Evidence map›Paper›PMID 27525053›Full record

ArticleOxidative medicine and cellular longevity2016

Oxidative Stress as Estimated by Gamma-Glutamyl Transferase Levels Amplifies the Alkaline Phosphatase-Dependent Risk for Mortality in ESKD Patients on Dialysis.

Claudia Torino, Francesco Mattace-Raso, Jan L C M van Saase, Maurizio Postorino, Giovanni Luigi Tripepi, Francesca Mallamaci, Carmine Zoccali, Progredire Study Group

Open access · hybridAbstract readMulticenter Study
In one paragraph

Article in Oxidative medicine and cellular longevity, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.8field-weighted citation impact, top 15% 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, 25 citations in OpenAlex.

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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

8 authors at 2 institutions in 2 countries.

Claudia TorinoCNR-IFC, Clinical Epidemiology and Physiopathology of Renal Diseases and Hypertension of Reggio Calabria, 89124 Reggio Calabria, Italy; Department of Internal Medicine, Erasmus University Medical Centre, 3015 CE Rotterdam, Netherlands.ORCID 0000-0002-4967-0916
Francesco Mattace-RasoDepartment of Internal Medicine, Erasmus University Medical Centre, 3015 CE Rotterdam, Netherlands.
Jan L C M van SaaseDepartment of Internal Medicine, Erasmus University Medical Centre, 3015 CE Rotterdam, Netherlands.
Maurizio PostorinoCNR-IFC, Clinical Epidemiology and Physiopathology of Renal Diseases and Hypertension of Reggio Calabria, 89124 Reggio Calabria, Italy.
Giovanni Luigi TripepiCNR-IFC, Clinical Epidemiology and Physiopathology of Renal Diseases and Hypertension of Reggio Calabria, 89124 Reggio Calabria, Italy.
Francesca MallamaciCNR-IFC, Clinical Epidemiology and Physiopathology of Renal Diseases and Hypertension of Reggio Calabria, 89124 Reggio Calabria, Italy.
Carmine ZoccaliCNR-IFC and Nephrology, Dialysis and Transplantation Unit, Ospedali Riuniti, c/o EUROLINE S.r.l., Via Vallone Petrara 57-59, 89124 Reggio Calabria, Italy.ORCID 0000-0002-6616-1996
Progredire Study GroupCNR-IFC, Clinical Epidemiology and Physiopathology of Renal Diseases and Hypertension of Reggio Calabria, 89124 Reggio Calabria, Italy.
Istituto di Fisiologia Clinica · ITErasmus University Rotterdam · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alkaline phosphatase (Alk-Phos) is a powerful predictor of death in patients with end-stage kidney disease (ESKD) and oxidative stress is a strong inducer of Alk-Phos in various tissues. We tested the hypothesis that oxidative stress, as estimated by a robust marker of systemic oxidative stress like γ-Glutamyl-Transpeptidase (GGT) levels, may interact with Alk-Phos in the high risk of death in a cohort of 993 ESKD patients maintained on chronic dialysis. In fully adjusted analyses the HR for mortality associated with Alk-Phos (50 IU/L increase) was progressively higher across GGT quintiles, being minimal in patients in the first quintile (HR: 0.89, 95% CI: 0.77-1.03) and highest in the GGT fifth quintile (HR: 1.13, 95% CI: 1.03-1.2) (P for the effect modification = 0.02). These findings were fully confirmed in sensitivity analyses excluding patients with preexisting liver disease, excessive alcohol intake, or altered liver disease biomarkers. GGT amplifies the risk of death associated with high Alk-Phos levels in ESKD patients. This observation is compatible with the hypothesis that oxidative stress is a strong modifier of the adverse biological effects of high Alk-Phos in this population.

Indexed as

Clinical Enzyme TestsAgedAlkaline PhosphataseBiomarkersFemalegamma-GlutamyltransferaseHumansItalyKidney Failure, ChronicMaleMiddle AgedPredictive Value of TestsProportional Hazards ModelsProspective StudiesRegistriesRenal DialysisAlkaline PhosphataseBiomarkersgamma-Glutamyltransferasegamma-glutamyltransferase, human

Identifiers

PMID27525053
PMCPMC4976170
OpenAlexW2500579017

What OpenQuestion holds

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Registered trials

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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.