Bowe Sophie, Mitlid-Mork Birgitte, Staff Anne Cathrine, Sugulle Meryam
Division of Obstetrics and Gynaecology, Oslo University Hospital Ullevål, P.O box 4956 Nydalen, 0424 Oslo, Norway; Faculty of Medicine, University of Oslo, P.O box 1078, Blindern, 0316 Oslo, Norway.
Division of Obstetrics and Gynaecology, Oslo University Hospital Ullevål, P.O box 4956 Nydalen, 0424 Oslo, Norway; Faculty of Medicine, University of Oslo, P.O box 1078, Blindern, 0316 Oslo, Norway.
Eur J Obstet Gynecol Reprod Biol. 2025 Apr;307:34-42. doi: 10.1016/j.ejogrb.2025.01.029. Epub 2025 Jan 22.
To assess the association between predelivery maternal placental growth factor (PlGF) and soluble fms-like tyrosine kinase-1 (sFlt-1) and adverse delivery outcome of a likely placental cause in women presenting with reduced fetal movements (RFM) in term and post-date pregnancies.
Prospective cohort study conducted in a single tertiary maternity unit from September 2016 to March 2020. PlGF and sFlt-1 were measured in maternal serum (n = 122) from prospectively included women presenting with RFM (gestational age ≥ 37). All neonatal and delivery outcomes were externally reviewed, blinded for biomarker results, and judged whether the adverse outcomes were most likely associated with placental dysfunction ("likely placental cause") or not.Predefined gestational age specific reference levels for PlGF, sFlt-1 and sFlt-1/PlGF ratio were used and multiple of the median (MoM) were calculated. Categorical variables were compared using Fisher's exact-test. Means were compared using one-way analysis of variance and medians were compared using the Kruskal-Wallis test. Pairwise comparisons between groups were Bonferroni corrected..
The pregnancies were assigned into three groups: the "complicated" (likely placental cause, n = 4), the "intermediate" (non-placental/undetermined cause, n = 9) and the "uncomplicated" (no adverse outcome, n = 109). Mean PlGF concentration differed significantly between the three groups (80, 144, and 213 pg/ml, p = 0.004). There was a higher proportion of PlGF levels < 10th centiles in the "complicated" compared to the "intermediate" and "uncomplicated" groups (50 % vs. 22 % and 11 %, p = 0.045). The median MoM of PlGF differed significantly between the three groups (0.43, 0.83 and 1.12, p = 0.006).
In women presenting with RFM in late pregnancy and beyond term (gestational age ≥ 37), a lower predelivery "proangiogenic" PlGF concentration was associated with a composite adverse delivery outcome of a likely placental cause. The diagnostic and predictive role of maternal circulating PlGF levels is promising.
评估足月及过期妊娠出现胎动减少(RFM)的孕妇产前母体胎盘生长因子(PlGF)和可溶性fms样酪氨酸激酶-1(sFlt-1)与可能由胎盘原因导致的不良分娩结局之间的关联。
2016年9月至2020年3月在一家三级妇产单位进行的前瞻性队列研究。对前瞻性纳入的出现RFM(孕周≥37周)的孕妇的母血(n = 122)进行PlGF和sFlt-1检测。所有新生儿和分娩结局均由外部人员进行审查,审查人员对生物标志物结果不知情,并判断不良结局是否最有可能与胎盘功能障碍(“可能由胎盘原因导致”)相关。使用PlGF、sFlt-1和sFlt-1/PlGF比值的预定义孕周特异性参考水平,并计算中位数倍数(MoM)。分类变量采用Fisher精确检验进行比较。均值采用单因素方差分析进行比较,中位数采用Kruskal-Wallis检验进行比较。组间两两比较采用Bonferroni校正。
这些妊娠被分为三组:“复杂组”(可能由胎盘原因导致,n = 4)、“中间组”(非胎盘/原因未明组,n = 9)和“非复杂组”(无不良结局,n = 109)。三组之间的平均PlGF浓度存在显著差异(80、144和213 pg/ml,p = 0.004)。与“中间组”和“非复杂组”相比,“复杂组”中PlGF水平低于第10百分位数的比例更高(50%对22%和11%,p = 0.045)。三组之间PlGF的中位数MoM存在显著差异(0.43、0.83和1.12,p = 0.006)。
在晚期妊娠及过期妊娠(孕周≥37周)出现RFM的孕妇中,产前较低的“促血管生成”PlGF浓度与可能由胎盘原因导致的综合不良分娩结局相关。母体循环PlGF水平的诊断和预测作用前景广阔。