Publication:
Alterations of erythrocyte rheology and cellular susceptibility in end stage renal disease: effects of peritoneal dialysis

dc.contributor.coauthorErtan, Nesrin Zeynep
dc.contributor.coauthorBozfakioglu, Semra
dc.contributor.coauthorSinan, Mukaddes
dc.contributor.departmentSchool of Medicine
dc.contributor.kuauthorUğurel, Elif
dc.contributor.kuauthorYalçın, Özlem
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2024-11-09T11:45:46Z
dc.date.issued2017
dc.description.abstractIn this study, we investigated the effects of peritoneal dialysis on hemorheological and hematological parameters and their relations with oxidant and antioxidant status of uremic patients. Hemorheological parameters (erythrocyte deformability, erythrocyte aggregation, osmotic deformability, blood and plasma viscosity) were measured in patients with renal insufficiency undergoing peritoneal dialysis (PD) and volunteers. Erythrocyte deformability, osmotic deformability and aggregation in both autologous plasma and 3% dextran 70 were measured by laser diffraction ektacytometry. Enzyme activities of glutathione peroxidase, superoxide dismutase and catalase were studied in erythrocytes; lipid peroxidation was studied by measuring the amount of malondialdehyde in both erythrocytes and plasma samples. Blood viscosity at native hematocrit was significantly lower in PD patients at all measured shear rates compared to controls, but it was high in PD patients at corrected (45%) hematocrit. Erythrocyte deformability did not show any difference between the two groups. Osmotic deformability was significantly lower in PD patients compared to controls. Aggregation index values were significantly high in PD patients in plasma Catalase and glutathione peroxidase activities in erythrocytes were decreased in PD patients whereas superoxide dismutase activity was increased compared to controls. Malondialdehyde was significantly increased in erythrocytes and plasma samples of PD patients which also shows correlations with aggregation parameters. It has been concluded that erythrocytes in PD patients are more prone to aggregation and this tendency could be influenced by lipid peroxidation activity in patient's plasma. These results imply that uremic conditions, loss of plasma proteins and an increased risk of oxidative stress because of decreasing levels of antioxidant enzymes affect erythrocyte rheology during peritoneal dialysis. This level of distortion may have crucial effects, impairing the blood flow dynamics and causing inadequate microcirculatory perfusion.
dc.description.fulltextYES
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.issue2
dc.description.openaccessYES
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipSeed Fund of Koç University
dc.description.sponsorshipResearch Foundation of Istanbul University
dc.description.versionPublisher version
dc.description.volume12
dc.identifier.doi10.1371/journal.pone.0171371
dc.identifier.embargoNO
dc.identifier.filenameinventorynoIR01355
dc.identifier.issn1932-6203
dc.identifier.quartileQ2
dc.identifier.scopus2-s2.0-85011602227
dc.identifier.urihttps://doi.org/10.1371/journal.pone.0171371
dc.identifier.wos396161700070
dc.keywordsOsmotic gradient ektacytometry
dc.keywordsOxidative stress
dc.keywordsReplacement therapy
dc.keywordsElongation index
dc.keywordsAnalyzer lorca
dc.keywordsHemodialysis
dc.keywordsDeformability
dc.keywordsFailure
dc.keywordsErythropoietin
dc.keywordsEfficiency
dc.language.isoeng
dc.publisherPublic Library of Science
dc.relation.grantno00006
dc.relation.grantno55613
dc.relation.ispartofPLOS One
dc.relation.urihttp://cdm21054.contentdm.oclc.org/cdm/ref/collection/IR/id/8110
dc.subjectMedicine
dc.subjectPhysiology
dc.titleAlterations of erythrocyte rheology and cellular susceptibility in end stage renal disease: effects of peritoneal dialysis
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorUğurel, Elif
local.contributor.kuauthorYalçın, Özlem
local.publication.orgunit1SCHOOL OF MEDICINE
local.publication.orgunit2School of Medicine
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relation.isParentOrgUnitOfPublication17f2dc8e-6e54-4fa8-b5e0-d6415123a93e
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