Please use this identifier to cite or link to this item: https://olympias.lib.uoi.gr/jspui/handle/123456789/23518
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dc.contributor.authorTsouchnikas, I.en
dc.contributor.authorDounousi, E.en
dc.contributor.authorPapakonstantinou, S.en
dc.contributor.authorIoannou, K.en
dc.contributor.authorKelesidis, A.en
dc.contributor.authorKotzadamis, N.en
dc.contributor.authorXanthopoulou, K.en
dc.contributor.authorTsakiris, D.en
dc.date.accessioned2015-11-24T19:33:16Z-
dc.date.available2015-11-24T19:33:16Z-
dc.identifier.issn1440-1797-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/23518-
dc.rightsDefault Licence-
dc.subjectAgeden
dc.subjectC-Reactive Protein/analysisen
dc.subjectCholesterol, LDL/blooden
dc.subjectErythropoietin/*therapeutic useen
dc.subjectFemaleen
dc.subjectHeptanoic Acids/*therapeutic useen
dc.subjectHumansen
dc.subjectHydroxymethylglutaryl-CoA Reductase Inhibitors/*therapeutic useen
dc.subjectMaleen
dc.subjectMiddle Ageden
dc.subjectProspective Studiesen
dc.subjectPyrroles/*therapeutic useen
dc.subject*Renal Dialysisen
dc.titleBeneficial effect of atorvastatin on erythropoietin responsiveness in maintenance haemodialysis patientsen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primary10.1111/j.1440-1797.2009.01084.x-
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/19422526-
heal.identifier.secondaryhttp://onlinelibrary.wiley.com/store/10.1111/j.1440-1797.2009.01084.x/asset/j.1440-1797.2009.01084.x.pdf?v=1&t=h0ul4dos&s=c9a7a07acc74ae13c899051be2973569697b79ef-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.publicationDate2009-
heal.abstractAIM: To evaluate the effect of atorvastatin on erythropoietin responsiveness and whether this effect is mediated by C-reactive protein (CRP) reduction in prevalent dyslipidemic, haemodialysis patients. METHODS: We studied prospectively 33 stable, iron-repleted haemodialysis patients with low-density lipoprotein cholesterol (LDL) > or =2.58 mmol/L, who received 20 mg atorvastatin aiming to achieve the target of LDL <2.58 mmol/L, over a period of 9 months. Twenty-five patients completed the study, 15 men, with mean age 66.1 +/- 8.2 years. The duration of haemodialysis was 56.6 +/- 63.1 months and 5/25 patients were diabetics. Total serum cholesterol, triglycerides, high-density lipoprotein cholesterol, LDL, haemoglobin, albumin, intact parathyroid hormone, serum iron, ferritin, total iron binding capacity, CRP and weekly dose of erythropoietin/body weight/haemoglobin were analysed. RESULTS: Twenty of the 25 patients (80%) achieved the goal of LDL <2.58 mmol/L. There was a significant decrease in total cholesterol (5.77 +/- 0.88 to 4.16 +/- 0.96 mmol/L, P < 0.001) and LDL (3.59 +/- 0.77 to 1.94 +/- 0.77 mmol/L, P < 0.001). Haemoglobin increased from 121 +/- 11 to 126 +/- 7 g/L (P < 0.05), while weekly dose of erythropoietin/body weight/haemoglobin decreased significantly from 8.34 +/- 3.70 to 7.87 +/- 3.11 IU/kg per haemoglobin (P < 0.05). CRP decreased not significantly from 7.0 +/- 6.1 to 4.5 +/- 2.2 mg/L. CONCLUSION: Dyslipidemia of haemodialysis patients was treated safely and effectively with atorvastatin, but a fifth of the patients failed to achieve the therapeutic target. Statin therapy resulted in a significant increase of haemoglobin levels and improvement of erythropoietin responsiveness without a significant reduction in CRP levels, suggesting that the beneficial effect of statins on erythropoietin responsiveness may be driven by a mechanism other than CRP reduction.en
heal.journalNameNephrology (Carlton)en
heal.journalTypepeer-reviewed-
heal.fullTextAvailabilityTRUE-
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