Andraweera Prabha H, Dekker Gustaaf A, Thompson Steven D, Nowak Rachael C, Zhang Jamie V, McCowan Lesley M E, North Robyn A, Roberts Claire T
Discipline of Obstetrics and Gynaecology, Research Centre for Reproductive Health, University of Adelaide, Adelaide, Australia.
Arch Pediatr Adolesc Med. 2011 Dec;165(12):1123-30. doi: 10.1001/archpediatrics.2011.796.
To examine whether single-nucleotide polymorphisms (SNPs) in VEGFA (-2578 C/A and +936 C/T) associate with small-for-gestational-age (SGA) pregnancies and to identify their effects on first-trimester placental VEGFA expression.
Multicenter prospective cohort study.
Adelaide, Australia, and Auckland, New Zealand.
A total of 3234 nulliparous pregnant women, their partners, and their infants.
The SNPs in the parent-infant trios and first-trimester placentae (n = 74) were genotyped. Placental VEGFA messenger RNA expression was determined by quantitative reverse transcription-polymerase chain reaction. Small for gestational age was defined as a birth weight less than the 10th customized birth weight percentile adjusted for maternal height, weight, parity, and ethnicity and for gestational age at delivery and infant sex. Uterine and umbilical artery Doppler was performed at 20 weeks' gestation, and resistance indices greater than the 90th percentile were considered abnormal.
Of 2123 pregnancies, 1176 (55.4%) were uncomplicated and 216 (10.2%) had SGA infants. Neonatal VEGFA +936 C/T SNP associates with SGA (adjusted odds ratio [aOR], 1.6; 95% CI, 1.0-2.3), SGA with abnormal Doppler findings (aOR, 3.5; 95% CI, 1.8-7.1), lower birth weight (P = .006), customized birth weight percentile (P = .049), and abnormal uterine artery Doppler findings (OR, 2.5; 95% CI, 1.2-5.4). Maternal VEGFA +936 C/T associates with abnormal umbilical artery Doppler findings (OR, 1.5; 95% CI, 1.1-2.2). VEGFA +936 CT+TT first-trimester placentae have 36% lower VEGFA messenger RNA expression compared with CC (P = .045).
Neonatal VEGFA +936 C/T associates with SGA, and the association is stronger for SGA with abnormal uterine or umbilical artery Doppler findings. The SNP also associates with reduced first-trimester placental VEGFA expression, suggesting that it may have a role in the pathogenesis of SGA. Trial Registration clinicaltrials.gov Identifier: ACTRN12607000551493.
研究血管内皮生长因子A(VEGFA)基因的单核苷酸多态性(SNP)(-2578 C/A和+936 C/T)与小于胎龄儿(SGA)妊娠的相关性,并确定其对孕早期胎盘VEGFA表达的影响。
多中心前瞻性队列研究。
澳大利亚阿德莱德和新西兰奥克兰。
总共3234名初产妇、她们的伴侣及其婴儿。
对母婴三联体和孕早期胎盘(n = 74)中的SNP进行基因分型。通过定量逆转录-聚合酶链反应测定胎盘VEGFA信使核糖核酸表达。小于胎龄儿定义为出生体重低于根据母亲身高、体重、产次、种族以及分娩时的孕周和婴儿性别调整后的第10百分位定制出生体重。在妊娠20周时进行子宫和脐动脉多普勒检查,阻力指数大于第90百分位被视为异常。
在2123例妊娠中,1176例(55.4%)无并发症,216例(10.2%)有SGA婴儿。新生儿VEGFA +936 C/T SNP与SGA相关(校正比值比[aOR],1.6;95%可信区间[CI],1.0 - 2.3),SGA与异常多普勒检查结果相关(aOR,3.5;95% CI,1.8 - 7.1),出生体重较低(P = .006),定制出生体重百分位数较低(P = .049),以及子宫动脉多普勒检查结果异常(OR,2.5;95% CI,1.2 - 5.4)。母亲VEGFA +936 C/T与脐动脉多普勒检查结果异常相关(OR,1.5;95% CI,1.1 - 2.2)。与CC相比,VEGFA +936 CT+TT孕早期胎盘的VEGFA信使核糖核酸表达降低36%(P = .045)。
新生儿VEGFA +936 C/T与SGA相关,对于伴有子宫或脐动脉多普勒检查结果异常的SGA,这种相关性更强。该SNP还与孕早期胎盘VEGFA表达降低相关,表明其可能在SGA的发病机制中起作用。试验注册 clinicaltrials.gov标识符:ACTRN12607000551493。