Evidence map›Paper›PMID 36696784›Full record

ArticlePlacenta2023

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

Zahra Masoumi, Lucas R Hansson, Eva Hansson, Evelina Ahlm, Eva Mezey, Lena Erlandsson, Stefan R Hansson

Open access · hybridAbstract read
In one paragraph

Article in Placenta, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.1field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Trophoblast ferroptosis restricts SARS-CoV-2 spread in the placenta.bioRxiv : the preprint server for biology · 2026
    Article
  3. Article
  4. Article
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 2 countries.

Zahra MasoumiDivision of Obstetrics and Gynecology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden. Electronic address: zahra.masoumi@york.ac.uk.
Lucas R HanssonDivision of Obstetrics and Gynecology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.
Eva HanssonDivision of Obstetrics and Gynecology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.
Evelina AhlmDivision of Obstetrics and Gynecology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden.
Eva MezeyAdult Stem Cell Section, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, USA.
Lena ErlandssonDivision of Obstetrics and Gynecology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden. Electronic address: lena.erlandsson@med.lu.se.
Stefan R HanssonDivision of Obstetrics and Gynecology, Department of Clinical Sciences Lund, Lund University, Lund, Sweden; Skåne University Hospital, Obstetrics and Gynecology, Sweden.
Lund University · SENational Institutes of Health · US

Funding

Contribution of bone marrow cells to tissue regeneration, immune function and hematopoiesisZIADE000714 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI MEZEY, EVA M. · 2009 to 2025
$25.3M
Intramural NIH HHS ZIA DE000714
6 · The paper itself

Abstract

introductionPreeclampsia (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.

methodsIn 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.

resultsFocusing 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. DISCUSSION: 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.

Indexed as

PlacentaPre-EclampsiaFemaleHomeostasisHumansIronPregnancyRetrospective StudiesIronErythroferrone/iron homeostasis/preeclampsia/placenta

Identifiers

PMID36696784
PMCPMC11544558
OpenAlexW4317492959

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.