Lambert-Messerlian Geralyn, Eklund Elizabeth E, Chien Edward K, Rosene-Montella Karen, Neveux Louis M, Haddow Hamish R M, Palomaki Glenn E
Department of Pathology and Laboratory, Medicine Women and Infants Hospital and the Alpert Medical School at Brown University, 70 Elm Street, Providence, RI 02903, USA.
Division of Maternal Fetal Medicine, MetroHealth Medical Center, Case Western Reserve University, 2500 Metrohealth Drive, Cleveland, OH 44109, USA.
Pregnancy Hypertens. 2014 Oct;4(4):271-8. doi: 10.1016/j.preghy.2014.07.001. Epub 2014 Jul 29.
Preeclampsia is a serious complication of pregnancy, threatening fetal and maternal health. The aim of our study is to examine the association between preeclampsia and biochemical markers, in matched first and second trimester maternal serum samples.
This is a nested case/control study derived from the cohort of pregnancies delivering at Women & Infants Hospital. Cases were identified at a clinic or by hospital codes, and individually confirmed by record review. Stored samples were available from 'integrated' Down syndrome screening. Results were expressed as multiples of the median (MoM).
Preeclampsia was classified as early/severe, late/severe, or mild based on professional guidelines. An additional adverse outcome group had only gestational hypertension.
Ninety-eight cases were each matched with five control pregnancies. Population distribution parameters and within and between trimester correlations were derived for cases and controls for six markers, as well as in case subgroups. The strongest associations were for early/severe preeclampsia with second trimester PAPP-A (rank sum test 2.30, p<0.01); PlGF (2.60, p<0.05) inhibin A (4.45, p<0.05) and endoglin (4.25, p<0.05). No strong associations were found for sVEGF-R and FLRG. Second trimester associations were stronger than those in the first (e.g., PAPP-A 2.45, p<0.01). No between-trimester associations were found that would provide important improvements in prediction.
This matched analysis of the serum markers in early pregnancy allows for direct comparison of first and second trimester associations with preeclampsia. PAPP-A and PlGF are equally and highly predictive of early/severe preeclampsia.
子痫前期是一种严重的妊娠并发症,威胁着胎儿和母亲的健康。我们研究的目的是在匹配的孕早期和孕中期孕妇血清样本中,检测子痫前期与生化标志物之间的关联。
这是一项巢式病例对照研究,来源于在妇女与婴儿医院分娩的妊娠队列。病例通过诊所或医院编码识别,并通过病历审查进行个体确认。可从“综合”唐氏综合征筛查中获得储存样本。结果以中位数倍数(MoM)表示。
根据专业指南,子痫前期分为早发型/重度、晚发型/重度或轻度。另一个不良结局组仅为妊娠期高血压。
98例病例分别与5例对照妊娠匹配。得出了病例组和对照组六种标志物在人群分布参数以及孕早期和孕中期之间及之内的相关性,以及病例亚组中的情况。最强的关联是早发型/重度子痫前期与孕中期妊娠相关血浆蛋白-A(秩和检验2.30,p<0.01);胎盘生长因子(2.60,p<0.05)、抑制素A(4.45,p<0.05)和内皮糖蛋白(4.25,p<0.05)。未发现可溶性血管内皮生长因子受体和Fms样酪氨酸激酶与子痫前期有强关联。孕中期的关联比孕早期更强(例如,妊娠相关血浆蛋白-A为2.45,p<0.01)。未发现孕早期和孕中期之间的关联能在预测方面有重要改善。
这项对孕早期血清标志物的匹配分析允许直接比较孕早期和孕中期与子痫前期的关联。妊娠相关血浆蛋白-A和胎盘生长因子对早发型/重度子痫前期具有同等且高度的预测价值。