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Could sST2 Predict Contrast-Induced Nephropathy in ST-Segment Elevation Myocardial Infarction?

BACKGROUND AND AIM: One of the most worrying complications of primary percutaneous coronary interventions is contrast-induced nephropathy (CIN) that is associated with increased mortality and morbidity in myocardial infarction. In this study, we questioned whether soluble suppression of tumorigenesi...

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Autores principales: Avcı, Ahmet, Somuncu, Mustafa Umut, Can, Murat, Akgul, Ferit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7708263/
https://www.ncbi.nlm.nih.gov/pubmed/33273849
http://dx.doi.org/10.2147/IJGM.S287834
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author Avcı, Ahmet
Somuncu, Mustafa Umut
Can, Murat
Akgul, Ferit
author_facet Avcı, Ahmet
Somuncu, Mustafa Umut
Can, Murat
Akgul, Ferit
author_sort Avcı, Ahmet
collection PubMed
description BACKGROUND AND AIM: One of the most worrying complications of primary percutaneous coronary interventions is contrast-induced nephropathy (CIN) that is associated with increased mortality and morbidity in myocardial infarction. In this study, we questioned whether soluble suppression of tumorigenesis-2 (sST2), which has thought to play a role in inflammatory processes, cardiac remodeling, and fibrosis could give an idea about the development of CIN in ST-elevation myocardial infarction (STEMI) patients. PATIENTS AND METHODS: This study is a cross-sectional observational study and includes 357 consecutive STEMI patients. Demographic features, medical history, laboratory parameters, and procedural characteristics were compared according to CIN’s development. The multivariate logistic regression analysis was selected to detect independent risk factors of CIN. RESULTS: In the study, 81 patients (22.7%) who developed CIN were identified. The concentration of sST2 in CIN (+) group was higher than that of CIN (-) group (40.6±21.0 ng/mL vs 31.5±13.0 ng/L, p<0.001). Independent predictors of CIN development were diabetes mellitus (OR, 2.059; 95% CI, 1.093–3.879; p=0.025), eGFR (OR, 0.983; 95% CI, 0.972–0.995; p=0.006), lower systolic blood pressure (OR, 0.976; 95% CI, 0.960–0.993; p=0.006), total procedure time (OR, 1.030; 95% CI, 1.011–1.049; p=0.002), and sST2 (OR, 1.101; 95% CI; 1.046–1.160; p<0.001). Besides, the risk of developing CIN in the high sST2 group is 3.06 times higher than the low group sST2 group regardless of other risk factors. CONCLUSION: sST2 levels on admission in STEMI patients are useful in predicting CIN development.
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spelling pubmed-77082632020-12-02 Could sST2 Predict Contrast-Induced Nephropathy in ST-Segment Elevation Myocardial Infarction? Avcı, Ahmet Somuncu, Mustafa Umut Can, Murat Akgul, Ferit Int J Gen Med Original Research BACKGROUND AND AIM: One of the most worrying complications of primary percutaneous coronary interventions is contrast-induced nephropathy (CIN) that is associated with increased mortality and morbidity in myocardial infarction. In this study, we questioned whether soluble suppression of tumorigenesis-2 (sST2), which has thought to play a role in inflammatory processes, cardiac remodeling, and fibrosis could give an idea about the development of CIN in ST-elevation myocardial infarction (STEMI) patients. PATIENTS AND METHODS: This study is a cross-sectional observational study and includes 357 consecutive STEMI patients. Demographic features, medical history, laboratory parameters, and procedural characteristics were compared according to CIN’s development. The multivariate logistic regression analysis was selected to detect independent risk factors of CIN. RESULTS: In the study, 81 patients (22.7%) who developed CIN were identified. The concentration of sST2 in CIN (+) group was higher than that of CIN (-) group (40.6±21.0 ng/mL vs 31.5±13.0 ng/L, p<0.001). Independent predictors of CIN development were diabetes mellitus (OR, 2.059; 95% CI, 1.093–3.879; p=0.025), eGFR (OR, 0.983; 95% CI, 0.972–0.995; p=0.006), lower systolic blood pressure (OR, 0.976; 95% CI, 0.960–0.993; p=0.006), total procedure time (OR, 1.030; 95% CI, 1.011–1.049; p=0.002), and sST2 (OR, 1.101; 95% CI; 1.046–1.160; p<0.001). Besides, the risk of developing CIN in the high sST2 group is 3.06 times higher than the low group sST2 group regardless of other risk factors. CONCLUSION: sST2 levels on admission in STEMI patients are useful in predicting CIN development. Dove 2020-11-27 /pmc/articles/PMC7708263/ /pubmed/33273849 http://dx.doi.org/10.2147/IJGM.S287834 Text en © 2020 Avcı et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Avcı, Ahmet
Somuncu, Mustafa Umut
Can, Murat
Akgul, Ferit
Could sST2 Predict Contrast-Induced Nephropathy in ST-Segment Elevation Myocardial Infarction?
title Could sST2 Predict Contrast-Induced Nephropathy in ST-Segment Elevation Myocardial Infarction?
title_full Could sST2 Predict Contrast-Induced Nephropathy in ST-Segment Elevation Myocardial Infarction?
title_fullStr Could sST2 Predict Contrast-Induced Nephropathy in ST-Segment Elevation Myocardial Infarction?
title_full_unstemmed Could sST2 Predict Contrast-Induced Nephropathy in ST-Segment Elevation Myocardial Infarction?
title_short Could sST2 Predict Contrast-Induced Nephropathy in ST-Segment Elevation Myocardial Infarction?
title_sort could sst2 predict contrast-induced nephropathy in st-segment elevation myocardial infarction?
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7708263/
https://www.ncbi.nlm.nih.gov/pubmed/33273849
http://dx.doi.org/10.2147/IJGM.S287834
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