Evidence map›Paper›PMID 38287305›Full record

ArticleBMC nephrology2024

Longitudinal NGAL and cystatin C plasma profiles present a high level of heterogeneity in a mixed ICU population.

Daniela Jou-Valencia, Meint Volbeda, Jan G Zijlstra, Jenny E Kootstra-Ros, Jill Moser, Matijs van Meurs, Jacqueline Koeze

Open access · goldAbstract read
In one paragraph

Article in BMC nephrology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

6 citing papers in PubMed, 5 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

7 authors at 2 institutions in 1 country.

Daniela Jou-ValenciaDepartment of Critical Care, University of Groningen, University Medical Center Groningen (UMCG), Hanzeplein 1, Groningen, 9713GZ, The Netherlands.ORCID 0000-0003-2897-5056
Meint VolbedaDepartment of Critical Care, University of Groningen, University Medical Center Groningen (UMCG), Hanzeplein 1, Groningen, 9713GZ, The Netherlands.ORCID 0000-0001-7641-1330
Jan G ZijlstraDepartment of Critical Care, University of Groningen, University Medical Center Groningen (UMCG), Hanzeplein 1, Groningen, 9713GZ, The Netherlands.ORCID 0000-0001-9079-0795
Jenny E Kootstra-RosDepartment of Laboratory Medicine, UMCG, Groningen, The Netherlands.ORCID 0000-0002-1394-513X
Jill MoserDepartment of Critical Care, University of Groningen, University Medical Center Groningen (UMCG), Hanzeplein 1, Groningen, 9713GZ, The Netherlands.ORCID 0000-0002-9614-2577
Matijs van MeursDepartment of Critical Care, University of Groningen, University Medical Center Groningen (UMCG), Hanzeplein 1, Groningen, 9713GZ, The Netherlands.ORCID 0000-0002-7745-2772
Jacqueline KoezeDepartment of Critical Care, University of Groningen, University Medical Center Groningen (UMCG), Hanzeplein 1, Groningen, 9713GZ, The Netherlands. j.koeze@umcg.nl.ORCID 0000-0002-4660-3400
University Medical Center Groningen · NLDialyse Centrum Groningen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNGAL and Cystatin C (CysC) as biomarkers for the early detection of AKI are subject to both pathophysiological, as well as patient related heterogeneity. The aim of this study was to investigate the timeline of plasma levels of NGAL and CysC during the first seven days of ICU admission in a mixed ICU population and to relate these to AKI severity during ICU stay. Via these means we aimed to bring clarity to the previously reported heterogeneity of these renal biomarkers.

methodsProspective Observation Cohort. Consecutive patients admitted to adult ICU at an academic hospital in the Netherlands between 18-02-2014 and 31-03-2014 were included. Urine output, serum creatinine, plasma NGAL and CysC were recorded during the first seven days of ICU admission. Biomarker expression was analyzed based on KDIGO score and time of AKI diagnosis.

results335 patients were included, 110 met KDIGO criteria for AKI. NGAL and CysC plasma levels were higher in AKI patients compared to non-AKI, high variability in individual values resulted in 56% of AKI patients having a false negative, and 32% of non-AKI patients having a false positive. Individual biomarker levels were variable, and no pattern based on KDIGO score was observed.

conclusionsPlasma NGAL and CysC as biomarkers for the early AKI detection may be subject to pathophysiological, and patient related heterogeneity. Further understanding of individual biomarker profiles may help in their application amongst mixed ICU populations.

trial registrationThe need for informed consent was waived by the Institutional Ethical Review Board of the University Medical Center Groningen (METc 2013 - 174) by Prof. dr. W.A. Kamps on May 17th 2013.

Indexed as

Acute Kidney InjuryCystatin CAdultBiomarkersCreatinineHumansIntensive Care UnitsLipocalin-2Prospective StudiesBiomarkersCreatinineCystatin CLipocalin-2AKICystatin CHeterogeneityNGALTimeline

Identifiers

PMID38287305
PMCPMC10826252
OpenAlexW4391310264

What OpenQuestion holds

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LicenceCC BY
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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.