Abstract

Prenatal alcohol exposure (PAE) interferes with neurodevelopment. The brain is particularly susceptible to the adverse consequences of prenatal alcohol exposure, and numerous studies have documented changes to brain anatomy and function, as well as consequences for cognition, behavior, and mental health. Studies in typically developing individuals have shown that the brain undergoes dynamic developmental processes over an individual’s lifespan. Furthermore, magnetic resonance imaging (MRI) studies in other neurodevelopmental and psychiatric disorders have shown that their developmental trajectories differ from the typical pattern. Therefore, to understand long-term clinical outcomes of fetal alcohol spectrum disorders (FASD), it is necessary to investigate changes in neurodevelopmental trajectories in this population. Here we review studies that have used MRI to evaluate changes in brain structure and function over time via cross-sectional or longitudinal methods in individuals with PAE. Research demonstrates that individuals with PAE have atypical cortical and white matter microstructural developmental trajectories through childhood and adolescence. More research is needed to understand how factors such as sex and postnatal experiences may further mediate these trajectories. Furthermore, nothing is known about the trajectories beyond young adulthood.

Highlights

  • Alcohol can interfere with the development of an embryo/fetus and produce a wide range of adverse effects

  • A recent meta-analysis estimated that across the globe, 630,000 children are born with fetal alcohol spectrum disorders (FASD) every year and, out of 187 countries for which there is data available, 76 have an estimated prevalence of FASD that exceeds 1% (Lange et al, 2017)

  • This study found that while subcortical structures increased in volume across time in both the children with prenatal alcohol exposure (PAE) and controls, there was no difference in the trajectories

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Summary

Introduction

Alcohol can interfere with the development of an embryo/fetus and produce a wide range of adverse effects. While both the CIFASD longitudinal studies support group differences in developmental volume change, albeit differing in the affected brain regions, another study found no significant between group differences in age-related volume change when examining cortical development in children with FASD (Rajaprakash et al, 2014).

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