Aug 2026· Drug and Alcohol Dependence· Vol 287, pp.
113318
· 0 citations· 79 references
Medicine
TL;DR
These findings build upon previous reports of structural and developmental differences in youth with PAE, suggesting that gyrification may be more sensitive to the effects of PAE than cortical thickness.
Abstract
Background
Prenatal alcohol exposure (PAE) occurs in ~10% of pregnancies in North America and can alter brain development. Prior research on brain morphology in children with PAE shows mixed findings for cortical thickness, and only a few studies have investigated more complex morphological features, showing decreased gyrification with PAE. Here, we use four anatomical measures to provide a comprehensive characterization of cortical morphology in youth with PAE compared to unexposed youth.
Methods
T1-weighted Magnetic Resonance Imaging (MRI) was used to examine cortical morphology metrics in 163 scans from 121 youth (56 with PAE) aged 7-21 years. Each participant had between 1 and 3 scans. Images were processed to segment 98 cortical brain regions. Linear mixed-effects models were used to test the effects of PAE on cortical gyrification index, thickness, sulcal depth, and shape complexity index, as well as their relationships with age.
Results
Individuals with PAE had significantly lower gyrification (β=-0.17, q = 0.028) and sulcal depth (β=-0.60, q = 0.013) in the right pars triangularis, lower shape complexity in the right occipital pole (β=-0.019, q = 0.012), and higher shape complexity in the right medial orbital gyrus (β=0.017, q = 0.012), compared to unexposed youth. PAE moderated the relationship between age and both gyrification and sulcal depth in several regions such that sulcal depth and gyrification decreased with age in the PAE group but slightly increased with age (or remained stable) in the unexposed group.
Conclusion
These findings build upon previous reports of structural and developmental differences in youth with PAE, suggesting that gyrification may be more sensitive to the effects of PAE than cortical thickness.
Two distinct ACEs-related pathways influencing adolescent behavior through neurostructural and functional mediators, moderated by genetic risk are delineated, advances the understanding of ACEs mechanisms and highlights targets for early intervention.
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