Evidence map›Paper›PMID 36050405›Full record

ArticleScientific reports2022

Hepcidin discriminates sepsis from other critical illness at admission to intensive care.

Jon Olinder, Alex Börjesson, Jakob Norrman, Tobias West, Joakim Carlström, Alexander Gustafsson, Martin Annborn, Heiko Herwald, Cecilia Rydén

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.0field-weighted citation impact, top 7% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
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  6. Biomarkers as Beacons: Illuminating Sepsis-Associated Hepato-Renal Injury.International journal of molecular sciences · 2025
    Review
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  8. Article
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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

9 authors at 2 institutions in 1 country.

Jon OlinderDepartment of Infectious Diseases, Helsingborg Hospital, Helsingborg, Sweden. jon.olinder@skane.se.
Alex BörjessonDivision of Infection Medicine, Department of Clinical Sciences, Lund University, Lund, Sweden.
Jakob NorrmanDivision of Infection Medicine, Department of Clinical Sciences, Lund University, Lund, Sweden.
Tobias WestDivision of Infection Medicine, Department of Clinical Sciences, Lund University, Lund, Sweden.
Joakim CarlströmDivision of Infection Medicine, Department of Clinical Sciences, Lund University, Lund, Sweden.
Alexander GustafssonDivision of Infection Medicine, Department of Clinical Sciences, Lund University, Lund, Sweden.
Martin AnnbornDivision of Infection Medicine, Department of Clinical Sciences, Lund University, Lund, Sweden.
Heiko HerwaldDivision of Infection Medicine, Department of Clinical Sciences, Lund University, Lund, Sweden.
Cecilia RydénDepartment of Infectious Diseases, Helsingborg Hospital, Helsingborg, Sweden.
Lund University · SEHelsingborgs lasarett · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Initial differential diagnosis and prognosis for patients admitted to intensive care with suspected sepsis remain arduous. Hepcidin has emerged as a potential biomarker for sepsis. Here we report data on the relevance of levels of hepcidin versus other biomarkers as a diagnostic and prognostic tool for sepsis. 164 adult patients admitted to the intensive care unit (ICU) within 24 h upon arrival to the hospital were included. Blood samples collected daily for seven consecutive days and hepcidin levels, heparin binding protein (HBP) levels and standard biomarkers were determined. Blood cultures were initiated at inclusion. Clinical scores were evaluated daily and mortality after 28- and 180-days was recorded. One hundred of the patients were found to fulfil the criteria for sepsis whereas 64 did not. Hepcidin levels at admission were significantly higher in the septic than in the non-septic patients. In septic patients hepcidin levels declined significantly already at 24 h followed by a steady decline. A significant negative correlation was observed between hepcidin levels and SAPS 3 in patients with sepsis. Hepcidin levels at inclusion were significantly higher among septic patients that survived 180-days and predicted mortality. Our data show that hepcidin levels are indicative of sepsis in patients admitted to the ICU and has a prognostic value for mortality.

Indexed as

HepcidinsSepsisAdultBiomarkersCritical CareCritical IllnessHumansIntensive Care UnitsPrognosisShock, SepticBiomarkersHepcidins

Identifiers

PMID36050405
PMCPMC9434539
OpenAlexW4294032373

What OpenQuestion holds

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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.