Elevated suPAR Is an Independent Risk Marker for Incident Kidney Disease in Acute Medical Patients

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Elevated suPAR Is an Independent Risk Marker for Incident Kidney Disease in Acute Medical Patients. / Iversen, Esben; Houlind, Morten Baltzer; Kallemose, Thomas; Rasmussen, Line Jee Hartmann; Hornum, Mads; Feldt-Rasmussen, Bo; Hayek, Salim S.; Andersen, Ove; Eugen-Olsen, Jesper.

In: Frontiers in Cell and Developmental Biology, Vol. 8, 339, 2020.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Iversen, E, Houlind, MB, Kallemose, T, Rasmussen, LJH, Hornum, M, Feldt-Rasmussen, B, Hayek, SS, Andersen, O & Eugen-Olsen, J 2020, 'Elevated suPAR Is an Independent Risk Marker for Incident Kidney Disease in Acute Medical Patients', Frontiers in Cell and Developmental Biology, vol. 8, 339. https://doi.org/10.3389/fcell.2020.00339

APA

Iversen, E., Houlind, M. B., Kallemose, T., Rasmussen, L. J. H., Hornum, M., Feldt-Rasmussen, B., Hayek, S. S., Andersen, O., & Eugen-Olsen, J. (2020). Elevated suPAR Is an Independent Risk Marker for Incident Kidney Disease in Acute Medical Patients. Frontiers in Cell and Developmental Biology, 8, [339]. https://doi.org/10.3389/fcell.2020.00339

Vancouver

Iversen E, Houlind MB, Kallemose T, Rasmussen LJH, Hornum M, Feldt-Rasmussen B et al. Elevated suPAR Is an Independent Risk Marker for Incident Kidney Disease in Acute Medical Patients. Frontiers in Cell and Developmental Biology. 2020;8. 339. https://doi.org/10.3389/fcell.2020.00339

Author

Iversen, Esben ; Houlind, Morten Baltzer ; Kallemose, Thomas ; Rasmussen, Line Jee Hartmann ; Hornum, Mads ; Feldt-Rasmussen, Bo ; Hayek, Salim S. ; Andersen, Ove ; Eugen-Olsen, Jesper. / Elevated suPAR Is an Independent Risk Marker for Incident Kidney Disease in Acute Medical Patients. In: Frontiers in Cell and Developmental Biology. 2020 ; Vol. 8.

Bibtex

@article{c6fcae055c584f849997be2a47644253,
title = "Elevated suPAR Is an Independent Risk Marker for Incident Kidney Disease in Acute Medical Patients",
abstract = "Introduction Identifying patients at high risk of developing kidney disease could lead to early clinical interventions that prevent or slow disease progression. Soluble urokinase plasminogen activator receptor (suPAR) is an inflammatory biomarker thought to be involved in the pathogenesis and development of kidney disease. We aimed to determine whether elevated plasma suPAR measured at hospital admission is associated with incident kidney disease in patients presenting to the emergency department. Materials and Methods This was a retrospective registry-based cohort study performed at the Emergency Department of Copenhagen University Hospital Amager and Hvidovre, Hvidovre, Denmark. Patients were included in the study from November 2013 to March 2017 and followed until June 2017. Patients were excluded if they were diagnosed with kidney disease or died prior to index discharge. Plasma suPAR was measured at hospital admission, and the main outcome was time to incident kidney disease, defined by ICD-10 diagnosis codes for both chronic and acute kidney conditions. Association between suPAR and time to incident kidney disease was assessed by Cox proportional hazard regression analysis. Results In total, 25,497 patients (median age 58.1 years; 52.5% female) were admitted to the emergency department and followed for development of kidney disease. In multivariable Cox regression analysis adjusting for age, sex, eGFR, CRP, cardiovascular disease, hypertension, and diabetes, each doubling in suPAR at hospital admission was associated with a hazard ratio of 1.57 (95% CI: 1.38-1.78,P<0.001) for developing a chronic kidney condition and 2.51 (95% CI: 2.09-3.01,P<0.001) for developing an acute kidney condition. Discussion In a large cohort of acutely hospitalized medical patients, elevated suPAR was independently associated with incident chronic and acute kidney conditions. This highlights the potential for using suPAR in risk classification models to identify high-risk patients who could benefit from early clinical interventions. The main limitation of this study is its reliance on accurate reporting of ICD-10 codes for kidney disease.",
keywords = "chronic kidney disease, acute kidney injury, dialysis, soluble urokinase plasminogen activator receptor, glomerular filtration rate, emergency department, PLASMINOGEN-ACTIVATOR RECEPTOR, GLOMERULAR-FILTRATION-RATE, SOLUBLE UROKINASE RECEPTOR, CARDIOVASCULAR-DISEASE, EMERGENCY-DEPARTMENT, RENAL-FUNCTION, ALBUMINURIA, GUIDELINE, MORTALITY, GUIDANCE",
author = "Esben Iversen and Houlind, {Morten Baltzer} and Thomas Kallemose and Rasmussen, {Line Jee Hartmann} and Mads Hornum and Bo Feldt-Rasmussen and Hayek, {Salim S.} and Ove Andersen and Jesper Eugen-Olsen",
year = "2020",
doi = "10.3389/fcell.2020.00339",
language = "English",
volume = "8",
journal = "Frontiers in Cell and Developmental Biology",
issn = "2296-634X",
publisher = "Frontiers Media",

}

RIS

TY - JOUR

T1 - Elevated suPAR Is an Independent Risk Marker for Incident Kidney Disease in Acute Medical Patients

AU - Iversen, Esben

AU - Houlind, Morten Baltzer

AU - Kallemose, Thomas

AU - Rasmussen, Line Jee Hartmann

AU - Hornum, Mads

AU - Feldt-Rasmussen, Bo

AU - Hayek, Salim S.

AU - Andersen, Ove

AU - Eugen-Olsen, Jesper

PY - 2020

Y1 - 2020

N2 - Introduction Identifying patients at high risk of developing kidney disease could lead to early clinical interventions that prevent or slow disease progression. Soluble urokinase plasminogen activator receptor (suPAR) is an inflammatory biomarker thought to be involved in the pathogenesis and development of kidney disease. We aimed to determine whether elevated plasma suPAR measured at hospital admission is associated with incident kidney disease in patients presenting to the emergency department. Materials and Methods This was a retrospective registry-based cohort study performed at the Emergency Department of Copenhagen University Hospital Amager and Hvidovre, Hvidovre, Denmark. Patients were included in the study from November 2013 to March 2017 and followed until June 2017. Patients were excluded if they were diagnosed with kidney disease or died prior to index discharge. Plasma suPAR was measured at hospital admission, and the main outcome was time to incident kidney disease, defined by ICD-10 diagnosis codes for both chronic and acute kidney conditions. Association between suPAR and time to incident kidney disease was assessed by Cox proportional hazard regression analysis. Results In total, 25,497 patients (median age 58.1 years; 52.5% female) were admitted to the emergency department and followed for development of kidney disease. In multivariable Cox regression analysis adjusting for age, sex, eGFR, CRP, cardiovascular disease, hypertension, and diabetes, each doubling in suPAR at hospital admission was associated with a hazard ratio of 1.57 (95% CI: 1.38-1.78,P<0.001) for developing a chronic kidney condition and 2.51 (95% CI: 2.09-3.01,P<0.001) for developing an acute kidney condition. Discussion In a large cohort of acutely hospitalized medical patients, elevated suPAR was independently associated with incident chronic and acute kidney conditions. This highlights the potential for using suPAR in risk classification models to identify high-risk patients who could benefit from early clinical interventions. The main limitation of this study is its reliance on accurate reporting of ICD-10 codes for kidney disease.

AB - Introduction Identifying patients at high risk of developing kidney disease could lead to early clinical interventions that prevent or slow disease progression. Soluble urokinase plasminogen activator receptor (suPAR) is an inflammatory biomarker thought to be involved in the pathogenesis and development of kidney disease. We aimed to determine whether elevated plasma suPAR measured at hospital admission is associated with incident kidney disease in patients presenting to the emergency department. Materials and Methods This was a retrospective registry-based cohort study performed at the Emergency Department of Copenhagen University Hospital Amager and Hvidovre, Hvidovre, Denmark. Patients were included in the study from November 2013 to March 2017 and followed until June 2017. Patients were excluded if they were diagnosed with kidney disease or died prior to index discharge. Plasma suPAR was measured at hospital admission, and the main outcome was time to incident kidney disease, defined by ICD-10 diagnosis codes for both chronic and acute kidney conditions. Association between suPAR and time to incident kidney disease was assessed by Cox proportional hazard regression analysis. Results In total, 25,497 patients (median age 58.1 years; 52.5% female) were admitted to the emergency department and followed for development of kidney disease. In multivariable Cox regression analysis adjusting for age, sex, eGFR, CRP, cardiovascular disease, hypertension, and diabetes, each doubling in suPAR at hospital admission was associated with a hazard ratio of 1.57 (95% CI: 1.38-1.78,P<0.001) for developing a chronic kidney condition and 2.51 (95% CI: 2.09-3.01,P<0.001) for developing an acute kidney condition. Discussion In a large cohort of acutely hospitalized medical patients, elevated suPAR was independently associated with incident chronic and acute kidney conditions. This highlights the potential for using suPAR in risk classification models to identify high-risk patients who could benefit from early clinical interventions. The main limitation of this study is its reliance on accurate reporting of ICD-10 codes for kidney disease.

KW - chronic kidney disease

KW - acute kidney injury

KW - dialysis

KW - soluble urokinase plasminogen activator receptor

KW - glomerular filtration rate

KW - emergency department

KW - PLASMINOGEN-ACTIVATOR RECEPTOR

KW - GLOMERULAR-FILTRATION-RATE

KW - SOLUBLE UROKINASE RECEPTOR

KW - CARDIOVASCULAR-DISEASE

KW - EMERGENCY-DEPARTMENT

KW - RENAL-FUNCTION

KW - ALBUMINURIA

KW - GUIDELINE

KW - MORTALITY

KW - GUIDANCE

U2 - 10.3389/fcell.2020.00339

DO - 10.3389/fcell.2020.00339

M3 - Journal article

C2 - 32596235

VL - 8

JO - Frontiers in Cell and Developmental Biology

JF - Frontiers in Cell and Developmental Biology

SN - 2296-634X

M1 - 339

ER -

ID: 247544028