies published in English, conducted in populations residing in high-income countries with any measure of birth spacing, and child development outcomes among children aged <10 years were included. Two authors independently assessed the eligibility of studies and extracted data on the study design, setting and population, birth spacing, outcomes, and results. Results The search yielded 1,556 records, of which seven studies met the inclusion criteria. Five of these seven studies used birth intervals as the exposure measure. Definitions of exposure differed between the studies. Three studies reported an association between short birth spacing and poorer child development outcomes, and two studies reported an association between long birth spacing and poorer child development outcomes. Conclusion Currently, limited evidence suggests that the adverse effects of sub-optimal birth spacing are observable beyond infancy.
... 3 The World Health Organization (WHO) recommended that women should avoid pregnancy until at least 24 months after their previous live birth. 1 Short birth interval (SBI) (i.e, short birthto-birth interval) is, therefore, defined as occurring when the time interval between two successive live births is less than 33 months (i.e, 33 months=24 months of birth to conception period+9 months duration of pregnancy). However, there are some inconsistencies in the literature [4][5][6][7][8][9] with cutoff points for short birth/interpregnancy interval varying from 6 to 24 months. Our study will investigate the measurements and definitions 3 used by studies for SBI which are among the reasons for the inconsistency in the cut-off points. ...
Article
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Background Short birth interval (SBI) has been linked to an increased risk of adverse maternal, perinatal, infant and child health outcomes. However, the prevalence and maternal and child health impacts of SBI in the Asia-Pacific region have not been well understood. This study aims to identify and summarise the existing evidence on SBI including its definition, measurement prevalence, determinants and association with adverse maternal and child health outcomes in the Asia-Pacific region. Methods Five databases (MEDLINE, Scopus, Cumulative Index to Nursing and Allied Health Literature (CINAHL), Maternity and Infant Care, and Web of Science (WoS)) will be systematically searched from September 2000 up to May 2023. Data will be extracted, charted, synthesised and summarised based on the outcomes measured, and where appropriate, meta-analysis will be performed. The risk of bias will be assessed using Joanna Briggs Institute quality appraisal. Grading of Recommendation Assessment, Development and Evaluation framework will be used to evaluate the quality of cumulative evidence from the included studies. Ethics and dissemination This review does not require ethics approval. Findings will be disseminated through peer-reviewed publications, policy briefs and conference presentations. PROSPERO registration number A protocol will be registered on PROSPERO for each separate outcome before performing the review. Cite Now
... Finally, a more recent study (Dhamrait et al., 2020) found a nonlinear relationship (U-shape) between interpregnancy intervals and children's developmental vulnerability at age 5 years, with an age gap of under 6 months or over 24 months being associated with an increased risk in developmental vulnerability. Thus, there is a need for further investigation of age gap effects. ...
Article
The number of older siblings a child has is negatively correlated with the child's verbal skills, an effect that is well known in the literature. However, few studies have examined the effect of older siblings’ sex, of the age gap between siblings, of having foreign‐speaking parents, as well as the mediating role of parental interaction. Using data from 12,296 children (49.3% female) from the French ELFE birth cohort, we analyzed the effect of these characteristics of the siblings and their family on children's expressive vocabulary measured using the French MacArthur‐Bates Communicative Development Inventory. Children's vocabulary at age 2 years was negatively associated with the number of older siblings (−0.08 SD per additional sibling), and this effect was partly mediated by parental interactions. In analyses restricted to children with one older sibling, the vocabulary score was negatively correlated with the age gap between the target child and their older sibling. The vocabulary score was not correlated to their sibling's sex, contrary to the result of a previous study. In addition, the effect of the number of siblings was less negative in foreign speaking families that in French speaking families, suggesting that older siblings might partly compensate for the effect of having foreign‐speaking parents. Overall, our results are consistent with the resource dilution (stating that parents have limited resources to distribute among their children) and inconsistent with the confluence model (stating that a child's cognitive ability is correlated to the mean cognitive ability of the family). Research Highlights Our results are consistent with the resource dilution model and inconsistent with the confluence model The negative effect of the number of siblings on expressive vocabulary is partly mediated by parental interactions Larger age gaps between a child and their older sibling are associated with lower expressive vocabulary score
... Finally, a more recent study (Dhamrait et al., 2020) found a non-linear relationship (Ushape) between interpregnancy intervals and children's developmental vulnerability at age 5 years, with an age gap of under 6 months or over 24 months being associated with an increased risk in developmental vulnerability. Thus, there is a need for further investigation of age gap effects. ...
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Using data from 12,296 children (49.3% female) from the French ELFE birth cohort, we analyzed the effect of various characteristics of the siblings on children’s expressive vocabulary. Children’s vocabulary at age 2 years was negatively associated with the number of older siblings (-.08 SD per additional sibling), and this effect was partly mediated by parental interactions. In an analysis restricted to children with one older sibling, the vocabulary score was negatively correlated with the age gap between the target child and their older sibling. In addition, our results suggest that older siblings might partly compensate for the effect of having foreign-speaking parents. Overall, our results are consistent with the resource dilution model and inconsistent with the confluence model.
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School closures across Australia in response to COVID‐19 have persisted since 2020, with rising mental health problems in children and adolescents, alongside rising negative family health and socioeconomic outcomes. Further, some children and young people who were already experiencing disadvantage pre‐pandemic may be at heightened risk of poorer educational outcomes. Therefore, the aim of this study was to conduct a systematic review of the literature to identify the factors for poorer educational outcomes that may be exacerbated by COVID‐19 amongst disadvantaged school students. Key development stages of disadvantage were identified: young children who started school behind, older students already at risk of disengagement from school and children and young people who have had contact with the child protection system. Five databases were systematically searched, across two search periods. A total of 69 Australian, peer‐reviewed articles, published in 2005–2021, examining risk factors for poor educational outcomes for children attending school met the inclusion criteria and were included in final analyses. Our findings provide evidence of key risk factors that make these populations susceptible to worsening outcomes resulting from the COVID‐19 pandemic, and of the critical importance of ongoing research to guide policy and practice support for these at‐risk groups.
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Abstract Studies have reported a dose-dependent relationship between gestational age and poorer school readiness. The study objective was to quantify the risk of developmental vulnerability for children at school entry, associated with gestational age at birth and to understand the impact of sociodemographic and other modifiable risk factors on these relationships. Linkage of population-level birth registration, hospital, and perinatal datasets to the Australian Early Development Census (AEDC), enabled follow-up of a cohort of 64,810 singleton children, from birth to school entry in either 2009, 2012, or 2015. The study outcome was teacher-reported child development on the AEDC with developmental vulnerability defined as domain scores
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Previous research assessing consequences of interpregnancy intervals (IPIs) on child development is mixed. Utilizing a population-based US sample (n=5,339), we first estimated the associations between background characteristics (e.g., sociodemographic and maternal characteristics) and short (≤ 1 year) and long (> 3 years) IPI. Then, we estimated associations between IPI and birth outcomes, infant temperament, cognitive ability, and externalizing symptoms. Several background characteristics, such as maternal age at childbearing and previous pregnancy loss, were associated with IPI, indicating research on the putative effects of IPI must account for background characteristics. After covariate adjustment, short IPI was associated with poorer fetal growth and long IPI was associated with lower infant activity level; however, associations between short and long IPI and the other outcomes were neither large nor statistically significant. These findings indicate that rather than intervening to modify IPI, at-risk families may benefit from interventions aimed at other modifiable risk factors.
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Objective To investigate the prevalence of, and associations between, prenatal and perinatal risk factors and developmental vulnerability in twins at age 5. Design Retrospective cohort study using bivariate and multivariable logistic regression. Setting Western Australia (WA), 2002–2015. Participants 828 twin pairs born in WA with an Australian Early Development Census (AEDC) record from 2009, 2012 or 2015. Main outcome measures The AEDC is a national measure of child development across five domains. Children with scores <10th percentile were classified as developmentally vulnerable on, one or more domains (DV1), or two or more domains (DV2). Results In this population, 26.0% twins were classified as DV1 and 13.5% as DV2. In the multivariable model, risk factors for DV1 were maternal age <25 years (adjusted OR (aOR): 7.06, 95% CI: 2.29 to 21.76), child speaking a language other than English at home (aOR: 6.45, 95% CI: 2.17 to 19.17), male child (aOR: 5.08, 95% CI: 2.89 to 8.92), age younger than the reference category for the study sample (≥5 years 1 month to <5 years 10 months) at time of AEDC completion (aOR: 3.34, 95% CI: 1.55 to 7.22) and having a proportion of optimal birth weight (POBW) <15th percentile of the study sample (aOR: 2.06, 95% CI 1.07 to 3.98). Risk factors for DV2 were male child (aOR: 7.87, 95% CI: 3.45 to 17.97), maternal age <25 (aOR: 5.60, 95% CI: 1.30 to 24.10), age younger than the reference category (aOR: 5.36, 95% CI: 1.94 to 14.82), child speaking a language other than English at home (aOR: 4.65, 95% CI: 1.14 to 19.03), mother’s marital status as not married at the time of twins’ birth (aOR: 4.59, 95% CI: 1.13 to 18.55), maternal occupation status in the lowest quintile (aOR: 3.30, 95% CI: 1.11 to 9.81) and a POBW <15th percentile (aOR: 3.11, 95% CI: 1.26 to 7.64). Conclusion Both biological and sociodemographic risk factors are associated with developmental vulnerability in twins at 5 years of age.
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Purpose: The purpose of our study was to evaluate the effect of IPI on long-term neurological morbidity of the offspring. Methods: In this retrospective cohort study, 144,397 singleton infants born to multiparous mothers, between the years 1991 and 2014 in a tertiary medical center, were evaluated for different perinatal outcomes and were followed until 18 years of age for long-term neurological morbidity according to three IPI groups: Short IPI (< 6 months), long IPI (> 60 months) and intermediate IPI (6-60 months). We used a Kaplan-Meier survival curve to compare cumulative incidence of long-term neurological morbidity, and a Cox regression analysis to control for confounders such as gestational age, birth weight and maternal age. Results: Offspring born to mothers with long IPI had higher rates of neurological morbidity (3.62% among offspring born after long IPI vs. 3.18% and 3.19% among offspring born after short and intermediate IPI, respectively, p = 0.041). The cumulative incidence of long-term neurological morbidity was significantly higher in the long IPI group (Kaplan-Meier log-rank test p < 0.001). Being born after a long IPI was found to be an independent risk factor for long-term neurological morbidity of the offspring (adjusted hazard ratio 1.2; 95% confidence interval 1.1-1.4; p < 0.001). Conclusion: Long IPI is independently associated with an increased risk of long-term neurological morbidity of the offspring.
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While neurodevelopmental disorders (NDDs) are highly heritable, several environmental risk factors have also been suggested. However, the role of familial confounding is unclear. To shed more light on this, we reviewed the evidence from twin and sibling studies. A systematic review was performed on case control and cohort studies including a twin or sibling within-pair comparison of neurodevelopmental outcomes, with environmental exposures until the sixth birthday. From 7,315 screened abstracts, 140 eligible articles were identified. After adjustment for familial confounding advanced paternal age, low birth weight, birth defects, and perinatal hypoxia and respiratory stress were associated with autism spectrum disorder (ASD), and low birth weight, gestational age and family income were associated with attention-deficit/hyperactivity disorder (ADHD), categorically and dimensionally. Several previously suspected factors, including pregnancy-related factors, were deemed due to familial confounding. Most studies were conducted in North America and Scandinavia, pointing to a global research bias. Moreover, most studies focused on ASD and ADHD. This genetically informed review showed evidence for a range of environmental factors of potential casual significance in NDDs, but also points to a critical need of more genetically informed studies of good quality in the quest of the environmental causes of NDDs.
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The number of older siblings a child has is negatively correlated with the child’s verbal skills, perhaps because of competition for parents’ attention. In the current study, we examined the role of siblings’ sex and age gap as moderating factors, reasoning that they affect older siblings’ tendency to compensate for reduced parental attention. We hypothesized that children with an older sister have better language abilities than children with an older brother, especially when there is a large age gap between the two siblings. We reanalyzed data from the EDEN cohort ( N = 1,154) and found that children with an older sister had better language skills than those with an older brother. Contrary to predictions, results showed that the age gap between siblings was not associated with language skills and did not interact with sex. Results suggest that the negative effect of older siblings on language development may be entirely due to the role of older brothers. Our findings invite further research on the mechanisms involved in this effect.
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Objectives The goals of interconception care are to optimize women’s health and encourage adequate spacing between pregnancies. Our study calculated trends in interpregnancy interval (IPI) patterns and measured the association of differing intervals with birth outcomes in California. Methods Women with “non-first birth” deliveries in California hospitals from 2007 to 2009 were identified in a linked birth certificate and patient discharge dataset and divided into three IPI birth categories: <6, 6–17, and 18–50 months. Trends over the study period were tested using the Cochran-Armitage two-sided linear trend test. Chi square tests were used to test the association between IPI and patient characteristics and selected singleton adverse birth outcomes. Results Of 645,529 deliveries identified as non-first births, 5.6 % had an IPI <6 months, 33.1 % had an IPI of 6–17 months, and 61.3 % had an IPI of 18–50 months. The prevalence of IPI <6 months declined over the 3-year period (5.8 % in 2007 to 5.3 % in 2009, trend p value <0.0001).Women with an IPI <6 months had a significantly higher prevalence of early preterm birth (<34 weeks), low birthweight (<2500 g), neonatal complications, neonatal death and severe maternal complications than women with a 6–17 month or 18–50 month IPI (p < 0.005). Comparing those with a 6–17 month vs 18–50 month IPI, there were increased early preterm births and decreased maternal complications, complicated delivery, and stillbirth/intrauterine fetal deaths among those with a shorter IPI. Conclusions for Practice In California, women with an IPI <6 months were at increased risk for several birth outcomes, including composite morbidity measures.
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Context: Both short and long interpregnancy intervals (IPIs) have recently been associated with increased risk of autism spectrum disorder (ASD). However, this association has not been systematically evaluated. Objective: To examine the relationship between birth spacing and the risk of ASD and other neurodevelopmental disabilities. Data sources: Electronic databases from their inception to December 2015, bibliographies, and conference proceedings. Study selection: Observational studies with results adjusted for potential confounding factors that reported on the association between IPIs or birth intervals and neurodevelopmental disabilities. Data extraction: Two reviewers independently extracted data on study characteristics, IPIs/birth intervals, and outcome measures. Results: Seven studies (1 140 210 children) reported an association between short IPIs and increased risk of ASD, mainly the former subtype autistic disorder. Compared with children born to women with IPIs of ≥36 months, children born to women with IPIs of <12 months had a significantly increased risk of any ASD (pooled adjusted odds ratio [OR] 1.90, 95% confidence interval [CI] 1.16-3.09). This association was stronger for autistic disorder (pooled adjusted OR 2.62, 95% CI 1.53-4.50). Three of these studies also reported a significant association between long IPIs and increased risk of ASD. Short intervals were associated with a significantly increased risk of developmental delay (3 studies; 174 940 children) and cerebral palsy (2 studies; 19 419 children). Limitations: Substantial heterogeneity, and few studies assessing neurodevelopmental disabilities other than ASD. Conclusions: Short IPIs are associated with a significantly increased risk of ASD. Long IPIs also appear to increase the risk of ASD.
Article
Background: Short or long interpregnancy interval (IPI) may adversely impact conditions for foetal development. Whether attention deficit hyperactivity disorder (ADHD) is related to IPI has been largely unexplored. Objectives: To examine the association between IPI and ADHD in a large, population-based Finnish study. Methods: All children born in Finland between 1991 and 2005 and diagnosed with ADHD (ICD-9 314x or ICD-10 F90.x) from 1995 to 2011 were identified using data from linked national registers. Each subject with ADHD was matched to 4 controls based on sex, date of birth, and place of birth. A total of 9564 subjects with ADHD and 34,479 matched controls were included in analyses. IPI was calculated as the time interval between sibling birth dates minus the gestational age of the second sibling. The association between IPI and ADHD was determined using conditional logistic regression and adjusted for potential confounders. Results: Relative to births with an IPI of 24 to 59 months, those with the shortest IPI (<6 months) had an increased risk of ADHD (odds ratio [OR] 1.30, 95% confidence interval (CI) 1.12, 1.51) and the ORs for the longer IPI births (60-119 months and ≥120 months) were 1.12 (95% CI 1.02, 1.24) and 1.25 (95% CI 1.08, 1.45), respectively. The association of longer IPI with ADHD was attenuated by adjustment for maternal age at the preceding birth, and comorbid autism spectrum disorders did not explain the associations with ADHD. Conclusions: The risk of ADHD is higher among children born following short or long IPIs although further studies are needed to explain this association.
Article
Objective: To examine associations among interpregnancy interval, the duration from the preceding birth to the conception of the next-born index child, and adverse birth outcomes using designs that adjust for measured and unmeasured factors. Methods: In this prospective cohort study, we used population-based Swedish registries from 1973 to 2009 to estimate the associations between interpregnancy interval (referent 18-23 months) and adverse birth outcomes (ie, preterm birth [less than 37 weeks of gestation], low birth weight [LBW; less than 2,500 g], small for gestational age [SGA; greater than 2 SDs below average weight for gestational age]). Analyses included cousin and sibling comparisons and postbirth intervals (ie, the interval between secondborn and thirdborn offspring predicting secondborn outcomes) to address unmeasured familial confounding. Results: Traditional cohort-wide analyses showed higher odds of preterm birth (adjusted odds ratio [OR] 1.51, 99% CI 1.39-1.63, 5.99% preterm births]) and LBW (adjusted OR 1.25, 99% CI 1.13-1.39, 3.32% LBW) after a short interpregnancy interval (0-5 months) compared with offspring born after an interpregnancy interval of 18-23 months (3.21% preterm births, 1.92% LBW). Except for preterm birth (adjusted OR 1.72, 99% CI 1.26-2.35), associations were attenuated in cousin comparisons. A small association between a short interpregnancy interval and preterm birth remained in sibling comparisons (adjusted OR 1.22, 99% CI 1.11-1.35), but associations with LBW (adjusted OR 0.83, 99% CI 0.74-0.94) and SGA (adjusted OR 0.74, 99% CI 0.64-0.85) reversed direction. For pregnancy intervals of 60 months or more, odds of preterm birth (adjusted OR 1.51, 99% CI 1.43-1.60, 5.07% preterm births), LBW (adjusted OR 1.61, 99% CI 1.50-1.73, 3.43% low-birth-weight births), and SGA (adjusted OR 1.54, 99% CI 1.42-1.66, 2.49% SGA births) were also higher when compared with the reference interval (1.53% SGA). Associations between long interpregnancy interval and adverse birth outcomes remained through cousin and sibling comparisons. Postbirth interval analyses showed familial confounding is present for short interpregnancy intervals, but supported independent associations for long interpregnancy intervals. Conclusion: Familial confounding explains most of the association between a short interpregnancy interval and adverse birth outcomes, whereas associations with long interpregnancy intervals were independent of measured and unmeasured factors.
Article
Objective: To examine the association between interpregnancy interval and maternal-neonate health when matching women to their successive pregnancies to control for differences in maternal risk factors and compare these results with traditional unmatched designs. Methods: We conducted a retrospective cohort study of 38,178 women with three or more deliveries (two or greater interpregnancy intervals) between 2000 and 2015 in British Columbia, Canada. We examined interpregnancy interval (0-5, 6-11, 12-17, 18-23 [reference], 24-59, and 60 months or greater) in relation to neonatal outcomes (preterm birth [less than 37 weeks of gestation], small-for-gestational-age birth [less than the 10th centile], use of neonatal intensive care, low birth weight [less than 2,500 g]) and maternal outcomes (gestational diabetes, beginning the subsequent pregnancy obese [body mass index 30 or greater], and preeclampsia-eclampsia). We used conditional logistic regression to compare interpregnancy intervals within the same mother and unconditional (unmatched) logistic regression to enable comparison with prior research. Results: Analyses using the traditional unmatched design showed significantly increased risks associated with short interpregnancy intervals (eg, there were 232 preterm births [12.8%] in 0-5 months compared with 501 [8.2%] in the 18-23 months reference group; adjusted odds ratio [OR] for preterm birth 1.53, 95% confidence interval [CI] 1.35-1.73). However, these risks were eliminated in within-woman matched analyses (adjusted OR for preterm birth 0.85, 95% CI 0.71-1.02). Matched results indicated that short interpregnancy intervals were significantly associated with increased risk of gestational diabetes (adjusted OR 1.35, 95% CI 1.02-1.80 for 0-5 months) and beginning the subsequent pregnancy obese (adjusted OR 1.61, 95% CI 1.05-2.45 for 0-5 months and adjusted OR 1.43, 95% CI 1.10-1.87 for 6-11 months). Conclusion: Previously reported associations between short interpregnancy intervals and adverse neonatal outcomes may not be causal. However, short interpregnancy interval is associated with increased risk of gestational diabetes and beginning a subsequent pregnancy obese.