极早产儿动脉导管未闭的脑损伤与脑微结构发育。

IF 3
Neonatology Pub Date : 2025-10-04 DOI:10.1159/000548673
Christina Schreiner, Maria Sappler, Michaela Höck, Stephanie Mangesius, Miriam Michel, Elke Griesmaier, Ursula Kiechl-Kohlendorfer, Vera Neubauer
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引用次数: 0

摘要

引言:关于非常早产儿动脉导管未闭(PDA)与大脑发育之间关系的证据尚无定论。本研究的目的是系统地评估脑损伤和脑微结构成熟,通过磁共振成像(MRI)在足月等效年龄对有和没有PDA的当代极早产儿队列进行评估。方法:这是一项回顾性的单中心研究。结果:我们纳入了148名患有PDA的婴儿和148名匹配的对照组。我们发现两组之间脑损伤率没有显著差异。脑成熟度的显微结构评估显示了某些区域的差异。在调整新生儿特征的差异后,仅在右脑中小脑脚上观察到显著差异。在患有PDA的婴儿中,接受手术结扎的婴儿表现出小脑出血和严重IVH的发生率升高,并进一步表现出更不成熟的脑成熟模式。经GA调整后,所有变量的统计差异均消失。结论:我们的研究结果表明,PDA的存在与脑损伤或脑发育受损没有内在联系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Brain injury and microstructural brain development in very preterm infants with patent ductus arteriosus.

Introduction: Evidence regarding the association between patent ductus arteriosus (PDA) and brain development in very preterm infants is inconclusive. The aim of the current study was to systematically evaluate brain injury and microstructural brain maturation as assessed by magnetic resonance imaging (MRI) at term-equivalent age in a contemporary cohort of very preterm infants with and without PDA.

Methods: This was a retrospective, single-centre study. Preterm infants born at <32 weeks' gestation with PDA and cerebral MRI were eligible for this study. They were matched 1:1 according to gestational age (GA) to infants without PDA. MRI was assessed for brain injury. We measured fractional anisotropy and apparent diffusion coefficient in 12 brain regions as indicators for microstructural brain maturation.

Results: We included 148 infants with PDA and 148 matched controls. We found no significant differences in brain injury rates between the groups. The evaluation of microstructural brain maturation revealed differences in some regions. After adjusting for differences in neonatal characteristics, a significant difference was seen only in the right middle cerebellar peduncle. Among infants with PDA, those who underwent surgical ligation exhibited elevated rates of both, cerebellar hemorrhage and severe IVH, and further showed a more immature brain maturation pattern. Statistical difference was lost for all variables after adjusting for GA.

Conclusion: Our results indicate that the presence of PDA is not intrinsically associated with brain injury or impaired brain development.

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