Mir Imran N, Machie Michelle, Clarke Rebekah, Brown L Steven, Leon Rachel, Wisnowski Jessica L, Chalak Lina
Division of Neonatal-Perinatal Medicine, Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Department of Pediatric Neurology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Pediatr Res. 2025 Jun 24. doi: 10.1038/s41390-025-04230-7.
Neonates with fetal inflammatory response (FIR) are at increased risk of early-onset sepsis and death. We aimed to determine whether FIR and its severity are associated with brain abnormalities on MRI at term-equivalent age in extremely preterm infants.
A prospective cohort study of extremely preterm infants born between 2018 to 2021 with MRI scans completed at term equivalent age. Brain injury was assessed using the Kidokoro scoring, with MRIs independently scored by two blinded readers and adjudicated by a third. FIR severity was classified per the Amsterdam Placental Workshop Group Consensus Statement.
Among 141 infants, FIR was present in 59 (42%), with 46 (78%) having severe FIR ( ≥ stage 2). FIR was significantly associated with abnormal Kidokoro scores (P < 0.01), specifically white matter (P < 0.01) and cerebellar abnormalities (P = 0.01), but not cortical or deep gray matter abnormalities. Increasing FIR severity correlated with worse Kidokoro scores in both white and gray matter (P < 0.01). Other placental lesions showed no significant association. Inter-rater reliability was high (intraclass correlation coefficient >0.7).
This study is the first to link FIR severity to MRI brain abnormalities in extremely preterm infants, highlighting FIR as a risk factor for brain injury and delayed maturation.
Fetal Inflammatory Response (FIR) is associated with white matter and cerebellar injury by term-equivalent gestational age (TEA). There is significant relationship between severity and progression of FIR and brain abnormalities by TEA. This is the first study demonstrating the impact of progression and severity of FIR on abnormalities on MRI brain at term-equivalent gestational age. These observations provide additional insight into understanding the impact of intrauterine exposure to inflammation on the brain injury in extremely preterm infants.
患有胎儿炎症反应(FIR)的新生儿发生早发型败血症和死亡的风险增加。我们旨在确定FIR及其严重程度是否与极早产儿足月相当年龄时MRI上的脑异常有关。
对2018年至2021年间出生的极早产儿进行前瞻性队列研究,这些婴儿在足月相当年龄时完成了MRI扫描。使用Kidokoro评分评估脑损伤,MRI由两名不知情的阅片者独立评分,并由第三名阅片者进行裁定。根据阿姆斯特丹胎盘研讨会小组共识声明对FIR严重程度进行分类。
在141名婴儿中,59名(42%)存在FIR,其中46名(78%)患有严重FIR(≥2期)。FIR与异常的Kidokoro评分显著相关(P<0.01),特别是白质(P<0.01)和小脑异常(P=0.01),但与皮质或深部灰质异常无关。FIR严重程度的增加与白质和灰质中较差的Kidokoro评分相关(P<0.01)。其他胎盘病变无显著关联。阅片者间可靠性高(组内相关系数>0.7)。
本研究首次将FIR严重程度与极早产儿MRI脑异常联系起来,突出了FIR作为脑损伤和延迟成熟的危险因素。
胎儿炎症反应(FIR)与足月相当胎龄(TEA)时的白质和小脑损伤有关。FIR的严重程度和进展与TEA时的脑异常之间存在显著关系。这是第一项证明FIR的进展和严重程度对足月相当胎龄时MRI脑异常影响的研究。这些观察结果为理解宫内炎症暴露对极早产儿脑损伤的影响提供了更多见解。