Romero Roberto, Chaemsaithong Piya, Tarca Adi L, Korzeniewski Steven J, Maymon Eli, Pacora Percy, Panaitescu Bogdan, Chaiyasit Noppadol, Dong Zhong, Erez Offer, Hassan Sonia S, Chaiworapongsa Tinnakorn
a Perinatology Research Branch, Program for Perinatal Research and Obstetrics, Division of Intramural Research , Eunice Kennedy Shriver National Institute of Child Health and Human Development, NIH/DHHS , Bethesda , MD, and Detroit, MI , USA.
b Department of Obstetrics and Gynecology , University of Michigan , Ann Arbor , MI , USA.
J Matern Fetal Neonatal Med. 2018 Feb;31(4):418-432. doi: 10.1080/14767058.2017.1286319. Epub 2017 Mar 1.
The objectives of this study were to determine (1) the longitudinal profile of plasma soluble ST2 (sST2) concentrations in patients with preeclampsia and those with uncomplicated pregnancies; (2) whether the changes in sST2 occur prior to the diagnosis of preeclampsia; and (3) the longitudinal sST2 profile of women with early or late preeclampsia.
This longitudinal nested case-control study included singleton pregnancies in the following groups: (1) uncomplicated pregnancies (n = 160); and (2) those complicated by early (<34 weeks, n = 9) and late (≥34 weeks, n = 31) preeclampsia. sST2 concentrations were determined by enzyme-linked immunosorbent assays. Mixed-effects models were used for the longitudinal analysis.
(1) Plasma sST2 concentration profiles across gestation differed significantly among cases and controls (p < 0.0001); (2) women with early preeclampsia had higher mean sST2 concentrations than controls at >22 weeks of gestation; cases with late preeclampsia had higher mean concentrations at >33 weeks of gestation (both p < 0.05); and (3) these changes started approximately 6 weeks prior to clinical diagnosis.
Maternal plasma sST2 concentrations are elevated 6 weeks prior to the clinical diagnosis of preeclampsia. An increase in the maternal plasma concentration of sST2 may contribute to an exaggerated intravascular inflammatory response and/or the Th1/Th2 imbalance in some cases.
本研究的目的是确定:(1)先兆子痫患者和正常妊娠患者血浆可溶性ST2(sST2)浓度的纵向变化情况;(2)sST2的变化是否在先兆子痫诊断之前就已发生;(3)早发型或晚发型先兆子痫女性的sST2纵向变化情况。
这项纵向巢式病例对照研究纳入了以下几组单胎妊娠:(1)正常妊娠(n = 160);(2)早发型(<34周,n = 9)和晚发型(≥34周,n = 31)先兆子痫。通过酶联免疫吸附测定法测定sST2浓度。采用混合效应模型进行纵向分析。
(1)病例组和对照组整个孕期的血浆sST2浓度变化存在显著差异(p < 0.0001);(2)早发型先兆子痫女性在妊娠>22周时的平均sST2浓度高于对照组;晚发型先兆子痫患者在妊娠>33周时平均浓度更高(均p < 0.05);(3)这些变化在临床诊断前约6周开始出现。
先兆子痫临床诊断前6周母体血浆sST2浓度升高。母体血浆sST2浓度升高可能在某些情况下导致血管内炎症反应过度和/或Th1/Th2失衡。