Evidence map›Paper›PMID 37387487›Full record

ArticleAnnals of laboratory medicine2023

Neutrophil Gelatinase-Associated Lipocalin Cutoff Value Selection and Acute Kidney Injury Classification System Determine Phenotype Allocation and Associated Outcomes.

Annemarie Albert, Sebastian Radtke, Louisa Blume, Rinaldo Bellomo, Michael Haase, Philipp Stieger, Ulrich Paul Hinkel, Rüdiger C Braun-Dullaeus, Christian Albert

Abstract read
In one paragraph

Article in Annals of laboratory medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
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

9 authors.

Annemarie AlbertDepartment of Nephrology and Endocrinology, Ernst von Bergmann Hospital, Potsdam, Germany.ORCID 0000-0002-5611-1506
Sebastian RadtkeUniversity Clinic for Cardiology and Angiology, Otto-von-Guericke University Magdeburg, Germany.ORCID 0000-0002-1874-1937
Louisa BlumeUniversity Clinic for Cardiology and Angiology, Otto-von-Guericke University Magdeburg, Germany.ORCID 0000-0001-9612-7185
Rinaldo BellomoDepartment of Intensive Care, The Austin Hospital, Melbourne, Australia.ORCID 0000-0002-1650-8939
Michael HaaseMedical Faculty, Otto-von-Guericke University Magdeburg, Germany.ORCID 0000-0001-8212-7416
Philipp StiegerUniversity Clinic for Cardiology and Angiology, Otto-von-Guericke University Magdeburg, Germany.ORCID 0000-0001-6103-9038
Ulrich Paul HinkelDepartment of Nephrology, Central Clinic Bad Berka, Bad Berka, Germany.ORCID 0000-0002-2416-7003
Rüdiger C Braun-DullaeusUniversity Clinic for Cardiology and Angiology, Otto-von-Guericke University Magdeburg, Germany.ORCID 0000-0003-3888-6532
Christian AlbertUniversity Clinic for Cardiology and Angiology, Otto-von-Guericke University Magdeburg, Germany.ORCID 0000-0002-6956-9962

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: We explored the extent to which neutrophil gelatinase-associated lipocalin (NGAL) cutoff value selection and the acute kidney injury (AKI) classification system determine clinical AKI-phenotype allocation and associated outcomes. Methods: Cutoff values from ROC curves of data from two independent prospective cardiac surgery study cohorts (Magdeburg and Berlin, Germany) were used to predict Kidney Disease: Improving Global Outcome (KDIGO)- or Risk, Injury, Failure, Loss of kidney function, End-stage (RIFLE)-defined AKI. Statistical methodologies (maximum Youden index, lowest distance to [0, 1] in ROC space, sensitivity≍specificity) and cutoff values from two NGAL meta-analyses were evaluated. Associated risks of adverse outcomes (acute dialysis initiation and in-hospital mortality) were compared. Results: NGAL cutoff concentrations calculated from ROC curves to predict AKI varied according to the statistical methodology and AKI classification system (10.6-159.1 and 16.85-149.3 ng/mL in the Magdeburg and Berlin cohorts, respectively). Proportions of attributed subclinical AKI ranged 2%-33.0% and 10.1%-33.1% in the Magdeburg and Berlin cohorts, respectively. The difference in calculated risk for adverse outcomes (fraction of odds ratios for AKI-phenotype group differences) varied considerably when changing the cutoff concentration within the RIFLE or KDIGO classification (up to 18.33- and 16.11-times risk difference, respectively) and was even greater when comparing cutoff methodologies between RIFLE and KDIGO classifications (up to 25.7-times risk difference). Conclusions: NGAL positivity adds prognostic information regardless of RIFLE or KDIGO classification or cutoff selection methodology. The risk of adverse events depends on the methodology of cutoff selection and AKI classification system.

Indexed as

Acute Kidney InjuryHumansKidneyLipocalin-2PhenotypeRenal DialysisLipocalin-2Acute kidney injuryAKI phenotypesCardiac surgeryCutoffDichotomizationNeutrophil gelatinase-associated lipocalinRisk assessmentRisk predictionROCSubclinical AKI

Identifiers

PMID37387487
PMCPMC10345176

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.