Verma Manju Lata, Singh Uma, Yadav Geeta, Solanki Vandana, Sachan Rekha, Sankhwar Pushp Lata
Department of Obstetrics and Gynaecology, KGMU, Lucknow, India.
Department of Pathology, KGMU, Lucknow, India.
J Obstet Gynaecol India. 2022 Oct;72(5):396-401. doi: 10.1007/s13224-022-01636-9. Epub 2022 Apr 22.
Placental growth factor (PLGF) is an angiogenic factor in pregnancy. To find out correlation of plasma levels of placental growth factor in first trimester of pregnancy in Indian women who develop maternal and perinatal adverse outcomes was the aim of the study.
A prospective longitudinal noninterventional study was done in the department of Obstetrics and Gynecology after obtaining ethics approval. After enrolling patients in the first trimester (11 weeks to 13 weeks 6 days), a questionnaire was filled for demographic characteristics. Uterine artery doppler was done for every patient and blood sample (5 ml) was taken by venu puncture of median cubital vein. Serum levels of PLGF were measured by enzyme linked immunosorbent assay using Thermo Scientific Pierce Human PLGF kit (Thermo Fisher Scientific, Inc., Waltham, MA, USA). Patients were followed for their whole antenatal period and delivery outcomes.
Incidence of preeclampsia in our study was 9.3% (15/161) and fetal growth restriction (FGR) was 19.8% (32/161). Neither BMI nor nulliparity was found to have statistically significant correlation with development of preeclampsia. However, history of preeclampsia was found to be significant risk factor for prediction of preeclampsia ( value < 0.04). Plasma levels of PLGF were significantly lower in preeclampsia and FGR group and this difference was statistically significant ( value < 0.04). 7.5% still born occurred in complicated group and 10% needed NNU/NICU admission in this group.
Measuring PLGF levels in first trimester of pregnancy can help in prediction of preeclampsia and FGR.
胎盘生长因子(PLGF)是孕期的一种血管生成因子。本研究旨在找出印度孕妇孕早期血浆胎盘生长因子水平与发生孕产妇及围产期不良结局之间的相关性。
在获得伦理批准后,于妇产科进行了一项前瞻性纵向非干预性研究。在孕早期(11周零天至13周6天)纳入患者后,填写一份关于人口统计学特征的问卷。对每位患者进行子宫动脉多普勒检查,并通过肘正中静脉穿刺采集5毫升血样。使用赛默飞世尔科技公司(美国马萨诸塞州沃尔瑟姆市)的赛默飞世尔科学Pierce人PLGF试剂盒,通过酶联免疫吸附测定法测量血清PLGF水平。对患者进行整个孕期及分娩结局的随访。
本研究中先兆子痫的发生率为9.3%(15/161),胎儿生长受限(FGR)的发生率为19.8%(32/161)。未发现BMI和初产情况与先兆子痫的发生有统计学显著相关性。然而,先兆子痫病史被发现是预测先兆子痫的重要危险因素(P值<0.04)。先兆子痫组和FGR组的血浆PLGF水平显著较低,且这种差异具有统计学意义(P值<0.04)。复杂组中有7.5%发生死产,该组中有10%需要入住新生儿重症监护病房/新生儿重症加强护理病房。
测量孕早期的PLGF水平有助于预测先兆子痫和FGR。