Publication: Cinacalcet may improve oxidative DNA damage in maintenance hemodialysis patients: an observational study
| dc.contributor.author | AŞICIOĞLU, EBRU | |
| dc.contributor.author | ARIKAN, İZZET HAKKI | |
| dc.contributor.authors | Ari, Elif; Kaya, Yuksel; Demir, Halit; Asicioglu, Ebru; Eren, Zehra; Celik, Eray; Arikan, Hakki | |
| dc.date.accessioned | 2022-03-13T12:46:40Z | |
| dc.date.accessioned | 2026-01-10T20:45:46Z | |
| dc.date.available | 2022-03-13T12:46:40Z | |
| dc.date.issued | 2014 | |
| dc.description.abstract | Oxidative stress is accepted as a non-classical cardiovascular risk factor in patients on maintenance hemodialysis (HD). The aim of this study was to evaluate the impact of cinacalcet on oxidative stress biomarkers, oxidative DNA damage (8-hydroxy-2'-deoxyguanosine/deoxyguanosine), endothelial function (FMD %) and carotid artery intima-media thickness (CIMT) in HD patients. Forty-two chronic HD patients with secondary hyperparathyroidism undergoing 60 mg/day cinacalcet treatment with a follow-up of 6 months and 38 age- and sex-matched healthy individuals were included in this prospective study. Plasma malondialdehyde (MDA) levels and 8-hydroxy-2'-deoxyguanosine/deoxyguanosine ratio (8-OHdG/dG) were determined as oxidative stress markers. Superoxide dismutase (SOD), paraoxonase (PON), catalase (CAT), carbonic anhydrase (CAN) and glutathione peroxidase (GPx) activities were measured as antioxidants. FMD % and CIMT were assessed by ultrasonography. MDA levels were decreased; SOD, PON, CAT, CAN and GPx activities were increased after 6 months of cinacalcet treatment in HD patients. Although CIMT remained stabile, there was a significant improvement in FMD % as well as a notable reduction trend in 8-OHdG/dG ratio after 6 months of treatment. Our data have demonstrated that cinacalcet improves oxidative stress, genomic damage, endothelial function and increases antioxidant protection in HD patients after 6 months of treatment. | |
| dc.identifier.doi | 10.1007/s11255-014-0723-0 | |
| dc.identifier.eissn | 1573-2584 | |
| dc.identifier.issn | 0301-1623 | |
| dc.identifier.pubmed | 24811568 | |
| dc.identifier.uri | https://hdl.handle.net/11424/237960 | |
| dc.identifier.wos | WOS:000341430800025 | |
| dc.language.iso | eng | |
| dc.publisher | SPRINGER | |
| dc.relation.ispartof | INTERNATIONAL UROLOGY AND NEPHROLOGY | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.subject | Cinacalcet | |
| dc.subject | DNA damage | |
| dc.subject | Hemodialysis | |
| dc.subject | Oxidative stress | |
| dc.subject | CHRONIC-RENAL-FAILURE | |
| dc.subject | INTIMA-MEDIA THICKNESS | |
| dc.subject | ENDOTHELIAL FUNCTION | |
| dc.subject | SECONDARY HYPERPARATHYROIDISM | |
| dc.subject | CARDIOVASCULAR-DISEASE | |
| dc.subject | ALL-CAUSE | |
| dc.subject | RISK | |
| dc.subject | ATHEROSCLEROSIS | |
| dc.subject | DYSFUNCTION | |
| dc.subject | MORTALITY | |
| dc.title | Cinacalcet may improve oxidative DNA damage in maintenance hemodialysis patients: an observational study | |
| dc.type | article | |
| dspace.entity.type | Publication | |
| oaire.citation.endPage | 1849 | |
| oaire.citation.issue | 9 | |
| oaire.citation.startPage | 1843 | |
| oaire.citation.title | INTERNATIONAL UROLOGY AND NEPHROLOGY | |
| oaire.citation.volume | 46 |
