Associations of fetal and infant growth patterns with behavior and cognitive outcomes in early adolescence
Abstract
Background
Fetal life and infancy might be critical periods for brain development leading to increased risks of neurocognitive disorders and psychopathology later in life. We examined the associations of fetal and infant weight growth patterns and birth characteristics with behavior and cognitive outcomes at the age of 13 years.
Methods
Population-based prospective cohort study from fetal life until adolescence. Pregnant women with a delivery date between April 2002 and January 2006 were eligible. Follow-up measurements were available for 4716 children. Fetal weight was estimated in the second and third trimesters of pregnancy by ultrasonography. Infant weight was measured at birth and at 6, 12, and 24 months. Fetal and infant weight acceleration or deceleration were defined as a change in SD greater than 0.67 between time points. Total, internalizing and externalizing problems and attention-deficit hyperactivity disorder (ADHD) symptoms were measured using Child Behavior Checklist (CBCL/6–18), autistic traits by the Social Responsiveness Scale (SRS) and intelligence quotient (IQ) by the Wechsler Intelligence Scale for Children-Fifth Edition (WISC-V).
Results
One week longer gestational age at birth was associated with a −0.03 SDS (95% Confidence Interval (CI): −0.04, −0.01) lower total behavior problems score, a −0.02 SDS (95% CI: −0.04, −0.01) lower ADHD symptoms score. Also an increase in birth weight of 500 g was associated with a lower odds of having high externalizing problems (OR 0.92 (95% CI: 0.86, 0.98) and of having a low IQ score (OR 0.79 (95% CI: 0.71, 0.88). Compared to children with normal fetal and infant growth, those with accelerated fetal and infant growth had a 0.27 SDS higher IQ (95% Confidence Interval 0.11, 0.44).
Conclusions
Both fetal and infant weight development are associated with behavioral and cognitive outcomes in early adolescence. Follow-up studies are needed to assess whether these associations link to later life mental health outcomes.
Key points
What’s known?
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In early life rapid development of the central nervous system takes place. Fetal and early life weight growth might be important for neurocognitive development.
What’s new?
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In this large population-based prospective study we observed that both birth characteristics and fetal and infant growth patterns are associated with behavior and cognitive outcomes in early adolescence. compared to children with normal fetal and infant growth, those with accelerated fetal and infant growth had the highest iq.
What’s relevant?
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Fetal and early life growth patterns that effect neurocognitive development have not yet been identified. This study gives an insight into the possible window of opportunity in early adolescent behavioral and cognitive development provided by fetal and early life weight growth.
INTRODUCTION
Preterm birth and low birth weight are associated with increased risks of impaired cognitive development, psychopathology and intellectual disabilities (Anderson et al., 2021; Hack et al., 2005; Johnson & Marlow, 2011). Low birth weight is also associated with poor performance on tests for neurocognitive function, attention-deficit hyperactivity disorder (ADHD) and autism spectrum disorder (ASD) among children, adolescents and adult (Sacchi et al., 2020; Song et al., 2022; Talmi et al., 2020). These associations are stronger among the extremes of birth characteristics but present across the normal range of gestational age and weight at birth (Anderson et al., 2021; Cortese et al., 2021; Pettersson et al., 2019; van Mil et al., 2015). Gestational age and weight at birth may not be causal factors per se leading to behavior and cognition later in life, but are merely markers of a continuous growth process that started before birth. A recent study from our group reported that among small for gestational age (SGA) children, those consistently small from mid-pregnancy onwards had the lowest IQ and most ADHD symptoms (Ferguson et al., 2021). Another, large individual participant data meta-analysis in very preterm and low birthweight children showed much higher risks of meeting the criteria for ADHD, ASD, Anxiety disorder and Mood disorder (Anderson et al., 2021). Also, a recent study in Belarus among 11,000 children reported that faster weight growth from birth to 5 years was positively associated with intelligence quotient (IQ) at 6 years old (Yang et al., 2011). Fetal life and early childhood are characterized by rapid development of the central nervous system (Konkel, 2018). Both early life weight and head circumference are related to cognitive skills in childhood (Bach et al., 2020; Geraedts et al., 2011). We have previously reported that increased weight gain during the fetal period and in infancy is associated with larger brain volumes on MRI scans at 10 years of age (Silva et al., 2021). Prospective studies on the associations of different fetal and infant growth characteristics with neurocognitive and psychopathology outcomes in childhood may contribute to identification of specific critical periods and windows of opportunity in fetal and infant growth. We hypothesize that birth characteristics and different fetal and infant growth patterns are associated with behavior and cognitive outcomes in early adolescence.
In this population-based prospective cohort study among 4716 children, we examined the associations of fetal and infant weight growth patterns and birth characteristics with behavior and cognitive outcomes at the age of 13 years. Main outcomes included parent-reported scores for total behavior problems, internalizing behavior problems reflecting anxiety, depressive and somatic symptoms and externalizing behavior problems reflecting rule breaking and aggressive behavior, ADHD symptoms, ASD traits and observed IQ. We were specifically interested in identification of specific fetal and infant growth patterns.
METHODS
Study population
This study was embedded in the Generation R Study, a population-based prospective cohort study from early fetal life onwards (Kooijman et al., 2016). Pregnant women with a delivery date between April 2002 and January 2006, living in Rotterdam, the Netherlands, were eligible. Details on response and follow-up were described previously (Kooijman et al., 2016). We had information on fetal or infant growth in 8624 singleton births. Analyses were restricted to a subgroup of (n = 4716) children for whom we had follow-up information at 13 years (follow-up rate 54.7%). A flowchart is given in the Supplemental Figure S1.
Ethical considerations
Written informed consent was provided by all parents and children. The Medical Ethics Committee of Erasmus Medical Center approved the study (MEC-2012-165). This study followed the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) reporting guideline (Vandenbroucke et al., 2007).
Fetal and infant growth measures
As previously described, fetal ultrasound examinations were performed in second trimester (median 20.5, range 18.6, 23.3 weeks), and third trimester (median 30.4, range 28.5, 32.9 weeks) (Kooijman et al., 2016). By standardized ultrasound procedures fetal head circumference, abdominal circumference, and femur length were measured (Kooijman et al., 2016; Verburg et al., 2008). The Hadlock formula was used to calculate gestational age adjusted estimated fetal weight and calculate standard deviation scores (SDS) using Dutch growth charts (Hadlock et al., 1985; Verburg et al., 2008).
Sex, expected date of delivery and birth weight was collected from midwives. Sex and gestational age adjusted birth weight SDS were constructed using World Health Organization growth charts (Kiserud et al., 2018). We used gestational age, birth weight and size for gestational age both continuous and categorized into clinically relevant categories. Gestational age was categorized into preterm (<37 weeks), term (37–42 weeks) and postterm (>42 weeks). Birth weight was categorized in low birth weight (<2500 g), normal birth weight (2500–4500 g) and high birth weight (>4500 g). Children with birth weight SDS <10th percentile were classified as small for gestational age (SGA), and those with birth weight SDS >90th percentile were classified as large for gestational age (LGA).
Infant weight was measured at approximately 6 months (median 6.2, range 5.0, 10.0 months), 12 months (median 11.1, range 10.0, 13.0 months), and 24 months of age (median 24.9, range 23.0, 29.0 months). Head circumference was measured between birth and approximately 3 months (median postconceptional age 41.1, range 33.0, 58.4 weeks) and at approximately 12 months (median 11.0, range 10.0, 13.0 months). We created age and sex-adjusted SDS using Dutch reference growth charts in Growth Analyzer 4.0 (Kooijman et al., 2016).
We constructed individual-based fetal and infant weight change variables by using estimated fetal weight, age and sex-adjusted birth weight and infant weight. Fetal weight change was defined as growth in SDS between the second trimester and birth. Infant weight change was defined as growth in SDS from birth to 24 months (n = 3097 of n = 3891 children). If weight at 24 months was not available, we used weight at 12 months (n = 639 of n = 3891 children) and if weight at 12 months was not available, we used weight at 6 months (n = 155 of n = 3891 children). We considered an increase of more than 0.67 SD between time points as growth acceleration and a decrease of more than 0.67 SD between time points as growth deceleration, reflecting the difference between two percentile lines on the growth charts commonly used to define growth deceleration or acceleration in population and clinical research (Cole & Lanham, 2011).
Emotional, behavioral and cognitive outcomes
At the age of 13 years (range 13.1, 14.7), the primary caregiver (91.3% mothers) was asked to complete the Child Behavior Checklist (CBCL)/6–18. The CBCL is an internationally validated and reliable measure of emotional and behavioral problems (Achenbach & Ruffle, 2000; Hofstra et al., 2002). Based on the behavior of the child in the preceding 6 months, each of the 112 items is rated on a 3-point scale: 0 (not true), 1 (somewhat true), 2 (very true or often true). Together the 112 items result in the total behavior problems score, a higher score indicating more emotional and behavioral problems. This total behavior problems sum score can be subdivided into the internalizing and externalizing problems scale. Internalizing problems consist of the subscales, emotionally reactive and anxious/depressed symptoms, as well as somatic complaints and symptoms of being withdrawn. Externalizing problems consist of the subscales rule breaking and aggressive behavior (Achenbach & Ruffle, 2000; Blok et al., 2022). The sum scores for the internalizing and externalizing problem scale were derived by summing the raw scores for each respective subscale of which the scale consists. We used the sum score of total behavior problems (n = 4133), internalizing problems (n = 4136), externalizing problems (n = 4125) and of the Diagnostic and Statistical Manual of Mental Disorders (DSM)-oriented ADHD symptoms (n = 4117). We used continuous values and dichotomous cut-off scores. As in previous analyses conducted in the same study population, a non-optimal score was defined as the highest 20% and used as the dichotomous cut-off scores (Cents et al., 2011; Velders et al., 2011). Using the individual-based CBCL cut-offs of the 95th and 98th percentile would in our relatively healthy population result in insufficient statistical power Achenbach & Rescorla, 2001).
At the same visit, the primary caregiver also completed an adapted version of the Social Responsiveness Scale, consisting of 18 items. The SRS is a quantitative measure of autistic traits for children 4–18 years old, with higher scores indicating greater social behavior impairment (Lyall et al., 2021; Wagner et al., 2019). The authors of the scale recommend cutoffs for screening consistent with 1.078 for boys and 1.000 for girls (Constantino & Gruber, 2005).
Children’s intelligence quotient (IQ) was assessed using a subset of the Wechsler Intelligence Scale for Children-Fifth Edition (WISC-V). The WISC-V is an instrument assessing cognitive functioning in 6 to 16-year-olds. Four core subtests: vocabulary, matrix reasoning, digit span and coding were selected to assess specific cognitive domains and to derive an estimated full scale intelligence quotient (FSIQ) (Kaufman et al., 2016). We used IQ estimates as continuous and dichotomous outcomes, using a cut-off of <80, as defined in the WISC-V manual, to distinguish borderline low IQ scores (Kaufman et al., 2016).
For all outcomes, we constructed standard deviation scores ((observed value−mean)/SD) within the population to enable comparison of effect estimates.
A detailed description of the Methods section can be found in the Supplementary Methods.
Covariates
We used a directed acyclic graphs (DAG) to identify potential covariates (Supplemental Figure S2). We obtained information on maternal age, pre-pregnancy weight, parity, ethnicity, educational level, smoking, alcohol use and folic acid supplementation using questionnaires and registries during pregnancy (Kooijman et al., 2016). Maternal educational level was self-reported as the highest completed educational level and categorized as lower (primary plus first 3 years of secondary education), medium (upper secondary and vocational training or management and specialist education) and higher education (associate degree, bachelor or master degree programs). During the 6-year follow-up visit we used the 12-item reliable and validated computerized short version of the Raven’s Progressive Matrices to assess maternal non-verbal cognitive ability (Raven, 2021).
Statistical analysis
First, we described maternal, fetal and childhood characteristics. We performed a non-response analysis by comparing characteristics of children with and without outcome assessments by using Independent Student T-test, Mann-Whitney U and χ2 tests. Second, we used linear and logistic regression models to assess the associations of birth characteristics with continuous and dichotomous scores of behavior and cognitive outcomes at the age of 13 years. We have added scatter plots of the associations to the Supplemental Figures S3-S5. For all analyses, the continuous scores for total, internalizing and externalizing behavior problems, ADHD symptoms and ASD traits were natural log-transformed to deal with a skewed distribution. Third, we used estimated fetal weight growth, gestational age adjusted birth weight and infant weight and categorized both fetal weight growth (second trimester to birth) and infant weight growth (birth to 24 months) change each into three groups (growth deceleration, normal growth, and growth acceleration), and created a combined 3 x 3 variable leading to nine different growth patterns. We used multivariable linear or logistic regression models to explore associations of fetal and infant weight changes with continuous and dichotomous behavior and cognitive outcomes. We performed a sensitivity analysis restricting the study population to only children with weight measurements at 24 months (n = 3097). Last, to test the robustness of our findings for different growth measures, we performed a sensitivity analysis for fetal and infant head circumference. We categorized head circumference at birth (0–3 months) and during infancy (12 months) into tertiles (smallest, middle and largest) and created a combined variable that reflects 9 different head circumference patterns. Participants were included if they had head circumference data at both time points. Because of the structural difference in the fetal and childhood head circumference reference charts, we did not combine these charts. For all analyses, basic models were adjusted for child’s sex and age at outcome assessment. The confounder-adjusted model, which we considered the main model, was additionally adjusted for maternal age, parity, pre-pregnancy body mass index, educational level, ethnicity, prenatal folic acid use, smoking, alcohol use and maternal IQ at 6 years old. Potential confounders were identified based on previous literature and we selected those that fulfilled the graphical criteria for confounding in a DAG and changed the effect estimates >10% after addition to the crude model. Consistently associated with fetal growth, birth weight and infancy weight were maternal educational level, ethnicity, folic acid supplementation, smoking during pregnancy, maternal IQ and BMI at age of outcome measurement. As fetal and infant growth are highly correlated and we considered three groups of outcomes, namely CBCL derivatives, SRS scores and IQ, we took account for multiple testing by specifying significant p-values as p < (0.05/3) 0.017. We tested for statistical interaction of maternal educational level, ethnicity, smoking, alcohol use and folic acid supplementation during pregnancy and maternal IQ in these associations but no statistically significant interactions were observed (p > 0.05). Missing data in covariates (ranging from 0.4% to 36.9%) were multiple imputed using the Markov Chain Monte Carlo method. Ten imputed datasets were created and analyzed together (Sterne et al., 2009). Statistical analyses were performed using the Statistical Package of Social Sciences version 25.0 for Windows (SPSS Inc., Chicago, IL, USA).
RESULTS
Participant characteristics
Table 1 shows the subject characteristics from imputed data. Follow-up measurements were available for 4716 children with a median age of 13.5 (range 13.1, 14.7) years, of whom 2400 (50.9%) were girls and 2744 (58.2%) were of Dutch ethnicity. Supplementary Table S1 shows subjects characteristics from the observed data. Supplementary Table S2 shows that compared to the study population (n = 4716), mothers of children without outcome measurements (n = 3906) were younger, less often primipara, of European ethnicity, had lower IQ and lower education, used less alcohol, smoked more often, used folic acid supplements less often, and had higher pre-pregnancy BMI. Children who were lost to follow-up were more often male, born preterm and born with a lower birth weight.
Characteristic |
(N = 4716) N (%) |
---|---|
Maternal | |
Age at enrollment, median (95% range), years | 31.4 (20.2, 39.6) |
Pre-pregnancy BMI, median (95% range), kg/m2 | 22.7 (17.8, 34.1) |
Parity nulliparous, N (%) | 2757 (58.5) |
Education level, N (%) | |
Primary education | 388 (8.4) |
Secondary education | 1930 (40.9) |
Higher education | 2398 (50.7) |
Ethnicity, No. (%) | |
Dutch | 2744 (58.2) |
Non-Dutch, Western | 392 (8.3) |
Non-Dutch, Non-Western | 1580 (33.5) |
Smoking during pregnancy, N (%) | 1108 (23.5) |
Alcohol during pregnancy, N (%) | 2753 (58.4) |
Folic acid supplement use, did not use N (%) | 1066 (22.6) |
Maternal IQ, mean (SD) | 99.8 (18.0) |
Fetal | |
Second trimester | |
Gestational age, median (95% range), weeks | 20.5 (18.6, 23.3) |
Estimated fetal weight, median (95% range), grams | 362 (260, 534) |
Third trimester | |
Gestational age, median (95% range), weeks | 30.4 (28.5, 32.9) |
Estimated fetal weight, median (95% range), grams | 1602 (1211, 2214) |
Birth | |
Child sex, female N (%) | 2400 (50.9) |
Gestational age at birth, median (95% range), weeks | 40.1 (35.9, 42.4) |
<37 weeks, N (%) | 216 (4.6) |
37–42 weeks, N (%) | 4162 (88.3) |
>42 weeks, N (%) | 338 (7.2) |
Birth weight, median (95% range), grams | 3470 (2254, 4500) |
<2500 g, N (%) | 201 (4.3) |
2500–4500 g, N (%) | 4388 (93.2) |
>4500 g, N (%) | 121 (2.6) |
Sex and gestational age adjusted birth weight | |
Small (<10th percentile), N (%) | 471 (10.0) |
Appropriate (10th - 90th percentile), N (%) | 3768 (80.0) |
Large (>90th percentile), N (%) | 471 (10.0) |
Postconceptional age at head circumference measurement, median (95% range), weeks | 41.1 (37.6, 52.9) |
Head circumference, mean (SD), cm | 35.2 (2.4) |
Infant | |
At 6-month visit | |
Age at visit, median (95% range), months | 6.2 (5.2, 8.3) |
Weight, median (95% range), kg | 7.8 (6.2, 9.7) |
At 12-month visit | |
Age at visit, median (95% range), years | 11.1 (10.1, 12.5) |
Weight, median (95% range), kg | 9.6 (7.6, 11.8) |
Head circumference, mean (SD), cm | 46.1 (1.4) |
At 2-year visit | |
Age at visit, median (95% range), years | 24.9 (23.4, 28.2) |
Weight, median (95% range), kg | 12.8 (10.3, 16.0) |
Childhood | |
Age at follow-up, median (95% range), years | 13.5 (13.1, 14.7) |
CBCL total behavior problems score, median (95% range) | 14.0 (0.0, 63.0) |
CBCL internalizing problems score, median (95% range) | 4.0 (0.0, 21.4) |
CBCL externalizing problems score, median (95% range) | 2.0 (0.0, 18.0) |
CBCL ADHD symptoms score, median (95% range) | 2.0 (0.0, 10.0) |
SRS autism traits score, median (95% range) | 4.0 (0.0, 16.0) |
Estimated WISC-V intelligence quotient, mean (SD) | 101.6 (13.9) |
- Note: Values are mean (SD), median (95% range), or number (valid %). WISC-V.
- Abbreviations: ADHD, attention-deficit hyperactivity disorder; BMI, body mass index; CBCL, Child Behavior Checklist; DSM, Diagnostic and Statistical Manual of Mental Disorders; SRS, Social Responsiveness Scale; WISC-V, Wechsler Intelligence Scale for Children-Fifth Edition.
- a Characteristics are based on the pooled datasets after multiple imputations.
Birth characteristics and behavioral and cognitive outcomes
Tables 2 and 3 show the associations of birth characteristics with behavior and cognitive outcomes at 13 years of age (basic models are shown in Supplementary Table S3 and Table S4). One week longer gestational age at birth was associated with a −0.03 SDS (95% Confidence Interval (CI): −0.04, −0.01) lower total behavior problems score, a −0.02 SDS (95% CI: −0.04, −0.01) lower ADHD symptoms score and a lower odds of a low IQ score (Odds Ratio (OR) 0.91 (95% CI: 0.86, 0.97). Compared to children born at term, those born preterm had a 0.20 SDS (95% Confidence Interval (CI) 0.06, 0.35) higher total behavior problems score. An increase in birth weight of 500 g was associated with a −0.04 SDS (95% CI: −0.07, −0.01) lower total behavior problems score, a −0.04 SDS (95% CI: −0.07, −0.01) lower ADHD symptoms score and a 0.06 SDS (95% CI: 0.04, 0.09) higher IQ score. Also an increase in birth weight of 500 g was associated with a lower odds of having high externalizing problems (OR 0.92 (95% CI: 0.86, 0.98), of having high ADHD symptoms (OR 0.91 (95% CI: 0.85, 0.98) and of having a low IQ score (OR 0.79 (95% CI: 0.71, 0.88). A 1-SDS higher birth weight for gestational age was associated with a 0.07 SDS (95% CI: 0.04, 0.10) higher IQ score and a lower odds of having a low IQ score (OR 0.82 (95% CI: 0.72, 0.94). As compared to children born appropriate size for gestational age (AGA), those born SGA had a 0.13 SDS (95% CI: 0.03, 0.23) higher total behavior problems score, a 0.16 (95% CI: 0.06, 0.27) higher internalizing problems score, a 0.13 SDS (95% CI: 0.03, 0.24) higher ADHD symptoms score and a −0.15 SDS (95% CI: −0.24, −0.05) lower IQ score. In line with these findings, SGA born children had a higher odds of an increased total behavior problems score (OR 1.35 (95% CI: 1.06, 1.72) and internalizing problems score (OR 1.58 [95% CI: 1.26, 1.99]). The associations of preterm birth, postterm birth, low birth weight, and LGA with behavior and cognitive outcomes attenuated into non-significance after correction for multiple testing.
Total problems (n = 4133) | Total problems >80th percentile (n = 845)a | Internalizing problems (n = 4136) | Internalizing problems >80th percentile (n = 932)b | Externalizing problems (n = 4125) | Externalizing problems >80th percentile (n = 972)c | ||
---|---|---|---|---|---|---|---|
Birth characteristics | N | Difference in SDS (95 CI) | OR (95% CI) | Difference in SDS (95 CI) | OR (95% CI) | Difference in SDS (95 CI) | OR (95% CI) |
Gestational age at birth, wk | −0.03 (−0.04 to −0.01)** | 0.96 (0.92–1.00)* | −0.02 (−0.04 to −0.00)* | 0.99 (0.94–1.03) | −0.02 (−0.04 to −0.00)* | 0.95 (0.91–0.99)* | |
<37 | 216 | 0.20 (0.06–0.35)** | 1.17 (0.82–1.67) | 0.15 (−0.00–0.29) | 1.14 (0.81–1.61) | 0.10 (−0.05–0.25) | 1.18 (0.84–1.66) |
37–42 | 4162 | Reference | Reference | Reference | Reference | Reference | Reference |
>42 | 338 | 0.03 (−0.10–0.14) | 0.96 (0.71–1.30) | 0.01 (−0.11–0.13) | 1.00 (0.74–1.34) | 0.02 (−0.10–0.14) | 0.99 (0.74–1.31) |
Birth weight, 500 gr | −0.04 (−0.07 to −0.01)** | 0.92 (0.86–0.99)* | −0.03 (−0.06 to −0.01)* | 0.93 (0.87–0.99)* | −0.02 (−0.05 to 0.01) | 0.92 (0.86–0.98)** | |
<2500 | 201 | 0.15 (0.00–0.30)* | 1.15 (0.80–1.65) | 0.06 (−0.09–0.22) | 1.05 (0.73–1.50) | 0.10 (−0.05–0.25) | 1.25 (0.88–1.76) |
2500–4500 | 4388 | Reference | Reference | Reference | Reference | Reference | Reference |
>4500 | 121 | 0.08 (−0.12–0.27) | 0.91 (0.55–1.50) | −0.01 (−0.20 to 0.19) | 0.99 (0.61–1.60) | 0.14 (−0.05–0.34) | 0.88 (0.55–1.41) |
Size for gestational age at birth, SD score | −0.02 (−0.05 to 0.02) | 0.94 (0.87–1.02) | −0.03 (−0.06 to 0.01) | 0.92 (0.86–0.99)* | 0.00 (−0.03 to 0.03) | 0.94 (0.88–1.02) | |
Small <10th percentile | 471 | 0.13 (0.03–0.23)** | 1.35 (1.06–1.72)** | 0.16 (0.06–0.27)** | 1.58 (1.26–1.99)** | 0.06 (−0.04–0.17) | 1.19 (0.94–1.51) |
Appropriate 10th-90th percentile | 3768 | Reference | Reference | Reference | Reference | Reference | Reference |
Large >90th percentile | 470 | 0.01 (−0.09–0.11) | 0.99 (0.77–1.29) | −0.03 (−0.13 to 0.08) | 0.87 (0.67–1.12) | 0.04 (−0.06–0.15) | 0.99 (0.77–1.27) |
- Note: Values are regression coefficients (95% confidence interval) or odds ratios (95% confidence interval) obtained from multivariable linear respectively logistic regression models and reflect the differences in parent-reported behavioral problems, the total problems (SDS), internalizing problems (SDS) and externalizing problems (SDS) for birth characteristics. For the logistic regressions the top 20% of the total score, the internalizing and the externalizing problem score was used. Pooled estimates are from multiple imputed datasets. The confounder model is adjusted for age at time of measurement and sex of the child, maternal age in pregnancy, parity, pre-pregnancy body mass index, educational level, ethnicity, folic acid use, smoking, alcohol and maternal IQ measured at the child age of 6 years old.
- Abbreviations: CI, confidence interval, OR, odds ratio; SDS, standard deviation score; wk, weeks.
- Total number of available cases; a: n = 4133, b: n = 4136, c: n = 4125.
- *p value < 0.05, **p value < 0.017.
ADHD symptoms score (n = 4117) | ADHD symptoms score >80th percentile (n = 1009)a | Autistic traits score (n = 4130) | Autistic traitsscore cut-off (n = 362)b | IQ score (n = 4292) | IQ score <80 (n = 261)c | ||
---|---|---|---|---|---|---|---|
Birth characteristics | N | Difference in SDS (95 CI) | OR (95% CI) | Difference in SDS (95 CI) | OR (95% CI) | Difference in SDS (95 CI) | OR (95% CI) |
Gestational age at birth, wk | −0.02 (−0.04 to −0.01)** | 0.96 (0.92–0.99)* | −0.02 (−0.03 to 0.00) | 0.95 (0.90–1.01) | 0.02 (0.00–0.03)* | 0.91 (0.86–0.97)** | |
<37 | 216 | 0.18 (0.03–0.32)* | 1.31 (0.94–1.82) | 0.03 (−0.12–0.18) | 1.16 (0.71–1.90) | −0.04 (−0.18 to 0.09) | 1.70 (1.03–2.81)* |
37–42 | 4162 | Reference | Reference | Reference | Reference | Reference | Reference |
>42 | 338 | −0.01 (−0.13 to 0.10) | 0.96 (0.72–1.27) | −0.12 (−0.24 to −0.00)* | 0.94 (0.61–1.45) | 0.11 (−0.00–0.21) | 0.87 (0.50–1.51) |
Birth weight, 500 gr | −0.04 (−0.07 to −0.01)** | 0.91 (0.85–0.98)** | −0.03 (−0.05 to 0.00) | 0.91 (0.83–1.01) | 0.06 (0.04–0.09)** | 0.79 (0.71–0.88)** | |
<2500 | 201 | 0.18 (0.03–0.33)* | 1.33 (0.94–1.87) | 0.08 (−0.07–0.23) | 1.49 (0.93–2.39) | −0.06 (−0.20 to 0.08) | 1.79 (1.07–2.99)* |
2500–4500 | 4388 | Reference | Reference | Reference | Reference | Reference | Reference |
>4500 | 121 | 0.04 (−0.16–0.23) | 0.84 (0.53–1.35) | −0.01 (−0.20 to 0.18) | 0.70 (0.32–1.53) | 0.13 (−0.05–0.31) | 0.52 (0.18–1.47) |
Size for gestational age at birth, SD score | −0.02 (−0.05 to 0.01) | 0.94 (0.87–1.01) | −0.02 (−0.05 to 0.01) | 0.94 (0.84–1.06) | 0.07 (0.04–0.10)** | 0.82 (0.72–0.94)** | |
Small <10th percentile | 471 | 0.13 (0.03–0.24)** | 1.22 (0.96–1.54) | 0.07 (−0.04–0.17) | 1.18 (0.84–1.66) | −0.15 (−0.24 to −0.05)** | 1.47 (1.00–2.15)* |
Appropriate 10th-90th percentile | 3768 | Reference | Reference | Reference | Reference | Reference | Reference |
Large >90th percentile | 470 | −0.01 (−0.11 to 0.09) | 0.95 (0.74–1.21) | −0.01 (−0.11 to 0.10) | 0.85 (0.57–1.26) | 0.11 (0.02–0.21)* | 1.07 (0.67–1.71) |
- Note: Values are regression coefficients (95% confidence interval) or odds ratio’s (95% confidence interval) obtained from multivariable linear respectively logistic regression models and reflect the differences in parent-reported behavioral problems, ADHD symptoms score (SDS), autistic traits score (SDS) and IQ (SDS) for birth characteristics. For the logistic regressions the top 20% of the ADHD symptoms score, autistic traits score (weighted scores of >1.078 for boys and >1.000 for girls) and IQ (score <80) was used. Pooled estimates are from multiple imputed datasets. The confounder model is adjusted for age at time of measurement and sex of the child, maternal age in pregnancy, parity, pre-pregnancy body mass index, educational level, ethnicity, folic acid use, smoking, alcohol and maternal IQ measured at the child age of 6 years old.
- Abbreviations: ADHD, attention-deficit hyperactivity disorder; CI, confidence interval; IQ, intelligence quotient; OR, odds ratio; SDS, standard deviation score.
- Total number of available cases; a: n = 4117, b: n = 4130, c: n = 4292.
- *p value < 0.05, **p value < 0.017.
Fetal and infant growth and behavioral and cognitive outcomes
Tables 4 and 5 show that as compared to children with normal fetal and infant growth, those with fetal growth deceleration, followed by normal infant growth had at age 13 years decreased odds of a high total behavior problems score (OR 0.66 [95% CI: 0.48, 0.91]). Children with fetal growth acceleration followed by normal infant growth had a −0.15 SDS (95% CI: −0.26, −0.03) lower total behavior problems score and a lower odds of having a high total behavior problems score (OR 0.65 (95% CI: 0.48, 0.88). Children with fetal and infant growth acceleration had the highest IQ score (difference with reference group 0.27 SDS [95% CI: 0.11, 0.44]). The following associations of fetal and infant growth patterns with ASD traits and IQ attenuated into non-significance after correction for multiple testing was applied. Children with fetal growth acceleration followed by infant growth deceleration also had lower odds of ASD traits above the screening cut-off (OR 0.62 [95% CI: 0.39, 0.99]). Children with normal fetal growth followed by infant growth acceleration had lower odds of ASD traits above the screening cut-off (OR 0.58 [95% CI: 0.34–0.96]). Children with fetal growth deceleration followed by infant growth acceleration had lower odds of a low IQ score (OR: 0.48 [95% CI: 0.25, 0.93]). The corresponding basic models are shown in Supplementary Tables S5 and S6. The results were largely similar when we restricted the analyses for the associations of fetal and infant growth patterns with behavioral and cognitive outcomes to only children with weight measurements at 24 months (Supplementary Table S9 and S10). Supplementary Table S11 shows the distribution of different fetal and infant growth patterns in children born preterm, with low birth weight and small for gestational age.
Total problems (n = 3315) | Total problems >80th percentile (n = 644)a | Internalizing problems (n = 3318) | Internalizing problems >80th percentile (n = 723)b | Externalizing problems (n = 3309) | Externalizing problems >80th percentile (n = 747)c | ||
---|---|---|---|---|---|---|---|
Fetal and infant growth patterns | N | Difference in SDS (95 CI) | OR (95% CI) | Difference in SDS (95 CI) | OR (95% CI) | Difference in SDS (95 CI) | OR (95% CI) |
Fetal growth deceleration | |||||||
Infant growth deceleration | 129 | 0.04 (−0.15–0.24) | 0.90 (0.56–1.47) | 0.07 (−0.12–0.27) | 0.83 (0.51–1.35) | −0.12 (−0.31 to 0.08) | 0.72 (0.44–1.18) |
Infant normal growth | 408 | −0.06 (−0.18 to 0.06) | 0.66 (0.48–0.91)** | −0.01 (−0.14 to 0.11) | 0.78 (0.57–1.06) | −0.10 (−0.22 to 0.03) | 0.85 (0.63–1.14) |
Infant growth acceleration | 419 | −0.03 (−0.15 to 0.10) | 0.82 (0.60–1.12) | 0.01 (−0.12–0.13) | 0.92 (0.68–1.24) | −0.01 (−0.13 to 0.12) | 0.92 (0.68–1.24) |
Fetal normal growth | |||||||
Infant growth deceleration | 351 | 0.02 (−0.11–0.15) | 0.93 (0.68–1.28) | 0.02 (−0.11–0.15) | 1.02 (0.75–1.39) | 0.02 (−0.11–0.15) | 1.01 (0.74–1.37) |
Infant normal growth | 869 | Reference | Reference | Reference | Reference | Reference | Reference |
Infant growth acceleration | 398 | −0.06 (−0.19 to 0.07) | 0.69 (0.50–0.97)* | −0.01 (−0.13 to 0.12) | 0.85 (0.63–1.16) | −0.06 (−0.19 to 0.06) | 0.74 (0.54–1.02) |
Fetal growth acceleration | |||||||
Infant growth deceleration | 479 | 0.02 (−0.10–0.13) | 0.77 (0.57–1.05) | −0.03 (−0.15 to 0.09) | 0.85 (0.64–1.14) | 0.01 (−0.11–0.12) | 0.80 (0.60–1.07) |
Infant normal growth | 505 | −0.15 (−0.26 to −0.03)** | 0.65 (0.48–0.88)** | −0.13 (−0.24 to −0.01)* | 0.78 (0.59–1.04) | −0.10 (−0.21 to 0.02) | 0.77 (0.58–1.03) |
Infant growth acceleration | 150 | −0.09 (−0.28 to 0.09) | 0.82 (0.51–1.30) | −0.07 (−0.25 to 0.11) | 0.74 (0.47–1.18) | −0.03 (−0.21 to 0.16) | 0.77 (0.49–1.22) |
- Note: Values are regression coefficients (95% confidence interval) or odds ratio’s (95% confidence interval) obtained from multivariable linear respectively logistic regression models and reflect the differences in parent-reported behavioral problems, the total problems (SDS), internalizing problems (SDS) and externalizing problems (SDS) for fetal and infant growth patterns. For the logistic regressions the top 20% of the total problems, the internalizing and the externalizing problems was used. Pooled estimates are from multiple imputed datasets. The confounder model is adjusted for age at time of measurement and sex of the child, maternal age in pregnancy, parity, pre-pregnancy body mass index, educational level, ethnicity, folic acid use, smoking, alcohol and maternal IQ measured at the child age of 6 years old.
- Abbreviations: CI, confidence interval; OR, odds ratio; SDS, standard deviation score.
- Total number of available cases; a: n = 3315, b: n = 3318, c: n = 3309.
- *p value < 0.05, **p value < 0.017.
ADHD symptoms score (n = 3304) | ADHD symptoms score >80th percentile (n = 764)a | Autistic traits score (n = 3315) | Autistic traits score cut-off (n = 274)b | IQ score (n = 3348) | IQ score cut off <80 (n = 171)c | ||
---|---|---|---|---|---|---|---|
Fetal and infant growth patterns | N | Difference in SDS (95 CI) | OR (95% CI) | Difference in SDS (95 CI) | OR (95% CI) | Difference in SDS (95 CI) | OR (95% CI) |
Fetal growth deceleration | |||||||
Infant growth deceleration | 129 | −0.05 (−0.24 to 0.14) | 0.93 (0.58–1.49) | −0.10 (−0.29 to 0.10) | 0.62 (0.28–1.34) | −0.05 (−0.23 to 0.13) | 1.95 (0.95–4.01) |
Infant normal growth | 408 | 0.04 (−0.08–0.16) | 0.99 (0.74–1.32) | −0.00 (−0.12 to 0.12) | 0.84 (0.54–1.31) | −0.07 (−0.18 to 0.05) | 1.17 (0.69–1.97) |
Infant growth acceleration | 419 | −0.02 (−0.14 to 0.11) | 0.99 (0.73–1.33) | −0.09 (−0.21 to 0.04) | 0.82 (0.52–1.29) | 0.04 (−0.08–0.15) | 0.48 (0.25–0.93)* |
Fetal normal growth | |||||||
Infant growth deceleration | 351 | −0.00 (−0.13 to 0.12) | 0.80 (0.58–1.10) | −0.01 (−0.14 to 0.12) | 1.05 (0.68–1.63) | 0.08 (−0.04–0.20) | 0.70 (0.37–1.35) |
Infant normal growth | 869 | Reference | Reference | Reference | Reference | Reference | Reference |
Infant growth acceleration | 398 | −0.05 (−0.17 to 0.08) | 0.83 (0.61–1.14) | −0.05 (−0.18 to 0.08) | 0.58 (0.34–0.96)* | 0.10 (−0.02–0.21) | 0.87 (0.50–1.53) |
Fetal growth acceleration | |||||||
Infant growth deceleration | 479 | 0.07 (−0.05–0.19) | 0.94 (0.71–1.25) | −0.07 (−0.19 to 0.05) | 0.62 (0.39–0.99)* | 0.09 (−0.02–0.20) | 0.92 (0.52–1.62) |
Infant normal growth | 505 | −0.09 (−0.20 to 0.02) | 0.85 (0.64–1.13) | −0.08 (−0.19 to 0.04) | 0.95 (0.63–1.43) | 0.08 (−0.03–0.19) | 0.84 (0.48–1.47) |
Infant growth acceleration | 150 | −0.14 (−0.32 to 0.04) | 0.83 (0.53–1.32) | −0.07 (−0.25 to 0.12) | 0.83 (0.43–1.62) | 0.27 (0.11–0.44)** | 0.52 (0.20–1.36) |
- Note: Values are regression coefficients (95% confidence interval) or odds ratio’s (95% confidence interval) obtained from multivariable linear respectively logistic regression models and reflect the differences in parent-reported behavioral problems, ADHD symptoms score (SDS), autistic traits score (SDS) and IQ (SDS) for fetal and infant growth patterns. For the logistic regressions the top 20% of the ADHD symptoms score, autistic traits score (weighted scores of >1.078 for boys and >1.000 for girls) and IQ (score <80) was used. Pooled estimates are from multiple imputed datasets. The confounder model is adjusted for age at time of measurement and sex of the child, maternal age in pregnancy, parity, pre-pregnancy body mass index, educational level, ethnicity, folic acid use, smoking, alcohol and maternal IQ measured at the child age of 6 years old.
- Abbreviations: ADHD, attention-deficit hyperactivity disorder; CI, confidence interval; IQ, intelligence quotient; OR, odds ratio; SDS, standard deviation score.
- Total number of available cases; a: n = 3304, b: n = 3315, c: n = 3348.
- *p value < 0.05, **p value < 0.017.
Birth and infant head circumference and childhood outcomes
Supplementary Tables S7 and S8 show the associations of birth and infant head circumference patterns with emotional, behavioral and cognitive outcomes at age 13 years. Children with a head circumference in the smallest tertile at birth and in infancy had a 0.26 SDS (95% CI: 0.10, 0.42) higher total behavior problems score, a 0.24 SDS (95% CI: 0.07, 0.40) higher externalizing problems score and higher odds of a high ADHD symptoms score (OR: 1.77 [95% CI: 1.22, 2.57]) and low IQ score (OR: 2.64 [95% CI: 1.48–4.70]). Overall the associations were similar in direction but stronger for birth and infant head circumference patterns than for fetal and infant weight growth patterns.
DISCUSSION
In this population-based prospective cohort study, we observed that a longer gestational age at birth was associated with lower parent-reported scores for total behavior problems and ADHD symptoms in early adolescence. Increased birth weight was associated with lower odds of parent-reported high externalizing problems and ADHD symptoms, and lower odds of a low IQ. Children born SGA had higher parent-reported total and internalizing behavior problems, ADHD symptoms, and lower IQ in early adolescence, compared to those born AGA. Children with accelerated fetal and infant growth had a higher IQ in early adolescence, whereas those with decelerated fetal growth followed by normal infant growth had lower odds of a high parent-reported total behavior problems score. The associations of fetal and infant head circumference with behavior and cognitive outcomes were stronger than those of fetal and infant weight growth patterns with the same behavioral and cognitive outcomes.
Small size for gestational age, low birth weight and prematurity are associated with increased risks of impaired cognitive development, behavioral problems, psychopathology and intellectual disabilities (Anderson et al., 2021; El Marroun et al., 2012; Grootendorst-van Mil et al., 2015; Hack et al., 2005; Johnson & Marlow, 2011). In a large meta-analysis, 81% of studies showed increased internalizing and externalizing problems in preterm born children (Bhutta et al., 2002). The estimated prevalence’s of behavioral problems depends on the severity of prematurity and low birth weight and range from 13% to 46% (Johnson & Marlow, 2011). We observed that preterm birth and being born SGA were associated with higher scores for total behavior problems, being born SGA was also associated with higher scores for internalizing problems in children aged 13 years. Also, a longer gestational duration and higher birth weight were associated with lower scores for total behavior problems. Longitudinal growth analyses suggest that children who experienced fetal growth deceleration or acceleration followed by normal infant growth had lower odds of high total behavior problems. Thus, our results suggest that next to birth characteristics, patterns of fetal and infant body growth might be important for the risks of behavioral problems in early adolescence.
Previous studies suggest that children born preterm or SGA are at higher risk of ADHD (Allotey et al., 2018; Anderson et al., 2021; Bhutta et al., 2002; Cortese et al., 2021; Pettersson et al., 2019; van Mil et al., 2015). A previous study conducted in Canada among 274 children showed that children who were fetal growth restricted but showed childhood catch-up growth had increased impulsivity at 5 years of age, as compared to normal birth weight children (Silveira et al., 2018). Also, results from a previous study in the same study population as the current, showed that those who were small from mid pregnancy until birth had slightly more ADHD symptoms at 6 year old, as compared to children appropriate size for gestational age (Ferguson et al., 2021). In line with previous studies, our results suggest that older gestational age and higher weight at birth are associated with lower ADHD symptoms, whereas being born SGA is associated with higher ADHD symptoms at 13 years old. However, we did not observe any association between fetal and infant weight growth patterns and ADHD in childhood. The differences in results might be explained by the differences in underlying populations and different approaches to assess growth.
A previous international cohort study of more than 3,500,000 individuals, including over 50,000 individuals with ASD, showed that both preterm and postterm birth are risk factors for ASD (Persson et al., 2020). In addition to gestational age at birth, also early life growth might be related to ASD (Dhaliwal et al., 2019). One Japanese case-control study with 280 ASD cases and 609 controls reported that children with ASD were heavier in infancy (Yang et al., 2011). We observed lower ASD traits in postterm born children as compared to term born. Also, we observed a lower odds of ASD traits above the screenings cut-off in children with fetal normal growth followed by infant growth acceleration and children with fetal growth acceleration followed by infant deceleration. However, these results attenuated into non-significance after correction for multiple testing was applied. Previous studies seem to suggest that gestational age on both ends of the spectrum is associated with ASD in childhood (Persson et al., 2020). Children with ASD might follow a different growth pattern in fetal life and infancy (Dhaliwal et al., 2019; Yang et al., 2011). However, from our study we cannot conclude that gestational age or a specific early life growth pattern is associated with ASD traits.
Childhood and adulthood IQ tend to be lower in individuals born preterm or with low birth weight (Cortese et al., 2021; Ferguson et al., 2021; Grootendorst-van Mil et al., 2015; Kirkegaard et al., 2020; Sacchi et al., 2020). A study conducted in Belarus among 11,899 healthy singletons observed positive associations of increased birth weight and increased childhood weight gain with IQ (Yang et al., 2011). We observed lower IQ for children born SGA. In contrast, longer gestational age, higher birth weight, and size for gestational age were all positively associated with IQ. Additionally, we found the highest IQ in early adolescence among children with fetal and infant growth acceleration. These findings suggest that higher fetal and infant growth are important for cognitive development in later life.
Altogether, we observed that preterm birth and lower weight gain in both fetal life and infancy seem to be related to unfavorable behavioral and cognitive outcomes. To ensure sufficient power in our analyses our main results are based on fetal and infant weight growth. However, sensitivity analyses on early life head circumference growth showed associations of similar direction but stronger than the observed associations of early life weight growth with behavioral and cognitive outcomes. This suggests that head circumference in itself is a growth parameter of great value which could be a proxy for brain development in these associations. In previous research, we have reported that increased weight gain during the fetal period and in infancy is associated with larger brain volumes on MRI scans at 10 years of age, suggesting that brain development is reflected by head circumference and weight growth in fetal life and infancy (Silva et al., 2021). Furthermore, previous research has shown that larger head circumference at birth and in infancy is associated with higher adult IQ and that this association is even stronger in children born very preterm or very low birth weight (Jaekel et al., 2019). Both fetal life and infancy are characterized by rapid body and brain growth. During the fetal life rapid maturation of the fetal brain occurs. Between a gestational age of 12–20 weeks, neuronal migration takes place and around 34 weeks of gestation approximately 40,000 synapses are being formed every second (Monk et al., 2019). This process continues in early childhood. Fetal and infant growth might be explained by various environmental and genetic factors, which might both also affect brain development. Previous studies have shown that growth acceleration following low birth weight of SGA can be both beneficial and detrimental (Ong, 2007). Interestingly, the beneficial effects of growth acceleration seem to be cognitive development whereas the detrimental effects seem to be related to the risk of obesity and adverse metabolic health (Ong, 2007). Previous research has shown the importance of fetal development and reaching growth potential during pregnancy, but has also shown that this potential is dependent on genetic and environmental factors making it difficult to define optimal individual growth potential (Grantz et al., 2018). Especially since excessive childhood weight gain is associated with many childhood and later life complications, such as higher risk of cardiovascular and metabolic diseases (Aggoun, 2007; Goncalves et al., 2022). Although, the observed effects are small, our results also suggest that optimizing growth and development from early fetal life onwards might be important for childhood brain, behavior and cognitive development on a population-based level. To balance optimal growth versus inadequate or excessive weight gain, individualized growth patterns related to different health outcomes would be most suited. Unfortunately, these have not yet been developed and further research should be focused on identification of such growth patterns.
Strengths of this study include the study design, large number of participants, detailed data on weight measurements from second trimester up to 2 years of age and extensive report on behavioral and cognitive outcomes. In addition to previous research conducted in our study population examining similar associations, this study is of added value since it is conducted in older children and adds fetal-infant growth patterns. This study also has limitations. Of the 8624 singleton live births with information on fetal or infant growth, 4716 children had data regarding behavior and cognitive outcome measurements. Mothers of children not included in our analyses were younger, less often primipara, higher educated and of European ethnicity, had lower IQ and less often used alcohol during pregnancy. This seems to suggest bias to a relatively more healthy population and might affect the generalizability of our results. Previous research has shown that the association of birth weight and gestational age at birth with IQ or behavior in later life might not be linear. The positive effect of gestational age on IQ seems greater below 34 weeks of gestation as compared to 34–37 weeks of gestation (Eves et al., 2023; MacKay et al., 2010; Wolke et al., 2015). In our population the number of preterm born children is small (4.6%) and an even smaller number of those born preterm was below <34 weeks (1.1%). Therefore we did not have enough numbers to stratify on gestational age or even on term birth versus preterm birth. Such stratification might be relevant for studies with larger numbers since rapid infant weight gain may be stronger associated with neurodevelopmental benefits for preterm infants than term infants (Belfort et al., 2010). Furthermore, the measurement of estimated fetal weight can be inaccurate and random error might be high, especially in the extreme values of estimated fetal weight (Dudley, 2005; Ewington et al., 2024). The stronger effects of postnatal weight growth than fetal weight growth might be due to biological effects or the results of better precision for postnatal measurements. We were interested in the combination between fetal and infant growth delta’s, which are in line with clinical guidelines regarding growth curves and the cut-offs used for growth deceleration and acceleration respectively. Further studies might focused on more detailed growth modeling aiming to identify the optimal growth patterns in early life for mental health outcomes. Although we adjusted for a large number of potential confounders, residual confounding might still be a possibility due to the observational nature of the study.
CONCLUSION
In a population-based sample of children followed from fetal life to adolescence, both gestational age at birth and fetal and infant growth were associated with behavioral and cognitive outcomes in early adolescence. Identification of healthy growth patterns is an important step, which might provide an opportunity in preventing psychopathology. Follow-up studies are needed to assess the underlying mechanisms and long term consequences of the observed associations.
AUTHOR CONTRIBUTIONS
Romy Gonçalves: Conceptualization; Data curation; Formal analysis; Investigation; Methodology; Project administration; Validation; Visualization; Writing – original draft; Writing – review & editing. Romy Gaillard: Conceptualization; Funding acquisition; Supervision; Validation; Writing – review & editing. Kelly Ferguson: Funding acquisition; Methodology; Validation; Writing – review & editing. Sara Sammallahti: Funding acquisition; Validation; Writing – review & editing. Manon Hillegers: Funding acquisition; Methodology; Validation; Writing – review & editing. Eric Steegers: Funding acquisition; Methodology; Supervision; Validation; Visualization; Writing – review & editing. Hanan El Marroun: Conceptualization; Methodology; Visualization; Writing – review & editing. Vincent Jaddoe: Conceptualization; Funding acquisition; Methodology; Supervision; Writing – review & editing.
ACKNOWLEDGMENTS
The Generation R Study is conducted by the Erasmus University Medical Center in close collaboration with the Erasmus University Rotterdam and the Municipal Health Service Rotterdam area, Rotterdam. We gratefully acknowledge the contribution of children and parents, general practitioners, hospitals, midwives and pharmacies in Rotterdam. R. Gonçalves is responsible for the study design, performed the statistical analyses and wrote the manuscript and had primary responsibility for the final content. V.W.V.J. and H.E.M contributed to the design of the study, interpretation of the results and were responsible for critical review of the manuscript. R. Gaillard, S.S, K.F, M.H.H. and E.A.P.S contributed to the interpretation of the results and critically reviewed the manuscript. All authors have read and approved the final manuscript and agree to be accountable for all aspects of the work.
This work was supported by the European Research Council [Consolidator Grant, ERC-2014-CoG-648916, received by Prof. Vincent V.W. Jaddoe], the European Joint Programming Initiative “A Healthy Diet for a Healthy Life” (JPI HDHL) the Netherlands, [EndObesity, ZonMW grant number 529051026, received by Dr Romy Gaillard], the European Union’s Horizon 2020 Research and Innovation Program grant agreement, 733206 (LifeCycle) and 874583 (ATHLETE Project). The Netherlands Organization for Health Research and Development [NWO, ZonMW, grant number 543003109, received by Dr Romy Gaillard], and the LEaDing Fellows EU Marie Skłodowska-Curie COFUND Program grant 707404 (Dr Sammallahti). Hanan El Marroun was supported by Stichting Volksbond Rotterdam, the Brain & Behavior Research Foundation (NARSAD Young Investigator Grant 27853), the Netherlands Organization for Health Research and Development (Aspasia grant No. 015.016.056). Support for Kelly K. Ferguson was provided by the Intramural Research Program of the National Institute of Environmental Health Sciences, National Institutes of Health. The Generation R Study is financially supported by the Erasmus Medical Center, Rotterdam, the Erasmus University Rotterdam and the Netherlands Organization for Health Research and Development and the Ministry of Health, Welfare and Sport.
CONFLICT OF INTEREST STATEMENT
The authors have declared no competing or potential conflicts of interest.
ETHICAL CONSIDERATIONS
Nil.
Open Research
DATA AVAILABILITY STATEMENT
Data from the Generation R study are available upon request to the director ([email protected]), subject to local rules and regulations.