Evidence map›Paper›PMID 41384696›Full record

ArticleJournal of pediatric gastroenterology and nutrition2026

Acute kidney injury markers in pediatric pancreatitis: Differentiating disease states and assessing severity.

Vineet Garlapally, Xiaojia Guo, Lindsey Hornung, Kenneth Delgado, Zobeida Cruz-Monserrate, Robert Safirstein, Fred Gorelick, Gary Desir, Stuart L Goldstein, Maisam Abu-El-Haija

Abstract read
In one paragraph

Article in Journal of pediatric gastroenterology and nutrition, 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Vineet GarlapallyDivision of Gastroenterology, Hepatology and Nutrition, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.ORCID https://orcid.org/0009-0008-6100-0414
Xiaojia GuoDepartment of Medicine, Section of Nephrology Yale University School of Medicine, New Haven, Connecticut, USA.
Lindsey HornungDivision of Biostatistics and Epidemiology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
Kenneth DelgadoDivision of Nephrology and Hypertension, The Heart Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
Zobeida Cruz-MonserrateDepartment of Internal Medicine, Division of Gastroenterology, Hepatology and Nutrition, and The Comprehensive Cancer Center-Arthur G, James Cancer Hospital and Richard J. Solove Research Institute, The Ohio State University Wexner Medical Center, Columbus, Ohio, USA.
Robert SafirsteinDepartment of Medicine, Section of Nephrology VA Medical Center, and Yale University School of Medicine, New Haven, Connecticut, USA.
Fred GorelickDepartment of Medicine, Section of Digestive Diseases, VA Medical Center, and Yale University School of Medicine, New Haven, Connecticut, USA.
Gary DesirDepartment of Medicine, Section of Nephrology Yale University School of Medicine, New Haven, Connecticut, USA.
Stuart L GoldsteinDivision of Nephrology and Hypertension, The Heart Institute, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
Maisam Abu-El-HaijaDivision of Gastroenterology, Hepatology and Nutrition, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.ORCID https://orcid.org/0000-0002-8968-7851

Funding

Predicting Severity and Improving the Outcomes of Pediatric PancreatitisK23DK118190 · NIDDK · CINCINNATI CHILDRENS HOSP MED CTR · PI ABU-EL-HAIJA, MAISAM · 2018 to 2022
$947k
NIDDK NIH HHS K23 DK118190NIDDK NIH HHS K23DK118190Veterans Administration Merit Senior Clinical Scientist Award BX003250
6 · The paper itself

Abstract

objectivesAcute kidney injury (AKI) is a complication commonly observed in adults with acute pancreatitis (AP) but remains poorly studied in pediatric patients. We investigated the utility of AKI biomarkers-kidney injury molecule-1 (KIM-1), lipocalin 2 (NGAL), cystatin-C (CYS-C), and renalase (RNLS) in acute and chronic pancreatitis (CP), and to assess AP severity, and evaluate kidney function.

methodsPlasma and urine samples were collected from children with AP (n = 49), CP (n = 50), and healthy controls (HC; n = 20). AKI biomarkers levels were measured using enzyme-linked immunosorbent assays (ELISA). AP patients were categorized into two groups: mild AP (MAP) and moderate/severe AP (SAP). Kidney function was evaluated using plasma creatinine (pCre) and CYS-C-based enhanced glomerular filtration rate (eGFR) formulas.

resultsPlasma KIM-1 and pCYS-C were elevated in AP versus CP and HCs (p < 0.0001). Urinary NGAL (uNGAL) was elevated in AP subjects, with 14% of patients exceeding the value of 125 ng/mL. Plasma A-RNLS remained same between AP and HCs (p = 0.78) but was elevated in CP cohort (p < 0.0001). However, pF-RNLS levels declined in AP compared to HCs and CP (p < 0.0001). SAP subjects (20% of AP cohort) had elevated pKIM-1 and pCYS-C compared to MAP (p = 0.002, p = 0.003). eGFR declined in AP subjects with 84% of AP patients showing CYS-C eGFR <90 mL/min/1.73 m². Plasma CYS-C, pA-RNLS, and pF-RNLS predicted AP from CP with area under the receiving operating curve of 0.86 (95% CL).

conclusionElevated pKIM-1, pCYS-C, and uNGAL, along with declining pF-RNLS, are helpful in distinguishing pediatric AP from CP. Quantifying the Levels of pKIM-1 and pCYS-C within the first 48 h can help predict development of SAP.

Indexed as

Acute Kidney InjuryPancreatitisAcute-Phase ProteinsAdolescentBiomarkersCase-Control StudiesChildChild, PreschoolCreatinineCystatin CFemaleGlomerular Filtration RateHepatitis A Virus Cellular Receptor 1HumansLipocalin-2LipocalinsAcute-Phase ProteinsBiomarkersCreatinineCystatin CHAVCR1 protein, humanHepatitis A Virus Cellular Receptor 1LCN2 protein, humanLipocalin-2LipocalinsMembrane GlycoproteinsProto-Oncogene ProteinsReceptors, Viruschildrenkidneypancreas

Identifiers

PMID41384696
PMCPMC13185510

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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.