Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/7325
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dc.contributor.authorDursun, Belda.-
dc.contributor.authorDursun, E.-
dc.contributor.authorCapraz, I.-
dc.contributor.authorOzben, T.-
dc.contributor.authorApaydin, A.-
dc.contributor.authorSuleymanlar, G.-
dc.date.accessioned2019-08-16T12:19:53Z
dc.date.available2019-08-16T12:19:53Z
dc.date.issued2008-
dc.identifier.issn1708-8267-
dc.identifier.urihttps://hdl.handle.net/11499/7325-
dc.identifier.urihttps://doi.org/10.2310/JIM.0b013e3181641ce3-
dc.description.abstractBackground: Oxidative stress is a new risk factor for atherosclerosis. Increased oxidative stress in hemodialysis (HD) patients may arise from uremia-associated metabolic/ humoral abnormalities and bioincompatibility of dialysis. Patients with diabetes mellitus (DM) may be subject to an additional risk. Respective influences of uremia, diabetes, and HD duration in accelerated atherosclerosisa nd oxidative stress have not been clarified yet. Methods: The study was performed on 24 nondiabetic HD patients, 23 diabetic HD patients, 20 stages 3 to 4 chronic kidney disease patients, and 21 diabetic patients without overt nephropathy. Carotid intima-media thickness, a surrogate of atherosclerosis, was measured by high-resolution B-mode ultrasonography. Oxidant status was determined by lipid peroxidation as expressed by malondialdehyde (MDA); antioxidant status was determined by superoxide dismutase, catalase, glutathione peroxidase, reduced intracellular glutathione, and plasma thiol. Results: Intima-media thi kness (IMT) was higher in patients undergoing HD but not different between nondiabetic HD patients and diabetic HD patients. No correlation was found between the duration of HD and intima-media thickness. Antioxidants were generally lower in HD patients. Intima-media thickness was positively correlated with MDA and negatively correlated with plasma thiol. Among other risk factors, only age was correlated with intima-media thickness. Conclusions: Increased carotid IMT in HD patients is independent of duration of HD or diabetes status. Age and MDA are the significant predictors of carotid IMT. Increased oxidative stress due to impaired antioxidant mechanisms, particularly reduced plasma thiol redox potential, may account for accelerated atherosclerosis in high-risk patients with chronic kidney failure and/or DM. ©2008 American Federation for Medical Research.en_US
dc.language.isoenen_US
dc.publisherBMJ Publishing Groupen_US
dc.relation.ispartofJournal of Investigative Medicineen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAntioxidant mechanismsen_US
dc.subjectAtherosclerosisen_US
dc.subjectUremiaen_US
dc.subjectcatalaseen_US
dc.subjectglutathioneen_US
dc.subjectglutathione peroxidaseen_US
dc.subjectsuperoxide dismutaseen_US
dc.subjectthiolen_US
dc.subjectantioxidanten_US
dc.subjectthiol derivativeen_US
dc.subjectadulten_US
dc.subjectantioxidant activityen_US
dc.subjectartery intima proliferationen_US
dc.subjectarticleen_US
dc.subjectatherosclerosisen_US
dc.subjectcontrolled studyen_US
dc.subjectdiabetes mellitusen_US
dc.subjectdiabetic patienten_US
dc.subjectdisease severityen_US
dc.subjectechographyen_US
dc.subjectfemaleen_US
dc.subjecthumanen_US
dc.subjectkidney diseaseen_US
dc.subjectlipid peroxidationen_US
dc.subjectmajor clinical studyen_US
dc.subjectmaleen_US
dc.subjectoxidative stressen_US
dc.subjectrisk factoren_US
dc.subjecturemiaen_US
dc.subjectcarotid arteryen_US
dc.subjectcarotid artery diseaseen_US
dc.subjectdiabetic angiopathyen_US
dc.subjectdiabetic nephropathyen_US
dc.subjectmetabolismen_US
dc.subjectmiddle ageden_US
dc.subjectphysiologyen_US
dc.subjectAntioxidantsen_US
dc.subjectCarotid Arteriesen_US
dc.subjectCarotid Artery Diseasesen_US
dc.subjectDiabetic Angiopathiesen_US
dc.subjectDiabetic Nephropathiesen_US
dc.subjectFemaleen_US
dc.subjectHumansen_US
dc.subjectMaleen_US
dc.subjectMiddle Ageden_US
dc.subjectOxidative Stressen_US
dc.subjectRisk Factorsen_US
dc.subjectSulfhydryl Compoundsen_US
dc.titleAre uremia, diabetes, and atherosclerosis linked with impaired antioxidant mechanisms?en_US
dc.typeArticleen_US
dc.identifier.volume56en_US
dc.identifier.issue2en_US
dc.identifier.startpage545
dc.identifier.startpage545en_US
dc.identifier.endpage552en_US
dc.identifier.doi10.2310/JIM.0b013e3181641ce3-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.pmid18317439en_US
dc.identifier.scopus2-s2.0-84940322742en_US
dc.identifier.wosWOS:000253061700014en_US
dc.identifier.scopusqualityQ2-
dc.ownerPamukkale University-
item.languageiso639-1en-
item.openairetypeArticle-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
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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