Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/10475
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dc.contributor.authorOrdu, S.-
dc.contributor.authorYildiz, B.S.-
dc.contributor.authorAlihanoglu, Y.I.-
dc.contributor.authorOzsoy, A.-
dc.contributor.authorTosun, M.-
dc.contributor.authorEvrengül, Harun-
dc.contributor.authorKaftan, Havane Asuman-
dc.date.accessioned2019-08-16T13:19:14Z-
dc.date.available2019-08-16T13:19:14Z-
dc.date.issued2015-
dc.identifier.issn1897-5593-
dc.identifier.urihttps://hdl.handle.net/11499/10475-
dc.identifier.urihttps://doi.org/10.5603/CJ.a2015.0012-
dc.description.abstractBackground: 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.isoenen_US
dc.publisherVia Medicaen_US
dc.relation.ispartofCardiology Journalen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectCA-125en_US
dc.subjectCystatin-Cen_US
dc.subjectIvabradineen_US
dc.subjectNT-proBNPen_US
dc.subjectSystolic heart failureen_US
dc.subjectbiochemical markeren_US
dc.subjectbrain natriuretic peptideen_US
dc.subjectCA 125 antigenen_US
dc.subjectcreatinineen_US
dc.subjectcystatin Cen_US
dc.subjectivabradineen_US
dc.subjectbenzazepine derivativeen_US
dc.subjectbiological markeren_US
dc.subjectcardiovascular agenten_US
dc.subjectCST3 protein, humanen_US
dc.subjectpeptide fragmenten_US
dc.subjectpro-brain natriuretic peptide (1-76)en_US
dc.subjectadulten_US
dc.subjectArticleen_US
dc.subjectblood analysisen_US
dc.subjectclinical assessmenten_US
dc.subjectdemographyen_US
dc.subjectdisease associationen_US
dc.subjectfollow upen_US
dc.subjectglomerulus filtration rateen_US
dc.subjectheart failureen_US
dc.subjectheart left ventricle ejection fractionen_US
dc.subjectheart rateen_US
dc.subjecthumanen_US
dc.subjectmajor clinical studyen_US
dc.subjectmaleen_US
dc.subjectmedical record reviewen_US
dc.subjectNew York Heart Association classen_US
dc.subjectprospective studyen_US
dc.subjectquantitative analysisen_US
dc.subjecttreatment outcomeen_US
dc.subjectageden_US
dc.subjectblooden_US
dc.subjectcontrolled studyen_US
dc.subjectdown regulationen_US
dc.subjectdrug effectsen_US
dc.subjectfemaleen_US
dc.subjectHeart Failure, Systolicen_US
dc.subjectheart left ventricle functionen_US
dc.subjectheart stroke volumeen_US
dc.subjectmiddle ageden_US
dc.subjectpathophysiologyen_US
dc.subjectrandomized controlled trialen_US
dc.subjecttime factoren_US
dc.subjectTurkeyen_US
dc.subjectAgeden_US
dc.subjectBenzazepinesen_US
dc.subjectBiomarkersen_US
dc.subjectCA-125 Antigenen_US
dc.subjectCardiovascular Agentsen_US
dc.subjectCystatin Cen_US
dc.subjectDown-Regulationen_US
dc.subjectFemaleen_US
dc.subjectHeart Rateen_US
dc.subjectHumansen_US
dc.subjectMaleen_US
dc.subjectMiddle Ageden_US
dc.subjectNatriuretic Peptide, Brainen_US
dc.subjectPeptide Fragmentsen_US
dc.subjectProspective Studiesen_US
dc.subjectStroke Volumeen_US
dc.subjectTime Factorsen_US
dc.subjectTreatment Outcomeen_US
dc.subjectVentricular Function, Leften_US
dc.titleEffects of ivabradine therapy on heart failure biomarkersen_US
dc.typeArticleen_US
dc.identifier.volume22en_US
dc.identifier.issue5en_US
dc.identifier.startpage501-
dc.identifier.startpage501en_US
dc.identifier.endpage509en_US
dc.identifier.doi10.5603/CJ.a2015.0012-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.pmid25733317en_US
dc.identifier.scopus2-s2.0-84944116507en_US
dc.identifier.wosWOS:000364706900007en_US
dc.identifier.scopusqualityQ2-
dc.ownerPamukkale University-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextWith Fulltext-
item.grantfulltextopen-
crisitem.author.dept10.10. Computer Engineering-
crisitem.author.dept14.02. Internal Medicine-
crisitem.author.dept14.02. 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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