Department of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, Georgia.
Department of Obstetrics and Gynecology, School of Medicine, University of Utah, Salt Lake City, Utah.
Paediatr Perinat Epidemiol. 2019 Jul;33(4):274-383. doi: 10.1111/ppe.12563.
Stillbirth, defined as foetal death ≥20 weeks' gestation, is associated with poor foetal growth and is often attributed to placental abnormalities, which are also associated with poor foetal growth. Evaluating inter-relationships between placental abnormalities, poor foetal growth, and stillbirth may improve our understanding of the underlying mechanisms for some causes of stillbirth.
Our primary objective was to determine whether poor foetal growth, operationalised as small for gestational age (SGA), mediates the relationship between placental abnormalities and stillbirth.
We used data from the Stillbirth Collaborative Research Network study, a population-based case-control study conducted from 2006-2008. Our analysis included 266 stillbirths and 1135 livebirths. We evaluated associations of stillbirth with five types of placental characteristics (developmental disorders, maternal and foetal inflammatory responses, and maternal and foetal circulatory disorders) and examined mediation of these relationships by SGA. We also assessed exposure-mediator interaction. Models were adjusted for maternal age, race/ethnicity, education, body mass index, parity, and smoking status.
All five placental abnormalities were more prevalent in cases than controls. After adjustment for potential confounders, maternal inflammatory response (odds ratio [OR] 2.58, 95% confidence interval [CI] 1.77, 3.75), maternal circulatory disorders OR 4.14, 95% CI 2.93, 5.84, and foetal circulatory disorders OR 4.58, 95% CI 3.11, 6.74 were strongly associated with stillbirth, and the relationships did not appear to be mediated by SGA status. Associations for developmental disorders and foetal inflammatory response diverged for SGA and non-SGA births, and strong associations were only observed when SGA was not present.
Foetal growth did not mediate the relationships between placental abnormalities and stillbirth. The relationships of stillbirth with maternal and foetal circulatory disorders and maternal inflammatory response appear to be independent of poor foetal growth, while developmental disorders and foetal inflammatory response likely interact with foetal growth to affect stillbirth risk.
死产定义为胎儿死亡≥20 周,与胎儿生长不良有关,通常归因于胎盘异常,胎盘异常也与胎儿生长不良有关。评估胎盘异常、胎儿生长不良和死产之间的相互关系可能有助于我们更好地理解某些死产原因的潜在机制。
我们的主要目的是确定胎儿生长不良(小胎龄儿)是否调节胎盘异常与死产之间的关系。
我们使用了 Stillbirth Collaborative Research Network 研究的数据,这是一项 2006-2008 年进行的基于人群的病例对照研究。我们的分析包括 266 例死产和 1135 例活产。我们评估了死产与五种胎盘特征(发育障碍、母婴炎症反应、母婴循环障碍)的关系,并检查了 SGA 对这些关系的调节作用。我们还评估了暴露-中介相互作用。模型调整了母亲年龄、种族/民族、教育程度、体重指数、产次和吸烟状况。
所有五种胎盘异常在病例组中比对照组更常见。在调整潜在混杂因素后,母亲炎症反应(比值比 [OR] 2.58,95%置信区间 [CI] 1.77,3.75)、母亲循环障碍(OR 4.14,95% CI 2.93,5.84)和胎儿循环障碍(OR 4.58,95% CI 3.11,6.74)与死产密切相关,且这些关系似乎不受 SGA 状态的调节。发育障碍和胎儿炎症反应与 SGA 和非 SGA 出生的关系存在差异,仅在不存在 SGA 时才观察到强烈的关联。
胎儿生长不良并未调节胎盘异常与死产之间的关系。死产与母婴循环障碍和母婴炎症反应的关系似乎与胎儿生长不良无关,而发育障碍和胎儿炎症反应可能与胎儿生长相互作用,影响死产风险。