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Association between serum hepcidin-25 and primary resistance to erythropoiesis-stimulating agents in chronic kidney disease: a secondary analysis of the HERO trial.
Gummer, Joel; Trengove, Robert; Pascoe, Elaine M; Badve, Sunil V; Cass, Alan; Clarke, Philip; McDonald, Stephen P; Morrish, Alicia T; Pedagogos, Eugenie; Perkovic, Vlado; Reidlinger, Donna; Scaria, Anish; Walker, Rowan; Vergara, Liza A; Hawley, Carmel M; Johnson, David W; Olynyk, John K; Ferrari, Paolo.
Afiliación
  • Gummer J; Separation Science and Metabolomics Laboratory and Metabolomics Australia, Murdoch University Node, Perth, Australia.
  • Trengove R; Separation Science and Metabolomics Laboratory and Metabolomics Australia, Murdoch University Node, Perth, Australia.
  • Pascoe EM; Australasian Kidney Trials Network, University of Queensland, Brisbane, Australia.
  • Badve SV; Australasian Kidney Trials Network, University of Queensland, Brisbane, Australia.
  • Cass A; Department of Nephrology, St George Hospital, Sydney, Australia.
  • Clarke P; Australasian Kidney Trials Network, University of Queensland, Brisbane, Australia.
  • McDonald SP; Menzies School of Health Research, Darwin, Australia.
  • Morrish AT; Centre for Health Policy, Programs and Economics, University of Melbourne, Melbourne, Australia.
  • Pedagogos E; Department of Nephrology and Transplantation Services, University of Adelaide at Central Northern Adelaide Renal and Transplantation Services, Adelaide, Australia.
  • Perkovic V; Australasian Kidney Trials Network, University of Queensland, Brisbane, Australia.
  • Reidlinger D; Department of Nephrology, Royal Melbourne Hospital, Melbourne, Australia.
  • Scaria A; Australasian Kidney Trials Network, University of Queensland, Brisbane, Australia.
  • Walker R; The George Institute for Global Health, Sydney, Australia.
  • Vergara LA; Australasian Kidney Trials Network, University of Queensland, Brisbane, Australia.
  • Hawley CM; Australasian Kidney Trials Network, University of Queensland, Brisbane, Australia.
  • Johnson DW; Department of Renal Medicine, The Alfred Hospital, Melbourne, Australia.
  • Olynyk JK; Australasian Kidney Trials Network, University of Queensland, Brisbane, Australia.
  • Ferrari P; Australasian Kidney Trials Network, University of Queensland, Brisbane, Australia.
Nephrology (Carlton) ; 22(7): 548-554, 2017 Jul.
Article en En | MEDLINE | ID: mdl-27171136
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.
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Texto completo: 1 Colección: 01-internacional Asunto principal: Pentoxifilina / Resistencia a Medicamentos / Eritropoyesis / Insuficiencia Renal Crónica / Hepcidinas / Darbepoetina alfa / Hematínicos / Anemia Tipo de estudio: Clinical_trials / Diagnostic_studies / Risk_factors_studies Límite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Nephrology (Carlton) Asunto de la revista: NEFROLOGIA Año: 2017 Tipo del documento: Article País de afiliación: Australia

Texto completo: 1 Colección: 01-internacional Asunto principal: Pentoxifilina / Resistencia a Medicamentos / Eritropoyesis / Insuficiencia Renal Crónica / Hepcidinas / Darbepoetina alfa / Hematínicos / Anemia Tipo de estudio: Clinical_trials / Diagnostic_studies / Risk_factors_studies Límite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Nephrology (Carlton) Asunto de la revista: NEFROLOGIA Año: 2017 Tipo del documento: Article País de afiliación: Australia