Evidence map›Paper›PMID 34703482›Full record

ArticleARYA atherosclerosis2021

Increased circulating platelet and endothelial-derived microparticles in patients with cardiac syndrome X.

Fereshteh Ghaffari, Yousef Rasmi, Mir Hossein Seyed Mohammadzad, Shahram Seyedi, Alireza Shirpoor, Elmira Roshani-Asl, Ehsan Saboory

Open access · greenAbstract read
In one paragraph

Article in ARYA atherosclerosis, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.1field-weighted citation impact, top 56% 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

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

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

7 authors at 2 institutions in 1 country.

Fereshteh GhaffariDepartment of Biochemistry, School of Medicine, Urmia University of Medical Sciences, Urmia, Iran.
Yousef RasmiProfessor, Cellular and Molecular Research Center AND Department of Biochemistry, School of Medicine, Urmia University of Medical Sciences, Urmia, Iran.
Mir Hossein Seyed MohammadzadAssociate Professor, Department of Cardiology, School of Medicine, Urmia University of Medical Sciences, Urmia, Iran.
Shahram SeyediAssistant Professor, Department of Immunology, School of Medicine, Urmia University of Medical Sciences, Urmia, Iran.
Alireza ShirpoorProfessor, Department of Physiology, School of Medicine, Urmia University of Medical Sciences, Urmia, Iran.
Elmira Roshani-AslDepartment of Biochemistry, School of Medicine, Urmia University of Medical Sciences, Urmia, Iran.
Ehsan SabooryProfessor, Zanjan Metabolic Diseases Research Center, Zanjan University of Medical Sciences, Zanjan, Iran.
Urmia University · IRUrmia University of Medical Sciences

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCardiac syndrome X (CSX) has been associated with endothelial dysfunction and inflammation. We conducted a case-control study to evaluate the association between plateletý and endothelial-derived microparticles (PMPs and EMPs), as specific quantitative plasma markers of endothelial dysfunction, and the presence of CSX.

methodsThe present study was conducted on 40 CSX patients and 19 healthy individuals. C-reactive protein (CRP), and hematological and biochemical parameters were evaluated. The MP concentration in platelet-poor plasma (PPP) was quantitatively determined through flow cytometry using specific anti-human CD31, CD41a, CD62E, and CD144 antibodies.

resultsThe mean platelet volume (MPV) and positive CRP rate (≥ 3.8 mg/l) were higher in patients compared to controls (P = 0.020 and P = 0.010, respectively). The CD62E+, CD144+, and CD31+41- EMPs, as well as CD41+ and CD31+CD41+ PMPs showed significant increase in CSX patients compared to controls (P < 0.050). There were direct correlations between the mean percentage of detected EMPs and PMPs as well as between their expression intensity; however, a reverse correlation was seen between the percentage of MPs and CD144 and CD41. Moreover, the MP level was reversely associated with prothrombin time (PT) and partial thromboplastin time (PTT) values. Only CD31+CD41+ PMP was correlated with CRP.

conclusionIt seems that EMPs and PMPs increase in CSX, which may contribute to various processes involved in the development of this syndrome.

Indexed as

Cardiac Syndrome XDysfunctionEndotheliumInflammationMicroparticles

Identifiers

PMID34703482
PMCPMC8519618
OpenAlexW3150457272

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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.