Reference centiles for maternal placental growth factor levels at term from a low-risk population

被引:2
作者
Dunn, Liam [1 ]
Sherrell, Helen [1 ]
Bligh, Larissa [1 ]
Alsolai, Amal [1 ]
Flatley, Christopher [1 ]
Kumar, Sailesh [1 ,2 ]
机构
[1] Univ Queensland, Mater Res Inst, Level 3,Aubigny Pl,Raymond Terrace, South Brisbane, Qld 4101, Australia
[2] Univ Queensland, Fac Med, 288 Herston Rd, Herston, Qld 4006, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
Placental growth factor; Placental function; Placental biomarker; CIRCULATING ANGIOGENIC FACTORS; GESTATIONAL-AGE; BIOCHEMICAL MARKERS; FACTOR PIGF; HYPERTENSIVE DISORDERS; ADVERSE INTRAPARTUM; TYROSINE KINASE-1; FETAL WEIGHT; BIRTH-WEIGHT; FACTOR PLGF;
D O I
10.1016/j.placenta.2019.08.086
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Introduction: Placental growth factor (PLGF) is a biomarker of placental function. The aim of this study was to define reference ranges for maternal PLGF levels in a normotensive cohort >= 36 + 0 weeks. Method: Prospective observational data from Mater Mothers' Hospital, Brisbane. PLGF levels were measured in women at >= 36 + 0 weeks with singleton, non-anomalous pregnancies. Women with hypertension and fetal growth restriction were excluded. PLGF (pg/mL) was assayed using DELFIA (R) Xpress (PerkinElmer Inc). The Generalised Additive Model for Location, Shape and Scale (GAMLSS) method was used for the calculation of gestational age-adjusted centiles. Data analysis was performed with Stata 13 (StataCorp, LLC) and R software (R Foundation for Statistical Computing, Vienna, Austria). In all women, PLGF was measured within 2 weeks of delivery. Results: The study cohort comprised of 845 women (36 weeks n = 73, 37 weeks n = 230, 38 weeks n = 214, 39 weeks n = 172, 40 weeks n = 115, 41 weeks n = 41). PLGF levels were negatively correlated with gestational age (r = -0.20, p < 0.001). Median PLGF levels dropped significantly from 36 weeks to 41 weeks (169.0 pg/mL to 96.6 pg/mL, p < 0.001). Gestational age specific maternal PLGF centiles were reported using fractional polynomial additive term and Box-Cox t distribution. PLGF did not perform adequately as a predictive test for adverse perinatal outcomes (AUC < 0.6). Discussion: We have created gestational centile reference ranges for maternal PLGF from a normotensive cohort. These novel data suggest maternal PLGF levels decline >= 36 + 0 weeks. The utility of PLGF as a predictor of adverse perinatal outcomes at term, should be further investigated with clinical trials.
引用
收藏
页码:15 / 19
页数:5
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