Urinary sFlt-1 and PlGF as preeclampsia predictors: sFlt-1/creatinine ratio improves the prediction value

被引:0
|
作者
Martin-Palumbo, Giovanna [1 ]
Alcorta, Marta Duque [2 ]
de Aguado, Marta Perez [1 ]
Antolin, Eugenia [1 ]
Bartha, Jose Luis [1 ,3 ,4 ]
机构
[1] La Paz Univ Hosp, Dept Obstet & Gynecol, Div Maternal & Fetal Med, Paseo Castellana 261, Madrid 28046, Spain
[2] La Paz Univ Hosp, Div Clin Chem, Madrid, Spain
[3] Autonomous Univ Madrid, Obstet & Gynecol, Madrid, Spain
[4] La Paz Univ Hosp, Fdn Invest Biomed, Maternal & Fetal Res Grp, Madrid, Spain
关键词
Preeclampsia; Fetal growth restriction; Soluble Fms-like tyrosine kinase-1; Placental growth factor; Middle cerebral artery pulsatility index; PLACENTAL GROWTH-FACTOR; ANGIOGENIC FACTORS; HYPERTENSIVE DISORDERS; FETAL-GROWTH; DIAGNOSIS; WEIGHT; CLASSIFICATION; RESTRICTION; MANAGEMENT; UPDATE;
D O I
10.1016/j.ejogrb.2024.05.002
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objectives: To evaluate the correlation between maternal serum and urinary soluble Fms-like tyrosine kinase-1 (sFlt-1) and placental growth factor (PlGF) levels and to assess their potential value in preeclampsia and fetal growth restriction. Study Design: This case-control longitudinal prospective study was performed in 49 singleton pregnant women, divided into two clinical groups, low risk pregnancy (n = 23) and pregnancy complicated by preeclampsia (n = 26). Maternal serum and urinary sFlt-1 and PlGF levels were quantified by electrochemiluminescence. Every patient underwent an ultrasound for fetal biometry. Doppler assessment was done when estimated fetal weight was under the 10th centile. ROC curves were used to evaluate the predictive capability of serum and urinary angiogenic biomarkers and their ratios on preeclampsia. Linear regression was used to compare the values of serum and urinary sFlt-1 and PlGF and their ratios. Results: Urine biomarkers were positively associated with their serum values, being the best associated urinary PlGF (R2 = 0.73), which also showed the highest predictive capability of preeclampsia of urine biomarkers (AUC 0.866). The predictive capability of urinary sFlt-1 was much lower (AUC 0.640), but increased when adjusting by serum creatinine, a more precise parameter (AUC 0.863). Conclusions: Urinary PlGF could be a lesser invasive alternative to circulating biomarkers to monitor pregnancies complicated with preeclampsia that need repeated controls of their pregnancy complication. Urinary sFlt-1 values need adjustment by serum creatinine to be reliable.
引用
收藏
页码:53 / 60
页数:8
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