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https://hdl.handle.net/11499/10475
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DC Field | Value | Language |
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dc.contributor.author | Ordu, S. | - |
dc.contributor.author | Yildiz, B.S. | - |
dc.contributor.author | Alihanoglu, Y.I. | - |
dc.contributor.author | Ozsoy, A. | - |
dc.contributor.author | Tosun, M. | - |
dc.contributor.author | Evrengül, Harun | - |
dc.contributor.author | Kaftan, Havane Asuman | - |
dc.date.accessioned | 2019-08-16T13:19:14Z | - |
dc.date.available | 2019-08-16T13:19:14Z | - |
dc.date.issued | 2015 | - |
dc.identifier.issn | 1897-5593 | - |
dc.identifier.uri | https://hdl.handle.net/11499/10475 | - |
dc.identifier.uri | https://doi.org/10.5603/CJ.a2015.0012 | - |
dc.description.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. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Via Medica | en_US |
dc.relation.ispartof | Cardiology Journal | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | CA-125 | en_US |
dc.subject | Cystatin-C | en_US |
dc.subject | Ivabradine | en_US |
dc.subject | NT-proBNP | en_US |
dc.subject | Systolic heart failure | en_US |
dc.subject | biochemical marker | en_US |
dc.subject | brain natriuretic peptide | en_US |
dc.subject | CA 125 antigen | en_US |
dc.subject | creatinine | en_US |
dc.subject | cystatin C | en_US |
dc.subject | ivabradine | en_US |
dc.subject | benzazepine derivative | en_US |
dc.subject | biological marker | en_US |
dc.subject | cardiovascular agent | en_US |
dc.subject | CST3 protein, human | en_US |
dc.subject | peptide fragment | en_US |
dc.subject | pro-brain natriuretic peptide (1-76) | en_US |
dc.subject | adult | en_US |
dc.subject | Article | en_US |
dc.subject | blood analysis | en_US |
dc.subject | clinical assessment | en_US |
dc.subject | demography | en_US |
dc.subject | disease association | en_US |
dc.subject | follow up | en_US |
dc.subject | glomerulus filtration rate | en_US |
dc.subject | heart failure | en_US |
dc.subject | heart left ventricle ejection fraction | en_US |
dc.subject | heart rate | en_US |
dc.subject | human | en_US |
dc.subject | major clinical study | en_US |
dc.subject | male | en_US |
dc.subject | medical record review | en_US |
dc.subject | New York Heart Association class | en_US |
dc.subject | prospective study | en_US |
dc.subject | quantitative analysis | en_US |
dc.subject | treatment outcome | en_US |
dc.subject | aged | en_US |
dc.subject | blood | en_US |
dc.subject | controlled study | en_US |
dc.subject | down regulation | en_US |
dc.subject | drug effects | en_US |
dc.subject | female | en_US |
dc.subject | Heart Failure, Systolic | en_US |
dc.subject | heart left ventricle function | en_US |
dc.subject | heart stroke volume | en_US |
dc.subject | middle aged | en_US |
dc.subject | pathophysiology | en_US |
dc.subject | randomized controlled trial | en_US |
dc.subject | time factor | en_US |
dc.subject | Turkey | en_US |
dc.subject | Aged | en_US |
dc.subject | Benzazepines | en_US |
dc.subject | Biomarkers | en_US |
dc.subject | CA-125 Antigen | en_US |
dc.subject | Cardiovascular Agents | en_US |
dc.subject | Cystatin C | en_US |
dc.subject | Down-Regulation | en_US |
dc.subject | Female | en_US |
dc.subject | Heart Rate | en_US |
dc.subject | Humans | en_US |
dc.subject | Male | en_US |
dc.subject | Middle Aged | en_US |
dc.subject | Natriuretic Peptide, Brain | en_US |
dc.subject | Peptide Fragments | en_US |
dc.subject | Prospective Studies | en_US |
dc.subject | Stroke Volume | en_US |
dc.subject | Time Factors | en_US |
dc.subject | Treatment Outcome | en_US |
dc.subject | Ventricular Function, Left | en_US |
dc.title | Effects of ivabradine therapy on heart failure biomarkers | en_US |
dc.type | Article | en_US |
dc.identifier.volume | 22 | en_US |
dc.identifier.issue | 5 | en_US |
dc.identifier.startpage | 501 | - |
dc.identifier.startpage | 501 | en_US |
dc.identifier.endpage | 509 | en_US |
dc.identifier.doi | 10.5603/CJ.a2015.0012 | - |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.identifier.pmid | 25733317 | en_US |
dc.identifier.scopus | 2-s2.0-84944116507 | en_US |
dc.identifier.wos | WOS:000364706900007 | en_US |
dc.identifier.scopusquality | Q2 | - |
dc.owner | Pamukkale University | - |
item.cerifentitytype | Publications | - |
item.languageiso639-1 | en | - |
item.openairetype | Article | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.fulltext | With Fulltext | - |
item.grantfulltext | open | - |
crisitem.author.dept | 10.10. Computer Engineering | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
crisitem.author.dept | 14.02. Internal Medicine | - |
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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Evrengül Kaftan.pdf | 242.25 kB | Adobe PDF | View/Open |
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