Please use this identifier to cite or link to this item: 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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