Evidence map›Paper›PMID 26323096›Full record

ArticlePloS one2015

Urinary Hepcidin Levels in Iron-Deficient and Iron-Supplemented Piglets Correlate with Hepcidin Hepatic mRNA and Serum Levels and with Body Iron Status.

Robert Staroń, Rachel P L Van Swelm, Paweł Lipiński, Anna Gajowiak, Małgorzata Lenartowicz, Aleksandra Bednarz, Małgorzata Gajewska, Marek Pieszka, Coby M M Laarakkers, Dorine W Swinkels and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

11 citing papers in PubMed, 22 citations in OpenAlex.

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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

11 authors at 6 institutions in 2 countries.

Robert StarońInstitute of Genetics and Animal Breeding PAS, Department of Molecular Biology, Jastrzębiec, Poland.
Rachel P L Van SwelmDepartment of Laboratory Medicine (LGEM 830), Radboud University Medical Centre, Nijmegen, The Netherlands.
Paweł LipińskiInstitute of Genetics and Animal Breeding PAS, Department of Molecular Biology, Jastrzębiec, Poland.
Anna GajowiakInstitute of Genetics and Animal Breeding PAS, Department of Molecular Biology, Jastrzębiec, Poland.
Małgorzata LenartowiczDepartment of Genetics and Evolution, Institute of Zoology, Jagiellonian University, Kraków, Poland.
Aleksandra BednarzDepartment of Genetics and Evolution, Institute of Zoology, Jagiellonian University, Kraków, Poland.
Małgorzata GajewskaWarsaw University of Life Sciences, Faculty of Veterinary Medicine, Department of Physiological Sciences, Warsaw, Poland.
Marek PieszkaDepartment of Animal Nutrition & Feed Science, National Research Institute of Animal Production, Kraków, Poland.
Coby M M LaarakkersDepartment of Laboratory Medicine (LGEM 830), Radboud University Medical Centre, Nijmegen, The Netherlands.
Dorine W SwinkelsDepartment of Laboratory Medicine (LGEM 830), Radboud University Medical Centre, Nijmegen, The Netherlands.
Rafał R StarzyńskiInstitute of Genetics and Animal Breeding PAS, Department of Molecular Biology, Jastrzębiec, Poland.
Institute of Plant Genetics, Polish Academy of Sciences · PLJagiellonian University · PLRadboud University Nijmegen · NLNational Research Institute of Animal Production · PLRadboud University Medical Center · NLWarsaw University of Life Sciences · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Among livestock, domestic pig (Sus scrofa) is a species, in which iron metabolism has been most intensively examined during last decade. The obvious reason for studying the regulation of iron homeostasis especially in young pigs is neonatal iron deficiency anemia commonly occurring in these animals. Moreover, supplementation of essentially all commercially reared piglets with iron entails a need for monitoring the efficacy of this routine practice followed in the swine industry for several decades. Since the discovery of hepcidin many studies confirmed its role as key regulator of iron metabolism and pointed out the assessment of its concentrations in biological fluids as diagnostic tool for iron-related disorder. Here we demonstrate that urine hepcidin-25 levels measured by a combination of weak cation exchange chromatography and time-of-flight mass spectrometry (WCX-TOF MS) are highly correlated with mRNA hepcidin expression in the liver and plasma hepcidin-25 concentrations in anemic and iron-supplemented 28-day old piglets. We also found a high correlation between urine hepcidin level and hepatic non-heme iron content. Our results show that similarly to previously described transgenic mouse models of iron disorders, young pigs constitute a convenient animal model to explore accuracy and relationship between indicators for assessing systemic iron status.

Indexed as

Anemia, Iron-DeficiencyAnimalsChromatography, Ion ExchangeDietary SupplementsHepcidinsIronLiverMass SpectrometryRNA, MessengerSus scrofaSwineSwine DiseasesHepcidinsIronRNA, Messenger

Identifiers

PMID26323096
PMCPMC4556373
OpenAlexW1903894494

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.