Maternal anxiety and infants’ hippocampal development: timing matters.
Open accessAbstract
Exposure to maternal anxiety predicts offspring brain development. However, because children’s brains are commonly assessed years after birth, the timing of such maternal influences in humans is unclear. This study aimed to examine the consequences of antenatal and postnatal exposure to maternal anxiety upon early infant development of the hippocampus, a key structure for stress regulation. A total of 175 neonates underwent magnetic resonance imaging (MRI) at birth and among them 35 had repeated scans at 6 months of age. Maternal anxiety was assessed using the State-Trait Anxiety Inventory (STAI) at week 26 of pregnancy and 3 months after delivery. Regression analyses showed that antenatal maternal anxiety did not influence bilateral hippocampal volume at birth. However, children of mothers reporting increased anxiety during pregnancy showed slower growth of both the left and right hippocampus over the first 6 months of life. This effect of antenatal maternal anxiety upon right hippocampal growth became statistically stronger when controlling for postnatal maternal anxiety. Furthermore, a strong positive association between postnatal maternal anxiety and right hippocampal growth was detected, whereas a strong negative association between postnatal maternal anxiety and the left hippocampal volume at 6 months of life was found. Hence, the postnatal growth of bilateral hippocampi shows distinct responses to postnatal maternal anxiety. The size of the left hippocampus during early development is likely to reflect the influence of the exposure to perinatal maternal anxiety, whereas right hippocampal growth is constrained by antenatal maternal anxiety, but enhanced in response to increased postnatal maternal anxiety.
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Exposure to prenatal maternal stress has enduring and wide-ranging consequences on brain development in the offspring, including altered regional brain volumetric growth, cortical folding, metabolism, microstructure, and functional connectivity.
“Importantly, exposure to prenatal maternal stress is shown to have enduring and wide-ranging consequences on brain development in the offspring, including altered regional brain volumetric growth, cortical folding, metabolism, microstructure, and functional connectivity [4, 15, 19, 23–27, 35–39].”
From Brain structural and functional outcomes in the offspring of women experiencing psychological distress during pregnancy (2024) · cites this paper as [36]
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Experimental — accuracy not yet measuredElevated prenatal maternal anxiety is associated with slower growth of the left and right hippocampus during the first 6 months of life.
“In the hippocampus, elevated prenatal maternal anxiety is associated with slower growth of the left and right hippocampus during the first 6 months of life [36].”
From Brain structural and functional outcomes in the offspring of women experiencing psychological distress during pregnancy (2024) · cites this paper as [36]
Maternal anxiety is associated with slower hippocampal growth between birth and 6 months of age.
“Maternal anxiety is associated with slower hippocampal growth between birth and 6 months of age178”
From Imaging structural and functional brain development in early childhood (2018) · cites this paper as [178]
Prenatal maternal stress exposure has enduring consequences on offspring brain development and long-term neurodevelopment.
“Prenatal maternal stress exposure has been shown to have enduring consequences on brain development in the offspring”
From Association of Elevated Maternal Psychological Distress, Altered Fetal Brain, and Offspring Cognitive and Social-Emotional Outcomes at 18 Months (2022) · cites this paper as [9]
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References 51 · Cited by 214
Research works printed but not linked: 1
- Pruessner JC Dedovic K Khalili-Mahani N Engert V Pruessner M Buss C Deactivation of the limbic system during acute psychosocial stress: evidence from positron emission tomography and functional magnetic resonance imaging studies Biol Psychiatry 2008 63 234 240 17686466
- Authors
- Qiu, A., Rifkin-Graboi, A., Chen, H., Chong, Y.-S., Kwek, K., Gluckman, P. D., Fortier, M. V., & Meaney, M. J.
- Affiliations
- Agency for Science, Technology and Research (SG)
- KK Women's and Children's Hospital (SG)
- National University of Singapore (SG)
- University of Auckland (NZ)
- Corresponding author
- Qiu, A
- Venue
- Translational Psychiatry
- Published
- 2013-09-24
- Volume
- 3
- Issue
- 9
- Pages
- e306-e306
- ISSN
- 2158-3188 (ISSN-L)
- PMC
- PMC3784768
- OpenAlex
- W2068991614
- Cited by
- 214
- References
- 51
- Citations by year
- 2026: 9 · 2025: 14 · 2024: 15 · 2023: 21 · 2022: 24 · 2021: 26 · 2020: 27 · 2019: 16 · 2018: 17 · 2017: 15 · 2016: 12 · 2015: 9 · 2014: 8 · 2013: 1
- FWCI
- 10.23
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Translational Psychiatry (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- National University of Singapore (submittedVersion, cc-by)
- Funders
- Agency for Science, Technology and Research (SICS-09/1/1/001, NMRC/CBRG/0039/2013)
- National University of Singapore (Tier 1, NUSYIA FY10 P07)
- Ministry of Education, India
- Medical Research Council
- National Medical Research Council (NMRC /CBRG/0039/2013)
- Topics
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Maternal Mental Health During Pregnancy and Postpartum
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Social Sciences › Psychology › Clinical Psychology › Child and Adolescent Psychosocial and Emotional Development
- Keywords
- maternal anxiety, hippocampus, infant brain development, hippocampal asymmetry, neonatal brain imaging, perinatal stress, stress regulation
- MeSH terms
- Anxiety, Child Development, Female, Hippocampus, Humans, Infant, Infant, Newborn, Magnetic Resonance Imaging, Male, Maternal Behavior, Mothers, Pregnancy, Pregnancy Complications, Prenatal Exposure Delayed Effects, Regression Analysis, Singapore, Cohort Studies, Fetal Development
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