Evidence map›Paper›PMID 33684239›Full record

ArticleAmerican journal of hematology2021

Marginally reduced maternal hepatic and splenic ferroportin under severe nutritional iron deficiency in pregnancy maintains systemic iron supply.

Rafał Mazgaj, Paweł Lipiński, Eunice Sindhuvi Edison, Aleksandra Bednarz, Robert Staroń, Olga Haberkiewicz, Małgorzata Lenartowicz, Ewa Smuda, Aneta Jończy, Rafał R Starzyński

Open access · hybridAbstract readComparative Study
In one paragraph

Article in American journal of hematology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

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  11. Iron Metabolism and Ferroptosis in Physiological and Pathological Pregnancy.International journal of molecular sciences · 2022
    Review
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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

10 authors at 3 institutions in 2 countries.

Rafał MazgajInstitute of Genetics and Animal Biotechnology, Polish Academy of Sciences, Magdalenka, Poland.
Paweł LipińskiInstitute of Genetics and Animal Biotechnology, Polish Academy of Sciences, Magdalenka, Poland.ORCID 0000-0002-0121-4460
Eunice Sindhuvi EdisonDepartment of Hematology, Christian Medical College, Vellore, India.ORCID 0000-0002-9726-1324
Aleksandra BednarzDepartment of Genetics and Evolution, Institute of Zoology and Biomedical Research, Jagiellonian University, Kraków, Poland.
Robert StarońInstitute of Genetics and Animal Biotechnology, Polish Academy of Sciences, Magdalenka, Poland.
Olga HaberkiewiczDepartment of Genetics and Evolution, Institute of Zoology and Biomedical Research, Jagiellonian University, Kraków, Poland.
Małgorzata LenartowiczDepartment of Genetics and Evolution, Institute of Zoology and Biomedical Research, Jagiellonian University, Kraków, Poland.
Ewa SmudaInstitute of Genetics and Animal Biotechnology, Polish Academy of Sciences, Magdalenka, Poland.
Aneta JończyInstitute of Genetics and Animal Biotechnology, Polish Academy of Sciences, Magdalenka, Poland.
Rafał R StarzyńskiInstitute of Genetics and Animal Biotechnology, Polish Academy of Sciences, Magdalenka, Poland.
Institute of Genetics and Animal Biotechnology of the Polish Academy of Sciences · PLJagiellonian University · PLChristian Medical College, Vellore · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The demand for iron is high in pregnancy to meet the increased requirements for erythropoiesis. Even pregnant females with initially iron-replete stores develop iron-deficiency anemia, due to inadequate iron absorption. In anemic females, the maternal iron supply is dedicated to maintaining iron metabolism in the fetus and placenta. Here, using a mouse model of iron deficiency in pregnancy, we show that iron recycled from senescent erythrocytes becomes a predominant source of this microelement that can be transferred to the placenta in females with depleted iron stores. Ferroportin is a key protein in the molecular machinery of cellular iron egress. We demonstrate that under iron deficiency in pregnancy, levels of ferroportin are greatly reduced in the duodenum, placenta and fetal liver, but not in maternal liver macrophages and in the spleen. Although low expression of both maternal and fetal hepcidin predicted ferroportin up-regulation in examined locations, its final expression level was very likely correlated with tissue iron status. Our results argue that iron released into the circulation of anemic females is taken up by the placenta, as evidenced by high expression of iron importers on syncytiotrophoblasts. Then, a substantial decrease in levels of ferroportin on the basolateral side of syncytiotrophoblasts, may be responsible for the reduced transfer of iron to the fetus. As attested by the lowest decrease in iron content among analyzed tissues, some part is retained in the placenta. These findings confirm the key role played by ferroportin in tuning iron turnover in iron-deficient pregnant mouse females and their fetuses.

Indexed as

Iron DeficienciesAnimalsCarrier ProteinsCation Transport ProteinsCytokinesDuodenumErythrocyte AgingErythrocyte IndicesFemaleFerroportinFetusHemoglobinsHepcidinsIronIron, DietaryLiverCarrier ProteinsCation Transport ProteinsCend1 protein, mouseCytokinesErfe protein, mouseFerroportinHamp protein, mouseHemoglobinsHepcidinsIronIron, DietaryMembrane ProteinsMuscle ProteinsNerve Tissue Proteins

Identifiers

PMID33684239
PMCPMC8251567
OpenAlexW3135256698

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Registered trials

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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.