Placental dysfunction is associated with a decrease in nutrients and oxygen to the fetus; the gestational age at which this happens varies depending on severity but is an important factor in outcome as it relates to when and which brain structures are most at risk. Evidence from Doppler ultrasonography of fetuses affected by severe placental dysfunction leading to intrauterine growth restriction (IUGR) suggests blood flow distribution occurs in a hierarchical manner. In IUGR, oxygenated blood is directed toward the brain, away from other fetal organs (except the fetal heart), a process referred to as brain sparing. Further evidence suggests that subcortical regions critical for homeostasis receive more blood flow, at the cost of cortical regions involved in higher-order functions. Although Doppler findings suggest that cortical regions show more variability to placental oxygenation changes, a Cochrane review found that the evidence was of moderate to low quality,
1 indicating the need for more sensitive techniques to study how placental function affects the brain. Recent work has demonstrated an association between a magnetic resonance imaging (MRI)–based measure of placental oxygenation, transverse relaxation time (T2*), and birth weight,
2 suggesting that T2* may similarly estimate variations in fetal brain development.