Kennedy Eleanor, Guo Ting, Williams Sian, Selvanathan Thiviya, Alsweiler Jane M, Bloomfield Frank H, Battin Malcolm, Dubowitz David, Miller Steven P, Morgan Catherine, Perry David, Stott Ngaire Susan, Harding Jane E
Liggins Institute, University of Auckland, Auckland, New Zealand.
Neurosciences and Mental Health, The Hospital for Sick Children Research Institute, Toronto, Canada.
Ann Neurol. 2025 Aug;98(2):329-340. doi: 10.1002/ana.27261. Epub 2025 Jun 9.
Moderate-to-late preterm (MLP) infants contribute to the greatest proportion of preterm children with neurodevelopmental impairments. White matter injury (WMI) is common and predicts adverse outcomes in very preterm (VP) infants. However, little is known about white matter abnormality (WMA) in MLP infants. We investigated the burden and distribution of WMA in MLP infants.
MLP infants were recruited from a randomized trial on neonatal nutrition and a prospective observational cohort in New Zealand, and underwent brain magnetic resonance imaging (MRI) soon after birth and at term-equivalent age (TEA). WMA was manually segmented using an established method. Total and regional WMA volumes and percentage of WMA to total cerebral volume were calculated. Probabilistic WMA maps were generated and compared with WMI in VP infants and term infants with congenital heart disease.
Of 101 infants (32 females), 40 (39.6%) had WMA on at least 1 scan. In 37 infants with WMA who had both scans, WMA was less visible in 22 (59.5%) or undetectable in 7 (18.9%) infants with a mean reduction of 72.7 ± 207.5 mm in WMA volume from early-life to term. Infants with and without WMA had mostly comparable pregnancy and neonatal characteristics. Probabilistic maps demonstrated a characteristic WMA topology, with most lesions in posterior followed by central and anterior regions. Trigonal areas were vulnerable across neonatal populations.
WMA is much more common in MLP infants than previously reported and occurs in a characteristic topology. WMA may be missed on TEA MRI, and its relationship with outcomes in MLP infants warrants attention. ANN NEUROL 2025;98:329-340.
中度至晚期早产儿(MLP)是神经发育障碍早产儿中占比最大的群体。白质损伤(WMI)在极早产儿(VP)中很常见,且可预测不良预后。然而,关于MLP婴儿白质异常(WMA)的情况却知之甚少。我们研究了MLP婴儿WMA的负担和分布情况。
从新西兰一项关于新生儿营养的随机试验和一个前瞻性观察队列中招募MLP婴儿,这些婴儿在出生后不久和足月等效年龄(TEA)时接受脑磁共振成像(MRI)检查。使用既定方法手动分割WMA。计算WMA的总体积和区域体积以及WMA占总脑体积的百分比。生成概率性WMA图谱,并与VP婴儿和患有先天性心脏病的足月儿的WMI图谱进行比较。
在101名婴儿(32名女性)中,40名(39.6%)在至少一次扫描中发现有WMA。在37名两次扫描都有WMA的婴儿中,22名(59.5%)婴儿的WMA在后期扫描中不太明显,7名(18.9%)婴儿的WMA不可检测到,从早期到足月时WMA体积平均减少72.7±207.5mm³。有和没有WMA的婴儿在妊娠和新生儿特征方面大多具有可比性。概率性图谱显示了WMA的特征性拓扑结构,大多数病变位于后部,其次是中部和前部区域。三角区在各新生儿群体中都很脆弱。
WMA在MLP婴儿中比之前报道的更为常见,且具有特征性拓扑结构。TEA MRI可能会漏诊WMA,其与MLP婴儿预后的关系值得关注。《神经病学年鉴》2025年;98:329 - 340。