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孕中期和孕晚期早期的母体细胞因子谱不能预测早产。

Maternal cytokine profiles in second and early third trimester are not predictive of preterm birth.

作者信息

Hornaday Kylie K, Stephenson Nikki L, Canning Mary T, Tough Suzanne C, Slater Donna M

机构信息

Department of Physiology and Pharmacology, Cumming School of Medicine, University of Calgary, Alberta, Canada.

Department of Community Health Sciences, Cumming School of Medicine, University of Calgary, Alberta, Canada.

出版信息

PLoS One. 2024 Dec 19;19(12):e0311721. doi: 10.1371/journal.pone.0311721. eCollection 2024.

Abstract

Previous studies have investigated whether inflammatory cytokines in maternal circulation are associated with preterm birth. However, many have reported inconsistent results, and few have investigated cytokine trends through gestation, particularly with respect to subtypes of preterm birth. We explored levels of 15 inflammatory cytokines and growth factors in plasma and serum collected in the second (17-23 weeks, timepoint 1 (T1)) and third (28-32 weeks, timepoint 2 (T2)) trimesters with respect to subtypes of preterm birth: spontaneous preterm labour (sPTL), preterm premature rupture of membranes (PPROM), and medically indicated preterm birth (mPTB). The change in TNFα levels over time (T2/T1) significantly classified mPTB from term birth with an AUC of 0.79. While elevated sICAM-1 levels were significantly associated with sPTL, sICAM-1 was not an effective biomarker for prediction. While statistical differences in some biomarkers, such as TNFα and sICAM-1 were found, these are likely not clinically meaningful for prediction. These results did not reveal a relationship between spontaneous labour and circulating maternal inflammatory biomarkers, however, do suggest distinct inflammatory profiles between subtypes of preterm birth.

摘要

既往研究已探讨母体循环中的炎性细胞因子是否与早产相关。然而,许多研究报告的结果并不一致,且很少有研究通过孕期来调查细胞因子的变化趋势,尤其是关于早产的亚型。我们探讨了在孕中期(17 - 23周,时间点1(T1))和孕晚期(28 - 32周,时间点2(T2))采集的血浆和血清中15种炎性细胞因子和生长因子的水平,涉及早产的亚型:自发性早产(sPTL)、胎膜早破早产(PPROM)和医源性早产(mPTB)。TNFα水平随时间的变化(T2/T1)能够显著区分mPTB和足月产,曲线下面积(AUC)为0.79。虽然sICAM - 1水平升高与sPTL显著相关,但sICAM - 1并非有效的预测生物标志物。虽然发现了一些生物标志物(如TNFα和sICAM - 1)存在统计学差异,但这些差异可能在临床上对预测并无意义。这些结果并未揭示自发分娩与母体循环中的炎性生物标志物之间的关系,不过,确实提示了不同早产亚型之间存在不同的炎性特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44f2/11658620/eade213e18c8/pone.0311721.g001.jpg

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