Placental growth factor as a marker of fetal growth restriction caused by placental dysfunction

被引:149
作者
Benton, Samantha J. [1 ]
McCowan, Lesley M. [2 ]
Heazell, Alexander E. P. [3 ]
Grynspan, David [4 ]
Hutcheon, Jennifer A. [1 ]
Senger, Christof [5 ]
Burke, Orlaith [6 ]
Chan, Yuen [2 ]
Harding, Jane E. [7 ]
Yockell-Lelievre, Julien [8 ]
Hu, Yuxiang
Chappell, Lucy C. [9 ]
Griffin, Melanie J. [9 ]
Shennan, Andrew H. [9 ]
Magee, Laura A. [1 ,11 ]
Gruslin, Andree [10 ]
von Dadelszen, Peter [1 ,11 ]
机构
[1] Univ British Columbia, Fac Med, Dept Obstet & Gynaecol, 4500 Oak St, Vancouver, BC V6H 3N1, Canada
[2] Univ Auckland, Fac Med & Hlth Sci, Dept Obstet & Gynaecol, Private Bag 92019, Auckland 1142, New Zealand
[3] Univ Manchester, St Marys Hosp, Maternal & Fetal Hlth Res Ctr, 5th Floor,Oxford Rd, Manchester M13 9WL, Lancs, England
[4] Childrens Hosp Eastern Ontario, Dept Pathol, 401 Smyth Rd, Ottawa, ON K1H 8L1, Canada
[5] Childrens & Womens Hlth Ctr British Columbia, Dept Pathol, 4500 Oak St, Vancouver, BC V6H 2N9, Canada
[6] Univ Oxford, Inst Hlth Sci, Nuffield Dept Populat Hlth, Old Rd, Oxford OX3 7LF, England
[7] Univ Auckland, Liggins Inst, Private Bag 92019,Victoria St West, Auckland 1142, New Zealand
[8] Ottawa Hosp Res Inst, Sprott Ctr Stem Cell Res, 501 Smyth Rd, Ottawa, ON K1H 8L6, Canada
[9] Kings Coll London, St Thomas Hosp, Womens Hlth Acad Ctr, 10th Floor North Wing,Westminster Bridge Rd, London SE1 7EH, England
[10] Univ Ottawa, Dept Obstet & Gynaecol, 501 Smyth Rd, Ottawa, ON K1H 8L6, Canada
[11] St Georges Univ London, Inst Cardiovasc & Cell Sci, Rm J0-27 Jenner Wing,Cranmer Terrace, London SW17 0RE, England
基金
美国国家卫生研究院; 比尔及梅琳达.盖茨基金会; 加拿大健康研究院;
关键词
Fetal growth restriction; Placental growth factor; Placental dysfunction; Placental lesions; Diagnosis; FOR-GESTATIONAL-AGE; UMBILICAL ARTERY DOPPLER; BIRTH-WEIGHT; DIAGNOSTIC-ACCURACY; WOMEN; SERUM; REPRODUCIBILITY; PREECLAMPSIA; PREGNANCIES; NOSOLOGY;
D O I
10.1016/j.placenta.2016.03.010
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Introduction: Discriminating between placentally-mediated fetal growth restriction and constitutionally-small fetuses is a challenge in obstetric practice. Placental growth factor (PlGF), measurable in the maternal circulation, may have this discriminatory capacity. Methods: Plasma PlGF was measured in women presenting with suspected fetal growth restriction (FGR; ultrasound fetal abdominal circumference <10th percentile for gestational age) at sites in Canada, New Zealand and the United Kingdom. When available, placenta tissue underwent histopathological examination for lesions indicating placental dysfunction, blinded to PlGF and clinical outcome. Lesions were evaluated according to pre-specified severity criteria and an overall severity grade was assigned (0-3, absent to severe). Low PlGF (concentration <5th percentile for gestational age) to identify placental FGR (severity grade >= 2) was assessed and compared with routine parameters for fetal assessment. For all cases, the relationship between PlGF and the sampling-to-delivery interval was determined. Results: Low PlGF identified placental FGR with an area under the receiver-operator characteristic curve of 0.96 [95% CI 0.93-0.98], 98.2% [95% CI 90.5-99.9] sensitivity and 75.1% [95% CI 67.6-81.7] specificity. Negative and positive predictive values were 99.2% [95% CI 95.4-99.9] and 58.5% [95% CI 47.9-68.6], respectively. Low PlGF outperformed gestational age, abdominal circumference and umbilical artery resistance index in predicting placental FGR. Very low PlGF (<12 pg/mL) was associated with shorter sampling-to-delivery intervals than normal PlGF (13 vs. 29.5 days, P < 0.0001). Discussion: Low PlGF identifies small fetuses with significant underlying placental pathology and is a promising tool for antenatal discrimination of FGR from fetuses who are constitutionally-small. (C) 2016 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
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页码:1 / 8
页数:8
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