脐-门静脉血流动力学在糖尿病并发妊娠的胎儿巨大儿发病机制中的作用

Q4 Medicine
E. Shelaeva, E. Kopteeva, E. Alekseenkova, R. Kapustin, I. Kogan
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引用次数: 0

摘要

背景:妊娠合并糖尿病期间,胎儿出现巨大儿和其他围产期并发症的风险会增加。胎儿脐-门静脉系统血流的再分布可能是影响巨大胎儿生长的一个重要但鲜为人知的代偿机制。目的:本研究旨在确定患有各种类型糖尿病且无碳水化合物代谢紊乱的孕妇的胎儿脐-门静脉血流动力学特征,同时考虑胎龄和巨大胎儿的生长情况。材料与方法:在这项前瞻性队列研究中,86 名妊娠前期糖尿病孕妇、44 名妊娠期糖尿病孕妇和 58 名无碳水化合物代谢紊乱的患者在妊娠 30+0 至 41+3 周期间接受了超声波检查。在超声检查过程中,我们对脐-门静脉系统血管的静脉血流动力学参数进行了多普勒评估,并计算了每条血管的容积血流量。此外,还计算了肝脏总容积血流量和静脉导管分流分数。结果:与正常体重胎儿相比,妊娠前期糖尿病组胎儿出现巨大胎儿时,脐静脉容积血流量增加了89.5毫升/分钟(p = 0.003),左门静脉容积血流量增加了33.3毫升/分钟(p = 0.008),胎儿肝脏总容积血流量增加了95.7毫升/分钟(p = 0.001)。同时,巨大胎儿的静脉导管分流率下降了3.83%(p = 0.001)。在妊娠糖尿病组和对照组中,尽管这些参数在巨大胎儿中有增加的趋势,但差异未达到统计学意义。以左门静脉容积流量阈值 94.51 毫升/分钟为标准,预测巨大胎儿的敏感性和特异性分别为 84.46% 和 72.09%。结论:母亲妊娠期糖尿病与胎儿肝脏血流的优先再分配有关,并伴随着静脉导管分流分数的下降。这些血流动力学变化的严重程度在出现巨大胎儿时会增加,这证实了肝脏灌注在无并发症妊娠和母体糖尿病的胎儿生长调节中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The role of umbilical-portal venous hemodynamics in fetal macrosomia pathogenesis in pregnancy complicated by diabetes mellitus
BACKGROUND: During pregnancy complicated by diabetes mellitus, the risks of developing fetal macrosomia and other perinatal complications increase. Redistribution of blood flow in the fetal umbilical-portal venous system may be an important but poorly understood compensatory mechanism that affects macrosomic fetal growth. AIM: The aim of this study was to determine the features of the fetal umbilical-portal venous hemodynamics in pregnant women with various types of diabetes mellitus and the absence of carbohydrate metabolism disorders, taking into account the gestational age and the macrosomic fetal growth. MATERIALS AND METHODS: In this prospective cohort study, 86 pregnant women with pregestational diabetes mellitus, 44 pregnant women with gestational diabetes mellitus and 58 patients without carbohydrate metabolism disorders underwent ultrasound examinations from 30+0 to 41+3 weeks of gestation. During ultrasound, we performed Doppler assessment of venous hemodynamic parameters in the vessels of the umbilical-portal venous system, with volumetric blood flow calculated for each vessel. Additionally, the total liver volumetric blood flow and ductus venosus shunt fraction were calculated. RESULTS: The presence of fetal macrosomia in patients from the pregestational diabetes mellitus group is associated with an increase in the volumetric blood flow of the umbilical vein by 89.5 ml/min (p = 0.003) and the left portal vein by 33.3 ml/min (p = 0.008), as well as the total volumetric blood flow of the fetal liver by 95.7 ml/min (p = 0.001) compared with normal-weight fetuses. At the same time, the ductus venosus shunt fraction decreased in macrosomic fetuses by 3.83% (p = 0.001). In the gestational diabetes mellitus and control groups, despite the tendency for these parameters to increase in fetuses with macrosomia, the differences did not reach statistical significance. With a left portal vein volume flow threshold of 94.51 ml/min, the sensitivity and specificity for predicting large births were 84.46 and 72.09%, respectively. CONCLUSIONS: Pregestational diabetes mellitus in the mother is associated with a priority redistribution of blood flow to the fetal liver and is accompanied by a decrease in the ductus venosus shunt fraction. The severity of these hemodynamic changes increases in the presence of fetal macrosomia, which confirms the role of liver perfusion in the regulation of fetal growth in uncomplicated pregnancy and maternal diabetes mellitus.
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来源期刊
Journal of obstetrics and women's diseases
Journal of obstetrics and women's diseases Medicine-Obstetrics and Gynecology
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