Assessing erythroferrone and iron homeostasis in preeclamptic and normotensive pregnancies: A retrospective study.


Journal

Placenta
ISSN: 1532-3102
Titre abrégé: Placenta
Pays: Netherlands
ID NLM: 8006349

Informations de publication

Date de publication:
03 03 2023
Historique:
received: 29 08 2022
revised: 15 01 2023
accepted: 18 01 2023
pubmed: 26 1 2023
medline: 25 2 2023
entrez: 25 1 2023
Statut: ppublish

Résumé

Preeclampsia (PE) is a pregnancy-related disorder associated with maternal hypertension and placental dysfunction. A significant micronutrient during pregnancy is iron, which is important in cellular functions. While iron absorption increases in pregnancy, little is known about the exact mechanisms regulating maternal iron levels and transfer through the placenta in normal and complicated pregnancies. In this retrospective study, we investigated the regulation of maternal and placental iron availability and storage, in normotensive and pregnancies complicated by early- or late-onset PE. Methods used were analysis of clinical records, ELISA analysis on plasma samples, immunofluorescent and Prussian Blue analysis on placenta biopsies. Focusing on erythroferrone (ERFE) as a new marker and hormonal regulator of iron, our results demonstrated altered maternal ERFE levels in PE. We are the first to report the expression of ERFE in trophoblasts and indicate its lower levels in early-onset PE placentas. These changes were associated with lower placental transferrin receptor 1 (TfR1) in syncytiotrophoblasts in both early- and late-onset PE. In addition, maternal plasma ERFE levels were elevated in both early- and late-onset PE and hepcidin levels reduced in early-onset PE. Unaltered maternal plasma IL-6 levels suggest mechanism other than inflammation being involved in altered iron regulation in PE pregnancy. Our data supports a deregulation in maternal iron bioavailability in early- and late-onset PE vs normotensive pregnancies. The exact role of placental ERFE in regulating maternal-placental-fetal iron transport axis requires further investigation.

Identifiants

pubmed: 36696784
pii: S0143-4004(23)00018-8
doi: 10.1016/j.placenta.2023.01.008
pii:
doi:

Substances chimiques

Iron E1UOL152H7

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, N.I.H., Intramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

10-18

Subventions

Organisme : Intramural NIH HHS
ID : ZIA DE000714
Pays : United States

Informations de copyright

Copyright © 2023 The Authors. Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest S.R.H. is a co-founder of Guard Therapeutics International AB (formerly named A1M Pharma AB). All other authors declare no conflict of interest.

Auteurs

Zahra Masoumi (Z)

Division of Obstetrics and Gynecology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden. Electronic address: zahra.masoumi@york.ac.uk.

Lucas R Hansson (LR)

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

Eva Hansson (E)

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

Evelina Ahlm (E)

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

Eva Mezey (E)

Adult Stem Cell Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, USA.

Lena Erlandsson (L)

Division of Obstetrics and Gynecology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden. Electronic address: lena.erlandsson@med.lu.se.

Stefan R Hansson (SR)

Division of Obstetrics and Gynecology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden; Skåne University Hospital, Obstetrics and Gynecology, Sweden.

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Classifications MeSH