Effects of G-CSF on systemic inflammation, coagulation and platelet activation in patients with acute myocardial infarction |
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Authors: | Steppich Birgit A Demetz Gabriele Schulz Stefanie von Wedel Jasper Pogatsa-Murray Giesela Braun Siegmund-Lorenz Stein Andreas Kastrati Adnan Schömig Albert Ott Ilka |
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Affiliation: | a 1. Medizinische Klinik, Klinikums rechts der Isar der Technischen Universität München, Ismaninger Str 22, 81675 München, Germanyb Deutsches Herzzentrum der Technischen Universität München, Lazarettstr, 36, 80636 München, Germanyc Insitut für Laboratoriumsmedizin des Deutschen Herzzentrums der Technischen Universität München, Lazarettstr, 36, 80636 München, Germany |
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Abstract: | IntroductionIn the prospective, randomised, double-blind, placebo-controlled Regenerate Vital Myocardium by Vigorous Activation of Bone Marrow Stem Cells (REVIVAL)-2 trial patients with acute myocardial infarction (AMI) and successful mechanical reperfusion received granulocyte-colony stimulating factor (G-CSF, 10 μg/kg KG s.c.) or placebo for 5 days. Aim of this substudy was to assess the impact of G-CSF on systemic inflammatory and procoagulant responses and platelet activation.Methods and ResultsBefore and five days after G-CSF (n = 56) or placebo (n = 58) circulating cytokine concentrations of interleukin (IL)-1ß, IL-6, IL-8, IL-10, IL-12 and Tumor-Necrosis Factor-α (TNF-α? were measured. Prothrombin fragment F1 + 2 and Tissue Factor activity served as a measure for activated coagulation. Platelet activation was characterized by cell surface expression of the activated fibrinogen receptor (PAC-1), P-selectin and CD40L by flow cytometry. Administration of G-CSF was associated with elevated TNF-α and CRP?concentrations compared to the placebo group after 5 days. Other cytokines (IL-1ß, IL-6, IL-8, IL-10, IL-12) were comparable after treatment with G-SCF or placebo. Similarly, circulating prothrombin fragments F1 + 2, TF activity and platelet activation did not differ in both groups.ConclusionTreatment with G-CSF in patients with AMI was associated with enhanced proinflammatory TNF-α and CRP levels but no activation of coagulation. |
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