Activation of the Nitric Oxide Pathway and Acute Myocardial Infarction Complicated by Acute Kidney Injury
Jazyk angličtina Země Švýcarsko Médium print-electronic
Typ dokumentu srovnávací studie, časopisecké články, pozorovací studie, práce podpořená grantem
PubMed
31958795
DOI
10.1159/000503718
PII: 000503718
Knihovny.cz E-zdroje
- Klíčová slova
- Acute kidney injury, Cardio renal, Myocardial infarction, Nitric oxide, Oxidative stress,
- MeSH
- akutní poškození ledvin etiologie metabolismus patofyziologie MeSH
- biologické markery krev MeSH
- infarkt myokardu s elevacemi ST úseků patofyziologie chirurgie MeSH
- infarkt myokardu komplikace metabolismus mortalita patofyziologie MeSH
- kardiogenní šok komplikace metabolismus MeSH
- kardiorenální syndrom komplikace MeSH
- koronární angioplastika škodlivé účinky metody MeSH
- lidé středního věku MeSH
- lidé MeSH
- multivariační analýza MeSH
- natriuretický peptid typu B metabolismus MeSH
- oxid dusnatý metabolismus MeSH
- oxidační stres fyziologie MeSH
- prediktivní hodnota testů MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- troponin metabolismus MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- pozorovací studie MeSH
- práce podpořená grantem MeSH
- srovnávací studie MeSH
- Názvy látek
- biologické markery MeSH
- natriuretický peptid typu B MeSH
- oxid dusnatý MeSH
- troponin MeSH
BACKGROUND/AIMS: The pathophysiology of acute kidney injury (AKI) in ST-elevation myocardial infarction (STEMI) patients remains poorly explored. The involvement of the nitric oxide (NO) pathway has been demonstrated in experimental ischemic AKI. The aim of this study was to assess the predictive value of circulating biomarkers of the NO pathway for AKI in STEMI patients. METHODS: Four hundred and twenty-seven STEMI patients treated with primary percutaneous coronary intervention were included. The primary end point was AKI. Biomarkers of the NO pathway (plasma superoxide dismutase [SOD], uric acid, nitrite/nitrate [NOx], neopterin) as well as cardiac biomarkers (B-type natriuretic peptide [BNP] and troponin) were sampled 12 h after admission. The predictive value of circulating biomarkers was evaluated in addition to the multivariate clinical model. RESULTS: AKI developed in 8.9% of patients. The 3-month mortality was significantly higher in patients with AKI (34.2 vs. 4.1%; p < 0.001). SOD, uric acid, NOx, neopterin, BNP and troponin were significantly associated with the development of AKI (area under curve [AUC]-receiver operating curve [ROC] ranging between 0.70 and 0.81). In multivariate analysis cardiogenic shock, neopterin, NOx and troponin were independent predictors of AKI. AUC-ROC of the association of multibiomarkers and clinical model was 0.90 and outperformed the predictive value of the clinical model alone. OR of NOx ≥45 µmol/L was 8.0 (95% CI 3.1-20.6) for AKI. CONCLUSION: Biomarkers of the NO pathway are associated with the development of AKI in STEMI patients. These results provide insights into the pathophysiology of AKI and may serve at developing preventing strategies for AKI targeting this pathway.
Department of Anaesthesiology and Intensive Care St Anne's University Hospital Brno Czechia
Department of Biochemistry Faculty of Medicine Masaryk University Brno Czechia
Department of Biochemistry University Hospital Brno Brno Czechia
Department of Internal Medicine and Cardiology University Hospital Brno Brno Czechia
Department of Laboratory Methods Faculty of Medicine Masaryk University Brno Czechia
Department of Translational Physiology Academic Medical Center Amsterdam The Netherlands
F CRIN INI CRCT Network Nancy France
Faculty of Medicine Masaryk University Brno Czechia
Institute of Biostatistics and Analyses Faculty of Medicine Masaryk University Brno Czechia
Institute of Pathological Physiology Faculty of Medicine Masaryk University Brno Czechia
Intensive Care Research International Clinical Research Centre Brno Czechia
Université Paris Diderot PRES Sorbonne Paris Cité Paris France
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