Smith Gordon C S, Crossley Jennifer A, Aitken David A, Jenkins Nicola, Lyall Fiona, Cameron Alan D, Connor J Michael, Dobbie Richard
Department of Obstetrics and Gynaecology, Cambridge University, Cambridge, United Kingdom.
Obstet Gynecol. 2007 Jun;109(6):1316-24. doi: 10.1097/01.AOG.0000265804.09161.0d.
To estimate the relationship between maternal serum levels of placental growth factor (PlGF) and soluble fms-like tyrosine kinase-1 (sFlt-1) in early pregnancy with the risk of subsequent adverse outcome.
A nested, case-control study was performed within a prospective cohort study of Down syndrome screening. Maternal serum levels of sFlt-1 and PlGF at 10-14 weeks of gestation were compared between 939 women with complicated pregnancies and 937 controls. Associations were quantified as the odds ratio for a one decile increase in the corrected level of the analyte.
Higher levels of sFlt-1 were not associated with the risk of preeclampsia but were associated with a reduced risk of delivery of a small for gestational age infant (odds ratio [OR] 0.92, 95% confidence interval [CI] 0.88-0.96), extreme (24-32 weeks) spontaneous preterm birth (OR 0.90, 95% CI 0.83-0.99), moderate (33-36 weeks) spontaneous preterm birth (OR 0.93, 95% CI 0.88-0.98), and stillbirth associated with abruption or growth restriction (OR 0.77, 95% CI 0.61-0.95). Higher levels of PlGF were associated with a reduced risk of preeclampsia (OR 0.95, 95% CI 0.90-0.99) and delivery of a small for gestational age infant (OR 0.95, 95% CI 0.91-0.99). Associations were minimally affected by adjustment for maternal characteristics.
Higher early pregnancy levels of sFlt-1 and PlGF were associated with a decreased risk of adverse perinatal outcome.
评估孕早期孕妇血清胎盘生长因子(PlGF)和可溶性fms样酪氨酸激酶-1(sFlt-1)水平与随后不良结局风险之间的关系。
在一项唐氏综合征筛查的前瞻性队列研究中进行了一项巢式病例对照研究。比较了939例妊娠合并症妇女和937例对照在妊娠10 - 14周时血清sFlt-1和PlGF水平。关联强度以分析物校正水平每增加一个十分位数的比值比来量化。
较高水平的sFlt-1与子痫前期风险无关,但与小于胎龄儿分娩风险降低相关(比值比[OR] 0.92,95%置信区间[CI] 0.88 - 0.96)、极早早产(24 - 32周)(OR 0.90,95% CI 0.83 - 0.99)、中度早产(33 - 36周)(OR 0.93,95% CI 0.88 - 0.98)以及与胎盘早剥或生长受限相关的死产风险降低相关(OR 0.77,95% CI 0.61 - 0.95)。较高水平的PlGF与子痫前期风险降低相关(OR 0.95,95% CI 0.90 - 0.99)以及小于胎龄儿分娩风险降低相关(OR 0.95,95% CI 0.91 - 0.99)。这些关联受孕妇特征调整的影响最小。
孕早期较高水平的sFlt-1和PlGF与不良围产期结局风险降低相关。