Yoon Young Mi, Shin Seung Han, Park Chan-Wook, Kim Ee-Kyung, Kim Han-Suk
Department of Pediatrics, Chungnam National University Sejong Hospital, Sejong, Korea.
Department of Pediatrics, Seoul National University College of Medicine, Seoul National University Children's Hospital, Seoul, Korea.
Pediatr Res. 2025 May 16. doi: 10.1038/s41390-025-04093-y.
Retinopathy of prematurity (ROP) is influenced by factors, including gestational age (GA), oxygen exposure, and chorioamnionitis. However, the association between histologic chorioamnionitis (HCA) and ROP remains controversial. This study aimed to investigate the association between HCA and severe ROP.
This retrospective cohort study utilized data from the National Korean Neonatal Network registry, focusing on infants with birthweights < 1500 g and GA < 32 weeks. Univariate and multivariate logistic regression analyses assessed the association between HCA and severe ROP. Sub-cohort analyses were performed to evaluate the effect of HCA on severe ROP across different GA groups.
Infants in the HCA cohort had lower GA and birth weights, with a higher prevalence of any-stage and severe ROP compared to those in the without-HCA cohort. However, multivariate logistic regression showed an inverse association between HCA and severe ROP. Sub-cohort analyses revealed that HCA was associated with an increased risk of severe ROP in infants born at 26-28 and 28-31 weeks, while no significant association was observed in infants born at 23-25 weeks.
HCA may reduce the risk of severe ROP, suggesting that intrauterine inflammation could play a protective role. Further research is needed to elucidate underlying mechanisms.
Retinopathy of prematurity (ROP) is influenced by numerous perinatal and postnatal factors, including low gestational age, oxygen exposure, and chorioamnionitis. However, the association between chorioamnionitis and ROP remains controversial. Our study showed that histologic chorioamnionitis (HCA) was negatively correlated with severe ROP in preterm infants, even after adjusting for confounding factors such as gestational age and birth weight. These findings suggest that HCA may have a protective effect against severe ROP, potentially mediated by inflammatory markers.
早产儿视网膜病变(ROP)受多种因素影响,包括胎龄(GA)、氧暴露和绒毛膜羊膜炎。然而,组织学绒毛膜羊膜炎(HCA)与ROP之间的关联仍存在争议。本研究旨在调查HCA与重度ROP之间的关联。
这项回顾性队列研究利用了韩国国家新生儿网络登记处的数据,重点关注出生体重<1500g且GA<32周的婴儿。单因素和多因素逻辑回归分析评估了HCA与重度ROP之间的关联。进行亚队列分析以评估HCA对不同GA组重度ROP的影响。
与无HCA队列的婴儿相比,HCA队列中的婴儿GA和出生体重较低,任何阶段和重度ROP的患病率较高。然而,多因素逻辑回归显示HCA与重度ROP之间存在负相关。亚队列分析显示,HCA与26 - 28周和28 - 31周出生的婴儿发生重度ROP的风险增加有关,而在23 - 25周出生的婴儿中未观察到显著关联。
HCA可能降低重度ROP的风险,提示宫内炎症可能起保护作用。需要进一步研究以阐明潜在机制。
早产儿视网膜病变(ROP)受多种围产期和产后因素影响,包括低胎龄、氧暴露和绒毛膜羊膜炎。然而,绒毛膜羊膜炎与ROP之间的关联仍存在争议。我们的研究表明,即使在调整了胎龄和出生体重等混杂因素后,组织学绒毛膜羊膜炎(HCA)与早产儿重度ROP呈负相关。这些发现表明,HCA可能对重度ROP具有保护作用,可能由炎症标志物介导。