Department of Pediatrics, Maastricht University Medical Center (MUMC+), School for Oncology and Developmental Biology (GROW), Maastricht, the Netherlands.
Neonatal Intensive Care Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Università degli Studi di Milano, Milan, Italy.
PLoS One. 2018 Oct 17;13(10):e0205838. doi: 10.1371/journal.pone.0205838. eCollection 2018.
The role of chorioamnionitis (CA) in the development of retinopathy of prematurity (ROP) is difficult to establish, because CA-exposed and CA-unexposed infants frequently present different baseline characteristics. We performed an updated systematic review and meta-analysis of studies reporting on the association between CA and ROP. We searched PubMed and EMBASE for relevant articles. Studies were included if they examined preterm or very low birth weight (VLBW, <1500g) infants and reported primary data that could be used to measure the association between exposure to CA and the presence of ROP. Of 748 potentially relevant studies, 50 studies met the inclusion criteria (38,986 infants, 9,258 CA cases). Meta-analysis showed a significant positive association between CA and any stage ROP (odds ratio [OR] 1.39, 95% confidence interval [CI] 1.11 to 1.74). CA was also associated with severe (stage ≥3) ROP (OR 1.63, 95% CI 1.41 to 1.89). Exposure to funisitis was associated with a higher risk of ROP than exposure to CA in the absence of funisitis. Additional meta-analyses showed that infants exposed to CA had lower gestational age (GA) and lower birth weight (BW). Meta-regression showed that lower GA and BW in the CA-exposed group was significantly associated with a higher risk of ROP. Meta-analyses of studies with data adjusted for confounders could not find a significant association between CA and ROP. In conclusion, our study confirms that CA is a risk factor for developing ROP. However, part of the effects of CA on the pathogenesis of ROP may be mediated by the role of CA as an etiological factor for very preterm birth.
绒毛膜羊膜炎(CA)在早产儿视网膜病变(ROP)发展中的作用难以确定,因为暴露于 CA 和未暴露于 CA 的婴儿经常具有不同的基线特征。我们对报告 CA 与 ROP 之间关联的研究进行了更新的系统评价和荟萃分析。我们在 PubMed 和 EMBASE 上搜索了相关文章。如果研究检查了早产儿或极低出生体重(VLBW,<1500g)婴儿,并报告了可用于衡量暴露于 CA 与 ROP 存在之间关联的原始数据,则将这些研究纳入。在 748 篇潜在相关的研究中,有 50 项研究符合纳入标准(38986 名婴儿,9258 例 CA 病例)。荟萃分析显示,CA 与任何阶段 ROP 之间存在显著的正相关(优势比 [OR] 1.39,95%置信区间 [CI] 1.11 至 1.74)。CA 还与严重(≥3 期)ROP 相关(OR 1.63,95% CI 1.41 至 1.89)。与无脐带炎的 CA 暴露相比,暴露于脐带炎与 ROP 的风险增加相关。进一步的荟萃分析表明,暴露于 CA 的婴儿的胎龄(GA)和出生体重(BW)较低。Meta 回归显示,CA 暴露组的 GA 和 BW 较低与 ROP 风险增加显著相关。对经过混杂因素调整的数据进行的研究的荟萃分析未能发现 CA 与 ROP 之间存在显著关联。总之,我们的研究证实 CA 是 ROP 发病的危险因素。然而,CA 对 ROP 发病机制的部分影响可能是由 CA 作为极早产的病因的作用介导的。