Soluble urokinase receptor as a predictor of non-cardiac mortality in patients with percutaneous coronary intervention treated ST-segment elevation myocardial infarction

Standard

Soluble urokinase receptor as a predictor of non-cardiac mortality in patients with percutaneous coronary intervention treated ST-segment elevation myocardial infarction. / Sandø, Andreas; Schultz, Martin; Eugen-Olsen, Jesper; Køber, Lars; Engstrøm, Thomas; Kelbæk, Henning; Jørgensen, Erik; Saunamäki, Kari; Holmvang, Lene; Pedersen, Frants; Tilsted, Hans Henrik; Høfsten, Dan; Helqvist, Steffen; Clemmensen, Peter; Iversen, Kasper.

in: CLIN BIOCHEM, Jahrgang 80, 06.2020, S. 8-13.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Sandø, A, Schultz, M, Eugen-Olsen, J, Køber, L, Engstrøm, T, Kelbæk, H, Jørgensen, E, Saunamäki, K, Holmvang, L, Pedersen, F, Tilsted, HH, Høfsten, D, Helqvist, S, Clemmensen, P & Iversen, K 2020, 'Soluble urokinase receptor as a predictor of non-cardiac mortality in patients with percutaneous coronary intervention treated ST-segment elevation myocardial infarction', CLIN BIOCHEM, Jg. 80, S. 8-13. https://doi.org/10.1016/j.clinbiochem.2020.03.013

APA

Sandø, A., Schultz, M., Eugen-Olsen, J., Køber, L., Engstrøm, T., Kelbæk, H., Jørgensen, E., Saunamäki, K., Holmvang, L., Pedersen, F., Tilsted, H. H., Høfsten, D., Helqvist, S., Clemmensen, P., & Iversen, K. (2020). Soluble urokinase receptor as a predictor of non-cardiac mortality in patients with percutaneous coronary intervention treated ST-segment elevation myocardial infarction. CLIN BIOCHEM, 80, 8-13. https://doi.org/10.1016/j.clinbiochem.2020.03.013

Vancouver

Bibtex

@article{a852c89df9cf48f6897a84acfea98b90,
title = "Soluble urokinase receptor as a predictor of non-cardiac mortality in patients with percutaneous coronary intervention treated ST-segment elevation myocardial infarction",
abstract = "BACKGROUND: Identification of patients at high risk of non-cardiac mortality following ST-segment elevation myocardial infarction (STEMI) could guide clinicians to identify patients who require attention due to serious non-cardiac conditions after the acute phase of STEMI. The purpose of this study was to evaluate if the non-specific and prognostic biomarker of inflammation and comorbidity, soluble urokinase receptor (suPAR), could predict non-cardiac mortality in a cohort of STEMI patients.METHODS: SuPAR was measured in 1,190 STEMI patients who underwent primary percutaneous coronary intervention (pPCI). The primary endpoint was non-cardiac mortality, secondary endpoints were cardiac mortality, all-cause mortality, reinfarction and periprocedural acute kidney injury. Backwards elimination of potential confounders significantly associated with the respective outcome was used to adjust associations.RESULTS: Patients were followed for a median of 3.0 years (interquartile range 2.5- 3.6 years). Multivariate cox regression revealed that a plasma suPAR level above 3.70 ng mL-1 was associated with non-cardiac and cardiac mortality at hazard ratios 3.33 (95% confidence interval 1.67-6.63, p = 0.001, adjusted for age) and 0.99 (0.18-5.30, p = 0.98, adjusted for previous myocardial infarction and left ventricular ejection fraction), respectively.CONCLUSION: In patients with pPCI treated STEMI, suPAR was an independent prognostic biomarker of non-cardiac but not cardiac mortality and may identify patients with high risk of non-cardiac mortality.",
keywords = "Aged, Biomarkers/blood, Cohort Studies, Female, Humans, Male, Middle Aged, Percutaneous Coronary Intervention/mortality, Prognosis, Receptors, Urokinase Plasminogen Activator/blood, Risk Factors, ST Elevation Myocardial Infarction/surgery, Treatment Outcome",
author = "Andreas Sand{\o} and Martin Schultz and Jesper Eugen-Olsen and Lars K{\o}ber and Thomas Engstr{\o}m and Henning Kelb{\ae}k and Erik J{\o}rgensen and Kari Saunam{\"a}ki and Lene Holmvang and Frants Pedersen and Tilsted, {Hans Henrik} and Dan H{\o}fsten and Steffen Helqvist and Peter Clemmensen and Kasper Iversen",
note = "Copyright {\textcopyright} 2020 The Canadian Society of Clinical Chemists. Published by Elsevier Inc. All rights reserved.",
year = "2020",
month = jun,
doi = "10.1016/j.clinbiochem.2020.03.013",
language = "English",
volume = "80",
pages = "8--13",
journal = "CLIN BIOCHEM",
issn = "0009-9120",
publisher = "Elsevier Inc.",

}

RIS

TY - JOUR

T1 - Soluble urokinase receptor as a predictor of non-cardiac mortality in patients with percutaneous coronary intervention treated ST-segment elevation myocardial infarction

AU - Sandø, Andreas

AU - Schultz, Martin

AU - Eugen-Olsen, Jesper

AU - Køber, Lars

AU - Engstrøm, Thomas

AU - Kelbæk, Henning

AU - Jørgensen, Erik

AU - Saunamäki, Kari

AU - Holmvang, Lene

AU - Pedersen, Frants

AU - Tilsted, Hans Henrik

AU - Høfsten, Dan

AU - Helqvist, Steffen

AU - Clemmensen, Peter

AU - Iversen, Kasper

N1 - Copyright © 2020 The Canadian Society of Clinical Chemists. Published by Elsevier Inc. All rights reserved.

PY - 2020/6

Y1 - 2020/6

N2 - BACKGROUND: Identification of patients at high risk of non-cardiac mortality following ST-segment elevation myocardial infarction (STEMI) could guide clinicians to identify patients who require attention due to serious non-cardiac conditions after the acute phase of STEMI. The purpose of this study was to evaluate if the non-specific and prognostic biomarker of inflammation and comorbidity, soluble urokinase receptor (suPAR), could predict non-cardiac mortality in a cohort of STEMI patients.METHODS: SuPAR was measured in 1,190 STEMI patients who underwent primary percutaneous coronary intervention (pPCI). The primary endpoint was non-cardiac mortality, secondary endpoints were cardiac mortality, all-cause mortality, reinfarction and periprocedural acute kidney injury. Backwards elimination of potential confounders significantly associated with the respective outcome was used to adjust associations.RESULTS: Patients were followed for a median of 3.0 years (interquartile range 2.5- 3.6 years). Multivariate cox regression revealed that a plasma suPAR level above 3.70 ng mL-1 was associated with non-cardiac and cardiac mortality at hazard ratios 3.33 (95% confidence interval 1.67-6.63, p = 0.001, adjusted for age) and 0.99 (0.18-5.30, p = 0.98, adjusted for previous myocardial infarction and left ventricular ejection fraction), respectively.CONCLUSION: In patients with pPCI treated STEMI, suPAR was an independent prognostic biomarker of non-cardiac but not cardiac mortality and may identify patients with high risk of non-cardiac mortality.

AB - BACKGROUND: Identification of patients at high risk of non-cardiac mortality following ST-segment elevation myocardial infarction (STEMI) could guide clinicians to identify patients who require attention due to serious non-cardiac conditions after the acute phase of STEMI. The purpose of this study was to evaluate if the non-specific and prognostic biomarker of inflammation and comorbidity, soluble urokinase receptor (suPAR), could predict non-cardiac mortality in a cohort of STEMI patients.METHODS: SuPAR was measured in 1,190 STEMI patients who underwent primary percutaneous coronary intervention (pPCI). The primary endpoint was non-cardiac mortality, secondary endpoints were cardiac mortality, all-cause mortality, reinfarction and periprocedural acute kidney injury. Backwards elimination of potential confounders significantly associated with the respective outcome was used to adjust associations.RESULTS: Patients were followed for a median of 3.0 years (interquartile range 2.5- 3.6 years). Multivariate cox regression revealed that a plasma suPAR level above 3.70 ng mL-1 was associated with non-cardiac and cardiac mortality at hazard ratios 3.33 (95% confidence interval 1.67-6.63, p = 0.001, adjusted for age) and 0.99 (0.18-5.30, p = 0.98, adjusted for previous myocardial infarction and left ventricular ejection fraction), respectively.CONCLUSION: In patients with pPCI treated STEMI, suPAR was an independent prognostic biomarker of non-cardiac but not cardiac mortality and may identify patients with high risk of non-cardiac mortality.

KW - Aged

KW - Biomarkers/blood

KW - Cohort Studies

KW - Female

KW - Humans

KW - Male

KW - Middle Aged

KW - Percutaneous Coronary Intervention/mortality

KW - Prognosis

KW - Receptors, Urokinase Plasminogen Activator/blood

KW - Risk Factors

KW - ST Elevation Myocardial Infarction/surgery

KW - Treatment Outcome

U2 - 10.1016/j.clinbiochem.2020.03.013

DO - 10.1016/j.clinbiochem.2020.03.013

M3 - SCORING: Journal article

C2 - 32213303

VL - 80

SP - 8

EP - 13

JO - CLIN BIOCHEM

JF - CLIN BIOCHEM

SN - 0009-9120

ER -