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Increased visfatin in hemodialysis patients is associated with decreased demands for recombinant human erythropoietin.

TitleIncreased visfatin in hemodialysis patients is associated with decreased demands for recombinant human erythropoietin.
Publication TypeJournal Article
Year of Publication2013
AuthorsEleftheriadis, T., Pissas G., Remoundou M., Antoniadi G., Liakopoulos V., & Stefanidis I.
JournalRen Fail
Volume35
Issue10
Pagination1399-403
Date Published2013
ISSN1525-6049
KeywordsAged, Anemia, Case-Control Studies, Cytokines, Erythropoietin, Female, Healthy Volunteers, Humans, Insulin Resistance, Iron, Kidney Failure, Chronic, Male, Middle Aged, Nicotinamide Phosphoribosyltransferase, Recombinant Proteins, Renal Dialysis
Abstract

BACKGROUND: Studies detected an association between visfatin and markers of iron metabolism in patients with insulin resistance. In this study, such a relation was evaluated in hemodialysis (HD) patients. Also relations between visfatin and hepcidin, demands for recombinant human erythropoietin (rHuEpo), inflammation, and situations characterized by insulin resistance were evaluated.METHODS: After a four-week washout period from iron treatment, 33 HD patients and 20 healthy volunteers enrolled in the study. Serum visfatin, hepcidin, and interleukin-6 (IL-6) were assessed by means of enzyme-linked immunosorbent assay. Hemoglobin, serum iron, ferritin, and transferrin saturation (TSAT) were also measured.RESULTS: Visfatin was markedly increased in HD patients. Visfatin levels did not differ between diabetics and non-diabetics. No relation was detected between visfatin and body mass index or IL-6 in HD patients. From the markers of iron metabolism, the hepcidin included, visfatin was related only to TSAT. A strong positive relation was revealed between visfatin and hemoglobin, whereas visfatin was inversely related to rHuEpo dose. Resistance to rHuEpo index was inversely and independently of TSAT related to visfatin.CONCLUSION: Visfatin is increased in HD patients and it is associated with decreased demands for rHuEpo.

DOI10.3109/0886022X.2013.828268
Alternate JournalRen Fail
PubMed ID23964827

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