Jancsura McKenzie K, Helsabeck Nathan P, Anderson Cindy M, Conley Yvette P, Hubel Carl A, Roberts James M
Martha S. Pitzer Center for Women, Children and Youth, College of Nursing, The Ohio State University, Columbus, USA.
College of Nursing, The Ohio State University, Columbus, USA.
Hypertens Pregnancy. 2025 Dec;44(1):2492084. doi: 10.1080/10641955.2025.2492084. Epub 2025 Apr 17.
Preeclampsia is a leading contributor to maternal and infant mortality, and early risk identification is a high priority. Inflammatory markers have shown potential as biomarkers for preeclampsia prediction, though optimal timing and marker selection remain unclear.
We measured 20 inflammatory markers using the Luminex platform across all three trimesters in 37 participants who developed preeclampsia and 74 normotensive controls, matched for pre-pregnancy body mass index (>25), smoking status, and race. We examined individual markers by trimester, changes in marker levels between trimesters, and ratios of pro- to anti-inflammatory markers, adjusting analyses for maternal age, gestational age, and fetal sex.
First-trimester levels of proinflammatory cytokines (GM-CSF, IFN-α, IFN-γ, IL-1α, IL-1β, IL-8, IL-12p70, IL-17a, TNF-α) and anti-inflammatory cytokines (IL-4, IL-10, and IL-13) were strongly associated with preeclampsia (standardized odds ratios > 2). First-trimester pro-anti-inflammatory ratios (e.g. TNF-α:IL-10 and IFN-γ:IL-10) also correlated with preeclampsia. Changes in inflammatory markers across trimesters and interactions with fetal sex were not significant.
Our results suggest that the first trimester inflammatory markers and ratios may offer utility for preeclampsia prediction. Future research should explore these associations in diverse populations and validate their clinical utility. Early risk identification can inform interventions to prevent preeclampsia and improve perinatal outcomes.
子痫前期是母婴死亡的主要原因之一,早期风险识别是当务之急。炎症标志物已显示出作为子痫前期预测生物标志物的潜力,尽管最佳时机和标志物选择仍不明确。
我们使用Luminex平台在37例发生子痫前期的参与者和74例血压正常的对照者的三个孕期中测量了20种炎症标志物,这些对照者在孕前体重指数(>25)、吸烟状况和种族方面相匹配。我们按孕期检查单个标志物、孕期之间标志物水平的变化以及促炎与抗炎标志物的比率,并针对产妇年龄、孕周和胎儿性别进行分析调整。
孕早期促炎细胞因子(GM-CSF、IFN-α、IFN-γ、IL-1α、IL-1β、IL-8、IL-12p70、IL-17a、TNF-α)和抗炎细胞因子(IL-4、IL-10和IL-13)的水平与子痫前期密切相关(标准化比值比>2)。孕早期促炎与抗炎比率(如TNF-α:IL-10和IFN-γ:IL-10)也与子痫前期相关。孕期炎症标志物的变化以及与胎儿性别的相互作用不显著。
我们的结果表明,孕早期炎症标志物和比率可能有助于子痫前期的预测。未来的研究应在不同人群中探索这些关联,并验证其临床实用性。早期风险识别可为预防子痫前期的干预措施提供依据,并改善围产期结局。