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Relationship between lncRNA-Ang362 and prognosis of patients with coronary heart disease after percutaneous coronary intervention

The severity and complexity evaluation of coronary artery disease in patients with coronary heart disease (CHD) require objective and accurate prognosis indexes. We assessed the relationship between lncRNA-Ang362 and prognosis of CHD patients after percutaneous coronary intervention (PCI). Clinical...

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Autores principales: Wang, Hui, Gong, Huichao, Liu, Yingwu, Feng, Limin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7383831/
https://www.ncbi.nlm.nih.gov/pubmed/32686826
http://dx.doi.org/10.1042/BSR20201524
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author Wang, Hui
Gong, Huichao
Liu, Yingwu
Feng, Limin
author_facet Wang, Hui
Gong, Huichao
Liu, Yingwu
Feng, Limin
author_sort Wang, Hui
collection PubMed
description The severity and complexity evaluation of coronary artery disease in patients with coronary heart disease (CHD) require objective and accurate prognosis indexes. We assessed the relationship between lncRNA-Ang362 and prognosis of CHD patients after percutaneous coronary intervention (PCI). Clinical follow-up data of CHD patients were prospectively collected. LncRNA-Ang362 levels were detected by real-time quantitative polymerase chain reaction. Survival rate was calculated by the Kaplan–Meier method, and risk ratios and 95% confidence intervals were computed using univariate and multivariate COX proportional hazard models. Finally, 434 patients were included in the follow-up cohort. The median follow-up time was 24.8 months (6.7–40). The incidence of adverse cardiovascular events was 13.6%. The high expression group significantly tended to be smoker and higher body mass index, low-density lipoprotein cholesterol, high-sensitivity C-reactive protein, creatinine, and uric acid levels compared with the low expression group. According to the SYNTAX grade, the high-risk and medium-risk groups had significantly higher lncRNA expression levels than the low-risk group. The univariate COX regression analysis indicated that high lncRAN-Ang362 expression significantly increased the risk of adverse cardiovascular events in CHD patients after PCI (hazard risk (HR) = 3.19, 95% confidence interval (CI): 1.29–7.92). Multivariate analysis found high lncRNA-Ang362 expression was independently related to worse prognosis in CHD patients after PCI (HR = 2.83, 95%CI: 1.34–6.02). Plasma lncRNA-Ang362 may be a prognosis factor in CHD patients after PCI. The patients with higher lncRNA-Ang362 expression usually have poor prognosis.
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spelling pubmed-73838312020-08-04 Relationship between lncRNA-Ang362 and prognosis of patients with coronary heart disease after percutaneous coronary intervention Wang, Hui Gong, Huichao Liu, Yingwu Feng, Limin Biosci Rep Diagnostics & Biomarkers The severity and complexity evaluation of coronary artery disease in patients with coronary heart disease (CHD) require objective and accurate prognosis indexes. We assessed the relationship between lncRNA-Ang362 and prognosis of CHD patients after percutaneous coronary intervention (PCI). Clinical follow-up data of CHD patients were prospectively collected. LncRNA-Ang362 levels were detected by real-time quantitative polymerase chain reaction. Survival rate was calculated by the Kaplan–Meier method, and risk ratios and 95% confidence intervals were computed using univariate and multivariate COX proportional hazard models. Finally, 434 patients were included in the follow-up cohort. The median follow-up time was 24.8 months (6.7–40). The incidence of adverse cardiovascular events was 13.6%. The high expression group significantly tended to be smoker and higher body mass index, low-density lipoprotein cholesterol, high-sensitivity C-reactive protein, creatinine, and uric acid levels compared with the low expression group. According to the SYNTAX grade, the high-risk and medium-risk groups had significantly higher lncRNA expression levels than the low-risk group. The univariate COX regression analysis indicated that high lncRAN-Ang362 expression significantly increased the risk of adverse cardiovascular events in CHD patients after PCI (hazard risk (HR) = 3.19, 95% confidence interval (CI): 1.29–7.92). Multivariate analysis found high lncRNA-Ang362 expression was independently related to worse prognosis in CHD patients after PCI (HR = 2.83, 95%CI: 1.34–6.02). Plasma lncRNA-Ang362 may be a prognosis factor in CHD patients after PCI. The patients with higher lncRNA-Ang362 expression usually have poor prognosis. Portland Press Ltd. 2020-07-24 /pmc/articles/PMC7383831/ /pubmed/32686826 http://dx.doi.org/10.1042/BSR20201524 Text en © 2020 The Author(s). https://creativecommons.org/licenses/by/4.0/ This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY).
spellingShingle Diagnostics & Biomarkers
Wang, Hui
Gong, Huichao
Liu, Yingwu
Feng, Limin
Relationship between lncRNA-Ang362 and prognosis of patients with coronary heart disease after percutaneous coronary intervention
title Relationship between lncRNA-Ang362 and prognosis of patients with coronary heart disease after percutaneous coronary intervention
title_full Relationship between lncRNA-Ang362 and prognosis of patients with coronary heart disease after percutaneous coronary intervention
title_fullStr Relationship between lncRNA-Ang362 and prognosis of patients with coronary heart disease after percutaneous coronary intervention
title_full_unstemmed Relationship between lncRNA-Ang362 and prognosis of patients with coronary heart disease after percutaneous coronary intervention
title_short Relationship between lncRNA-Ang362 and prognosis of patients with coronary heart disease after percutaneous coronary intervention
title_sort relationship between lncrna-ang362 and prognosis of patients with coronary heart disease after percutaneous coronary intervention
topic Diagnostics & Biomarkers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7383831/
https://www.ncbi.nlm.nih.gov/pubmed/32686826
http://dx.doi.org/10.1042/BSR20201524
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