Literature DB >> 18585516

Platelet collagen receptor glycoprotein VI as a possible novel indicator for the acute coronary syndrome.

Boris Bigalke1, Tobias Geisler, Konstantinos Stellos, Harald Langer, Karin Daub, Elisabeth Kremmer, Peter Seizer, Andreas E May, Stephan Lindemann, Meinrad Gawaz.   

Abstract

BACKGROUND: Platelet collagen receptor glycoprotein VI (GPVI) plays a critical role in acute coronary thrombosis. This prospective study examined the predictive value of GPVI for acute coronary syndromes (ACS) in a large consecutive group of patients with symptomatic coronary artery disease to identify the high-risk cohort with imminent coronary events.
METHODS: We evaluated 1,003 patients with symptomatic coronary artery disease, verified by coronary angiography, and determined the surface expression of GPVI using flow cytometry. In a subgroup of 471 patients, who were treated with aspirin plus clopidogrel for coronary stenting, adenosine disphosphate (20 micromol/L)-induced platelet aggregation was evaluated.
RESULTS: Patients with ACS (n = 485) showed a significantly enhanced GPVI expression compared to patients with stable angina pectoris (SAP; n = 518) (mean fluorescence intensity for ACS 19.8 +/- 5.9; SAP 18.7 +/- 8.5, P = .01). Patients with elevated GPVI levels on admission (GPVI cutoff value > or =18.6 mean fluorescence intensity) had a 1.4-fold relative risk for ACS. Logistic regression analysis showed that an elevated platelet GPVI level may indicate ACS independent of biomarkers of myocardial necrosis including troponin, creatine kinase, and creatine kinase-MB. Patients with increased platelet activation (GPVI expression level > or =18.6) showed significant enhanced residual platelet aggregation despite dual antiplatelet therapy compared to patients with low GPVI levels (P = .028).
CONCLUSIONS: Surface expression of GPVI is enhanced in patients with ACS and indicates an imminent acute coronary event before irreversible myocardial necrosis is evident. High GPVI levels are associated with increased residual platelet aggregation despite antiplatelet therapy. Therefore, GPVI is useful to identify the subgroup of patients with a high risk for coronary stent thrombosis and thromboischemic events.

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Year:  2008        PMID: 18585516     DOI: 10.1016/j.ahj.2008.02.010

Source DB:  PubMed          Journal:  Am Heart J        ISSN: 0002-8703            Impact factor:   4.749


  5 in total

Review 1.  A review of antiplatelet drugs, coronary artery diseases and cardiopulmonary bypass.

Authors:  Yajun Ren; Kirti Patel; Terry Crane
Journal:  J Extra Corpor Technol       Date:  2010-06

2.  Glycoprotein VI as a prognostic biomarker for cardiovascular death in patients with symptomatic coronary artery disease.

Authors:  Boris Bigalke; Konstantinos Stellos; Tobias Geisler; Stephan Lindemann; Andreas E May; Meinrad Gawaz
Journal:  Clin Res Cardiol       Date:  2010-01-05       Impact factor: 5.460

3.  Alteration of platelet GPVI signaling in ST-elevation myocardial infarction patients demonstrated by a combination of proteomic, biochemical, and functional approaches.

Authors:  Paula Vélez; Raymundo Ocaranza-Sánchez; Diego López-Otero; Lilian Grigorian-Shamagian; Isaac Rosa; Esteban Guitián; José María García-Acuña; José Ramón González-Juanatey; Ángel García
Journal:  Sci Rep       Date:  2016-12-22       Impact factor: 4.379

4.  Prenatal lead exposure is associated with decreased cord blood DNA methylation of the glycoprotein VI gene involved in platelet activation and thrombus formation.

Authors:  Karin Engström; Filip Rydbeck; Maria Kippler; Tomasz K Wojdacz; Shams Arifeen; Marie Vahter; Karin Broberg
Journal:  Environ Epigenet       Date:  2015-11-27

5.  Platelet Carcinoembryonic Antigen Cell Adhesion Molecule 5 (CEACAM5) as a Possible Novel Diagnostic Tool for Evaluation of Acute Coronary Syndrome.

Authors:  Wen Wan; Yujia Ye; Huawei Wang; Longjun Li; Yajuan Gu; Lai Yang; Lihong Yang; Han Liu; Chao Meng; Deng Li; Zhe Wang; Zhaohui Meng
Journal:  Med Sci Monit       Date:  2019-12-22
  5 in total

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