Evidence map›Paper›PMID 25970343›Full record

ArticlePloS one2015

Calprotectin and platelet aggregation in patients with stable coronary artery disease.

Sanne Bøjet Larsen, Erik Lerkevang Grove, Manan Pareek, Steen Dalby Kristensen, Anne-Mette Hvas

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 26% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
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  12. Serum Calprotectin Levels and Outcome Following Percutaneous Coronary Intervention in Patients with Diabetes and Acute Coronary Syndrome.Medical science monitor : international medical journal of experimental and clinical research · 2019
    Article
  13. Zinc Homeostasis in Platelet-Related Diseases.International journal of molecular sciences · 2019
    Review
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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

5 authors at 2 institutions in 1 country.

Sanne Bøjet LarsenDepartment of Cardiology, Aarhus University Hospital, DK-8200, Aarhus N, Denmark.
Erik Lerkevang GroveDepartment of Cardiology, Aarhus University Hospital, DK-8200, Aarhus N, Denmark.
Manan PareekDepartment of Cardiology, Aarhus University Hospital, DK-8200, Aarhus N, Denmark.
Steen Dalby KristensenDepartment of Cardiology, Aarhus University Hospital, DK-8200, Aarhus N, Denmark; Faculty of Health Sciences, Aarhus University, DK-8200, Aarhus N, Denmark.
Anne-Mette HvasFaculty of Health Sciences, Aarhus University, DK-8200, Aarhus N, Denmark; Department of Clinical Biochemistry, Aarhus University Hospital, DK-8200, Aarhus N, Denmark.
Aarhus University Hospital · DKAarhus University · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRecent studies suggest that the inflammation-associated protein calprotectin may be implicated in the pathogenesis of coronary artery disease (CAD). However, the impact of calprotectin levels on platelet aggregation in CAD patients has never been investigated.

objectivesWe investigated the association between calprotectin levels and platelet aggregation in stable, high-risk CAD patients receiving aspirin as mono antiplatelet therapy. Furthermore, we aimed to investigate independent clinical and laboratory determinants of calprotectin levels.

methodsWe performed a cross-sectional study including 581 stable, high-risk CAD patients. All patients received 75 mg aspirin daily as mono antiplatelet therapy. Platelet aggregation was assessed by 1) impedance aggregometry (Multiplate Analyzer) using arachidonic acid (AA) and collagen as agonists and by 2) the VerifyNow Aspirin Assay. Low-grade inflammation was evaluated by calprotectin, high-sensitive C-reactive-protein (hs-CRP) and interleukin-6. Platelet activation was assessed by soluble P-selectin, and cyclooxygenase-1 inhibition was evaluated by serum thromboxane B2, both measured by ELISA.

resultsCalprotectin levels correlated positively with platelet aggregation according to Multiplate Analyzer (r=0.12, p=0.01). Additionally, calprotectin was positively associated with leukocytes (r=0.33, p<0.0001), hs-CRP (r=0.31, p<0.0001), interleukin-6 (r=0.28, p<0.0001), soluble P-selectin (r=0.10, p=0.02) and serum thromboxane B2 (r=0.10, p=0.02). Type 2 diabetes mellitus was an independent predictor of increased calprotectin levels (p=0.004), and trends were seen for body mass index (p=0.06) and smoking (p=0.07). Compliance with aspirin was confirmed by low serum thromboxane B2 levels in all patients (median [25%;75%]: 1.07 [0.52;1.87] ng/mL).

conclusionCalprotectin levels correlated positively, though weakly, with platelet aggregation and activation as well as serum thromboxane B2 in high-risk, stable CAD patients treated with aspirin.

Indexed as

Platelet AggregationAgedAspirinCoronary Artery DiseaseC-Reactive ProteinCross-Sectional StudiesFemaleHumansInterleukin-6Leukocyte L1 Antigen ComplexMaleMedication AdherenceMiddle AgedPlatelet Aggregation InhibitorsThromboxane B2AspirinC-Reactive ProteinIL6 protein, humanInterleukin-6Leukocyte L1 Antigen ComplexPlatelet Aggregation InhibitorsThromboxane B2

Identifiers

PMID25970343
PMCPMC4430524
OpenAlexW1599433215

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.