Departments of Obstetrics & Gynecology, Maternal-Fetal Medicine Division, University of Toronto, Toronto, Ontario, Canada.
Department of Obstetrics & Gynecology, University of Toronto, Toronto, Ontario, Canada.
JAMA Netw Open. 2024 Nov 4;7(11):e2444454. doi: 10.1001/jamanetworkopen.2024.44454.
Early preterm birth (ie, at less than 34 weeks' gestation) confers a high risk for adverse health outcomes, yet no universal screening strategy exists, preventing targeted delivery of effective interventions.
To evaluate the ability of midpregnancy placental growth factor (PlGF) screening to identify pregnancies at highest risk for early preterm birth.
DESIGN, SETTING, AND PARTICIPANTS: This prospective cohort study was conducted at an urban, tertiary care center from 2020 to 2023. Participants were unselected, pregnant people with singleton pregnancies, receiving universal-access prenatal care from obstetricians, family physicians, or midwives, who underwent a PlGF test at the time of routine gestational diabetes screening, typically at 24 to 28 weeks' gestation. Data were analyzed from January to May 2024.
PlGF level less than 100 pg/mL at the time of gestational diabetes screen.
The primary outcome was all early preterm birth, defined as less than 34 weeks' gestation. Secondary outcomes included iatrogenic preterm birth, spontaneous preterm birth, preeclampsia, stillbirth, and small-for-gestational-age birth weight.
Among 9037 unique pregnant individuals, 156 (1.7%) experienced early preterm birth (52 spontaneous births; 104 iatrogenic births). The area under the curve (AUC) for PlGF and early preterm birth was 0.80 (95% CI, 0.75-0.85). Low PlGF level was associated with early preterm birth (positive likelihood ratio [LR], 79.400 [95% CI, 53.434-115.137]; negative LR, 0.606 [95% CI, 0.494-0.742]; specificity, 99.5% [95% CI, 99.3%-99.6%]; negative predictive value, 98.9% [95% CI, 98.8%-99.1%]). Time to birth from PlGF test was significantly reduced among patients with a PlGF level less than 100 pg/mL, among whom more than 50% delivered within 50 days of testing. Individuals with a low PlGF level made up more than 30% of subsequent stillbirths (aRR, 36.78 [95% CI, 18.63-72.60]) and more than half of patients requiring iatrogenic early preterm birth (aRR, 92.11 [95% CI, 64.83-130.87]). The AUC for iatrogenic early preterm birth was 0.90 (95% CI, 0.85-0.94).
These findings suggest that low PlGF level (<100 pg/mL), identified at the time of routine gestational diabetes screening, may be a powerful clinical tool to identify pregnant people at risk of early preterm birth, especially in iatrogenic births. Strategic redirection of tertiary health care resources to this high-risk group could improve maternal and perinatal outcomes.
极早产(即妊娠 34 周前)会导致不良健康后果的风险很高,但目前尚无普遍的筛查策略,无法针对极早产进行有效的干预。
评估中孕期胎盘生长因子(PlGF)筛查识别极早产风险最高的妊娠的能力。
设计、地点和参与者:这是一项前瞻性队列研究,于 2020 年至 2023 年在一个城市的三级保健中心进行。参与者为未选择的、单胎妊娠的孕妇,她们接受来自妇产科医生、家庭医生或助产士的普遍获得的产前护理,并在常规妊娠期糖尿病筛查时进行 PlGF 检测,通常在 24 至 28 周妊娠时进行。数据分析于 2024 年 1 月至 5 月进行。
妊娠期糖尿病筛查时 PlGF 水平<100 pg/mL。
主要结局是所有极早产,定义为妊娠 34 周前分娩。次要结局包括医源性早产、自发性早产、子痫前期、死胎和小于胎龄儿。
在 9037 名独特的孕妇中,有 156 名(1.7%)发生极早产(52 例自发性分娩;104 例医源性分娩)。PlGF 和极早产的曲线下面积(AUC)为 0.80(95%CI,0.75-0.85)。低 PlGF 水平与极早产相关(阳性似然比[LR],79.400[95%CI,53.434-115.137];阴性 LR,0.606[95%CI,0.494-0.742];特异性,99.5%[95%CI,99.3%-99.6%];阴性预测值,98.9%[95%CI,98.8%-99.1%])。PlGF 水平<100 pg/mL 的患者从 PlGF 检测到分娩的时间明显缩短,其中超过 50%的患者在检测后 50 天内分娩。PlGF 水平较低的患者中,超过 30%的患者发生了后续死胎(ARR,36.78[95%CI,18.63-72.60]),超过一半需要医源性极早产的患者(ARR,92.11[95%CI,64.83-130.87])。医源性极早产的 AUC 为 0.90(95%CI,0.85-0.94)。
这些发现表明,在常规妊娠期糖尿病筛查时检测到的低 PlGF 水平(<100 pg/mL)可能是识别极早产风险的孕妇的有力临床工具,尤其是医源性早产。将三级保健资源战略性地转向这一高风险群体,可能会改善母婴围产期结局。