Department Obstetrics, Gynecology and Reproductive Sciences, University of Manitoba, Winnipeg, Canada R3A 1R9.
Children's Hospital Research Institute of Manitoba, University of Manitoba, Winnipeg, Canada R3E 3P4.
Dis Markers. 2021 Jun 4;2021:5566234. doi: 10.1155/2021/5566234. eCollection 2021.
Multiple-marker, maternal serum screening (MSS) has been the cornerstone of prenatal diagnosis since the 1980s. While combinations of these markers are used to predict fetal risk of Down syndrome and other genetic conditions, there is some evidence that individual markers may also predict nongenetic pregnancy complications, particularly those related to placental dysfunction. The objective of this meta-analysis was to investigate the utility of false-positive, second-trimester MSS for Down syndrome as a marker of placentally mediated complications amongst singleton pregnancies globally.
Electronic searches of PubMed, Medline, Embase, CINAHL, Web of Science, Scopus, and grey literature to 2019 were performed to identify observational studies comparing risk of pregnancy complications amongst pregnancies with false-positive MSS versus controls. A random-effects model of pooled odds ratios by outcome of interest (stillbirth, preeclampsia, fetal growth restriction, and preterm birth) and subgrouped by type of MSS test (double-, triple-, and quadruple-marker MSS) was used.
16 studies enrolling 68515 pregnancies were included. There were increased odds of preeclampsia (OR 1.28, 95% CI 1.09-1.51) and stillbirth (OR 2.46, 95% CI 1.94-3.12) amongst pregnancies with false-positive MSS. There was no significant association with preterm birth or growth restriction.
There is some evidence of an association between false-positive, second-trimester MSS for Down syndrome and increased odds of preeclampsia and stillbirth. Future large-scale prospective studies are still needed to best determine the predictive value of false-positive MSS as a marker of placentally mediated complications later in pregnancy and evaluate potential clinical interventions to reduce these risks.
自 20 世纪 80 年代以来,多种母体血清标志物筛查(MSS)一直是产前诊断的基石。虽然这些标志物的组合用于预测唐氏综合征和其他遗传疾病的胎儿风险,但有一些证据表明,个别标志物也可能预测非遗传的妊娠并发症,特别是那些与胎盘功能障碍有关的并发症。本荟萃分析的目的是研究全球单胎妊娠中,作为胎盘介导并发症标志物的假阳性二联中期 MSS 对唐氏综合征的预测价值。
对 PubMed、Medline、Embase、CINAHL、Web of Science、Scopus 和灰色文献进行电子检索,检索范围截至 2019 年,以确定比较假阳性 MSS 妊娠与对照妊娠妊娠并发症风险的观察性研究。采用按感兴趣的结局(死胎、子痫前期、胎儿生长受限和早产)和 MSS 测试类型(二联、三联和四联 MSS)分层的汇总优势比的随机效应模型。
纳入了 16 项研究,共纳入了 68515 例妊娠。假阳性 MSS 妊娠的子痫前期(OR 1.28,95%CI 1.09-1.51)和死胎(OR 2.46,95%CI 1.94-3.12)的发生风险较高。与早产或生长受限无关。
有一些证据表明,唐氏综合征假阳性二联中期 MSS 与子痫前期和死胎发生风险增加之间存在关联。仍需要未来进行大规模的前瞻性研究,以确定假阳性 MSS 作为妊娠晚期胎盘介导并发症的预测价值,并评估潜在的临床干预措施以降低这些风险。