Evidence map›Paper›PMID 30300910›Full record

ArticleThrombosis and haemostasis2018

Monocytes of Different Subsets in Complexes with Platelets in Patients with Myocardial Infarction.

Marina Loguinova, Natalia Pinegina, Valeria Kogan, Murad Vagida, Anush Arakelyan, Alexander Shpektor, Leonid Margolis, Elena Vasilieva

Open access · greenAbstract read
In one paragraph

Article in Thrombosis and haemostasis, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

17 citing papers in PubMed, 36 citations in OpenAlex.

  1. Thromborepair: the tissue repair partner to thromboinflammation.Blood vessels, thrombosis & hemostasis · 2026
    Review
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  12. PScientific reports · 2021
    Article
  13. Article
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  15. Platelet Extracellular Vesicles: Beyond the Blood.Arteriosclerosis, thrombosis, and vascular biology · 2021
    Review
  16. Review
  17. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 3 countries.

Marina LoguinovaLaboratory of Atherothrombosis, Moscow State University of Medicine and Dentistry, Moscow, Russia.
Natalia PineginaLaboratory of Atherothrombosis, Moscow State University of Medicine and Dentistry, Moscow, Russia.
Valeria KoganAriel University, Institute for Translational Research, Ariel, Israel.
Murad VagidaLaboratory of Atherothrombosis, Moscow State University of Medicine and Dentistry, Moscow, Russia.
Anush ArakelyanSection on Intercellular Interactions, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, United States.
Alexander ShpektorLaboratory of Atherothrombosis, Moscow State University of Medicine and Dentistry, Moscow, Russia.
Leonid MargolisSection on Intercellular Interactions, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, United States.
Elena VasilievaLaboratory of Atherothrombosis, Moscow State University of Medicine and Dentistry, Moscow, Russia.
Moscow State University of Medicine and Dentistry · RUNational Institutes of Health · USAriel University · IL

Funding

Viral transmission and pathogenesis in human tissuesZIAHD008968 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI MARGOLIS, LEONID B. · 2018 to 2023
$12.2M
Intramural NIH HHS Z99 HD999999
6 · The paper itself

Abstract

Acute myocardial infarction (AMI) is associated with activation of various cells, including platelets that form monocyte-platelet complexes (MPCs). Here, we analysed MPC in vivo and in vitro and investigated the abilities of different monocyte subclasses to form MPC, the characteristics of the cells involved in MPC formation and MPC changes in AMI. We identified MPC by co-staining for platelet antigen CD41a and monocyte antigens CD14 and CD16. Platelet activation was evaluated from expression of phosphatidylserine as revealed by annexin V. Our results confirm published data and provide new information regarding the patterns of MPC in AMI patients. We found that the patterns of platelet aggregation with monocytes were different in AMI patients and controls: (1) in AMI patients, MPC formed by intermediate monocytes carry more platelets whereas in healthy controls more platelets aggregated with classical monocytes; (2) the numbers of MPC in AMI patients, being already higher than in controls, were further increased if these patients suffered various in-hospital complications; (3) on the basis of the CD41a fluorescence of the antibody-stained MPC, some of the aggregates seem to consist of monocytes and platelet-derived extracellular vesicles (EVs); (4) aggregation of monocytes with platelet EV occurred in in vitro experiments; and (5) these experiments demonstrated that monocytes from AMI patients aggregate with both platelets and platelet EVs more efficiently than do monocytes from controls. MPC in AMI patients may play an important role in this pathology.

Indexed as

AgedAntigens, CDBlood PlateletsCell CommunicationCells, CulturedFemaleFlow CytometryGPI-Linked ProteinsHumansLipopolysaccharide ReceptorsMaleMiddle AgedMonocytesMyocardial InfarctionPlatelet AggregationPlatelet Glycoprotein GPIb-IX ComplexAntigens, CDCD160 protein, humanGPI-Linked ProteinsLipopolysaccharide ReceptorsPlatelet Glycoprotein GPIb-IX ComplexReceptors, Immunologic

Identifiers

PMID30300910
PMCPMC7000167
OpenAlexW2897887484

What OpenQuestion holds

Textmetadata
LicenceTDM
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.