Serum and urinary biomarkers to predict acute kidney injury in premature infants: a systematic review and meta-analysis of diagnostic accuracy.


Journal

Journal of nephrology
ISSN: 1724-6059
Titre abrégé: J Nephrol
Pays: Italy
ID NLM: 9012268

Informations de publication

Date de publication:
11 2022
Historique:
received: 13 01 2022
accepted: 05 03 2022
pubmed: 7 4 2022
medline: 25 10 2022
entrez: 6 4 2022
Statut: ppublish

Résumé

Premature infants are at high risk for acute kidney injury (AKI) and current diagnostic criteria are flawed. The objective of this study was to determine the diagnostic accuracy of urine and serum biomarkers not currently used in routine clinical practice to predict AKI in premature infants. A systematic review was performed that followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses of Diagnostic Test Accuracy Studies (PRISMA-DTA). Data were extracted on the diagnostic accuracy of AKI biomarkers using serum creatinine or urine output as the reference standard. Quality and validity were assessed using modified Standards for Reporting Diagnostic Accuracy (STARD) criteria. We identified 1024 articles, with 15 studies (791 infants) eligible for inclusion. Twenty-seven biomarkers were identified including serum cystatin C and urinary neutrophil gelatinase-associated lipocalin (uNGAL), osteopontin, kidney injury molecule-1, epidermal growth factor, and protein S100-P. However, many were only reported by one study each. A meta-analysis could only be conducted on uNGAL (288 infants from 6 studies) using a hierarchical, random-effects logistic-regression model. uNGAL had a summary sensitivity of 77% (95% CI 58-89%), specificity of 76% (95% CI 57-88%) and AUC-SROC of 0.83 (95% CI 0.80-0.86) for the diagnosis of AKI. By utilising uNGAL, the post-test probability of AKI increased to 52% (95% CI 37-66%) with a positive test and decreased to 9% (95% CI 5-16%) with a negative test if the pre-test probability was 25%. uNGAL shows promise as a diagnostically accurate biomarker for AKI in premature infants.

Sections du résumé

BACKGROUND
Premature infants are at high risk for acute kidney injury (AKI) and current diagnostic criteria are flawed. The objective of this study was to determine the diagnostic accuracy of urine and serum biomarkers not currently used in routine clinical practice to predict AKI in premature infants.
METHOD
A systematic review was performed that followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses of Diagnostic Test Accuracy Studies (PRISMA-DTA). Data were extracted on the diagnostic accuracy of AKI biomarkers using serum creatinine or urine output as the reference standard. Quality and validity were assessed using modified Standards for Reporting Diagnostic Accuracy (STARD) criteria.
RESULTS
We identified 1024 articles, with 15 studies (791 infants) eligible for inclusion. Twenty-seven biomarkers were identified including serum cystatin C and urinary neutrophil gelatinase-associated lipocalin (uNGAL), osteopontin, kidney injury molecule-1, epidermal growth factor, and protein S100-P. However, many were only reported by one study each. A meta-analysis could only be conducted on uNGAL (288 infants from 6 studies) using a hierarchical, random-effects logistic-regression model. uNGAL had a summary sensitivity of 77% (95% CI 58-89%), specificity of 76% (95% CI 57-88%) and AUC-SROC of 0.83 (95% CI 0.80-0.86) for the diagnosis of AKI. By utilising uNGAL, the post-test probability of AKI increased to 52% (95% CI 37-66%) with a positive test and decreased to 9% (95% CI 5-16%) with a negative test if the pre-test probability was 25%.
CONCLUSION
uNGAL shows promise as a diagnostically accurate biomarker for AKI in premature infants.

Identifiants

pubmed: 35384606
doi: 10.1007/s40620-022-01307-y
pii: 10.1007/s40620-022-01307-y
pmc: PMC9584850
doi:

Substances chimiques

Lipocalin-2 0
Cystatin C 0
Creatinine AYI8EX34EU
Osteopontin 106441-73-0
Biomarkers 0
EGF Family of Proteins 0

Types de publication

Meta-Analysis Systematic Review Journal Article Review Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2001-2014

Subventions

Organisme : National Health and Medical Research Council
ID : APP1078164
Organisme : Children's Hospital Foundation
ID : 50331

Informations de copyright

© 2022. The Author(s).

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Auteurs

Jenny Kuo (J)

Child Health Research Centre, The University of Queensland, South Brisbane, QLD, Australia.

Lisa K Akison (LK)

Child Health Research Centre, The University of Queensland, South Brisbane, QLD, Australia.
School of Biomedical Sciences, The University of Queensland, Sir William MacGregor Building, St Lucia, QLD, 4072, Australia.

Mark D Chatfield (MD)

Child Health Research Centre, The University of Queensland, South Brisbane, QLD, Australia.

Peter Trnka (P)

Child Health Research Centre, The University of Queensland, South Brisbane, QLD, Australia.
Queensland Child and Adolescent Renal Service, Queensland Children's Hospital, South Brisbane, QLD, Australia.

Karen M Moritz (KM)

Child Health Research Centre, The University of Queensland, South Brisbane, QLD, Australia. k.moritz@uq.edu.au.
School of Biomedical Sciences, The University of Queensland, Sir William MacGregor Building, St Lucia, QLD, 4072, Australia. k.moritz@uq.edu.au.

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