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Infant subcortical brain volumes associated with maternal obesity and diabetes: a large multicohort human study
Ann M Alex1,2, Jerod M Rasmussen3,4, Jetro J Tuulari5,6,7,8,9
1Department of Neuroscience and Experimental Therapeutics, Texas A&M Health Science Center, College of Medicine, Bryan, TX, USA.
Insights
Maternal obesity and diabetes impact infant brain development, with obesity showing stronger effects on subcortical volumes. These effects differ by infant sex, highlighting the importance of maternal metabolic health.
Area of Science:
- Neuroscience
- Developmental Biology
- Public Health
Background:
- Maternal diabetes and obesity are known risk factors for adverse child health outcomes.
- Fetal programming effects of these conditions may vary by infant sex.
- The independent and interactive influences on early brain development require further investigation.
Purpose of the Study:
- To investigate the independent and interactive effects of maternal obesity and diabetes on infant subcortical brain volumes.
- To examine sex-specific associations between maternal metabolic conditions and infant brain development.
Main Methods:
- Prospective study of 1,965 infants from six international cohorts.
- Infant brain MRI was used to measure subcortical volumes (thalamus, amygdala, hippocampus, etc.).
- Statistical analyses included multiple linear regression with interaction terms, controlling for covariates and applying FDR corrections.
Main Results:
- Maternal obesity was associated with smaller hippocampal and thalamic volumes.
- In females, maternal obesity was linked to smaller hippocampal and amygdala volumes.
- A three-way interaction (maternal diabetes x obesity x sex) affected thalamus volume; combined exposure was linked to smaller thalamic volumes in males.
Conclusions:
- Maternal obesity has a more significant impact on infant subcortical volumes than maternal diabetes.
- Sex-specific effects were observed, with maternal obesity impacting female infants' amygdala and hippocampus, and combined exposures affecting male infants' thalamus.
- Maternal metabolic health and infant sex are crucial factors in early neurodevelopment.
Background:
Maternal diabetes and obesity are established risk factors for adverse offspring health. Emerging evidence suggests that these fetal programming effects vary by sex, yet it remains unclear whether these factors independently or interactively influence early brain development.
Methods:
This prospective study included 1,965 infants from six international cohorts. Infant MRI was used to derive subcortical volumes (thalamus, amygdala, hippocampus, pallidum, putamen, caudate). ComBat harmonization was applied. Multiple linear regression tested main and interaction effects of maternal obesity, maternal diabetes, and sex, controlling for covariates with false discovery rate (FDR) corrections.
Results:
Of the sample, 46% were female (N = 909), 9% were exposed to maternal diabetes (N = 172), 22% to maternal obesity (N = 386), and 3% to both (N = 61). MRI scans were performed at 25.9 ± 18.8 days. Maternal diabetes was associated with smaller thalamic volume (standardized β = -0.09, 95%CI -0.16 to -0.01, FDR P = 0.020), but this association was attenuated after adjusting for maternal obesity. Maternal obesity was associated with smaller hippocampal (standardized β = -0.13, 95%CI -0.21 to -0.05, FDR P = 0.009) and thalamic volumes (standardized β = -0.09, 95%CI -0.14 to -0.03, FDR P = 0.007). Sex-specific associations were observed. In females, maternal obesity was associated with smaller hippocampal (standardized β = -0.24, 95%CI -0.36 to -0.13, FDR P < 0.001) and amygdala volumes (standardized β = -0.18, 95% CI = -0.30 to -0.06, FDR P = 0.016). A three-way interaction (diabetes x obesity x sex) was observed for thalamus volume (standardized β = -0.50, 95%CI -0.81 to -0.18, FDR P = 0.017). In males, combined exposure had lower thalamic volume compared to those with one or neither exposure (all Ps < 0.05). In females, maternal obesity (standardized β = -0.12, 95%CI -0.20 to -0.04, FDR P = 0.015) and diabetes (standardized β = -0.16, 95%CI -0.30 to -0.02, FDR P = 0.042) showed independent associations with thalamic volume, without a significant interaction (standardized β = 0.23, 95%CI -0.01 to 0.46, FDR P = 0.092).
Conclusions:
Maternal obesity shows stronger associations with infant subcortical volumes than maternal diabetes. It is associated with smaller hippocampal and amygdala volumes in females, while combined exposure to maternal diabetes and obesity is associated with smaller thalamic volumes in males. These findings highlight the role of maternal metabolic health and infant sex in early neurodevelopment.
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