Evidence map›Paper›PMID 26111529›Full record

ArticleCritical care (London, England)2015

Persistently elevated osteopontin serum levels predict mortality in critically ill patients.

Christoph Roderburg, Fabian Benz, David Vargas Cardenas, Matthias Lutz, Hans-Joerg Hippe, Tom Luedde, Christian Trautwein, Norbert Frey, Alexander Koch, Frank Tacke and 1 more

Open access · goldAbstract read
In one paragraph

Article in Critical care (London, England), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
5.1field-weighted citation impact, top 5% 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

32 citing papers in PubMed, 49 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Christoph RoderburgDepartment of Medicine III, University Hospital RWTH Aachen, Pauwelsstrasse 30, 52074, Aachen, Germany. croderburg@ukaachen.de.
Fabian BenzDepartment of Medicine III, University Hospital RWTH Aachen, Pauwelsstrasse 30, 52074, Aachen, Germany. fabian.benz@rwth-aachen.de.
David Vargas CardenasDepartment of Medicine III, University Hospital RWTH Aachen, Pauwelsstrasse 30, 52074, Aachen, Germany. david.vargas@rwth-aachen.de.
Matthias LutzDepartment of Internal Medicine III, University of Kiel, Schittenhelmstrasse 12, 24105, Kiel, Germany. matthias.lutz@uk-sh.de.
Hans-Joerg HippeDepartment of Internal Medicine III, University of Kiel, Schittenhelmstrasse 12, 24105, Kiel, Germany. hans-joerg.hippe@uksh.de.
Tom LueddeDepartment of Medicine III, University Hospital RWTH Aachen, Pauwelsstrasse 30, 52074, Aachen, Germany. tluedde@ukaachen.de.
Christian TrautweinDepartment of Medicine III, University Hospital RWTH Aachen, Pauwelsstrasse 30, 52074, Aachen, Germany. ctrautwein@ukaachen.de.
Norbert FreyDepartment of Internal Medicine III, University of Kiel, Schittenhelmstrasse 12, 24105, Kiel, Germany. norbert.frey@uksh.de.
Alexander KochDepartment of Medicine III, University Hospital RWTH Aachen, Pauwelsstrasse 30, 52074, Aachen, Germany. akoch@ukaachen.de.
Frank TackeDepartment of Medicine III, University Hospital RWTH Aachen, Pauwelsstrasse 30, 52074, Aachen, Germany. frank.tacke@gmx.net.
Mark LueddeDepartment of Internal Medicine III, University of Kiel, Schittenhelmstrasse 12, 24105, Kiel, Germany. mark.luedde@uksh.de.
RWTH Aachen University · DEKiel University · DE

Funding

European Research Council 208237
6 · The paper itself

Abstract

introductionInflammatory, autoimmune and metabolic disorders have been associated with alterations in osteopontin (OPN) serum levels. Furthermore, elevated serum levels of OPN were reported from a small cohort of patients with sepsis. We therefore analyzed OPN serum concentrations in a large cohort of critically ill medical patients.

methodsA total of 159 patients (114 with sepsis, 45 without sepsis) were studied prospectively upon admission to the medical intensive care unit (ICU) as well as after 3 days of ICU treatment and compared to 50 healthy controls. Clinical data, various laboratory parameters as well as investigational inflammatory cytokine profiles were assessed. Patients were followed for approximately 1 year.

resultsWe found significantly elevated serum levels of OPN at admission to the ICU and after 3 days of treatment in critically ill patients compared to healthy controls. OPN concentrations were related to disease severity and significantly correlated with established prognosis scores and classical as well as experimental markers of inflammation and multi-organ failure. In the total cohort, OPN levels decreased from admission to day 3 of ICU treatment. However, persistently elevated OPN levels at day 3 of ICU treatment were a strong independent predictor for an unfavorable prognosis, with similar or better diagnostic accuracy than routinely used markers of organ failure or prognostic scoring systems such as SAPS2 or APACHE II score.

conclusionsPersistently elevated OPN serum concentrations are associated with an unfavourable outcome in patients with critical illness, independent of the presence of sepsis. Besides a possible pathogenic role of OPN in critical illness, our study indicates a potential value for OPN as a prognostic biomarker in critically ill patients during the early course of ICU treatment.

Indexed as

AdultAgedAged, 80 and overBiomarkersCritical IllnessFemaleHumansIntensive Care UnitsMaleMiddle AgedMortalityOsteopontinPredictive Value of TestsProspective StudiesYoung AdultBiomarkersOsteopontin

Identifiers

PMID26111529
PMCPMC4490692
OpenAlexW1915726540

What OpenQuestion holds

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LicenceCC BY
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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.