Association of Low Placental Growth Factor Gene Expression with Maternal and Neonatal Outcomes in Type 1 Diabetes: A Single Center, Cross-Sectional Study

IF 0.7 Q4 ENDOCRINOLOGY & METABOLISM
R. Iciek, P. Gutaj, Sara Królik, G. Kurzawińska, A. Bogacz, A. Seremak-Mrozikiewicz, P. Mikołajczak, J. Brązert, E. Wender-Ożegowska
{"title":"Association of Low Placental Growth Factor Gene Expression with Maternal and Neonatal Outcomes in Type 1 Diabetes: A Single Center, Cross-Sectional Study","authors":"R. Iciek, P. Gutaj, Sara Królik, G. Kurzawińska, A. Bogacz, A. Seremak-Mrozikiewicz, P. Mikołajczak, J. Brązert, E. Wender-Ożegowska","doi":"10.5603/dk.a2022.0056","DOIUrl":null,"url":null,"abstract":"Objective: The placental growth factor (PlGF) plays a crucial role in early and late pregnancy placental development. Pregestational type 1 diabetes (T1D) is a pregnancy complication that may lead to serious fetomaternal complications. Our study analyzed the association between placental PlGF mRNA expression and metabolic control, fetal weight and development in women with T1D. Materials and methods: A cross-sectional study on 65 pregnant women with T1D in singleton pregnancies admitted to the tertiary-level perinatal care unit. The study examined associations between the placental mRNA-PlGF gene expression measured with quantitative real-time PC and markers of maternal metabolism in the third trimester. The expression was also compared across maternal subgroups stratified according to the birth weight (small-vs. appropriate-vs. large-for-gestational age; SGA, AGA, LGA, respectively) and the following neonatal outcomes: mode of delivery, Apgar score and pH in the umbilical vessels. Results: Placental PlGF mRNA expression was significantly lower in SGA than in AGA and LGA patients (0.60 ± 0.34 vs. 0.63 ± 0.54 vs. 1.02 ± 0.15, respectively, p < 0.05). In the SGA group, the expression of the PlGF-mRNA correlated positively with maternal 3 rd trimester BMI (r = 0.49, p = 0.04), pH and BE cord blood values, and maternal 3 rd trimester mean BP. There was no correlation between 3 rd -trimester glycated hemoglobin and mean blood glucose levels (MBG) and PlGF expression. Conclusions: Our data suggest that lower PlGF mRNA expression may predict neonatal outcomes in women with T1D giving birth to SGA newborns. (Clin Diabetol 2023; 12; 1: 38–44)","PeriodicalId":10386,"journal":{"name":"Clinical Diabetology","volume":null,"pages":null},"PeriodicalIF":0.7000,"publicationDate":"2023-02-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Diabetology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5603/dk.a2022.0056","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
引用次数: 0

Abstract

Objective: The placental growth factor (PlGF) plays a crucial role in early and late pregnancy placental development. Pregestational type 1 diabetes (T1D) is a pregnancy complication that may lead to serious fetomaternal complications. Our study analyzed the association between placental PlGF mRNA expression and metabolic control, fetal weight and development in women with T1D. Materials and methods: A cross-sectional study on 65 pregnant women with T1D in singleton pregnancies admitted to the tertiary-level perinatal care unit. The study examined associations between the placental mRNA-PlGF gene expression measured with quantitative real-time PC and markers of maternal metabolism in the third trimester. The expression was also compared across maternal subgroups stratified according to the birth weight (small-vs. appropriate-vs. large-for-gestational age; SGA, AGA, LGA, respectively) and the following neonatal outcomes: mode of delivery, Apgar score and pH in the umbilical vessels. Results: Placental PlGF mRNA expression was significantly lower in SGA than in AGA and LGA patients (0.60 ± 0.34 vs. 0.63 ± 0.54 vs. 1.02 ± 0.15, respectively, p < 0.05). In the SGA group, the expression of the PlGF-mRNA correlated positively with maternal 3 rd trimester BMI (r = 0.49, p = 0.04), pH and BE cord blood values, and maternal 3 rd trimester mean BP. There was no correlation between 3 rd -trimester glycated hemoglobin and mean blood glucose levels (MBG) and PlGF expression. Conclusions: Our data suggest that lower PlGF mRNA expression may predict neonatal outcomes in women with T1D giving birth to SGA newborns. (Clin Diabetol 2023; 12; 1: 38–44)
低胎盘生长因子基因表达与1型糖尿病母婴结局的关系:一项单中心横断面研究
目的:胎盘生长因子(PlGF)在妊娠早期和晚期胎盘发育中起着至关重要的作用。妊娠期1型糖尿病(T1D)是一种妊娠并发症,可导致严重的母婴并发症。我们的研究分析了T1D女性胎盘PlGF mRNA表达与代谢控制、胎儿体重和发育之间的关系。材料与方法:对在三级围产儿监护病房就诊的65例单胎妊娠T1D孕妇进行横断面研究。本研究通过实时定量PC检测胎盘mRNA-PlGF基因表达与妊娠晚期母体代谢标志物之间的关系。还比较了根据出生体重分层的母亲亚组(小对大)的表达。appropriate-vs。large-for-gestational年龄;分别为SGA, AGA, LGA)和以下新生儿结局:分娩方式,Apgar评分和脐带血管pH。结果:SGA患者胎盘PlGF mRNA表达量显著低于AGA和LGA患者(分别为0.60±0.34∶0.63±0.54∶1.02±0.15,p < 0.05)。在SGA组中,PlGF-mRNA的表达与母体妊娠晚期BMI (r = 0.49, p = 0.04)、脐带血pH值和BE值以及母体妊娠晚期平均血压呈正相关。妊娠晚期糖化血红蛋白与平均血糖水平(MBG)和PlGF表达无相关性。结论:我们的数据表明,较低的PlGF mRNA表达可能预测T1D妇女分娩SGA新生儿的新生儿结局。《临床糖尿病杂志》2023;12;1: 38-44)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Clinical Diabetology
Clinical Diabetology ENDOCRINOLOGY & METABOLISM-
CiteScore
0.90
自引率
14.30%
发文量
49
审稿时长
25 weeks
期刊介绍: Clinical Diabetology hereinafter referred to as ‘CD’ or ′the Journal′, is a peer-reviewed, open access journal covering broad spectrum of topics in diabetology and aiming to advance the knowledge and science of this rapidly evolving field. The Journal is the official bimonthly of the Diabetes Poland (Polish Diabetes Association) and publishes review articles, original clinical and experimental investigations in the field of diabetology, case reports, letters and editorial comments . The Journal has been published in full text English since 2016.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信