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血红素结合蛋白和α1-微球蛋白这两种血红素清除剂在子痫前期和胎儿生长受限中发挥不同作用。

Hemopexin and α1-microglobulin heme scavengers with differential involvement in preeclampsia and fetal growth restriction.

机构信息

Section of Obstetrics and Gynecology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.

BCNatal | Fetal Medicine Research Center (Hospital Clínic and Hospital Sant Joan de Déu), Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), University of Barcelona, Barcelona, Spain.

出版信息

PLoS One. 2020 Sep 11;15(9):e0239030. doi: 10.1371/journal.pone.0239030. eCollection 2020.

Abstract

Hemopexin and α1-microglobulin act as scavengers to eliminate free heme-groups responsible for hemoglobin-induced oxidative stress. The present study evaluated maternal and fetal plasma concentrations of these scavengers in the different phenotypes of placenta-mediated disorders. Singleton pregnancies with normotensive fetal growth restriction [FGR] (n = 47), preeclampsia without FGR (n = 45) and preeclampsia with FGR (n = 51) were included prospectively as well as uncomplicated pregnancies (n = 49). Samples were collected at delivery and ELISA analysis was applied to measure the hemopexin and α1-microglobulin concentrations. In maternal blood in preeclampsia with and without FGR, hemopexin was significantly lower (p = 0.003 and p<0.001, respectively) and α1-microglobulin was significantly higher (p<0.001 in both) whereas no difference existed in normotensive FGR mothers compared to controls. In contrast, in fetal blood in growth restricted fetuses with and without preeclampsia, both hemopexin and α1-microglobulin were significantly lower (p<0.001 and p = 0.001 for hemopexin, p = 0.016 and p = 0.013 for α1-microglobulin, respectively) with no difference in fetuses from preeclampsia without FGR in comparison to controls. Thus, hemopexin and α1-microglobulin present significantly altered concentrations in maternal blood in the maternal disease -preeclampsia- and in cord blood in the fetal disease -FGR-, which supports their differential role in placenta-mediated disorders in accordance with the clinical presentation of these disorders.

摘要

血红素结合蛋白和α1-微球蛋白作为清除剂,可消除导致血红蛋白诱导的氧化应激的游离血红素基团。本研究评估了这些清除剂在不同胎盘介导的疾病表型中母血和胎血中的浓度。前瞻性纳入了单纯性胎儿生长受限[FGR](n = 47)、无 FGR 的子痫前期(n = 45)和有 FGR 的子痫前期(n = 51)的正常血压胎儿生长受限孕妇,以及单纯妊娠(n = 49)。分娩时采集样本,应用 ELISA 分析测定血红素结合蛋白和α1-微球蛋白浓度。在有和无 FGR 的子痫前期产妇血中,血红素结合蛋白显著降低(p = 0.003 和 p<0.001),α1-微球蛋白显著升高(两者均 p<0.001),而正常血压 FGR 产妇与对照组相比无差异。相反,在有和无子痫前期的生长受限胎儿的胎血中,血红素结合蛋白和α1-微球蛋白均显著降低(p<0.001 和 p = 0.001 用于血红素结合蛋白,p = 0.016 和 p = 0.013 用于α1-微球蛋白),而无 FGR 的子痫前期胎儿与对照组相比无差异。因此,血红素结合蛋白和α1-微球蛋白在母体疾病-子痫前期的母体血中和胎儿疾病-FGR 的脐血中浓度明显改变,这支持它们在胎盘介导的疾病中根据这些疾病的临床表现发挥不同的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3bf8/7485876/1b5cb9b19aaf/pone.0239030.g001.jpg

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