TY - JOUR
T1 - White matter microstructure and cognitive abilities in 28-year-old offspring prenatally exposed to maternal anxiety
T2 - A prospective exploratory multimodal brain imaging study
AU - Van den Bergh, Bea R.H.
AU - Sleurs, Charlotte
AU - Geusens, Birte
AU - Emsell, Louise
AU - Sunaert, Stefan
AU - Billiet, Thibo
PY - 2025/8
Y1 - 2025/8
N2 - Prenatal exposure to maternal psychological distress (PEMPD) can affect brain development and cognition, but its long-term impact on adult white matter (WM) microstructure and cognition remains unclear. In an exploratory study, we examined 28-year-old offspring (n = 52) exposed to high maternal anxiety (HA group; State Anxiety > 43) or low-to-medium maternal anxiety (LMA group; State Anxiety <= 43) at 12-22 weeks of gestation, a critical period for WM development. Whole WM voxel-based analysis assessed microstructural differences using diffusion magnetic resonance imaging (dMRI), including standard diffusion tensor imaging (DTI), advanced methods such as diffusion kurtosis imaging, neurite orientation dispersion and density imaging, and myelin water imaging. Group differences in WM and cognition (Vocabulary, Perceptual Organization, Processing Speed) were tested using ANCOVAs respectively MANOVA (Holm-Bonferroni-corrected) adjusting for birth weight and postnatal maternal anxiety. The HA group showed lower radial and mean diffusivity and a trend for lower isotropic volume fraction) in the left superior corona radiata. Vocabulary scores were consistently lower in the HA group across ages 14-15 and 28 (moderate effect). The left-lateralized WM differences may reflect altered axonal architecture or cellular composition, possibly originating in utero. The use of advanced and complementary microstructural metrics highlights subtle WM alterations that mayshape neurodevelopmental trajectories and underlie later cognitive outcomes.
AB - Prenatal exposure to maternal psychological distress (PEMPD) can affect brain development and cognition, but its long-term impact on adult white matter (WM) microstructure and cognition remains unclear. In an exploratory study, we examined 28-year-old offspring (n = 52) exposed to high maternal anxiety (HA group; State Anxiety > 43) or low-to-medium maternal anxiety (LMA group; State Anxiety <= 43) at 12-22 weeks of gestation, a critical period for WM development. Whole WM voxel-based analysis assessed microstructural differences using diffusion magnetic resonance imaging (dMRI), including standard diffusion tensor imaging (DTI), advanced methods such as diffusion kurtosis imaging, neurite orientation dispersion and density imaging, and myelin water imaging. Group differences in WM and cognition (Vocabulary, Perceptual Organization, Processing Speed) were tested using ANCOVAs respectively MANOVA (Holm-Bonferroni-corrected) adjusting for birth weight and postnatal maternal anxiety. The HA group showed lower radial and mean diffusivity and a trend for lower isotropic volume fraction) in the left superior corona radiata. Vocabulary scores were consistently lower in the HA group across ages 14-15 and 28 (moderate effect). The left-lateralized WM differences may reflect altered axonal architecture or cellular composition, possibly originating in utero. The use of advanced and complementary microstructural metrics highlights subtle WM alterations that mayshape neurodevelopmental trajectories and underlie later cognitive outcomes.
KW - Advanced Diffusion MRI
KW - Brain development and aging
KW - Developmental origins of health and disease (DOHaD)
KW - Diffusion kurtosis imaging (DKI)
KW - Myelin water imaging (MWI)
KW - Neurite orientation dispersion and density imaging (NODDI)
KW - Neurodevelopmental trajectories
KW - Perinatal mental health
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=wosstart_imp_pure20230417&SrcAuth=WosAPI&KeyUT=WOS:001507092700002&DestLinkType=FullRecord&DestApp=WOS_CPL
U2 - 10.1016/j.bandc.2025.106319
DO - 10.1016/j.bandc.2025.106319
M3 - Article
C2 - 40483834
SN - 0278-2626
VL - 188
JO - Brain and Cognition
JF - Brain and Cognition
M1 - 106319
ER -