Department of Obstetrics and Gynecology, Victor Babeş University of Medicine and Pharmacy, Timişoara, Romania;
Rom J Morphol Embryol. 2023 Apr-Jun;64(2):215-224. doi: 10.47162/RJME.64.2.12.
Early-onset fetal growth restriction (FGR), an identifiable variant of FGR, exhibits divergences in its severity, management, and placental pathologies when juxtaposed with late-onset FGR. The objective of this cross-sectional investigation was to scrutinize placental pathologies in pregnancies afflicted by early-onset FGR, emphasizing a comparative analysis between cohorts with and without preeclampsia (PE).
PATIENTS, MATERIALS AND METHODS: The study encompassed a cohort of 85 expectant mothers who received a diagnosis of early-onset FGR. Rigorous histopathological (HP) and immunohistochemical (IHC) assessments were conducted on the placentas. Comparative analyses were performed, distinguishing between individuals diagnosed with both PE and early-onset FGR, and those presenting normotensive early-onset FGR.
HP analysis unveiled a multitude of shared placental lesions, encompassing retroplacental hemorrhage, expedited villous maturation, infarctions, and calcification-associated fibrin deposits. IHC investigations displayed affirmative immunoreactivity for anti-hypoxia-inducible factor (HIF) and anti-vascular endothelial growth factor (VEGF) antibodies within the placental infarcted villitis. Moreover, noteworthy variances in placental measurements and distinctive lesions were discerned when comparing the PE and early-onset FGR cohort with the normotensive group.
Maternal malperfusion emerged as a pivotal determinant linked to placental lesions in pregnancies affected by early-onset FGR. Remarkably, the occurrence of infarctions, specifically delayed infarctions, exhibited a noteworthy correlation with PE. These findings accentuate the significance of pursuing additional research endeavors aimed at unraveling the intricate mechanisms governing maternal malperfusion and its consequential influence on placental health in the context of early-onset FGR, with particular attention to the interplay with PE.
早发型胎儿生长受限(FGR)是 FGR 的一种可识别变异,与晚发型 FGR 相比,其严重程度、管理和胎盘病理学存在差异。本横断面研究旨在检查早发型 FGR 妊娠的胎盘病理学,强调对伴有和不伴有子痫前期(PE)的队列进行比较分析。
患者、材料和方法:该研究纳入了 85 名被诊断为早发型 FGR 的孕妇。对胎盘进行了严格的组织病理学(HP)和免疫组织化学(IHC)评估。对伴有 PE 和早发型 FGR 的个体与表现为正常血压的早发型 FGR 的个体进行了比较分析。
HP 分析揭示了许多共同的胎盘病变,包括胎盘后出血、绒毛加速成熟、梗死和与钙化相关的纤维蛋白沉积。IHC 研究显示,胎盘梗死性绒毛膜炎中抗缺氧诱导因子(HIF)和抗血管内皮生长因子(VEGF)抗体呈阳性反应。此外,当将 PE 和早发型 FGR 队列与正常血压组进行比较时,还发现了胎盘测量值和特征性病变的显著差异。
母体灌注不良是导致早发型 FGR 妊娠胎盘病变的关键决定因素。值得注意的是,梗死的发生,特别是迟发性梗死,与 PE 有显著相关性。这些发现强调了开展更多研究工作的重要性,旨在揭示母体灌注不良及其对早发型 FGR 中胎盘健康的影响的复杂机制,并特别关注与 PE 的相互作用。