Inflammatory state does not affect the antiplatelet efficacy of potent P2Y12 inhibitors in ACS
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作者:
Biesinger, Benedikt S.
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Med Univ Vienna, Dept Internal Med 2, Div Cardiol, Vienna, AustriaMed Univ Vienna, Dept Internal Med 2, Div Cardiol, Vienna, Austria
Biesinger, Benedikt S.
[1
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Gasecka, Aleksandra
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Perkmann, Thomas
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Med Univ Vienna, Dept Lab Med, Vienna, AustriaMed Univ Vienna, Dept Internal Med 2, Div Cardiol, Vienna, Austria
Perkmann, Thomas
[3
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Wojta, Johann
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Lesiak, Maciej
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Poznan Univ Med Sci, Dept Cardiol 1, Pozna, PolandMed Univ Vienna, Dept Internal Med 2, Div Cardiol, Vienna, Austria
Lesiak, Maciej
[4
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Grygier, Marek
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Poznan Univ Med Sci, Dept Cardiol 1, Pozna, PolandMed Univ Vienna, Dept Internal Med 2, Div Cardiol, Vienna, Austria
Grygier, Marek
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Eyileten, Ceren
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Ctr Preclin Res & Technol, Dept Expt & Clin Pharmacol, Warsaw, PolandMed Univ Vienna, Dept Internal Med 2, Div Cardiol, Vienna, Austria
Eyileten, Ceren
[5
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Postula, Marek
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Med Univ Warsaw, Chair & Dept Cardiol 1, Warsaw, Poland
Ctr Preclin Res & Technol, Dept Expt & Clin Pharmacol, Warsaw, PolandMed Univ Vienna, Dept Internal Med 2, Div Cardiol, Vienna, Austria
Postula, Marek
[2
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Filipiak, Krzysztof J.
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Med Univ Warsaw, Chair & Dept Cardiol 1, Warsaw, PolandMed Univ Vienna, Dept Internal Med 2, Div Cardiol, Vienna, Austria
Filipiak, Krzysztof J.
[2
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Toma, Aurel
[1
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Hengstenberg, Christian
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Med Univ Vienna, Dept Internal Med 2, Div Cardiol, Vienna, AustriaMed Univ Vienna, Dept Internal Med 2, Div Cardiol, Vienna, Austria
Hengstenberg, Christian
[1
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Siller-Matula, Jolanta M.
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Med Univ Vienna, Dept Internal Med 2, Div Cardiol, Vienna, Austria
Ctr Preclin Res & Technol, Dept Expt & Clin Pharmacol, Warsaw, PolandMed Univ Vienna, Dept Internal Med 2, Div Cardiol, Vienna, Austria
Siller-Matula, Jolanta M.
[1
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机构:
[1] Med Univ Vienna, Dept Internal Med 2, Div Cardiol, Vienna, Austria
Inflammation leads to atherosclerosis and acute coronary syndromes (ACS). We performed a prospective, observational study to assess association between the concentrations of inflammatory markers (high sensitivity C-reactive protein, hsCRP; high sensitivity interleukin6, hsIL-6; soluble CD40 ligand, sCD40 L) and platelet reactivity in 338 patients with ACS treated with ticagrelor and prasugrel. We also assessed whether hsCRP, hsIL-6, and sCD40 L are associated with standard inflammatory markers (white blood cell [WBC] and fibrinogen), and whether they differ according to patient diabetic status and pre-treatment with statins. Concentrations of hsCRP and concentrations of hsIL-6 and sCD40 L were assessed using turbidimetric assay and enzyme-linked immunosorbent assay, respectively. Platelet reactivity was measured using multiple electrode aggregometry. There was only a weak inverse correlation between hsIL-6 and platelet reactivity (r <=-0.125). In contrast, concentration of hsIL6 and hsCRP positively correlated with WBC count and fibrinogen (r >= 0.199). Insulin-dependent diabetes mellitus (IDDM) was associated with higher concentration of hsIL-6 (p= .014), whereas pre-treatment with statins - with lower concentration of hsIL-6 (p= .035). In conclusion, inflammatory state does not affect the antiplatelet efficacy of potent P2Y12 inhibitors in the acute phase of ACS, confirming the safety and efficacy of potent P2Y12 inhibitors in patients with a high inflammatory burden.
机构:
Univ Milan, Osped San Paolo, Unita Med 3, Dipartimento Med Chirurg & Odontoiatria, I-20142 Milan, ItalyUniv Milan, Osped San Paolo, Unita Med 3, Dipartimento Med Chirurg & Odontoiatria, I-20142 Milan, Italy