Comparative Evaluation of Two NGAL Automated Immunoassays in Urine and Plasma.


Journal

The journal of applied laboratory medicine
ISSN: 2576-9456
Titre abrégé: J Appl Lab Med
Pays: England
ID NLM: 101693884

Informations de publication

Date de publication:
04 05 2022
Historique:
received: 11 06 2021
accepted: 25 10 2021
pubmed: 8 1 2022
medline: 10 5 2022
entrez: 7 1 2022
Statut: ppublish

Résumé

Acute kidney injury (AKI), a frequent and serious complication of hospitalized patients, is associated with increased mortality and morbidity. Neutrophil gelatinase-associated lipocalin (NGAL) is a biomarker for the early identification of AKI. We report a comparative laboratory verification of the Abbott Diagnostics (ARCHITECT® urine NGAL) and BioPorto Diagnostics (NGAL TestTM) assays including an assessment of the Abbott assay's performance in EDTA plasma. Intra-/interbatch imprecision, linearity, recovery, and limit of quantitation (LoQ) were assessed and an interassay comparison performed (n = 51). Between-laboratory agreement was assessed against other laboratories using the Abbott (n = 48) and BioPorto (n = 94) assays. Plasma NGAL (pNGAL) levels were measured in non-AKI patients with a range of estimated glomerular filtration rates (n = 80). Coefficients of variation (CVs) for intra- and interbatch imprecision were 0.7%-12.4% and 1.9%-27.5% for the BioPorto assay, respectively, and 1.4%-6.3%/3.4%-6.8%, respectively, for the Abbott assay. The BioPorto assay exhibited a higher LoQ (27.5 ng/mL vs 1.2 ng/mL). Both assays were linear over the range 5-6000 ng/mL. Recovery of recombinant NGAL was 113.1 ± 7.1% and 96.5 ± 7.8% for the Abbott and BioPorto assays, respectively. On average, the Abbott assay gave results 9.2% lower than the BioPorto assay. Mean differences of 0.2% (Abbott) and 20.2% (BioPorto) were observed in the between-laboratory comparison. In patients without AKI, pNGAL levels were inversely proportional to eGFR. Performance of the Abbott and BioPorto assays was similar although the latter performed less well at lower NGAL concentrations. The Abbott assay tended to yield lower results, exhibited a lower LoQ and over-recovered NGAL. Although only Conformité Européenne-marked and marketed for use in urine, the Abbott assay demonstrated equivalent performance to the BioPorto assay with EDTA plasma.

Sections du résumé

BACKGROUND
Acute kidney injury (AKI), a frequent and serious complication of hospitalized patients, is associated with increased mortality and morbidity. Neutrophil gelatinase-associated lipocalin (NGAL) is a biomarker for the early identification of AKI. We report a comparative laboratory verification of the Abbott Diagnostics (ARCHITECT® urine NGAL) and BioPorto Diagnostics (NGAL TestTM) assays including an assessment of the Abbott assay's performance in EDTA plasma.
METHODS
Intra-/interbatch imprecision, linearity, recovery, and limit of quantitation (LoQ) were assessed and an interassay comparison performed (n = 51). Between-laboratory agreement was assessed against other laboratories using the Abbott (n = 48) and BioPorto (n = 94) assays. Plasma NGAL (pNGAL) levels were measured in non-AKI patients with a range of estimated glomerular filtration rates (n = 80).
RESULTS
Coefficients of variation (CVs) for intra- and interbatch imprecision were 0.7%-12.4% and 1.9%-27.5% for the BioPorto assay, respectively, and 1.4%-6.3%/3.4%-6.8%, respectively, for the Abbott assay. The BioPorto assay exhibited a higher LoQ (27.5 ng/mL vs 1.2 ng/mL). Both assays were linear over the range 5-6000 ng/mL. Recovery of recombinant NGAL was 113.1 ± 7.1% and 96.5 ± 7.8% for the Abbott and BioPorto assays, respectively. On average, the Abbott assay gave results 9.2% lower than the BioPorto assay. Mean differences of 0.2% (Abbott) and 20.2% (BioPorto) were observed in the between-laboratory comparison. In patients without AKI, pNGAL levels were inversely proportional to eGFR.
CONCLUSIONS
Performance of the Abbott and BioPorto assays was similar although the latter performed less well at lower NGAL concentrations. The Abbott assay tended to yield lower results, exhibited a lower LoQ and over-recovered NGAL. Although only Conformité Européenne-marked and marketed for use in urine, the Abbott assay demonstrated equivalent performance to the BioPorto assay with EDTA plasma.

Identifiants

pubmed: 34993540
pii: 6498037
doi: 10.1093/jalm/jfab167
doi:

Substances chimiques

Acute-Phase Proteins 0
Lipocalin-2 0
Lipocalins 0
Proto-Oncogene Proteins 0
Edetic Acid 9G34HU7RV0

Types de publication

Comparative Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

747-761

Subventions

Organisme : Abbott Diagnostics and BioPorto Diagnostics provided NGAL reagents, calibrators

Informations de copyright

© American Association for Clinical Chemistry 2022. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

Simon J Whitehead (SJ)

Department of Blood Sciences, Royal Wolverhampton NHS Trust, New Cross Hospital, Wolverhampton, West Midlands, UK.

Katie Chadwick (K)

Department of Blood Sciences, Royal Wolverhampton NHS Trust, New Cross Hospital, Wolverhampton, West Midlands, UK.

Clare Ford (C)

Department of Blood Sciences, Royal Wolverhampton NHS Trust, New Cross Hospital, Wolverhampton, West Midlands, UK.

Ramesh Giri (R)

Department of Cardiac Anesthesia, Royal Wolverhampton NHS Trust, New Cross Hospital, Wolverhampton, West Midlands, UK.

Heyman Luckraz (H)

Department of Cardiac Surgery, Royal Wolverhampton NHS Trust, New Cross Hospital, Wolverhampton, West Midlands, UK.

Rousseau Gama (R)

Department of Blood Sciences, Royal Wolverhampton NHS Trust, New Cross Hospital, Wolverhampton, West Midlands, UK.
School of Medicine and Clinical Practice, Wolverhampton University, Wolverhampton, West Midlands, UK.

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Classifications MeSH