Kluivers Anna C M, Neuman Rugina I, Kalra Bhanu, Kumar Ajay, Visser Willy, Danser A H Jan, Saleh Langeza
Department of Internal Medicine, Division of Pharmacology and Vascular Medicine, Erasmus Medical Center Rotterdam, Rotterdam, the Netherlands; Department of Gynecology and Obstetrics, Erasmus MC University Hospital, Rotterdam, the Netherlands.
Department of Internal Medicine, Division of Pharmacology and Vascular Medicine, Erasmus Medical Center Rotterdam, Rotterdam, the Netherlands.
Pregnancy Hypertens. 2025 Mar;39:101177. doi: 10.1016/j.preghy.2024.101177. Epub 2024 Dec 10.
To evaluate glycosylated fibronectin (GlyFn) as a novel biomarker for preeclampsia and preeclampsia-related complications, and to compare GlyFn to traditional biomarkers, including soluble Fms-like tyrosine kinase-1 (sFlt-1) and placental growth factor (PlGF).
Secondary analysis of a prospective cohort study (n = 524) with suspected preeclampsia (control), gestational hypertension (GH), or confirmed preeclampsia/hemolysis, elevated liver enzymes and low platelets syndrome (PE/HELLP).
GlyFn levels in PE/HELLP versus control and GH. Its association with preeclampsia-related complications, and its added value on top of a traditional model incorporating gestational age, proteinuria, parity, and blood pressure. A comparison of all GlyFn-related performances versus those of sFlt-1 and PlGF.
A significant elevation in GlyFn levels in patients with GH and PE/HELLP was observed versus control. Notably, GlyFn displayed positive correlations with sFlt-1 and the sFlt-1/PlGF ratio, and a negative correlation with PlGF. GlyFn alone outperformed the traditional model in predicting maternal but not fetal complications. This pattern was also observed for sFlt-1, PlGF and their ratio. Combining GlyFn with the traditional model, enhanced the C-index for maternal complications. However, the GlyFn/PlGF ratio, when added to the traditional model, yielded the best results for predicting fetal complications in the overall cohort. In women with a GA < 37 weeks, the latter combination also showed the best predictive value for predicting maternal complications.
GlyFn is a novel biomarker for PE diagnosis and its complications, particularly at GA < 37 weeks. Prospective studies should evaluate to what degree it outperforms traditional biomarkers.
评估糖基化纤连蛋白(GlyFn)作为子痫前期及子痫前期相关并发症的新型生物标志物,并将GlyFn与传统生物标志物进行比较,包括可溶性Fms样酪氨酸激酶-1(sFlt-1)和胎盘生长因子(PlGF)。
对一项前瞻性队列研究(n = 524)进行二次分析,该研究对象为疑似子痫前期(对照)、妊娠期高血压(GH)或确诊的子痫前期/溶血、肝酶升高和血小板减少综合征(PE/HELLP)。
PE/HELLP组与对照组及GH组的GlyFn水平。其与子痫前期相关并发症的关联,以及在纳入孕周、蛋白尿、产次和血压的传统模型基础上的附加值。比较所有与GlyFn相关的指标与sFlt-1和PlGF的指标。
与对照组相比,观察到GH组和PE/HELLP组患者的GlyFn水平显著升高。值得注意的是,GlyFn与sFlt-1和sFlt-1/PlGF比值呈正相关,与PlGF呈负相关。单独使用GlyFn在预测母体并发症而非胎儿并发症方面优于传统模型。sFlt-1、PlGF及其比值也观察到这种模式。将GlyFn与传统模型相结合,提高了母体并发症的C指数。然而,将GlyFn/PlGF比值添加到传统模型中,在预测整个队列的胎儿并发症方面产生了最佳结果。在孕周<37周的女性中,后一种组合在预测母体并发症方面也显示出最佳预测价值。
GlyFn是子痫前期诊断及其并发症的新型生物标志物,特别是在孕周<37周时。前瞻性研究应评估其在多大程度上优于传统生物标志物。