Higher birth weights usually reflect better intrauterine health, nutrition, and growth. Higher birth weights are also associated with better cognitive outcomes for children (1). However, among pregnancies complicated by diabetes, being born large for gestational age may reflect different intrauterine disease processes, and it is unclear whether this carries the same benefits for education. Our objective is to examine whether diabetes during pregnancy modifies the association between birth weight and school achievement.

This whole-of-population study was conducted using deidentified administrative data that linked perinatal data to children’s school assessments. School assessments were obtained from the National Assessment Program – Literacy and Numeracy (NAPLAN), which involves assessments of reading, writing, spelling, grammar, and numeracy in grade three (age ∼8 years). Scores were dichotomized at performing above the national minimum standard or not. Children who perform at or below the standard typically require classroom learning support. Z scores of birth weight for gestational age (BWGA) were calculated using Australian norms. Diabetes was recorded as either preexisting (i.e., prior to pregnancy, including all types of diabetes) or gestational diabetes mellitus. Preexisting and gestational diabetes mellitus were combined for analyses due to small numbers.

The analysis explored whether the effect of BWGA on NAPLAN was modified by maternal diabetes. BWGA was categorized into the lowest (<20th), middle (20–79th), and highest (≥80th) quintiles. Risk ratios (RR) were calculated from log-Poisson regression models with robust errors and adjustment for confounding by stabilized inverse probability of treatment weights. We tested for effect measure modification by maternal diabetes on the additive scale using the relative excess risk due to interaction (RERI) (2) because the additive scale is important for public health outcomes. We also report the multiplicative scale using the ratio of relative risks (RRR). Potential confounders were identified based on evidence and content knowledge of common causes of birth weight and educational achievement. Analyses were conducted using Stata SE, version 14.0 (StataCorp., College Station, Texas).

The total sample included 73,642 children. Birth weight in grams (mean ± SD) was 3,419 ± 572 and 3,376 ± 572 for infants born to mothers with and without diabetes, respectively. Table 1 shows that, in the absence of diabetes, BWGA<20 had higher and BWGA≥80 had lower risks of poor school outcomes compared with BWGA20–79. For example, the risks of poor spelling scores were 17% higher for BWGA<20 (RR 1.17 [95% CI 1.13, 1.22]) and 6% lower for BWGA≥80 (0.94 [0.90, 0.98]). In the presence of diabetes, risks of poor scores were higher for BWGA≥80 than BWGA20–79, which was reflected in the RERI. For example, risk of poor scores on spelling was 38% higher than that for BWGA20–79 (1.38 [1.15, 1.67]); RERI 0.49 [95% CI 0.15, 0.83]).

Table 1

Associations between BWGA and meeting the national minimum standard score for NAPLAN assessments, according to the presence of maternal diabetes*

BWGA percentiles across the whole populationWithin stratum of diabetes
<20th20–79th≥80th<20th vs. 20–79th≥80th vs. 20–79th
n ≤ NMS/total N (%)RR (95% CI)*n ≤ NMS/total N (%)RR (95% CI)*n ≤ NMS/total N (%)RR (95% CI)*RR/RERI/RRR (95% CI)RR/RERI/RRR (95% CI)
Grammar         
 No diabetes 3,545/14,515 (24.4%) 1.17 (1.12, 1.21) 8,181/42,256 (19.4%) Reference 2,348/13,368 (17.6%) 0.93 (0.89, 0.97) RR 1.17 (1.12, 1.21) RR 0.93 (0.89, 0.97) 
 Diabetes 89/383 (23.2%) 1.05 (0.83, 1.32) 262/1,387 (18.9%) 0.98 (0.88, 1.10) 171/737 (23.2%) 1.40 (1.17, 1.70) RR 1.22 (0.97, 1.53) RR 1.30 (1.08, 1.57) 
        RERI −0.10 (−0.42, 0.22) RERI 0.49 (0.13, 0.84) 
        RRR 0.91 (0.63, 1.20) RRR 1.53 (1.10, 1.97)  
Reading  
 No diabetes 3,655/14,502 (25.2%) 1.19 (1.14, 1.23) 8,346/42,122 (19.8%) Reference 2,420/13,348 (18.1%) 0.95 (0.90, 0.99) RR 1.19 (1.14, 1.23) RR 0.95 (0.90, 0.99) 
 Diabetes 79/382 (20.7%) 0.91 (0.71, 1.16) 272/1,381 (19.7%) 1.00 (0.90, 1.11) 159/723 (22.0%) 1.19 (0.98, 1.45) RR 1.08 (0.85, 1.37) RR 1.13 (0.93, 1.37) 
        RERI −0.27 (−0.57, 0.02) RERI 0.25 (−0.08, 0.57) 
        RRR 0.77 (0.53, 1.01) RRR 1.26 (0.90, 1.62)  
Spelling  
 No diabetes 3,733/14,515 (25.7%) 1.17 (1.13, 1.22) 8,698/42,256 (20.6%) Reference 2,532/13,368 (18.9%) 0.94 (0.90, 0.98) RR 1.17 (1.13, 1.22) RR 0.94 (0.90, 0.98) 
 Diabetes 94/383 (24.5%) 1.10 (0.88, 1.38) 273/1,387 (19.7%) 0.95 (0.86, 1.06) 177/737 (24.0%) 1.38 (1.15, 1.67) RR 1.29 (1.04, 1.61) RR 1.30 (1.08, 1.55) 
        RERI −0.03 (−0.34, 0.29) RERI 0.49 (0.15, 0.83) 
        RRR 0.98 (0.69, 1.28) RRR 1.54 (1.12, 1.97)  
Writing  
 No diabetes 2,266/14,413 (15.7%) 1.16 (1.10, 1.22) 5,191/42,069 (12.3%) Reference 1,460/13,295 (11.0%) 0.91 (0.86, 0.97) RR 1.16 (1.10, 1.22) RR 0.91 (0.86, 0.97) 
 Diabetes 50/379 (13.2%) 0.94 (0.68, 1.29) 168/1,380 (12.2%) 0.98 (0.85, 1.14) 122/731 (16.7%) 1.60 (1.25, 2.05) RR 1.08 (0.79, 1.50) RR 1.46 (1.15, 1.86)  
        RERI −0.21 (−0.61, 0.19) RERI 0.71 (0.20, 1.22)  
        RRR 0.82 (0.48, 1.12) RRR 1.79 (1.13, 2.44)  
Numeracy  
 No diabetes 4,152/14,481 (28.7%) 1.20 (1.16, 1.24) 9,395/42,035 (22.4%) Reference 2,635/13,302 (19.8%) 0.92 (0.88, 0.96) RR 1.20 (1.16, 1.24) RR 0.92 (0.88, 0.96)  
 Diabetes 115/387 (29.7%) 1.10 (0.90, 1.33) 316/1,373 (23.0%) 1.03 (0.94, 1.14) 190/728 (26.1%) 1.27 (1.06, 1.51) RR 1.32 (1.08, 1.60) RR 1.16 (0.98, 1.38)  
        RERI −0.14 (−0.43, 0.15) RERI 0.32 (0.02, 0.62)  
        RRR 0.88 (0.65, 1.12) RRR 1.34 (1.00, 1.69)  
BWGA percentiles across the whole populationWithin stratum of diabetes
<20th20–79th≥80th<20th vs. 20–79th≥80th vs. 20–79th
n ≤ NMS/total N (%)RR (95% CI)*n ≤ NMS/total N (%)RR (95% CI)*n ≤ NMS/total N (%)RR (95% CI)*RR/RERI/RRR (95% CI)RR/RERI/RRR (95% CI)
Grammar         
 No diabetes 3,545/14,515 (24.4%) 1.17 (1.12, 1.21) 8,181/42,256 (19.4%) Reference 2,348/13,368 (17.6%) 0.93 (0.89, 0.97) RR 1.17 (1.12, 1.21) RR 0.93 (0.89, 0.97) 
 Diabetes 89/383 (23.2%) 1.05 (0.83, 1.32) 262/1,387 (18.9%) 0.98 (0.88, 1.10) 171/737 (23.2%) 1.40 (1.17, 1.70) RR 1.22 (0.97, 1.53) RR 1.30 (1.08, 1.57) 
        RERI −0.10 (−0.42, 0.22) RERI 0.49 (0.13, 0.84) 
        RRR 0.91 (0.63, 1.20) RRR 1.53 (1.10, 1.97)  
Reading  
 No diabetes 3,655/14,502 (25.2%) 1.19 (1.14, 1.23) 8,346/42,122 (19.8%) Reference 2,420/13,348 (18.1%) 0.95 (0.90, 0.99) RR 1.19 (1.14, 1.23) RR 0.95 (0.90, 0.99) 
 Diabetes 79/382 (20.7%) 0.91 (0.71, 1.16) 272/1,381 (19.7%) 1.00 (0.90, 1.11) 159/723 (22.0%) 1.19 (0.98, 1.45) RR 1.08 (0.85, 1.37) RR 1.13 (0.93, 1.37) 
        RERI −0.27 (−0.57, 0.02) RERI 0.25 (−0.08, 0.57) 
        RRR 0.77 (0.53, 1.01) RRR 1.26 (0.90, 1.62)  
Spelling  
 No diabetes 3,733/14,515 (25.7%) 1.17 (1.13, 1.22) 8,698/42,256 (20.6%) Reference 2,532/13,368 (18.9%) 0.94 (0.90, 0.98) RR 1.17 (1.13, 1.22) RR 0.94 (0.90, 0.98) 
 Diabetes 94/383 (24.5%) 1.10 (0.88, 1.38) 273/1,387 (19.7%) 0.95 (0.86, 1.06) 177/737 (24.0%) 1.38 (1.15, 1.67) RR 1.29 (1.04, 1.61) RR 1.30 (1.08, 1.55) 
        RERI −0.03 (−0.34, 0.29) RERI 0.49 (0.15, 0.83) 
        RRR 0.98 (0.69, 1.28) RRR 1.54 (1.12, 1.97)  
Writing  
 No diabetes 2,266/14,413 (15.7%) 1.16 (1.10, 1.22) 5,191/42,069 (12.3%) Reference 1,460/13,295 (11.0%) 0.91 (0.86, 0.97) RR 1.16 (1.10, 1.22) RR 0.91 (0.86, 0.97) 
 Diabetes 50/379 (13.2%) 0.94 (0.68, 1.29) 168/1,380 (12.2%) 0.98 (0.85, 1.14) 122/731 (16.7%) 1.60 (1.25, 2.05) RR 1.08 (0.79, 1.50) RR 1.46 (1.15, 1.86)  
        RERI −0.21 (−0.61, 0.19) RERI 0.71 (0.20, 1.22)  
        RRR 0.82 (0.48, 1.12) RRR 1.79 (1.13, 2.44)  
Numeracy  
 No diabetes 4,152/14,481 (28.7%) 1.20 (1.16, 1.24) 9,395/42,035 (22.4%) Reference 2,635/13,302 (19.8%) 0.92 (0.88, 0.96) RR 1.20 (1.16, 1.24) RR 0.92 (0.88, 0.96)  
 Diabetes 115/387 (29.7%) 1.10 (0.90, 1.33) 316/1,373 (23.0%) 1.03 (0.94, 1.14) 190/728 (26.1%) 1.27 (1.06, 1.51) RR 1.32 (1.08, 1.60) RR 1.16 (0.98, 1.38)  
        RERI −0.14 (−0.43, 0.15) RERI 0.32 (0.02, 0.62)  
        RRR 0.88 (0.65, 1.12) RRR 1.34 (1.00, 1.69)  
*

RRs and 95% CI were calculated from a generalized linear model with log-Poisson links and inverse probability of treatment weighting to adjust for the following potential confounders: maternal age, smoking in pregnancy, ethnicity, occupation, birthing in private hospital, index of relative socioeconomic advantage and disadvantage, living in a remote area, maternal asthma, high blood pressure, singleton, parity, gestational age, and child’s sex. NMS, national minimum standard score for age.

Among women who had diabetes during pregnancy, infants with birth weights in the heaviest quintile for their gestational age had poorer school assessments. The evidence is less clear for mothers with diabetes whose infants are born in the lowest quintile due to smaller numbers and wide confidence intervals. Among women who do not have diabetes, lower birth weights for gestational age were linked to poorer assessments and higher birth weights were linked to better assessments. Our use of a population-based data set is less susceptible to recall and selection biases than cohort studies, and the large size is well powered for looking within subgroups of infants with higher/lower birth weights and presence/absence of diabetes. The analysis included adjustments for a wide range of confounders but not maternal BMI, as it was not collected. However, others have shown little change to point estimates after adjusting for BMI (3). Furthermore, adjusting for maternal BMI is more important for studies where child weight is an outcome, rather than education.

The current study may have implications for clinical management of pregnant women with diabetes. Large fetal size can reflect overnutrition due to hyperglycemia or healthy fetuses who are constitutionally large and not at risk for poor academic outcomes. The perinatal database does not include information on diabetes control, and women who have poorer control and larger babies may have children who have poorer school assessments. Births at 40–41 weeks’ gestation are optimal for school achievement (4). Ultrasound monitoring of fetal size during pregnancy in addition to diet and insulin (if required) may help reduce large-for-gestational-age births (5). Optimization of blood glucose levels for pregnant women with diabetes is key, and prevention of obesity, while difficult, might theoretically represent the best approach. However, studies involving dietary interventions for overweight or obese women have been largely unsuccessful; thus, preventing prepregnancy obesity is likely to be important but not achievable at the population level.

To summarize, on average, being born in the highest quintile of BWGA is linked to poorer school achievement if mothers have diabetes during pregnancy.

Acknowledgments. The authors acknowledge SA NT DataLink and data custodians and managers from government departments at state and federal levels that have contributed to the development of this work through the South Australian Early Childhood Data Project (ECDP). The authors specifically thank the Pregnancy Outcomes Unit at the South Australian Department for Health and Wellbeing, the Births Registry office at the South Australia Attorney General, and the Department for Education for contributing data that have been used in this project.

Funding. This work was funded by a National Health and Medical Research Council (NHMRC) of Australia Partnership Grant (1056888), the Centre for Clinical Research Excellence (1099422), an Australia Fellowship (570120) awarded to J.L., and a Practitioner Fellowship awarded to B.W.M. (1082548).

The views presented here do not necessarily reflect those of our government partners.

Duality of Interest. B.W.M. reports consultancy for ObsEva, Merck, and Guerbet. No other potential conflicts of interest relevant to this article were reported.

Author Contributions. L.G.S. conceptualized the study, conducted the analysis, interpreted the results, and drafted and revised the manuscript. M.N.M. provided advice on the analysis and revised the manuscript for intellectual content. G.D. and B.W.M. provided clinical advice, contributed to the interpretation, and revised the manuscript for intellectual content. J.L. procured the data from custodians, contributed to the conception and interpretation, and revised the manuscript for intellectual content. All authors approved the final submitted version. L.G.S. is the guarantor of this work and, as such, had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.

Prior Presentation. Parts of this work were presented in abstract form at the 32nd Annual Meeting of the Society for Pediatric and Perinatal Epidemiologic Research, Minneapolis, MN, 17–18 July 2019.

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