The Ritchie Centre, Hudson Institute of Medical Research, Melbourne, VIC, Australia.
Department of Obstetrics and Gynaecology, Monash University, Melbourne, VIC, Australia.
Front Endocrinol (Lausanne). 2024 Mar 13;15:1374897. doi: 10.3389/fendo.2024.1374897. eCollection 2024.
Fetal growth restriction (FGR) is a common pregnancy complication, caused by placental insufficiency, with serious adverse consequences for development and postnatal wellbeing. There are no antenatal treatments to improve growth or organ development in FGR, and animal models are essential to mimic the physiological adaptations in FGR and to assess potential interventions. This study aimed to identify the temporal nature of reduced developmental trajectory in fetuses with FGR, and to examine the effects of common factors that may mediate differential growth such as glucocorticoid treatment. We hypothesised that the trajectory of growth would be adversely impacted by FGR.
FGR was induced via surgical placental insufficiency in fetal sheep (89 days gestation/0.6 gestation; n=135) and compared to age-matched controls over the last third of gestation and into neonatal life (n=153).
Body weight of FGR fetuses/lambs was significantly reduced compared to controls (p<0.0001) from 127 days of gestation (term is 148 days), with increased brain:body weight ratio (p<0.0001) indicative of brain sparing. All biometric measures of body size were reduced in the FGR group with the exception of biparietal (head) diameter. The trajectory of body growth in the last trimester of sheep pregnancy was significantly reduced in the FGR group compared to controls, and stillbirth rate increased with longer gestation.
This work provides a well characterised FGR animal model that mimics the known physiological adaptations in human pregnancy and can be used to determine the efficacy of potential interventions.
胎儿生长受限(FGR)是一种常见的妊娠并发症,由胎盘功能不全引起,对发育和产后健康有严重的不良后果。目前尚无改善 FGR 生长或器官发育的产前治疗方法,动物模型对于模拟 FGR 中的生理适应以及评估潜在干预措施至关重要。本研究旨在确定 FGR 胎儿生长轨迹的时间性质,并研究可能影响生长差异的常见因素(如糖皮质激素治疗)的影响。我们假设 FGR 会对生长轨迹产生不利影响。
通过对胎儿羊(89 天妊娠/0.6 妊娠;n=135)进行手术性胎盘功能不全来诱导 FGR,并与同期出生的对照组在妊娠晚期和新生儿期(n=153)进行比较。
FGR 胎儿/羔羊的体重与对照组相比显著降低(p<0.0001),从妊娠 127 天(足月为 148 天)开始,大脑/体重比增加(p<0.0001),表明大脑得到了保护。FGR 组的所有身体大小的生物测量指标均降低,除了双径(头部)直径。FGR 组在妊娠晚期的身体生长轨迹明显低于对照组,并且随着妊娠时间的延长,死产率增加。
本研究提供了一种经过良好特征描述的 FGR 动物模型,模拟了人类妊娠中的已知生理适应,可用于确定潜在干预措施的疗效。