Evidence map›Paper›PMID 41063171›Full record

ArticleCritical care (London, England)2025

Discovery of a resistant cohort to acute kidney injury: insights from patients with septic shock.

Dana Y Fuhrman, Towia A Libermann, Neil A Hukriede, Luca Molinari, Samir M Parikh, John A Kellum, ProCESS and ProGReSS-AKI Investigators

Abstract read
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Article in Critical care (London, England), 2025. 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

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Dana Y Fuhrman *Department of Critical Care Medicine, UPMC Children's Hospital of Pittsburgh, Pittsburgh, PA, USA. dana.fuhrman@chp.edu.ORCID http://orcid.org/0000-0002-3672-7960
Towia A LibermannBeth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
Neil A HukriedeDepartment of Cell Biology, School of Medicine, University of Pittsburgh, Pittsburgh, PA, USA.
Luca Molinari *Program for Critical Care Nephrology, Department of Critical Care Medicine, University of Pittsburgh, Pittsburgh, PA, USA.
Samir M Parikh *Division of Nephrology, Department of Internal Medicine, UT Southwestern, Dallas, TX, USA. samir.parikh@utsouthwestern.edu.ORCID http://orcid.org/0000-0002-1038-981X
John A Kellum *Program for Critical Care Nephrology, Department of Critical Care Medicine, University of Pittsburgh, Pittsburgh, PA, USA. kellum@pitt.edu.ORCID http://orcid.org/0000-0003-1995-2653
ProCESS and ProGReSS-AKI Investigators

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAcute kidney injury (AKI) is a significant complication among critically ill patients, particularly those with sepsis, yet no specific therapies exist. Progress in some diseases has been achieved by analyzing individuals who appear resistant. This study sought to develop a framework to investigate AKI resistance using clinical phenotyping and biomarkers and applied this framework to a large cohort of patients with septic shock.

methodsWe performed a retrospective analysis of patients enrolled in the Protocolized Care for Early Septic Shock (ProCESS) trial. We measured urinary tissue inhibitor of metalloproteinase-2 (TIMP-2), insulin-like growth factor binding protein 7 (IGFBP7), and kidney injury molecule 1 (KIM-1) 6 h after the start of resuscitation. AKI was defined first as high risk by [TIMP-2]•[IGFBP7] > 1.0 (ng/mL)²/1000 and either meeting Kidney Disease Improving Global Outcomes Criteria (KDIGO) criteria within 7 days after the start of resuscitation or having [KIM-1] > 2.0 ng/ml. AKI resistance was defined as the combination of (a) high-risk by [TIMP-2]•[IGFBP7] > 1.0 (ng/mL)²/1000 but without meeting (b) KDIGO AKI criteria nor (c) [KIM-1] > 2.0 ng/ml. We compared clinical characteristics and outcomes across three groups: AKI-resistant, AKI, and reduced risk, which was defined as [TIMP-2]•[IGFBP7] < 1.0 (ng/mL)²/1000.

resultsAmong 573 patients, 339 (59.2%) had reduced risk, 194 (33.9%) developed AKI, and 40 (7%) were AKI-resistant. Median (IQR) non-renal SOFA scores were lower for patients at reduced risk for AKI (5 [2-7]) than for those with AKI resistance (6 [4.5-8], P < 0.01) or AKI (6 [5-9], P < 0.01). Baseline characteristics did not differ between AKI-resistant and AKI-affected individuals. However, AKI-resistant patients experienced significantly lower 30-day mortality (10% vs. 32%; adjusted OR 0.26, 95% CI: 0.09-0.80, P = 0.02) and shorter ICU stays when compared to those with AKI.

conclusionDespite greater illness severity, AKI-resistant patients had similar mortality and length of stay as lower-risk patients but better outcomes than those with AKI. Studying these patients may reveal novel therapeutic targets for AKI prevention and treatment.

Indexed as

Acute Kidney InjuryShock, SepticAgedBiomarkersCohort StudiesFemaleHepatitis A Virus Cellular Receptor 1HumansInsulin-Like Growth Factor Binding ProteinsMaleMiddle AgedRetrospective StudiesTissue Inhibitor of Metalloproteinase-2BiomarkersHAVCR1 protein, humanHepatitis A Virus Cellular Receptor 1insulin-like growth factor binding protein-related protein 1Insulin-Like Growth Factor Binding ProteinsTIMP2 protein, humanTissue Inhibitor of Metalloproteinase-2AKI resistanceBiomarkersSepsis associated AKISeptic shock

Identifiers

PMID41063171
PMCPMC12505998

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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.