Evidence map›Paper›PMID 30768153›Full record

ArticleCardiovascular research2019

Association of the coronary artery disease risk gene GUCY1A3 with ischaemic events after coronary intervention.

Thorsten Kessler, Bernhard Wolf, Niclas Eriksson, Daniel Kofink, Bakhtawar K Mahmoodi, Himanshu Rai, Vinicius Tragante, Axel Åkerblom, Richard C Becker, Isabell Bernlochner and 21 more

Open access · bronzeAbstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Cardiovascular research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 11% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. The Impact of Single Nucleotide Polymorphisms and Other Mechanisms on Aspirin Resistance.Cardiovascular & hematological disorders drug targets · 2025
    Review
  5. Genetic associations of cardiovascular risk genes in European patients with coronary artery spasm.Clinical research in cardiology : official journal of the German Cardiac Society · 2024
    Article
  6. Article
  7. Review
  8. Biomedicines · 2022
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

31 authors at 14 institutions in 5 countries.

Thorsten KesslerKlinik für Herz- und Kreislauferkrankungen, Deutsches Herzzentrum München, Technische Universität München, Munich, Germany.
Bernhard WolfKlinik für Herz- und Kreislauferkrankungen, Deutsches Herzzentrum München, Technische Universität München, Munich, Germany.
Niclas ErikssonUppsala Clinical Research Center, Uppsala University, Uppsala, Sweden.
Daniel KofinkDivision of Heart and Lungs, Department of Cardiology, University Medical Center Utrecht, University of Utrecht, The Netherlands.
Bakhtawar K MahmoodiCardiology Department, St. Antonius Hospital, Nieuwegein, The Netherlands.
Himanshu RaiKlinik für Herz- und Kreislauferkrankungen, Deutsches Herzzentrum München, Technische Universität München, Munich, Germany.
Vinicius TraganteDivision of Heart and Lungs, Department of Cardiology, University Medical Center Utrecht, University of Utrecht, The Netherlands.
Axel ÅkerblomUppsala Clinical Research Center, Uppsala University, Uppsala, Sweden.
Richard C BeckerDivision of Cardiovascular Health and Disease, University of Cincinnati Heart, Lung & Vascular Institute, Cincinnati, OH, USA.
Isabell BernlochnerI. Medizinische Klinik und Poliklinik, Klinikum rechts der Isar, Technische Universität München, Munich, Germany.
Roman BoppKlinik für Herz- und Kreislauferkrankungen, Deutsches Herzzentrum München, Technische Universität München, Munich, Germany.
Stefan JamesUppsala Clinical Research Center, Uppsala University, Uppsala, Sweden.
Hugo A KatusInnere Medizin III: Kardiologie, Angiologie und Pneumologie, Universität Heidelberg, and DZHK e.V., Partner Site Heidelberg, Heidelberg, Germany.
Katharina MayerKlinik für Herz- und Kreislauferkrankungen, Deutsches Herzzentrum München, Technische Universität München, Munich, Germany.
Matthias MunzInstitute for Cardiogenetics, University of Lübeck, Lübeck, Germany.
Francesco NordioTIMI Study Group, Brigham and Women's Hospital, Boston, MA, USA.
Michelle L O'DonoghueTIMI Study Group, Brigham and Women's Hospital, Boston, MA, USA.
Hendrik B SagerKlinik für Herz- und Kreislauferkrankungen, Deutsches Herzzentrum München, Technische Universität München, Munich, Germany.
Dirk SibbingDeutsches Zentrum für Herz-Kreislauf-Forschung (DZHK) e.V., Partner Site Munich Heart Alliance, Munich, Germany.
Linda SolakovKlinik für Herz- und Kreislauferkrankungen, Deutsches Herzzentrum München, Technische Universität München, Munich, Germany.
Robert F StoreyDepartment of Infection, Immunity & Cardiovascular Disease, University of Sheffield, Sheffield, UK.
Jana WobstKlinik für Herz- und Kreislauferkrankungen, Deutsches Herzzentrum München, Technische Universität München, Munich, Germany.
Folkert W AsselbergsDivision of Heart and Lungs, Department of Cardiology, University Medical Center Utrecht, University of Utrecht, The Netherlands.
Robert A ByrneKlinik für Herz- und Kreislauferkrankungen, Deutsches Herzzentrum München, Technische Universität München, Munich, Germany.
Jeanette ErdmannInstitute for Cardiogenetics, University of Lübeck, Lübeck, Germany.
Wolfgang KoenigKlinik für Herz- und Kreislauferkrankungen, Deutsches Herzzentrum München, Technische Universität München, Munich, Germany.
Karl-Ludwig LaugwitzDeutsches Zentrum für Herz-Kreislauf-Forschung (DZHK) e.V., Partner Site Munich Heart Alliance, Munich, Germany.
Jurrien M Ten BergCardiology Department, St. Antonius Hospital, Nieuwegein, The Netherlands.
Lars WallentinUppsala Clinical Research Center, Uppsala University, Uppsala, Sweden.
Adnan KastratiKlinik für Herz- und Kreislauferkrankungen, Deutsches Herzzentrum München, Technische Universität München, Munich, Germany.
Heribert SchunkertKlinik für Herz- und Kreislauferkrankungen, Deutsches Herzzentrum München, Technische Universität München, Munich, Germany.
Deutsches Herzzentrum München · DETechnical University of Munich · DEUppsala University · SEBrigham and Women's Hospital · USGerman Centre for Cardiovascular Research · DESt. Antonius Ziekenhuis · NLUtrecht University · NLCharité - Universitätsmedizin Berlin · DEHeidelberg University · DELudwig-Maximilians-Universität München · DEUniversity College London · GBUniversity of Cincinnati · USUniversity of Lübeck · DEUniversity of Sheffield · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimA common genetic variant at the GUCY1A3 coronary artery disease locus has been shown to influence platelet aggregation. The risk of ischaemic events including stent thrombosis varies with the efficacy of aspirin to inhibit platelet reactivity. This study sought to investigate whether homozygous GUCY1A3 (rs7692387) risk allele carriers display higher on-aspirin platelet reactivity and risk of ischaemic events early after coronary intervention. METHODS AND

resultsThe association of GUCY1A3 genotype and on-aspirin platelet reactivity was analysed in the genetics substudy of the ISAR-ASPI registry (n = 1678) using impedance aggregometry. The clinical outcome cardiovascular death or stent thrombosis within 30 days after stenting was investigated in a meta-analysis of substudies of the ISAR-ASPI registry, the PLATO trial (n = 3236), and the Utrecht Coronary Biobank (n = 1003) comprising a total 5917 patients. Homozygous GUCY1A3 risk allele carriers (GG) displayed increased on-aspirin platelet reactivity compared with non-risk allele (AA/AG) carriers [150 (interquartile range 91-209) vs. 134 (85-194) AU⋅min, P < 0.01]. More homozygous risk allele carriers, compared with non-risk allele carriers, were assigned to the high-risk group for ischaemic events (>203 AU⋅min; 29.5 vs. 24.2%, P = 0.02). Homozygous risk allele carriers were also at higher risk for cardiovascular death or stent thrombosis (hazard ratio 1.70, 95% confidence interval 1.08-2.68; P = 0.02). Bleeding risk was not altered.

conclusionWe conclude that homozygous GUCY1A3 risk allele carriers are at increased risk of cardiovascular death or stent thrombosis within 30 days after coronary stenting, likely due to higher on-aspirin platelet reactivity. Whether GUCY1A3 genotype helps to tailor antiplatelet treatment remains to be investigated.

Indexed as

Polymorphism, Single NucleotideAgedAged, 80 and overAspirinClinical Trials as TopicClopidogrelCoronary Artery DiseaseCoronary RestenosisCoronary ThrombosisDrug ResistanceEuropeFemaleGenetic Association StudiesGenetic Predisposition to DiseaseHemorrhageHomozygoteAspirinClopidogrelGUCY1A1 protein, humanPlatelet Aggregation InhibitorsSoluble Guanylyl CyclaseGenetic variationGenome-wide association studiesOn-aspirin platelet reactivityPlatelet aggregationStent thrombosis

Identifiers

PMID30768153
OpenAlexW2911805233

What OpenQuestion holds

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Read underepoch 390

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.