Infant subcortical brain volumes associated with maternal obesity and diabetes: a large multicohort human study

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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Journal
BMC Medicine
Published
2026-04-16
DOI
https://doi.org/10.1186/s12916-026-04860-6
Primary Topic
Gestational Diabetes Research and Management
Type
article
Field-Weighted Citation Impact
0.00

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article

Infant subcortical brain volumes associated with maternal obesity and diabetes: a large multicohort human study

Sonja Entringer, Rebecca Knickmeyer, Nynke A. Groenewold, Katherine E. Lawrence et al.
BMC Medicine
Gestational Diabetes Research and Management
article

Infant subcortical brain volumes associated with maternal obesity and diabetes: a large multicohort human study

Sonja Entringer, Rebecca Knickmeyer, Nynke A. Groenewold, Katherine E. Lawrence, A. David Edwards, Kirsten A. Donald, Inka Mattila, Gustavo de los Campos, Jerod M. Rasmussen, ENIGMA-ORIGINs working group, Hasse Karlsson, Shan Luo, Pathik D. Wadhwa, Ann M. Alex, John H. Gilmore, Jetro J. Tuulari, Xi Zhu, Linnea Karlsson, Julie Nihouarn Sigurdardottir, Paul Andrew Thompson, Heather J. Zar, Claudia Buss, Dan J. Stein, Martin Styner
article en

Abstract

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.

BMC Medicine
South African Medical Research Council (ZA), University of North Carolina at Chapel Hill (US), University of Southern California (US), Children's Hospital of Los Angeles (US), University of Turku (FI), University of Cape Town (ZA), King's College London (GB), The University of Texas at Arlington (US), University of California, Irvine (US), Diabetes Australia (AU), Turku University Hospital (FI), Zentrum für Seelische Gesundheit (AT), Texas A&M Health Science Center (US), Deutsche Akademie für Kinder- und Jugendmedizin (DE), Red Cross War Memorial Children's Hospital (ZA), Charité - Universitätsmedizin Berlin (DE), Michigan State University (US)
Carnegie Corporation of New York, Bill and Melinda Gates Foundation, Brain and Behavior Research Foundation, Suomen Lääketieteen Säätiö, National Alliance for Research on Schizophrenia and Depression, Newton Fund, Academy of Medical Sciences, South African Medical Research Council, Academy of Finland, Jane ja Aatos Erkon Säätiö, Signe ja Ane Gyllenbergin Säätiö, Emil Aaltosen Säätiö, Varsinais-Suomen Sairaanhoitopiiri, National Institutes of Health, National Institute of Mental Health, National Institute of Diabetes and Digestive and Kidney Diseases
Zero hunger
Openalex Percentile: Top 25%
Gestational Diabetes Research and Management
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