Department of Paediatrics I, Neonatology, University Hospital Essen, University Duisburg-Essen, Essen, Germany,
Department of Paediatrics I, Neonatology, University Hospital Essen, University Duisburg-Essen, Essen, Germany.
Neonatology. 2019;116(4):331-340. doi: 10.1159/000501799. Epub 2019 Aug 27.
Preterm infants are at increased risk of neurodevelopmental impairment due to the vulnerability of the immature brain. Early risk stratification is necessary for predicting outcome in the period of highest neuroplasticity. Several biomarkers in magnetic resonance imaging (MRI) at term equivalent age (TEA) have therefore been suggested.
To assess the predictive value of simple brain metrics and the total abnormality score (TAS) - a modified score for brain injury and growth - in relation to neurodevelopmental outcome of very preterm infants in MRI at TEA.
Single-centre cohort study including preterm infants with gestational age (GA) ≤32 weeks and birth weight ≤1,500 g. Biparietal width (BPW), interhemispheric distance, transcerebellar diameter (TCD) and TAS were assessed. To detect subtle haemorrhages, additional susceptibility-weighted imaging (SWI) was used in addition to conventional MRI to evaluate its clinical relevance. Neurodevelopment was tested by the Mental and Psychomotor Developmental Index (MDI/PDI) of the Bayley Scales of Infant Development II at a corrected age of 24 months.
One hundred twenty-nine children with median GA of 28.1 weeks and median birth weight of 980 g were included. BPW significantly correlated with PDI (p= 0.01, R2 = 0.06) and TCD with MDI (p < 0.01, R2 = 0.05) and PDI (p < 0.01, R2 = 0.06) but explained variances were low. TAS was not predictive of neurodevelopmental outcome. By using SWI, additional 4 cases of low grade haemorrhages were identified compared to conventional sequences. In one case this additional information was clinically relevant (MDI/PDI below average).
Simple brain metrics and TAS did not reliably predict neurodevelopmental outcome in a cohort with low prevalence of high grade brain injury. The additional value of SWI is yet to be determined in larger cohorts. The combination of imaging and functional biomarkers may be advisable for the prediction of neurodevelopmental outcome.
由于未成熟大脑的脆弱性,早产儿发生神经发育障碍的风险增加。早期风险分层对于预测最高神经可塑性时期的结果是必要的。因此,在足月等效龄(TEA)的磁共振成像(MRI)中提出了几种生物标志物。
评估简单脑指标和总异常评分(TAS)——一种用于评估脑损伤和生长的改良评分——在 TEA 时 MRI 中预测极早产儿神经发育结局的预测价值。
这是一项单中心队列研究,纳入胎龄(GA)≤32 周且出生体重≤1500g 的早产儿。评估了双额径(BPW)、大脑半球间距离、小脑横径(TCD)和 TAS。为了检测细微出血,除了常规 MRI 外,还使用了磁共振磁敏感加权成像(SWI)来评估其临床相关性。采用贝利婴幼儿发育量表第二版的精神和心理运动发育指数(MDI/PDI)在矫正年龄 24 个月时测试神经发育情况。
共纳入 129 名中位 GA 为 28.1 周和中位出生体重为 980g 的儿童。BPW 与 PDI 显著相关(p=0.01,R2=0.06),TCD 与 MDI(p<0.01,R2=0.05)和 PDI(p<0.01,R2=0.06)显著相关,但解释的方差较小。TAS 不能预测神经发育结局。与常规序列相比,SWI 可额外识别 4 例低级别出血病例。在一个病例中,这一额外信息具有临床意义(MDI/PDI 低于平均水平)。
在低等级脑损伤患病率较低的队列中,简单的脑指标和 TAS 不能可靠地预测神经发育结局。SWI 的额外价值有待在更大的队列中确定。影像学和功能生物标志物的联合应用可能有利于预测神经发育结局。