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MicroRNA‐21 was a promising biomarker for lung carcinoma diagnosis: An update meta‐analysis
OBJECTIVE: To investigate the diagnostic performance of microRNA‐21 detected in serum or sputum as a biomarker for lung carcinoma identification through pooling the open published data. METHODS: Clinical diagnostic studies related to microRNA‐21 as a biomarker for lung carcinoma identification were...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons Australia, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8807252/ https://www.ncbi.nlm.nih.gov/pubmed/34837469 http://dx.doi.org/10.1111/1759-7714.14242 |
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author | Wang, Haiyan Xu, Jia Ding, Ling |
author_facet | Wang, Haiyan Xu, Jia Ding, Ling |
author_sort | Wang, Haiyan |
collection | PubMed |
description | OBJECTIVE: To investigate the diagnostic performance of microRNA‐21 detected in serum or sputum as a biomarker for lung carcinoma identification through pooling the open published data. METHODS: Clinical diagnostic studies related to microRNA‐21 as a biomarker for lung carcinoma identification were electronically searched in the databases of Pubmed, EMBASE, Cochrane Library, Chinese National Knowledge Infrastructure, Wanfang, and Google Scholar. The data of the included studies was extracted and made pooling of diagnostic sensitivity, specificity, diagnostic odds ratio (DOR), area under the summary receiver operating characteristic curve (ROC) (AUC) for microRNA‐21 expression in serum or sputum as a biomarker for lung carcinoma identification. The publication bias was evaluated by Deek's funnel plot. RESULTS: Seventeen diagnostic studies were finally included and made data pooling. For the included 17 studies, 4 investigated the microRNA‐21 expression in sputum and 13 studies in serum. The pooled diagnostic sensitivity and specificity were 0.73 (95% CI, 0.67–0.78) and 0.81 (95% CI, 0.75–0.85), respectively, under random effect model. The combined DOR was 9.65 (95% CI, 6.64–14.03) with the AUC of 0.84 (95% CI, 0.80–0.87). Given a pre‐test probability of 50%, the post‐test positive probability and post‐test negative probability were 79% and 25%, respectively, by using microRNA‐21 as a biomarker for lung carcinoma diagnosis. Deek's funnel was obviously asymmetry and indicated significant publication bias (p < 0.05). CONCLUSION: MicroRNA‐21 in serum or sputum was a promising biomarker for lung cancer identification with relative high diagnostic sensitivity and specificity. |
format | Online Article Text |
id | pubmed-8807252 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley & Sons Australia, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-88072522022-02-04 MicroRNA‐21 was a promising biomarker for lung carcinoma diagnosis: An update meta‐analysis Wang, Haiyan Xu, Jia Ding, Ling Thorac Cancer Original Articles OBJECTIVE: To investigate the diagnostic performance of microRNA‐21 detected in serum or sputum as a biomarker for lung carcinoma identification through pooling the open published data. METHODS: Clinical diagnostic studies related to microRNA‐21 as a biomarker for lung carcinoma identification were electronically searched in the databases of Pubmed, EMBASE, Cochrane Library, Chinese National Knowledge Infrastructure, Wanfang, and Google Scholar. The data of the included studies was extracted and made pooling of diagnostic sensitivity, specificity, diagnostic odds ratio (DOR), area under the summary receiver operating characteristic curve (ROC) (AUC) for microRNA‐21 expression in serum or sputum as a biomarker for lung carcinoma identification. The publication bias was evaluated by Deek's funnel plot. RESULTS: Seventeen diagnostic studies were finally included and made data pooling. For the included 17 studies, 4 investigated the microRNA‐21 expression in sputum and 13 studies in serum. The pooled diagnostic sensitivity and specificity were 0.73 (95% CI, 0.67–0.78) and 0.81 (95% CI, 0.75–0.85), respectively, under random effect model. The combined DOR was 9.65 (95% CI, 6.64–14.03) with the AUC of 0.84 (95% CI, 0.80–0.87). Given a pre‐test probability of 50%, the post‐test positive probability and post‐test negative probability were 79% and 25%, respectively, by using microRNA‐21 as a biomarker for lung carcinoma diagnosis. Deek's funnel was obviously asymmetry and indicated significant publication bias (p < 0.05). CONCLUSION: MicroRNA‐21 in serum or sputum was a promising biomarker for lung cancer identification with relative high diagnostic sensitivity and specificity. John Wiley & Sons Australia, Ltd 2021-11-27 2022-02 /pmc/articles/PMC8807252/ /pubmed/34837469 http://dx.doi.org/10.1111/1759-7714.14242 Text en © 2021 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Articles Wang, Haiyan Xu, Jia Ding, Ling MicroRNA‐21 was a promising biomarker for lung carcinoma diagnosis: An update meta‐analysis |
title |
MicroRNA‐21 was a promising biomarker for lung carcinoma diagnosis: An update meta‐analysis |
title_full |
MicroRNA‐21 was a promising biomarker for lung carcinoma diagnosis: An update meta‐analysis |
title_fullStr |
MicroRNA‐21 was a promising biomarker for lung carcinoma diagnosis: An update meta‐analysis |
title_full_unstemmed |
MicroRNA‐21 was a promising biomarker for lung carcinoma diagnosis: An update meta‐analysis |
title_short |
MicroRNA‐21 was a promising biomarker for lung carcinoma diagnosis: An update meta‐analysis |
title_sort | microrna‐21 was a promising biomarker for lung carcinoma diagnosis: an update meta‐analysis |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8807252/ https://www.ncbi.nlm.nih.gov/pubmed/34837469 http://dx.doi.org/10.1111/1759-7714.14242 |
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