Evidence map›Paper›PMID 26885820›Full record

ArticlePloS one2016

The Ratio of ADP- to TRAP-Induced Platelet Aggregation Quantifies P2Y12-Dependent Platelet Inhibition Independently of the Platelet Count.

Christoph B Olivier, Melanie Meyer, Hans Bauer, Katharina Schnabel, Patrick Weik, Qian Zhou, Christoph Bode, Martin Moser, Philipp Diehl

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Trial
  2. Observational
  3. Article
  4. Observational
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

9 authors at 2 institutions in 1 country.

Christoph B OlivierHeart Center Freiburg University, Cardiology and Angiology I, Freiburg-Bad Krozingen, Germany.
Melanie MeyerHeart Center Freiburg University, Cardiology and Angiology I, Freiburg-Bad Krozingen, Germany.
Hans BauerMunich University Hospital, Institute and Outpatient Clinic for Occupational, Social, and Environmental Medicine, Munich, Germany.
Katharina SchnabelHeart Center Freiburg University, Cardiology and Angiology I, Freiburg-Bad Krozingen, Germany.
Patrick WeikHeart Center Freiburg University, Cardiology and Angiology I, Freiburg-Bad Krozingen, Germany.
Qian ZhouHeart Center Freiburg University, Cardiology and Angiology I, Freiburg-Bad Krozingen, Germany.
Christoph BodeHeart Center Freiburg University, Cardiology and Angiology I, Freiburg-Bad Krozingen, Germany.
Martin MoserHeart Center Freiburg University, Cardiology and Angiology I, Freiburg-Bad Krozingen, Germany.
Philipp DiehlHeart Center Freiburg University, Cardiology and Angiology I, Freiburg-Bad Krozingen, Germany.
Universitäts-Herzzentrum Freiburg-Bad Krozingen · DEMünchen Klinik · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis study aimed to assess the association of clinical factors with P2Y12-dependent platelet inhibition as monitored by the ratio of ADP- to TRAP-induced platelet aggregation and conventional ADP-induced aggregation, respectively.

backgroundControversial findings to identify and overcome high platelet reactivity (HPR) after coronary stent-implantation and to improve clinical outcome by tailored anti-platelet therapy exist. Monitoring anti-platelet therapy ex vivo underlies several confounding parameters causing that ex vivo platelet aggregation might not reflect in vivo platelet inhibition.

methodsIn a single centre observational study, multiple electrode aggregometry was performed in whole blood of patients after recent coronary stent-implantation. Relative ADP-induced aggregation (r-ADP-agg) was defined as the ratio of ADP- to TRAP- induced aggregation reflecting the individual degree of P2Y12-mediated platelet reactivity.

resultsPlatelet aggregation was assessed in 359 patients. Means (± SD) of TRAP-, ADP-induced aggregation and r-ADP-agg were 794 ± 239 AU*min, 297 ± 153 AU*min and 37 ± 14%, respectively. While ADP- and TRAP-induced platelet aggregation correlated significantly with platelet count (ADP: r = 0.302; p<0.001; TRAP: r = 0.509 p<0.001), r-ADP-agg values did not (r = -0.003; p = 0.960). These findings were unaltered in multivariate analyses adjusting for a range of factors potentially influencing platelet aggregation. The presence of an acute coronary syndrome and body weight were found to correlate with both ADP-induced platelet aggregation and r-ADP-agg.

conclusionThe ratio of ADP- to TRAP-induced platelet aggregation quantifies P2Y12-dependent platelet inhibition independently of the platelet count in contrast to conventional ADP-induced aggregation. Furthermore, r-ADP-agg was associated with the presence of an acute coronary syndrome and body weight as well as ADP-induced aggregation. Thus, the r-ADP-agg is a more valid reflecting platelet aggregation and potentially prognosis after coronary stent-implantation in P2Y12-mediated HPR than conventional ADP-induced platelet aggregation.

Indexed as

Adenosine DiphosphateAgedBiomarkersFemaleHumansMaleOligopeptidesPlatelet AggregationPlatelet CountReceptors, Purinergic P2Y12Regression AnalysisAdenosine DiphosphateBiomarkersOligopeptidesReceptors, Purinergic P2Y12thrombin receptor-activating peptide SFLLRNPNDKY

Identifiers

PMID26885820
PMCPMC4757031
OpenAlexW2284346804

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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.