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dc.contributor.authorGummer, J.
dc.contributor.authorTrengove, R.
dc.contributor.authorPascoe, E.
dc.contributor.authorBadve, S.
dc.contributor.authorCass, A.
dc.contributor.authorClarke, P.
dc.contributor.authorMcDonald, S.
dc.contributor.authorMorrish, A.
dc.contributor.authorPedagogos, E.
dc.contributor.authorPerkovic, V.
dc.contributor.authorReidlinger, D.
dc.contributor.authorScaria, A.
dc.contributor.authorWalker, R.
dc.contributor.authorVergara, L.
dc.contributor.authorHawley, C.
dc.contributor.authorJohnson, D.
dc.contributor.authorOlynyk, John
dc.contributor.authorFerrari, P.
dc.date.accessioned2017-08-24T02:23:12Z
dc.date.available2017-08-24T02:23:12Z
dc.date.created2017-08-23T07:21:29Z
dc.date.issued2017
dc.identifier.citationGummer, J. and Trengove, R. and Pascoe, E. and Badve, S. and Cass, A. and Clarke, P. and McDonald, S. et al. 2017. Association between serum hepcidin-25 and primary resistance to erythropoiesis-stimulating agents in chronic kidney disease: a secondary analysis of the HERO trial. Nephrology. 22 (7): pp. 548-554.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/56256
dc.identifier.doi10.1111/nep.12815
dc.description.abstract

Background: Pentoxifylline has been shown to increase haemoglobin levels in patients with chronic kidney disease (CKD) and erythropoietin-stimulating agent (ESA)-hyporesponsive anaemia in the Handling Erythropoietin Resistance with Oxpentifylline multicentre double-blind, randomized controlled trial. The present sub-study evaluated the effects of pentoxifylline on the iron-regulatory hormone hepcidin in patients with ESA-hyporesponsive CKD. Methods: This sub-study included 13 patients in the pentoxifylline arm (400 mg daily) and 13 in the matched placebo arm. Hepcidin-25 was measured by ultra performance liquid chromatography/quadrupole time-of-flight mass spectrometry following isolation from patient serum. Serum hepcidin-25, serum iron biomarkers, haemoglobin and ESA dosage were compared within and between the two groups. Results: Hepcidin-25 concentration at 4 months adjusted for baseline did not differ significantly in pentoxifylline versus placebo treated patients (adjusted mean difference (MD) -7.9 nmol, P = 0.114), although the difference between the groups mean translated into a > 25% reduction of circulating hepcidin-25 due to pentoxifylline compared with the placebo baseline. In paired analysis, serum hepcidin-25 levels were significantly decreased at 4 months compared with baseline in the pentoxifylline group (-5.47 ± 2.27 nmol/l, P < 0.05) but not in the placebo group (2.82 ± 4.29 nmol/l, P = 0.24). Pentoxifylline did not significantly alter serum ferritin (MD 55.4 mcg/l), transferrin saturation (MD 4.04%), the dosage of ESA (MD -9.93 U/kg per week) or haemoglobin concentration (MD 5.75 g/l). Conclusion: The reduction of circulating hepcidin-25 due to pentoxifylline did not reach statistical significance; however, the magnitude of the difference suggests that pentoxifylline may be a clinically and biologically meaningful modulator of hepcidin-25 in dialysis of patients with ESA-hyporesponsive anaemia. © 2016 Asian Pacific Society of Nephrology.

dc.publisherWiley-Blackwell
dc.titleAssociation between serum hepcidin-25 and primary resistance to erythropoiesis-stimulating agents in chronic kidney disease: a secondary analysis of the HERO trial
dc.typeJournal Article
dcterms.source.volume22
dcterms.source.number7
dcterms.source.startPage548
dcterms.source.endPage554
dcterms.source.issn1320-5358
dcterms.source.titleNephrology
curtin.accessStatusFulltext not available
curtin.facultyFaculty of Health Sciences


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