Evidence map›Paper›PMID 29512095›Full record

ArticleCardiology journal2019

Mast cell derived carboxypeptidase A3 is decreased among patients with advanced coronary artery disease.

Łukasz Lewicki, Janusz Siebert, Tomasz Koliński, Karolina Piekarska, Magdalena Reiwer-Gostomska, Radosław Targoński, Piotr Trzonkowski, Natalia Marek-Trzonkowska

Open access · goldAbstract read
In one paragraph

Article in Cardiology journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.2field-weighted citation impact, top 46% 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

7 citing papers in PubMed, 23 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

8 authors at 1 institution in 1 country.

Łukasz LewickiUniversity Center for Cardiology, Dębinki 2, 80-211 Gdańsk, Poland. luklewicki@gmail.com.
Janusz SiebertUniversity Center for Cardiology, Gdansk, Poland; Department of Family Medicine, Medical University of Gdansk, Gdansk, Poland, Poland.
Tomasz KolińskiLaboratory of Immunoregulation and Cellular Therapies, Department of Family Medicine, Medical University of Gdansk, Gdansk, Poland.
Karolina PiekarskaLaboratory of Immunoregulation and Cellular Therapies, Department of Family Medicine, Medical University of Gdansk, Gdansk, Poland.
Magdalena Reiwer-GostomskaDepartment of Family Medicine, Medical University of Gdansk, Gdansk, Poland.
Radosław TargońskiPomeranian Cardiology Centers, Wejherowo, Poland.
Piotr TrzonkowskiDepartment of Clinical Immunology and Transplantology, Medical University of Gdansk, Gdansk, Poland.
Natalia Marek-TrzonkowskaLaboratory of Immunoregulation and Cellular Therapies, Department of Family Medicine, Medical University of Gdansk, Gdansk, Poland.
Gdańsk Medical University · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCoronary artery disease (CAD) affects milions of people and can result in myocardial infarction (MI). Previously, mast cells (MC) have been extensively investigated in the context of hypersensitivity, however as regulators of the local inflammatory response they can potentially contribute to CAD and/or its progression. The aim of the study was to assess if serum concentration of MC proteases: carboxypeptidase A3, cathepsin G and chymase 1 is associated with the extension of CAD and MI.

methodsThe 44 patients with angiographically confirmed CAD (23 subjects with non-ST-segment elevation MI [NSTEMI] and 21 with stable CAD) were analyzed. Clinical data were obtained as well serum concentrations of carboxypeptidase A3, cathepsin G and chymase 1 were also measured.

resultsPatients with single vessel CAD had higher serum concentration of carboxypeptidase than those with more advanced CAD (3838.6 ± 1083.1 pg/mL vs. 2715.6 ± 442.5 pg/mL; p = 0.02). There were no significant differences in levels of any protease between patients with stable CAD and those with NSTEMI. Patients with hypertension had ≈2-fold lower serum levels of cathepsin G than normotensive individuals (4.6 ± 0.9 pg/mL vs. 9.4 ± 5.8 pg/mL; p = 0.001). Cathepsin G levels were also decreased in sera of the current smokers as compared with non-smokers (3.1 ± 1.2 ng/mL vs. 5.8 ± 1.2 ng/mL, p = 0.02).

conclusionsDecreased serum level of carboxypeptidase is a hallmark of more advanced CAD. Lower serum levels of carboxypeptidase A3 and catepsin G are associated with risk factors of blood vessel damage suggesting a protective role of these enzymes in CAD.

Indexed as

AgedBiomarkersCarboxypeptidases ACase-Control StudiesCathepsin GChymasesCoronary Artery DiseaseDown-RegulationFemaleHumansMaleMast CellsMiddle AgedNon-ST Elevated Myocardial InfarctionProspective StudiesBiomarkersCarboxypeptidases ACathepsin GChymasesCMA1 protein, humanCPA3 protein, humanCTSG protein, humancarboxypeptidase A3cathepsin Gchymase 1coronary artery diseasemast cells

Identifiers

PMID29512095
PMCPMC8083039
OpenAlexW2791354903

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.