Evidence map›Paper›PMID 26284153›Full record

ArticleCanadian journal of kidney health and disease2015

Association between serum alkaline phosphatase and primary resistance to erythropoiesis stimulating agents in chronic kidney disease: a secondary analysis of the HERO trial.

Sunil V Badve, Lei Zhang, Jeff S Coombes, Elaine M Pascoe, Alan Cass, Philip Clarke, Paolo Ferrari, Stephen P McDonald, Alicia T Morrish, Eugenie Pedagogos and 8 more

Open access · goldAbstract read
In one paragraph

Article in Canadian journal of kidney health and disease, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
0.4field-weighted citation impact, top 33% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 9 citations in OpenAlex.

  1. Antioxidants for adults with chronic kidney disease.The Cochrane database of systematic reviews · 2023
    Pooled it
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  3. Autoimmune processes and production of catalytically active antibodies-abzymes in prone to amyotrophic lateral sclerosis FUS(1-359) mice.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors at 8 institutions in 2 countries.

Sunil V BadveAustralasian Kidney Trials Network, University of Queensland, Brisbane, Australia ; Department of Nephrology, Princess Alexandra Hospital, Brisbane, Australia ; Department of Nephrology, Level 2, ARTS Building, Princess Alexandra Hospital, Ipswich Road, Woolloongabba, Queensland 4102 Australia.
Lei ZhangAustralasian Kidney Trials Network, University of Queensland, Brisbane, Australia ; Department of Nephrology, Guangdong Provincial Hospital of Chinese Medicine, Guangzhou, China.
Jeff S CoombesSchool of Human Movement Studies, University of Queensland, Brisbane, Australia.
Elaine M PascoeAustralasian Kidney Trials Network, University of Queensland, Brisbane, Australia.
Alan CassAustralasian Kidney Trials Network, University of Queensland, Brisbane, Australia ; Menzies School of Health Research, Darwin, Australia.
Philip ClarkeCentre for Health Policy, Programs & Economics, University of Melbourne, Melbourne, Australia.
Paolo FerrariDepartment of Nephrology, Prince of Wales Hospital, Sydney, Australia.
Stephen P McDonaldDepartment of Nephrology and Transplantation Services, University of Adelaide at Central Northern Adelaide Renal and Transplantation Services, Adelaide, Australia.
Alicia T MorrishAustralasian Kidney Trials Network, University of Queensland, Brisbane, Australia.
Eugenie PedagogosDepartment of Nephrology, Royal Melbourne Hospital, Melbourne, Australia.
Vlado PerkovicAustralasian Kidney Trials Network, University of Queensland, Brisbane, Australia ; The George Institute for Global Health, Sydney, Australia.
Donna ReidlingerAustralasian Kidney Trials Network, University of Queensland, Brisbane, Australia.
Anish ScariaAustralasian Kidney Trials Network, University of Queensland, Brisbane, Australia.
Rowan WalkerDepartment of Renal Medicine, The Alfred Hospital, Melbourne, Australia.
Liza A VergaraAustralasian Kidney Trials Network, University of Queensland, Brisbane, Australia.
Carmel M HawleyAustralasian Kidney Trials Network, University of Queensland, Brisbane, Australia ; Department of Nephrology, Princess Alexandra Hospital, Brisbane, Australia.
David W JohnsonAustralasian Kidney Trials Network, University of Queensland, Brisbane, Australia ; Department of Nephrology, Princess Alexandra Hospital, Brisbane, Australia.
HERO Study Collaborative Group
The University of Queensland · AUKidney Health Australia · AUPrince of Wales Hospital · AUPrincess Alexandra Hospital · AUThe Alfred Hospital · AUThe Royal Melbourne Hospital · AUThe University of Adelaide · AUThe University of Melbourne · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundErythropoiesis stimulating agent (ESA)-resistant anemia is common in chronic kidney disease (CKD).

objectivesTo evaluate the determinants of severity of ESA resistance in patients with CKD and primary ESA-resistance.

designSecondary analysis of a randomized controlled trial (the Handling Erythropoietin Resistance with Oxpentifylline, HERO). SETTING AND PATIENTS: 53 adult patients with CKD stage 4 or 5 and primary ESA-resistant anemia (hemoglobin ≤120 g/L, ESA resistance index [ERI] ≥1.0 IU/kg/week/gHb for erythropoietin or ≥0.005 μg/kg/week/gHb for darbepoeitin, no cause for ESA-resistance identified). MEASUREMENTS: Iron studies, parathyroid hormone, albumin, liver enzymes, phosphate or markers of oxidative stress and inflammation.

methodsParticipants were divided into tertiles of ERI. Multinomial logistic regression was used to analyse the determinants of ERI tertiles.

resultsAll patients, except one, were receiving dialysis for end-stage kidney disease. The mean ± SD ERI values in the low (n = 18), medium (n = 18) and high (n = 17) ERI tertiles were 1.4 ± 0.3, 2.3 ± 0.2 and 3.5 ± 0.8 IU/kg/week/gHb, respectively (P < 0.001). There were no significant differences observed in age, gender, ethnicity, cause of kidney disease, diabetes, iron studies, parathyroid hormone, albumin, liver enzymes, phosphate or markers of oxidative stress and inflammation between the ERI tertiles. The median [inter-quartile range] serum alkaline phosphatase concentrations in the low, medium and high ERI tertiles were 89 [64,121], 99 [76,134 and 148 [87,175] U/L, respectively (P = 0.054). There was a weak but statistically significant association between ERI and serum alkaline phosphatase (R(2) = 0.06, P = 0.03). Using multinomial logistic regression, the risk of being in the high ERI tertile relative to the low ERI tertile increased with increasing serum alkaline phosphatase levels (P = 0.02). No other variables were significantly associated with ERI. LIMITATIONS: Small sample size; bone-specific alkaline phosphatase, other markers of bone turnover and bone biopsies not evaluated.

conclusionsSerum alkaline phosphatase was associated with severity of ESA resistance in ESA-resistant patients with CKD. Large prospective studies are required to confirm this association. (

trial registrationAustralian New Zealand Clinical Trials Registry 12608000199314).

Indexed as

Alkaline phosphataseAnemiaBiological markerChronic kidney diseaseErythropoiesis stimulating agentsRandomized controlled trialRisk factors

Identifiers

PMID26284153
PMCPMC4538753
OpenAlexW2145713528

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.