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Prognostic value of serum soluble ST2 in stable coronary artery disease: a prospective observational study

The role of ST2 in stable coronary artery disease (CAD) has not yet been well defined. This study was performed to investigate baseline serum soluble ST2 (sST2) level can predict clinical outcomes in patients with stable CAD. A total of 388 consecutive patients with suspected CAD (65 years and 63.7%...

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Autores principales: Kim, Hack-Lyoung, Lee, Jung Pyo, Wong, Nathan, Lim, Woo-Hyun, Seo, Jae-Bin, Zo, Joo-Hee, Kim, Myung-A, Kim, Sang-Hyun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8313553/
https://www.ncbi.nlm.nih.gov/pubmed/34312471
http://dx.doi.org/10.1038/s41598-021-94714-3
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author Kim, Hack-Lyoung
Lee, Jung Pyo
Wong, Nathan
Lim, Woo-Hyun
Seo, Jae-Bin
Zo, Joo-Hee
Kim, Myung-A
Kim, Sang-Hyun
author_facet Kim, Hack-Lyoung
Lee, Jung Pyo
Wong, Nathan
Lim, Woo-Hyun
Seo, Jae-Bin
Zo, Joo-Hee
Kim, Myung-A
Kim, Sang-Hyun
author_sort Kim, Hack-Lyoung
collection PubMed
description The role of ST2 in stable coronary artery disease (CAD) has not yet been well defined. This study was performed to investigate baseline serum soluble ST2 (sST2) level can predict clinical outcomes in patients with stable CAD. A total of 388 consecutive patients with suspected CAD (65 years and 63.7% male) in stable condition referred for elective invasive coronary angiography (ICA) was prospectively recruited. Major adverse cardiovascular event (MACE), including cardiac death, non-fatal myocardial infarction, coronary revascularization (90 days after ICA), and ischemic stroke during clinical follow-up was assessed. Most of the patients (88.0%) had significant CAD (stenosis ≥ 50%). During median follow-up of 834 days, there was 29 case of MACE (7.5%). The serum sST2 level was significantly higher in patients with MACE than those without (47.3 versus 30.6 ng/ml, P < 0.001). In multiple Cox regression model, higher sST2 level (≥ 26.8 ng/ml) was an independent predictor of MACE even after controlling potential confounders (hazard ratio, 13.7; 95% confidence interval 1.80–104.60; P = 0.011). The elevated level of baseline sST2 is associated with an increased risk of adverse clinical events in stable CAD patients. Studies with larger sample size are needed to confirm our findings.
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spelling pubmed-83135532021-07-27 Prognostic value of serum soluble ST2 in stable coronary artery disease: a prospective observational study Kim, Hack-Lyoung Lee, Jung Pyo Wong, Nathan Lim, Woo-Hyun Seo, Jae-Bin Zo, Joo-Hee Kim, Myung-A Kim, Sang-Hyun Sci Rep Article The role of ST2 in stable coronary artery disease (CAD) has not yet been well defined. This study was performed to investigate baseline serum soluble ST2 (sST2) level can predict clinical outcomes in patients with stable CAD. A total of 388 consecutive patients with suspected CAD (65 years and 63.7% male) in stable condition referred for elective invasive coronary angiography (ICA) was prospectively recruited. Major adverse cardiovascular event (MACE), including cardiac death, non-fatal myocardial infarction, coronary revascularization (90 days after ICA), and ischemic stroke during clinical follow-up was assessed. Most of the patients (88.0%) had significant CAD (stenosis ≥ 50%). During median follow-up of 834 days, there was 29 case of MACE (7.5%). The serum sST2 level was significantly higher in patients with MACE than those without (47.3 versus 30.6 ng/ml, P < 0.001). In multiple Cox regression model, higher sST2 level (≥ 26.8 ng/ml) was an independent predictor of MACE even after controlling potential confounders (hazard ratio, 13.7; 95% confidence interval 1.80–104.60; P = 0.011). The elevated level of baseline sST2 is associated with an increased risk of adverse clinical events in stable CAD patients. Studies with larger sample size are needed to confirm our findings. Nature Publishing Group UK 2021-07-26 /pmc/articles/PMC8313553/ /pubmed/34312471 http://dx.doi.org/10.1038/s41598-021-94714-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Kim, Hack-Lyoung
Lee, Jung Pyo
Wong, Nathan
Lim, Woo-Hyun
Seo, Jae-Bin
Zo, Joo-Hee
Kim, Myung-A
Kim, Sang-Hyun
Prognostic value of serum soluble ST2 in stable coronary artery disease: a prospective observational study
title Prognostic value of serum soluble ST2 in stable coronary artery disease: a prospective observational study
title_full Prognostic value of serum soluble ST2 in stable coronary artery disease: a prospective observational study
title_fullStr Prognostic value of serum soluble ST2 in stable coronary artery disease: a prospective observational study
title_full_unstemmed Prognostic value of serum soluble ST2 in stable coronary artery disease: a prospective observational study
title_short Prognostic value of serum soluble ST2 in stable coronary artery disease: a prospective observational study
title_sort prognostic value of serum soluble st2 in stable coronary artery disease: a prospective observational study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8313553/
https://www.ncbi.nlm.nih.gov/pubmed/34312471
http://dx.doi.org/10.1038/s41598-021-94714-3
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