Woolcock Jane, Hennessy Annemarie, Xu Bei, Thornton Charlene, Tooher Jane, Makris Angela, Ogle Robert
Department of Obstetrics and Gynecology, Royal Prince Alfred Hospital, Camperdown, New South Wales, Australia.
Aust N Z J Obstet Gynaecol. 2008 Feb;48(1):64-70. doi: 10.1111/j.1479-828X.2007.00804.x.
Serum levels of soluble fms-like tyrosine kinase (sFlt-1) increase in pre-eclampsia (PE).
To determine whether concentrations of serum sFlt-1 can differentiate PE or superimposed PE (SPE) from gestational hypertension (GH) or chronic hypertension (CH).
Blood was collected from pregnant women being investigated for hypertension (blood pressure of > 140 and/or 90 mmHg). Normotensive (NP) and pre-eclamptic (PE-C) control ranges were measured.
Patients with evolving hypertension in pregnancy eventually fell into four groups: GH (n = 14), PE (n = 7), CH (n = 9) and SPE (n = 9). Patients who later developed pre-eclampsia had a higher sFlt-1 (PE: 2.61 ng/mL and SPE: 2.77 ng/mL, respectively) than GH (P < 0.001) or CH (1.05 ng/mL, P = 0.11). Women with established PE at recruitment (PE-C; (n = 18) (3.13 ng/mL; interquartile range (IQR): 2.14-4.17 ng/mL) had a median sFlt-1 higher than NP (n = 18) (0.47 ng/mL; IQR: 0.11-0.89) (P < 0.0008). Patients with GH compared to NP had a slight increase (1.33 ng/mL, P < 0.003). Using a sFlt-1 cut-off of > or = 1.9 ng/mL yielded a sensitivity of 94% (95% confidence interval (CI) 73-100%) and specificity of 78% (95% CI 64-82%).
sFlt-1 was elevated in women with PE compared to NP. The sFlt-1 also differentiated women destined to develop PE among those who presented with a diagnostic rise in maternal blood pressure. The sFlt-1 test is a useful diagnostic test for PE.
子痫前期(PE)患者血清中可溶性fms样酪氨酸激酶(sFlt-1)水平升高。
确定血清sFlt-1浓度能否区分PE或合并PE(SPE)与妊娠期高血压(GH)或慢性高血压(CH)。
采集因高血压(血压>140和/或90 mmHg)接受检查的孕妇血液。测量血压正常(NP)和子痫前期(PE-C)的对照范围。
妊娠期高血压病情进展的患者最终分为四组:GH(n = 14)、PE(n = 7)、CH(n = 9)和SPE(n = 9)。后来发展为子痫前期的患者sFlt-1水平(PE分别为2.61 ng/mL,SPE为2.77 ng/mL)高于GH(P < 0.001)或CH(1.05 ng/mL,P = 0.11)。招募时已确诊为PE的女性(PE-C;(n = 18)(3.13 ng/mL;四分位数间距(IQR):2.14 - 4.17 ng/mL)的sFlt-1中位数高于NP(n = 18)(0.47 ng/mL;IQR:0.11 - 0.89)(P < 0.0008)。与NP相比,GH患者sFlt-1略有升高(1.33 ng/mL,P < 0.003)。使用sFlt-1临界值≥1.9 ng/mL时,敏感性为94%(95%置信区间(CI)73 - 100%),特异性为78%(95% CI 64 - 82%)。
与NP相比,PE女性的sFlt-1升高。sFlt-1还能在出现母体血压诊断性升高的人群中区分出注定会发展为PE的女性。sFlt-1检测是一种用于PE的有用诊断检测方法。