Evidence map›Paper›PMID 40178654›Full record

ArticleIntensive care medicine experimental2025

Plasma endostatin at intensive care admission is independently associated with acute kidney injury, dialysis, and mortality in COVID-19.

Hazem Koozi, Jonas Engström, Ahmad Zwawi, Martin Spångfors, Ingrid Didriksson, Anders Larsson, Hans Friberg, Attila Frigyesi

Abstract read
In one paragraph

Article in Intensive care medicine experimental, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

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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

2 citing papers in PubMed.

  1. Article
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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

8 authors.

Hazem KooziDepartment of Clinical Sciences, Anaesthesiology and Intensive Care, Lund University, 22185, Lund, Sweden. hazem.koozi@med.lu.se.ORCID http://orcid.org/0000-0002-5892-3524
Jonas EngströmDepartment of Clinical Sciences, Anaesthesiology and Intensive Care, Lund University, 22185, Lund, Sweden.
Ahmad ZwawiFaculty of Medicine, Lund University, 22184, Lund, Sweden.
Martin SpångforsDepartment of Clinical Sciences, Anaesthesiology and Intensive Care, Lund University, 22185, Lund, Sweden.
Ingrid DidrikssonDepartment of Clinical Sciences, Anaesthesiology and Intensive Care, Lund University, 22185, Lund, Sweden.
Anders LarssonDepartment of Medical Sciences, Clinical Chemistry, Uppsala University, 75185, Uppsala, Sweden.
Hans FribergDepartment of Clinical Sciences, Anaesthesiology and Intensive Care, Lund University, 22185, Lund, Sweden.
Attila FrigyesiDepartment of Clinical Sciences, Anaesthesiology and Intensive Care, Lund University, 22185, Lund, Sweden.

Funding

Crafoordska Stiftelsen 2021-0833Government funding of clinical research within the Swedish National Health Service (ALF) 2021-10233Government funding of clinical research within the Swedish National Health Service (ALF) 2022-0226Government funding of clinical research within the Swedish National Health Service (ALF) 2022:YF0009 and 2022-0075Hjärt-Lungfonden 2022-0352Hjärt-Lungfonden 2022-0458Regional research support, Region Skåne 2022-1284
6 · The paper itself

Abstract

backgroundCritical COVID-19 is associated with high mortality, and acute kidney injury (AKI) is common. Endostatin has emerged as a promising prognostic biomarker for predicting AKI and mortality in intensive care. This study aimed to investigate plasma endostatin at intensive care unit (ICU) admission as a biomarker for AKI, renal replacement therapy (RRT), and 90-day mortality in COVID-19.

methodsA pre-planned retrospective analysis of a prospectively collected cohort of admissions with a primary SARS-CoV-2 infection to six ICUs in southern Sweden between May 2020 and May 2021 was undertaken. Endostatin at ICU admission was evaluated with multivariable logistic regression analyses adjusted for age, sex, C-reactive protein, and creatinine. Net reclassification index analyses were also performed.

resultsFour hundred eighty-four patients were included. Endostatin showed a non-linear association with AKI, RRT, and 90-day mortality. Endostatin levels of 100-200 ng/mL were associated with AKI on ICU day 1 (OR 5.1, 95% CI 1.5-18, p = 0.0097), RRT during the ICU stay (OR 3.5, 95% CI 1.1-12, p = 0.039), and 90-day mortality (OR 4.2, 95% CI 1.6-11, p = 0.0037). Adding endostatin to creatinine improved prediction of AKI on ICU day 1, while adding it to a model containing age, sex, CRP, and creatinine improved prediction of both AKI on ICU day 1 and 90-day mortality, but not RRT.

conclusionsEndostatin at ICU admission was independently associated with AKI, RRT, and 90-day mortality in ICU patients with COVID-19. In addition, endostatin improved the prediction of AKI and 90-day mortality, highlighting its potential as a biomarker for early risk stratification in intensive care.

Indexed as

Acute kidney injuryCOVID-19Critical careEndostatinIntensive careMortalityRenal replacement therapy

Identifiers

PMID40178654
PMCPMC11968582

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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.