Vrachnis Dionysios, Antonakopoulos Nikolaos, Fotiou Alexandros, Pergialiotis Vasilios, Loukas Nikolaos, Valsamakis Georgios, Iavazzo Christos, Stavros Sofoklis, Maroudias Georgios, Panagopoulos Periklis, Vlahos Nikolaos, Peppa Melpomeni, Stefos Theodoros, Mastorakos George
Department of Clinical Therapeutics, Alexandra Hospital, Medical School, National and Kapodistrian University of Athens, 115 28 Athens, Greece.
Third Department of Obstetrics and Gynecology, General University Hospital "Attikon", Medical School, National and Kapodistrian University of Athens, 124 62 Athens, Greece.
J Clin Med. 2023 Apr 28;12(9):3166. doi: 10.3390/jcm12093166.
Fetal growth disturbances place fetuses at increased risk for perinatal morbidity and mortality. As yet, little is known about the basic pathogenetic mechanisms underlying deranged fetal growth. Apelin is an adipokine with several biological activities. Over the past decade, it has been investigated for its possible role in fetal growth restriction. Most studies have examined apelin concentrations in maternal serum and amniotic fluid in the third trimester or during neonatal life. In this study, apelin concentrations were examined for the first time in early second-trimester fetuses. Another major regulator of tissue growth and metabolism is insulin.
This was a prospective observational cohort study. We measured apelin and insulin concentrations in the amniotic fluid of 80 pregnant women who underwent amniocentesis in the early second trimester. Amniotic fluid samples were stored in appropriate conditions until delivery. The study groups were then defined, i.e., gestations with different fetal growth patterns (SGA, AGA, and LGA). Measurements were made using ELISA kits.
Apelin and insulin levels were measured in all 80 samples. The analysis revealed statistically significant differences in apelin concentrations among groups ( = 0.007). Apelin concentrations in large for gestational age (LGA) fetuses were significantly lower compared to those in AGA and SGA fetuses. Insulin concentrations did not differ significantly among groups.
A clear trend towards decreasing apelin concentrations as birthweight progressively increased was identified. Amniotic fluid apelin concentrations in the early second trimester may be useful as a predictive factor for determining the risk of a fetus being born LGA. Future studies are expected/needed to corroborate the present findings and should ideally focus on the potential interplay of apelin with other known intrauterine metabolic factors.
胎儿生长紊乱会使胎儿围产期发病和死亡风险增加。然而,对于胎儿生长紊乱背后的基本发病机制,目前仍知之甚少。Apelin是一种具有多种生物学活性的脂肪因子。在过去十年中,人们对其在胎儿生长受限中可能发挥的作用进行了研究。大多数研究检测了孕晚期或新生儿期母体血清和羊水中的Apelin浓度。在本研究中,首次检测了孕中期早期胎儿羊水中的Apelin浓度。组织生长和代谢的另一个主要调节因子是胰岛素。
这是一项前瞻性观察队列研究。我们测量了80名在孕中期早期接受羊膜穿刺术的孕妇羊水中的Apelin和胰岛素浓度。羊水样本在适当条件下保存直至分娩。然后定义研究组,即具有不同胎儿生长模式(小于胎龄儿、适于胎龄儿和大于胎龄儿)的妊娠。使用酶联免疫吸附测定试剂盒进行测量。
对所有80个样本都测量了Apelin和胰岛素水平。分析显示各组之间Apelin浓度存在统计学显著差异(P = 0.007)。与适于胎龄儿和小于胎龄儿相比,大于胎龄儿的Apelin浓度显著降低。各组之间胰岛素浓度无显著差异。
确定了随着出生体重逐渐增加Apelin浓度呈明显下降趋势。孕中期早期羊水中的Apelin浓度可能作为预测胎儿出生为大于胎龄儿风险的一个因素。预计/需要未来的研究来证实目前的发现,并且理想情况下应关注Apelin与其他已知宫内代谢因子之间的潜在相互作用。