Plasma endostatin at intensive care admission is independently associated with acute kidney injury, dialysis, and mortality in COVID-19
(2025) In Intensive Care Medicine Experimental 13. p.1-11- Abstract
- Background
Critical 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.
Methods
A 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... (More) - Background
Critical 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.
Methods
A 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.
Results
Four 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.
Conclusions
Endostatin 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. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/d45f5327-2efe-44ca-894d-393b6755343b
- author
- Koozi, Hazem
LU
; Engström, Jonas
LU
; Zwawi, Ahmad ; Spångfors, Martin LU
; Didriksson, Ingrid LU
; Larsson, Anders ; Friberg, Hans LU and Frigyesi, Attila LU
- organization
- publishing date
- 2025-04-03
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Intensive Care Medicine Experimental
- volume
- 13
- article number
- 42
- pages
- 1 - 11
- publisher
- Springer Nature
- external identifiers
-
- scopus:105002877691
- pmid:40178654
- ISSN
- 2197-425X
- DOI
- 10.1186/s40635-025-00748-6
- language
- English
- LU publication?
- yes
- id
- d45f5327-2efe-44ca-894d-393b6755343b
- date added to LUP
- 2025-04-04 21:00:31
- date last changed
- 2025-07-05 03:00:09
@article{d45f5327-2efe-44ca-894d-393b6755343b, abstract = {{Background<br/>Critical 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.<br/><br/>Methods<br/>A 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.<br/><br/>Results<br/>Four 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.<br/><br/>Conclusions<br/>Endostatin 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.}}, author = {{Koozi, Hazem and Engström, Jonas and Zwawi, Ahmad and Spångfors, Martin and Didriksson, Ingrid and Larsson, Anders and Friberg, Hans and Frigyesi, Attila}}, issn = {{2197-425X}}, language = {{eng}}, month = {{04}}, pages = {{1--11}}, publisher = {{Springer Nature}}, series = {{Intensive Care Medicine Experimental}}, title = {{Plasma endostatin at intensive care admission is independently associated with acute kidney injury, dialysis, and mortality in COVID-19}}, url = {{http://dx.doi.org/10.1186/s40635-025-00748-6}}, doi = {{10.1186/s40635-025-00748-6}}, volume = {{13}}, year = {{2025}}, }