Evidence map›Paper›PMID 33051525›Full record

ArticleScientific reports2020

Circulating antibodies against age-modified proteins in patients with coronary atherosclerosis.

Edina Korça, Veronika Piskovatska, Jochen Börgermann, Alexander Navarrete Santos, Andreas Simm

Abstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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

12 citing papers in PubMed.

  1. Review
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  12. Integrative Role of Albumin: Evolutionary, Biochemical and Pathophysiological Aspects.Journal of evolutionary biochemistry and physiology · 2021
    Article
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

5 authors.

Edina KorçaDepartment of Cardiothoracic Surgery, University Hospital Halle (Saale), Martin-Luther University Halle-Wittenberg, Halle, Germany.
Veronika PiskovatskaDepartment of Cardiothoracic Surgery, University Hospital Halle (Saale), Martin-Luther University Halle-Wittenberg, Halle, Germany.
Jochen BörgermannDepartment of Cardiothoracic Surgery, University Hospital Halle (Saale), Martin-Luther University Halle-Wittenberg, Halle, Germany.
Alexander Navarrete SantosCenter for Medical Basic Research, Martin-Luther University Halle-Wittenberg, Halle, Germany.
Andreas SimmDepartment of Cardiothoracic Surgery, University Hospital Halle (Saale), Martin-Luther University Halle-Wittenberg, Halle, Germany. andreas.simm@uk-halle.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Advanced glycation endproducts (AGEs) are formed in a series of non-enzymatic reactions between reducing sugars and the amino groups of proteins and accumulate during aging, diabetes mellitus, chronic kidney disease and other chronic diseases. Accumulation of AGE-modifications alters protein structure and function, transforming these molecules into potential targets of the immune system, presumably triggering the production of autoantibodies against AGEs. In this study, we detected autoantibodies against AGE-modified proteins with ELISA in plasma samples of 91 patients with documented coronary artery disease (CAD), who underwent coronary artery bypass grafting (CABG) surgery. Patients with high levels of autoantibodies had a higher body mass index (BMI 28.6 vs 27.1 kg/m

Indexed as

AgedAntibody SpecificityAutoantibodiesBiomarkersCoronary Artery BypassCoronary Artery DiseaseEnzyme-Linked Immunosorbent AssayFemaleGlycation End Products, AdvancedHumansMaleAutoantibodiesBiomarkersGlycation End Products, Advanced

Identifiers

PMID33051525
PMCPMC7553914

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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.