Evidence map›Paper›PMID 32321351›Full record

ArticleJournal of the American Heart Association2020

Iron Metabolism Contributes to Prognosis in Coronary Artery Disease: Prognostic Value of the Soluble Transferrin Receptor Within the AtheroGene Study.

Henri Weidmann, Johannes H Bannasch, Christoph Waldeyer, Apurva Shrivastava, Sebastian Appelbaum, Francisco Miguel Ojeda-Echevarria, Renate Schnabel, Karl J Lackner, Stefan Blankenberg, Tanja Zeller and 1 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Journal of the American Heart Association, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. Pooled it
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  5. Circulating protein biomarkers and their association with vulnerable plaque characteristics - a PROSPECT II substudy.International journal of cardiology. Cardiovascular risk and prevention · 2025
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  18. Iron deficiency and cardiovascular disease.European heart journal · 2023
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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 2 institutions in 1 country.

Henri WeidmannDepartment of General and Interventional Cardiology University Heart Center Hamburg Hamburg Germany.
Johannes H BannaschDepartment of General and Interventional Cardiology University Heart Center Hamburg Hamburg Germany.
Christoph WaldeyerDepartment of General and Interventional Cardiology University Heart Center Hamburg Hamburg Germany.
Apurva ShrivastavaDepartment of General and Interventional Cardiology University Heart Center Hamburg Hamburg Germany.
Sebastian AppelbaumDepartment of General and Interventional Cardiology University Heart Center Hamburg Hamburg Germany.
Francisco Miguel Ojeda-EchevarriaDepartment of General and Interventional Cardiology University Heart Center Hamburg Hamburg Germany.
Renate SchnabelDepartment of General and Interventional Cardiology University Heart Center Hamburg Hamburg Germany.
Karl J LacknerDepartment of Laboratory Medicine University Medical Center Johannes Gutenberg University Mainz Mainz Germany.
Stefan BlankenbergDepartment of General and Interventional Cardiology University Heart Center Hamburg Hamburg Germany.
Tanja ZellerDepartment of General and Interventional Cardiology University Heart Center Hamburg Hamburg Germany.
Mahir KarakasDepartment of General and Interventional Cardiology University Heart Center Hamburg Hamburg Germany.
Universität Hamburg · DEJohannes Gutenberg University Mainz · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background Coronary heart disease is a leading cause of mortality worldwide. Iron deficiency, a frequent comorbidity of coronary heart disease, causes an increased expression of transferrin receptor and soluble transferrin receptor levels (sTfR) levels, while iron repletion returns sTfR levels to the normal physiological range. Recently, sTfR levels were proposed as a potential new marker of iron metabolism in cardiovascular diseases. Therefore, we aimed to evaluate the prognostic value of circulating sTfR levels in a large cohort of patients with coronary heart disease. Methods and Results The disease cohort comprised 3423 subjects who had angiographically documented coronary heart disease and who participated in the AtheroGene study. Serum levels of sTfR were determined at baseline using an automated immunoassay (Roche Cobas Integra 400). Two main outcomes were considered: a combined end point of myocardial infarction and cardiovascular death and cardiovascular death alone. During a median follow-up of 4.0 years, 10.3% of the patients experienced an end point. In Cox regression analyses for sTfR levels, the hazard ratio (HR) for future cardiovascular death and/or myocardial infarction was 1.27 (95% CI, 1.11-1.44,

Indexed as

AgedBiomarkersCoronary AngiographyCoronary Artery DiseaseFemaleGermanyHumansIronMaleMiddle AgedMyocardial InfarctionMyocardiumPredictive Value of TestsPrognosisReceptors, TransferrinRisk AssessmentBiomarkersIronReceptors, Transferrinbiomarkercoronary artery diseaseironprognosissoluble transferrin receptor

Identifiers

PMID32321351
PMCPMC7428563
OpenAlexW3017620857

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.