Department of Neurosurgery, Washington University in St. Louis, St. Louis, United States; Department of Pediatrics, Washington University in St. Louis, St. Louis, United States; Department of Orthopedic Surgery, Washington University in St. Louis, United States.
Department of Neurology, Washington University in St. Louis, St. Louis, United States.
Neuroimage Clin. 2019;22:101787. doi: 10.1016/j.nicl.2019.101787. Epub 2019 Mar 18.
Preterm infants are at high risk for brain injury during the perinatal period. Intraventricular hemorrhage and periventricular leukomalacia, the two most common patterns of brain injury in prematurely-born children, are associated with poor neurodevelopmental outcomes. The hippocampus is known to be critical for learning and memory; however, it remains unknown how these forms of brain injury affect hippocampal growth and how the resulting alterations in hippocampal development relate to childhood outcomes. To investigate these relationships, hippocampal segmentations were performed on term equivalent MRI scans from 55 full-term infants, 85 very preterm infants (born ≤32 weeks gestation) with no to mild brain injury and 73 very preterm infants with brain injury (e.g., grade III/IV intraventricular hemorrhage, post-hemorrhagic hydrocephalus, cystic periventricular leukomalacia). Infants then underwent standardized neurodevelopmental testing using the Bayley Scales of Infant and Toddler Development, 3rd edition at age 2 years, corrected for prematurity. To delineate the effects of brain injury on early hippocampal development, hippocampal volumes were compared across groups and associations between neonatal volumes and neurodevelopmental outcomes at age 2 years were explored. Very preterm infants with brain injury had smaller hippocampal volumes at term equivalent age compared to term and very preterm infants with no to mild injury, with the smallest hippocampi among those with grade III/IV intraventricular hemorrhage and post-hemorrhagic hydrocephalus. Further, larger ventricle size was associated with smaller hippocampal size. Smaller hippocampal volumes were related to worse motor performance at age 2 years across all groups. In addition, smaller hippocampal volumes in infants with brain injury were correlated with impaired cognitive scores at age 2 years, a relationship specific to this group. Consistent with our preclinical findings, these findings demonstrate that perinatal brain injury is associated with hippocampal size in preterm infants, with smaller volumes related to domain-specific neurodevelopmental impairments in this high-risk clinical population.
早产儿在围产期有很高的脑损伤风险。脑室出血和脑室周围白质软化,早产儿最常见的两种脑损伤模式,与不良的神经发育结果有关。海马体被认为对学习和记忆至关重要;然而,目前尚不清楚这些形式的脑损伤如何影响海马体的生长,以及由此导致的海马体发育变化如何与儿童的结果相关。为了研究这些关系,我们对 55 名足月婴儿、85 名无至轻度脑损伤的极早产儿(出生胎龄≤32 周)和 73 名脑损伤的极早产儿(如 3/4 级脑室出血、出血后脑积水、囊性脑室周围白质软化)的等效 MRI 扫描进行了海马体分割。然后,根据早产儿情况,使用贝利婴幼儿发育量表第 3 版对婴儿进行标准化神经发育测试,2 岁时进行校正。为了描述脑损伤对早期海马体发育的影响,我们比较了各组之间的海马体体积,并探讨了新生儿期体积与 2 岁时神经发育结果之间的关系。与无至轻度脑损伤的足月和极早产儿相比,脑损伤的极早产儿在等效胎龄时的海马体体积较小,其中 3/4 级脑室出血和出血后脑积水的早产儿海马体最小。此外,脑室越大,海马体越小。在所有组中,海马体体积较小与 2 岁时的运动表现较差有关。此外,脑损伤婴儿的海马体体积较小与 2 岁时的认知评分受损相关,这种关系是该组特有的。与我们的临床前研究结果一致,这些研究结果表明,围产期脑损伤与早产儿的海马体大小有关,在这一高危临床人群中,体积较小与特定领域的神经发育损伤有关。