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Diagnostic value of circRNAs as effective biomarkers in human cardiovascular disease: an updated meta-analysis

Background: A growing body of literature has demonstrated that circular RNAs (circRNAs) are the potential biomarkers in human cardiovascular disease (CVD). Therefore, a meta-analysis based on current studies was accomplished to appraise the role of circRNAs in the diagnostic of CVD patients. Methods...

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Autores principales: Zhang, Zhexiao, Guo, Runmin, Wang, Yuhui, Huang, Hairong, Liu, Jie, Wang, Chenfei, Wu, Hongfu, Zou, Tangbin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8964318/
https://www.ncbi.nlm.nih.gov/pubmed/35370465
http://dx.doi.org/10.7150/ijms.67094
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author Zhang, Zhexiao
Guo, Runmin
Wang, Yuhui
Huang, Hairong
Liu, Jie
Wang, Chenfei
Wu, Hongfu
Zou, Tangbin
author_facet Zhang, Zhexiao
Guo, Runmin
Wang, Yuhui
Huang, Hairong
Liu, Jie
Wang, Chenfei
Wu, Hongfu
Zou, Tangbin
author_sort Zhang, Zhexiao
collection PubMed
description Background: A growing body of literature has demonstrated that circular RNAs (circRNAs) are the potential biomarkers in human cardiovascular disease (CVD). Therefore, a meta-analysis based on current studies was accomplished to appraise the role of circRNAs in the diagnostic of CVD patients. Methods: Studies before October 30, 2021, were searched using PubMed, EMBASE, the Web of Science, and Cochrane Library. The diagnostic odds ratio (DOR) with a confidence interval (CI) of 95% was used to investigate the associations between circRNAs and CVDs. Results: A total of 27 eligible articles were selected, including 47 studies, with 6833 participants meeting the criteria standard constrain. The pooled overall sensitivity and specificity for circRNAs expression profile in differentiating CVD patients from controls (non-CVDs or healthy subjects) were 0.81 (95%CI 0.78-0.83) and 0.74 (95%CI 0.68-0.78), respectively; the overall positive likelihood ratio was 3.1 (95%CI 2.5-3.7); the negative likelihood ratio was 0.26 (95%CI 0.22-0.31); the overall diagnostic odds ratio corresponding to an area under the curve of 0.85 (95%CI 0.81-0.88) was 12 (95%CI 9-16). Subgroup analysis indicated that the serum rather than blood has higher diagnostic accuracy. Likewise, meta-regression analysis demonstrated that the specimen, detection method, sample size, and publication year were the main sources of heterogeneity. Sensitivity analysis and Deeks' funnel plot revealed that our results are relatively robust. Conclusions: Our evidence-based analysis results suggested that circRNAs provide higher diagnostic accuracy in the prediction of CVDs. Thus, circRNAs might be potential biomarkers in CVDs.
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spelling pubmed-89643182022-03-31 Diagnostic value of circRNAs as effective biomarkers in human cardiovascular disease: an updated meta-analysis Zhang, Zhexiao Guo, Runmin Wang, Yuhui Huang, Hairong Liu, Jie Wang, Chenfei Wu, Hongfu Zou, Tangbin Int J Med Sci Review Background: A growing body of literature has demonstrated that circular RNAs (circRNAs) are the potential biomarkers in human cardiovascular disease (CVD). Therefore, a meta-analysis based on current studies was accomplished to appraise the role of circRNAs in the diagnostic of CVD patients. Methods: Studies before October 30, 2021, were searched using PubMed, EMBASE, the Web of Science, and Cochrane Library. The diagnostic odds ratio (DOR) with a confidence interval (CI) of 95% was used to investigate the associations between circRNAs and CVDs. Results: A total of 27 eligible articles were selected, including 47 studies, with 6833 participants meeting the criteria standard constrain. The pooled overall sensitivity and specificity for circRNAs expression profile in differentiating CVD patients from controls (non-CVDs or healthy subjects) were 0.81 (95%CI 0.78-0.83) and 0.74 (95%CI 0.68-0.78), respectively; the overall positive likelihood ratio was 3.1 (95%CI 2.5-3.7); the negative likelihood ratio was 0.26 (95%CI 0.22-0.31); the overall diagnostic odds ratio corresponding to an area under the curve of 0.85 (95%CI 0.81-0.88) was 12 (95%CI 9-16). Subgroup analysis indicated that the serum rather than blood has higher diagnostic accuracy. Likewise, meta-regression analysis demonstrated that the specimen, detection method, sample size, and publication year were the main sources of heterogeneity. Sensitivity analysis and Deeks' funnel plot revealed that our results are relatively robust. Conclusions: Our evidence-based analysis results suggested that circRNAs provide higher diagnostic accuracy in the prediction of CVDs. Thus, circRNAs might be potential biomarkers in CVDs. Ivyspring International Publisher 2022-02-07 /pmc/articles/PMC8964318/ /pubmed/35370465 http://dx.doi.org/10.7150/ijms.67094 Text en © The author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Review
Zhang, Zhexiao
Guo, Runmin
Wang, Yuhui
Huang, Hairong
Liu, Jie
Wang, Chenfei
Wu, Hongfu
Zou, Tangbin
Diagnostic value of circRNAs as effective biomarkers in human cardiovascular disease: an updated meta-analysis
title Diagnostic value of circRNAs as effective biomarkers in human cardiovascular disease: an updated meta-analysis
title_full Diagnostic value of circRNAs as effective biomarkers in human cardiovascular disease: an updated meta-analysis
title_fullStr Diagnostic value of circRNAs as effective biomarkers in human cardiovascular disease: an updated meta-analysis
title_full_unstemmed Diagnostic value of circRNAs as effective biomarkers in human cardiovascular disease: an updated meta-analysis
title_short Diagnostic value of circRNAs as effective biomarkers in human cardiovascular disease: an updated meta-analysis
title_sort diagnostic value of circrnas as effective biomarkers in human cardiovascular disease: an updated meta-analysis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8964318/
https://www.ncbi.nlm.nih.gov/pubmed/35370465
http://dx.doi.org/10.7150/ijms.67094
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