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

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.

Publication types

  • Observational Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Alpha-Globulins / metabolism*
  • Biomarkers / blood
  • Case-Control Studies
  • Female
  • Fetal Blood / metabolism
  • Fetal Growth Retardation / blood*
  • Fetal Growth Retardation / etiology
  • Free Radical Scavengers / blood
  • Heme / metabolism*
  • Hemopexin / metabolism*
  • Humans
  • Infant, Newborn
  • Oxidative Stress
  • Pre-Eclampsia / blood*
  • Pre-Eclampsia / etiology
  • Pregnancy
  • Prospective Studies

Substances

  • Alpha-Globulins
  • Biomarkers
  • Free Radical Scavengers
  • alpha-1-microglobulin
  • Heme
  • Hemopexin

Grants and funding

This project has been partially funded with support of the Erasmus + Programme of the European Union (Framework Agreement number: 2013-0040). This publication reflects the views only of the authors, and the Commission cannot be held responsible for any use, which may be made of the information contained therein. Additionally, the research leading to these results has received funding form “la Caixa” Foundation under grant agreements LCF/PR/GN14/10270005 and LCF/PR/GN18/10310003, the Instituto de Salud Carlos III (PI14/00226, PI15/00130, PIE15/00027, PI17/00675, PI18/00073) integrados en el Plan Nacional de I+D+I y cofinanciados por el ISCIII-Subdirección General de Evaluación y el Fondo Europeo de Desarrollo Regional (FEDER) “Una manera de hacer Europa”, Cerebra Foundation for the Brain Injured Child (Carmarthen, Wales, UK) and AGAUR 2017 SGR grant n° 1531. This work was also funded by the Swedish Medical Research Council (VR), governmental ALF research grant to Lund University and Lund University hospital, the Royal Physiographic Society in Lund and the Swedish Foundation for Strategic Research (SSF).