Evidence map›Paper›PMID 42599955›Full record

Observational studyPloS one2026

Neutrophil gelatinase-associated lipocalin (NGAL) is a poor diagnostic marker for sepsis in the ICU - An observational multicentre study.

Lisa Boström, Sofie Hagström, Jonas Engström, Anders Olof Larsson, Hans Friberg, Maria Lengquist, Attila Frigyesi

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

7 authors.

Lisa BoströmDepartment of Clinical Sciences, Lund University, Lund, Sweden.ORCID https://orcid.org/0000-0002-2527-7167
Sofie HagströmDepartment of Clinical Sciences, Lund University, Lund, Sweden.
Jonas EngströmDepartment of Clinical Sciences, Lund University, Lund, Sweden.ORCID https://orcid.org/0000-0003-1421-3640
Anders Olof LarssonDepartment of Clinical Chemistry, Uppsala University Hospital, Uppsala, Sweden.ORCID https://orcid.org/0000-0003-3161-0402
Hans FribergDepartment of Clinical Sciences, Lund University, Lund, Sweden.
Maria LengquistDepartment of Clinical Sciences, Lund University, Lund, Sweden.
Attila FrigyesiDepartment of Clinical Sciences, Lund University, Lund, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSepsis is a major public health challenge, and reliable biomarkers are essential for distinguishing sepsis from other conditions. Neutrophil Gelatinase-Associated Lipocalin (NGAL) has shown promise as a diagnostic marker due to its role in the immune response. This study evaluates plasma NGAL as a diagnostic tool at the time of ICU admission.

methodsWe analysed plasma NGAL and C-reactive protein (CRP) levels in 2950 adult patients admitted to four ICUs between 2015 and 2018. All patients were retrospectively screened for Sepsis-3 criteria at ICU admission. The discriminative performance of NGAL and CRP for sepsis was assessed using receiver operating characteristic (ROC) analysis, with NGAL levels adjusted for chronic kidney disease (CKD) and age. Patients were stratified by renal function.

findingsPlasma NGAL levels were significantly higher in septic patients (p < 0.001). For the whole cohort, NGAL alone yielded an area under the curve (AUC) of 0.66 (confidence interval (CI) 0.64-0.68), CRP yielded an AUC of 0.71 (CI 0.69-0.73, p < 0.001), and combining NGAL with CRP nominally improved discriminative performance ([Formula: see text]AUC 0.018, 95% CI 0.011-0.027). Stratified analyses indicated that NGAL, together with CRP, significantly outperformed CRP alone in patients with no kidney injury and those with Acute Kidney Injury (AKI) only. In contrast, differences were not significant in patients with CKD only or CKD and AKI.

conclusionIn this large cohort, NGAL showed modest discrimination for sepsis, with a nominal improvement when combined with CRP. These findings do not indicate that NGAL meaningfully improves sepsis diagnosis in the ICU.

Indexed as

Lipocalin-2SepsisAgedBiomarkersC-Reactive ProteinFemaleHumansIntensive Care UnitsMaleMiddle AgedRetrospective StudiesROC CurveBiomarkersC-Reactive ProteinLCN2 protein, humanLipocalin-2

Identifiers

PMID42599955
PMCPMC13475940

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