Association between serum hepcidin-25 and primary resistance to erythropoiesis-stimulating agents in chronic kidney disease: a secondary analysis of the HERO trial
dc.contributor.author | Gummer, J. | |
dc.contributor.author | Trengove, R. | |
dc.contributor.author | Pascoe, E. | |
dc.contributor.author | Badve, S. | |
dc.contributor.author | Cass, A. | |
dc.contributor.author | Clarke, P. | |
dc.contributor.author | McDonald, S. | |
dc.contributor.author | Morrish, A. | |
dc.contributor.author | Pedagogos, E. | |
dc.contributor.author | Perkovic, V. | |
dc.contributor.author | Reidlinger, D. | |
dc.contributor.author | Scaria, A. | |
dc.contributor.author | Walker, R. | |
dc.contributor.author | Vergara, L. | |
dc.contributor.author | Hawley, C. | |
dc.contributor.author | Johnson, D. | |
dc.contributor.author | Olynyk, John | |
dc.contributor.author | Ferrari, P. | |
dc.date.accessioned | 2017-08-24T02:23:12Z | |
dc.date.available | 2017-08-24T02:23:12Z | |
dc.date.created | 2017-08-23T07:21:29Z | |
dc.date.issued | 2017 | |
dc.identifier.citation | Gummer, 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.uri | http://hdl.handle.net/20.500.11937/56256 | |
dc.identifier.doi | 10.1111/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.publisher | Wiley-Blackwell | |
dc.title | Association between serum hepcidin-25 and primary resistance to erythropoiesis-stimulating agents in chronic kidney disease: a secondary analysis of the HERO trial | |
dc.type | Journal Article | |
dcterms.source.volume | 22 | |
dcterms.source.number | 7 | |
dcterms.source.startPage | 548 | |
dcterms.source.endPage | 554 | |
dcterms.source.issn | 1320-5358 | |
dcterms.source.title | Nephrology | |
curtin.accessStatus | Fulltext not available | |
curtin.faculty | Faculty of Health Sciences |
Files in this item
Files | Size | Format | View |
---|---|---|---|
There are no files associated with this item. |