Elevated serum SDMA and ADMA at hospital admission predict in-hospital mortality of COVID-19 patients
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Elevated serum SDMA and ADMA at hospital admission predict in-hospital mortality of COVID-19 patients. / Hannemann, Juliane; Balfanz, Paul; Schwedhelm, Edzard; Hartmann, Bojan; Ule, Johanna; Müller-Wieland, Dirk; Dahl, Edgar; Dreher, Michael; Marx, Nikolaus; Böger, Rainer.
in: SCI REP-UK, Jahrgang 11, Nr. 1, 9895, 10.05.2021.Publikationen: SCORING: Beitrag in Fachzeitschrift/Zeitung › SCORING: Zeitschriftenaufsatz › Forschung › Begutachtung
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TY - JOUR
T1 - Elevated serum SDMA and ADMA at hospital admission predict in-hospital mortality of COVID-19 patients
AU - Hannemann, Juliane
AU - Balfanz, Paul
AU - Schwedhelm, Edzard
AU - Hartmann, Bojan
AU - Ule, Johanna
AU - Müller-Wieland, Dirk
AU - Dahl, Edgar
AU - Dreher, Michael
AU - Marx, Nikolaus
AU - Böger, Rainer
PY - 2021/5/10
Y1 - 2021/5/10
N2 - COVID-19 is a disease with a variable clinical course ranging from mild symptoms to critical illness, organ failure, and death. Prospective biomarkers may help to predict the severity of an individual's clinical course and mortality risk. We analyzed asymmetric (ADMA) and symmetric dimethylarginine (SDMA) in blood samples from 31 patients hospitalized for COVID-19. We calculated associations of ADMA and SDMA with mortality and organ failure, and we developed a predictive algorithm based upon these biomarkers to predict mortality risk. Nine patients (29%) experienced in-hospital death. SDMA and ADMA serum concentrations were significantly higher at admission in COVID-19 patients who died than in survivors. Cut-offs of 0.90 µmol/L for SDMA (AUC, 0.904, p = 0.0005) and 0.66 µmol/L for ADMA (AUC, 0.874, p = 0.0013) were found in ROC analyses to best discriminate both subgroups of patients. Hazard ratio for in-hospital mortality was 12.2 (95% CI: 2.2-31.2) for SDMA and 6.3 (1.1-14.7) for ADMA above cut-off. Sequential analysis of both biomarkers allowed discriminating a high-risk group (87.5% mortality) from an intermediate-risk group (25% mortality) and a low-risk group (0% mortality). Elevated circulating concentrations of SDMA and ADMA may help to better identify COVID-19 patients with a high risk of in-hospital mortality.
AB - COVID-19 is a disease with a variable clinical course ranging from mild symptoms to critical illness, organ failure, and death. Prospective biomarkers may help to predict the severity of an individual's clinical course and mortality risk. We analyzed asymmetric (ADMA) and symmetric dimethylarginine (SDMA) in blood samples from 31 patients hospitalized for COVID-19. We calculated associations of ADMA and SDMA with mortality and organ failure, and we developed a predictive algorithm based upon these biomarkers to predict mortality risk. Nine patients (29%) experienced in-hospital death. SDMA and ADMA serum concentrations were significantly higher at admission in COVID-19 patients who died than in survivors. Cut-offs of 0.90 µmol/L for SDMA (AUC, 0.904, p = 0.0005) and 0.66 µmol/L for ADMA (AUC, 0.874, p = 0.0013) were found in ROC analyses to best discriminate both subgroups of patients. Hazard ratio for in-hospital mortality was 12.2 (95% CI: 2.2-31.2) for SDMA and 6.3 (1.1-14.7) for ADMA above cut-off. Sequential analysis of both biomarkers allowed discriminating a high-risk group (87.5% mortality) from an intermediate-risk group (25% mortality) and a low-risk group (0% mortality). Elevated circulating concentrations of SDMA and ADMA may help to better identify COVID-19 patients with a high risk of in-hospital mortality.
KW - Aged
KW - Aged, 80 and over
KW - Arginine/analogs & derivatives
KW - Biomarkers/blood
KW - COVID-19/blood
KW - Cohort Studies
KW - Female
KW - Hospital Mortality
KW - Hospitalization/statistics & numerical data
KW - Humans
KW - Kaplan-Meier Estimate
KW - Male
KW - Middle Aged
KW - Risk Factors
KW - SARS-CoV-2/isolation & purification
U2 - 10.1038/s41598-021-89180-w
DO - 10.1038/s41598-021-89180-w
M3 - SCORING: Journal article
C2 - 33972591
VL - 11
JO - SCI REP-UK
JF - SCI REP-UK
SN - 2045-2322
IS - 1
M1 - 9895
ER -