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Role of circulating long non-coding RNA for the improvement of the predictive ability of the CHA(2)DS(2)–VASc score in patients with atrial fibrillation
BACKGROUND: The CHA(2)DS(2)–VASc score was initially applied to stratify stroke risk in patients with atrial fibrillation (AF) and was found to be effective in predicting all-cause mortality outcomes. To date, it is still unclear whether circulating long non-coding RNAs (lncRNAs) as emerging biomark...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9481441/ https://www.ncbi.nlm.nih.gov/pubmed/35869861 http://dx.doi.org/10.1097/CM9.0000000000002213 |
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author | Zhang, Yuanbo Wang, Duan Wu, Na Chen, Xinghua Yuan, Zhiquan Jia, Xiaoyue Li, Chengying Hu, Qin Chen, Yanxiu Zhang, Zhihui Zhong, Li Li, Yafei |
author_facet | Zhang, Yuanbo Wang, Duan Wu, Na Chen, Xinghua Yuan, Zhiquan Jia, Xiaoyue Li, Chengying Hu, Qin Chen, Yanxiu Zhang, Zhihui Zhong, Li Li, Yafei |
author_sort | Zhang, Yuanbo |
collection | PubMed |
description | BACKGROUND: The CHA(2)DS(2)–VASc score was initially applied to stratify stroke risk in patients with atrial fibrillation (AF) and was found to be effective in predicting all-cause mortality outcomes. To date, it is still unclear whether circulating long non-coding RNAs (lncRNAs) as emerging biomarkers, can improve the predictive power of the CHA(2)DS(2)–VASc score in stroke and all-cause mortality. METHODS: Candidate lncRNAs were screened by searching the literature and analyzing previous RNA sequencing results. After preliminary verification in 29 patients with AF, the final selected lncRNAs were evaluated by Cox proportional hazards regression in 192 patients to determine whether their relative expression levels were associated with stroke and all-cause mortality. The c-statistic, net reclassification improvement (NRI), and integrated discrimination improvement of the patients were calculated to evaluate the discrimination and reclassification power for stroke and all-cause mortality when adding lncRNA expression levels to the CHA(2)DS(2)–VASc score model. RESULTS: Five plasma lncRNAs associated with stroke and all-cause mortality in AF patients were selected in our screening process. Patients with elevated H19 levels were found to have a higher risk of stroke (hazard ratio [HR] 3.264, 95% confidence interval [CI]: 1.364–7.813, P = 0.008). Adding the H19 expression level to the CHA(2)DS(2)–VASc score significantly improved the discrimination and reclassification power of the CHA(2)DS(2)–VASc score for stroke in AF patients. In addition, the H19 level showed a marginally significant association with all-cause mortality (HR 2.263, 95% CI: 0.889–5.760, P = 0.087), although it appeared to have no significant improvement for the CHA(2)DS(2)–VASc model for predicting all-cause mortality. CONCLUSIONS: Plasma expression of H19 was associated with stroke risk in AF patients and improved the discriminatory power of the CHA(2)DS(2)–VASc score. Therefore, lncRNA H19 served as an emerging non-invasive biomarker for stroke risk prediction in patients with AF. |
format | Online Article Text |
id | pubmed-9481441 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-94814412022-09-19 Role of circulating long non-coding RNA for the improvement of the predictive ability of the CHA(2)DS(2)–VASc score in patients with atrial fibrillation Zhang, Yuanbo Wang, Duan Wu, Na Chen, Xinghua Yuan, Zhiquan Jia, Xiaoyue Li, Chengying Hu, Qin Chen, Yanxiu Zhang, Zhihui Zhong, Li Li, Yafei Chin Med J (Engl) Original Articles BACKGROUND: The CHA(2)DS(2)–VASc score was initially applied to stratify stroke risk in patients with atrial fibrillation (AF) and was found to be effective in predicting all-cause mortality outcomes. To date, it is still unclear whether circulating long non-coding RNAs (lncRNAs) as emerging biomarkers, can improve the predictive power of the CHA(2)DS(2)–VASc score in stroke and all-cause mortality. METHODS: Candidate lncRNAs were screened by searching the literature and analyzing previous RNA sequencing results. After preliminary verification in 29 patients with AF, the final selected lncRNAs were evaluated by Cox proportional hazards regression in 192 patients to determine whether their relative expression levels were associated with stroke and all-cause mortality. The c-statistic, net reclassification improvement (NRI), and integrated discrimination improvement of the patients were calculated to evaluate the discrimination and reclassification power for stroke and all-cause mortality when adding lncRNA expression levels to the CHA(2)DS(2)–VASc score model. RESULTS: Five plasma lncRNAs associated with stroke and all-cause mortality in AF patients were selected in our screening process. Patients with elevated H19 levels were found to have a higher risk of stroke (hazard ratio [HR] 3.264, 95% confidence interval [CI]: 1.364–7.813, P = 0.008). Adding the H19 expression level to the CHA(2)DS(2)–VASc score significantly improved the discrimination and reclassification power of the CHA(2)DS(2)–VASc score for stroke in AF patients. In addition, the H19 level showed a marginally significant association with all-cause mortality (HR 2.263, 95% CI: 0.889–5.760, P = 0.087), although it appeared to have no significant improvement for the CHA(2)DS(2)–VASc model for predicting all-cause mortality. CONCLUSIONS: Plasma expression of H19 was associated with stroke risk in AF patients and improved the discriminatory power of the CHA(2)DS(2)–VASc score. Therefore, lncRNA H19 served as an emerging non-invasive biomarker for stroke risk prediction in patients with AF. Lippincott Williams & Wilkins 2022-06-20 2022-07-23 /pmc/articles/PMC9481441/ /pubmed/35869861 http://dx.doi.org/10.1097/CM9.0000000000002213 Text en Copyright © 2022 The Chinese Medical Association, produced by Wolters Kluwer, Inc. under the CC-BY-NC-ND license. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | Original Articles Zhang, Yuanbo Wang, Duan Wu, Na Chen, Xinghua Yuan, Zhiquan Jia, Xiaoyue Li, Chengying Hu, Qin Chen, Yanxiu Zhang, Zhihui Zhong, Li Li, Yafei Role of circulating long non-coding RNA for the improvement of the predictive ability of the CHA(2)DS(2)–VASc score in patients with atrial fibrillation |
title | Role of circulating long non-coding RNA for the improvement of the predictive ability of the CHA(2)DS(2)–VASc score in patients with atrial fibrillation |
title_full | Role of circulating long non-coding RNA for the improvement of the predictive ability of the CHA(2)DS(2)–VASc score in patients with atrial fibrillation |
title_fullStr | Role of circulating long non-coding RNA for the improvement of the predictive ability of the CHA(2)DS(2)–VASc score in patients with atrial fibrillation |
title_full_unstemmed | Role of circulating long non-coding RNA for the improvement of the predictive ability of the CHA(2)DS(2)–VASc score in patients with atrial fibrillation |
title_short | Role of circulating long non-coding RNA for the improvement of the predictive ability of the CHA(2)DS(2)–VASc score in patients with atrial fibrillation |
title_sort | role of circulating long non-coding rna for the improvement of the predictive ability of the cha(2)ds(2)–vasc score in patients with atrial fibrillation |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9481441/ https://www.ncbi.nlm.nih.gov/pubmed/35869861 http://dx.doi.org/10.1097/CM9.0000000000002213 |
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