胎盘生长因子(PlGF)在加拿大西部三级中心的实施:与超声结果和围产期结局的关系。

Ernesto A Figueiro-Filho, Genevieve Dietrich, Adrielle P Souza Lira, Eman Ramadan, Adewumi Adanlawo, John Matelski, Joshua D Buse
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引用次数: 0

摘要

目的:评估加拿大西部三级转诊中心高危妊娠人群中胎盘生长因子(PlGF)水平、超声表现和围产期结局之间的关系,并评估PlGF检测的预测性能。方法:我们对389例妊娠12+0 ~ 36+0周间接受PlGF检测的高危孕妇进行了回顾性队列研究。参与者按PlGF水平分层:正常(≥10百分位)、不确定(5 -9百分位)和低(≤5百分位)。比较各组临床、生化、超声和围产期结局。计算比值比、敏感性、特异性和预测值。结果:低PlGF水平在33.9%的妊娠中被观察到,在中位胎龄为27.7周时进行检测。低PlGF水平与母亲较高的BMI、血压升高、肌酐、尿酸和蛋白尿水平升高显著相关。低PlGF组的超声检查结果显示胎儿生长受限率较高,多普勒检查异常,胎盘形态异常。结论:低PlGF水平与超声及胎盘功能障碍生化指标及不良围产期结局密切相关。PlGF检测可作为高危妊娠的有效风险分层工具,特别是在农村和服务不足的人群中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Implementation of Placental Growth Factor (PlGF) in a Tertiary Western Canadian Centre: Association with Ultrasound findings and Perinatal Outcomes.

Objective: To evaluate the association between placental growth factor (PlGF) levels, ultrasound findings, and perinatal outcomes in a high-risk pregnant population at a tertiary referral centre in Western Canada, and to assess the predictive performance of the PlGF test.

Methods: We conducted a retrospective cohort study of 389 high-risk pregnant individuals who underwent PlGF testing between 12+0 and 36+0 weeks' gestation. Participants were stratified by PlGF levels: normal (≥ 10th centile), inconclusive (5th-9th centile), and low (≤ 5th centile). Clinical, biochemical, ultrasound, and perinatal outcomes were compared across groups. Odds ratios, sensitivity, specificity, and predictive values were calculated.

Results: Low PlGF levels were observed in 33.9% pregnancies, with testing performed at a median gestational age of 27.7 weeks. Low PlGF levels were significantly associated with higher maternal BMI, elevated blood pressure, and increased creatinine, uric acid, and proteinuria levels. Ultrasound findings in the low PlGF group revealed higher rates of fetal growth restriction, abnormal Doppler studies, and abnormal placental morphology. These pregnancies had increased incidence of preterm birth <34 weeks (52/132 39.3%), preeclampsia (69/132 52.3%), NICU admissions (54/132 40.9%), and small-for-gestational-age neonates (15/132 11.4%). Most negative predictive values exceeded 90%.

Conclusion: Low maternal PlGF levels are strongly associated with ultrasound and biochemical indicators of placental dysfunction and adverse perinatal outcomes. PlGF testing may serve as an effective risk stratification tool in high-risk pregnancies, particularly in rural and underserved populations.

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