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https://hdl.handle.net/11499/10475
Title: | Effects of ivabradine therapy on heart failure biomarkers | Authors: | Ordu, S. Yildiz, B.S. Alihanoglu, Y.I. Ozsoy, A. Tosun, M. Evrengül, Harun Kaftan, Havane Asuman |
Keywords: | CA-125 Cystatin-C Ivabradine NT-proBNP Systolic heart failure biochemical marker brain natriuretic peptide CA 125 antigen creatinine cystatin C ivabradine benzazepine derivative biological marker cardiovascular agent CST3 protein, human peptide fragment pro-brain natriuretic peptide (1-76) adult Article blood analysis clinical assessment demography disease association follow up glomerulus filtration rate heart failure heart left ventricle ejection fraction heart rate human major clinical study male medical record review New York Heart Association class prospective study quantitative analysis treatment outcome aged blood controlled study down regulation drug effects female Heart Failure, Systolic heart left ventricle function heart stroke volume middle aged pathophysiology randomized controlled trial time factor Turkey Aged Benzazepines Biomarkers CA-125 Antigen Cardiovascular Agents Cystatin C Down-Regulation Female Heart Rate Humans Male Middle Aged Natriuretic Peptide, Brain Peptide Fragments Prospective Studies Stroke Volume Time Factors Treatment Outcome Ventricular Function, Left |
Publisher: | Via Medica | Abstract: | Background: Heart rate (HR) reduction is associated with improved outcomes in patients with heart failure (HF) and biomarkers can be a valuable diagnostic tool in HF management. The primary aim of our study was to evaluate the short-term (6 months) effect of ivabradine on N-terminal pro B-type natriuretic peptide (NT-proBNP), CA-125, and cystatin-C values in systolic HF outpatients, and secondary aim was to determine the relationship between baseline HR and the NT-proBNP, CA-125, cystatin-C, and clinical status variation with ivabradine therapy. Methods: Ninety-eight patients (mean age: 65.81 ± 10.20 years; 33 men), left ventricular ejection fraction < 35% with Simpson method, New York Heart Association (NYHA) class II–III, sinus rhythm and resting HR > 70/min, optimally treated before the study were included. Among them, two matched groups were formed: the ivabradine group and the control group. Patients received ivabradine with an average (range of 10–15) mg/day during 6 months of follow-up. Blood samples for NT-proBNP, CA-125, and cystatin-C were taken at baseline and at the end of a 6-month follow-up in both groups. Results: There was a significant decrease in NYHA class in the ivabradine group (2.67 ± ± 0.47 vs. 1.85 ± 0.61, p < 0.001). When ivabradine and control groups were compared, a significant difference was also found in NHYA class 6 months later (p = 0.013). A significant decrease was found in HR in the ivabradine and control groups (84.10 ± 8.76 vs. 68.36 ± ± 8.32 bpm, p = 0.001; 84.51 ± 10 vs. 80.40 ± 8.3 bpm, p = 0.001). When both groups were compared, a significant difference was also found in HR after 6 months (p = 0.001). A significant decrease was found in cystatin-C (2.10 ± 0.73 vs. 1.50 ± 0.44 mg/L, p < 0.001), CA-125 (30.09 ± 21.08 vs. 13.22 ± 8.51 U/mL, p < 0.001), and NT-proBNP (1,353.02 ± 1,453.77 vs. 717.81 ± 834.76 pg/mL, p < 0.001) in the ivabradine group. When ivabradine and control groups were compared after 6 months, a significant decrease was found in all HF parameters (respectively; cystatin-C: p = 0.001, CA-125: p = 0.001, NT-proBNP: p = 0.001). Creatinine level was significantly decreased and glomerular filtration rate (GFR) was significantly increased in the ivabradine group (1.02 ± 0.26 vs. 0.86 ± 0.17, creatinine: p = 0.001; 79.26 ± 18.58 vs. 92.48 ± 19.88, GFR: p = 0.001). There was no significant correlation between NYHA classes (before and after ivabradine therapy) and biochemical markers, or HR. Conclusions: In the outpatients with systolic HF, persistent resting HF > 70/min with optimal medical therapy, the NT-proBNP, CA-125, and cystatin-C reductions were obtained with ivabradine treatment. Measurement of NT-proBNP, CA-125, and cystatin-C may prove to be useful in biomarker panels evaluating ivabradine therapy response in HF patients. © 2015 Via Medica. | URI: | https://hdl.handle.net/11499/10475 https://doi.org/10.5603/CJ.a2015.0012 |
ISSN: | 1897-5593 |
Appears in Collections: | PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection Tıp Fakültesi Koleksiyonu WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection |
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