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Diagnostic Performance of DNA Hypermethylation Markers in Peripheral Blood for the Detection of Colorectal Cancer: A Meta-Analysis and Systematic Review

DNA hypermethylation in blood is becoming an attractive candidate marker for colorectal cancer (CRC) detection. To assess the diagnostic accuracy of blood hypermethylation markers for CRC in different clinical settings, we conducted a meta-analysis of published reports. Of 485 publications obtained...

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Autores principales: Li, Bingsheng, Gan, Aihua, Chen, Xiaolong, Wang, Xinying, He, Weifeng, Zhang, Xiaohui, Huang, Renxiang, Zhou, Shuzhu, Song, Xiaoxiao, Xu, Angao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4861294/
https://www.ncbi.nlm.nih.gov/pubmed/27158984
http://dx.doi.org/10.1371/journal.pone.0155095
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author Li, Bingsheng
Gan, Aihua
Chen, Xiaolong
Wang, Xinying
He, Weifeng
Zhang, Xiaohui
Huang, Renxiang
Zhou, Shuzhu
Song, Xiaoxiao
Xu, Angao
author_facet Li, Bingsheng
Gan, Aihua
Chen, Xiaolong
Wang, Xinying
He, Weifeng
Zhang, Xiaohui
Huang, Renxiang
Zhou, Shuzhu
Song, Xiaoxiao
Xu, Angao
author_sort Li, Bingsheng
collection PubMed
description DNA hypermethylation in blood is becoming an attractive candidate marker for colorectal cancer (CRC) detection. To assess the diagnostic accuracy of blood hypermethylation markers for CRC in different clinical settings, we conducted a meta-analysis of published reports. Of 485 publications obtained in the initial literature search, 39 studies were included in the meta-analysis. Hypermethylation markers in peripheral blood showed a high degree of accuracy for the detection of CRC. The summary sensitivity was 0.62 [95% confidence interval (CI), 0.56–0.67] and specificity was 0.91 (95% CI, 0.89–0.93). Subgroup analysis showed significantly greater sensitivity for the methylated Septin 9 gene (SEPT9) subgroup (0.75; 95% CI, 0.67–0.81) than for the non-methylated SEPT9 subgroup (0.58; 95% CI, 0.52–0.64). Sensitivity and specificity were not affected significantly by target gene number, CRC staging, study region, or methylation analysis method. These findings show that hypermethylation markers in blood are highly sensitive and specific for CRC detection, with methylated SEPT9 being particularly robust. The diagnostic performance of hypermethylation markers, which have varied across different studies, can be improved by marker optimization. Future research should examine variation in diagnostic accuracy according to non-neoplastic factors.
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spelling pubmed-48612942016-05-13 Diagnostic Performance of DNA Hypermethylation Markers in Peripheral Blood for the Detection of Colorectal Cancer: A Meta-Analysis and Systematic Review Li, Bingsheng Gan, Aihua Chen, Xiaolong Wang, Xinying He, Weifeng Zhang, Xiaohui Huang, Renxiang Zhou, Shuzhu Song, Xiaoxiao Xu, Angao PLoS One Research Article DNA hypermethylation in blood is becoming an attractive candidate marker for colorectal cancer (CRC) detection. To assess the diagnostic accuracy of blood hypermethylation markers for CRC in different clinical settings, we conducted a meta-analysis of published reports. Of 485 publications obtained in the initial literature search, 39 studies were included in the meta-analysis. Hypermethylation markers in peripheral blood showed a high degree of accuracy for the detection of CRC. The summary sensitivity was 0.62 [95% confidence interval (CI), 0.56–0.67] and specificity was 0.91 (95% CI, 0.89–0.93). Subgroup analysis showed significantly greater sensitivity for the methylated Septin 9 gene (SEPT9) subgroup (0.75; 95% CI, 0.67–0.81) than for the non-methylated SEPT9 subgroup (0.58; 95% CI, 0.52–0.64). Sensitivity and specificity were not affected significantly by target gene number, CRC staging, study region, or methylation analysis method. These findings show that hypermethylation markers in blood are highly sensitive and specific for CRC detection, with methylated SEPT9 being particularly robust. The diagnostic performance of hypermethylation markers, which have varied across different studies, can be improved by marker optimization. Future research should examine variation in diagnostic accuracy according to non-neoplastic factors. Public Library of Science 2016-05-09 /pmc/articles/PMC4861294/ /pubmed/27158984 http://dx.doi.org/10.1371/journal.pone.0155095 Text en © 2016 Li et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Li, Bingsheng
Gan, Aihua
Chen, Xiaolong
Wang, Xinying
He, Weifeng
Zhang, Xiaohui
Huang, Renxiang
Zhou, Shuzhu
Song, Xiaoxiao
Xu, Angao
Diagnostic Performance of DNA Hypermethylation Markers in Peripheral Blood for the Detection of Colorectal Cancer: A Meta-Analysis and Systematic Review
title Diagnostic Performance of DNA Hypermethylation Markers in Peripheral Blood for the Detection of Colorectal Cancer: A Meta-Analysis and Systematic Review
title_full Diagnostic Performance of DNA Hypermethylation Markers in Peripheral Blood for the Detection of Colorectal Cancer: A Meta-Analysis and Systematic Review
title_fullStr Diagnostic Performance of DNA Hypermethylation Markers in Peripheral Blood for the Detection of Colorectal Cancer: A Meta-Analysis and Systematic Review
title_full_unstemmed Diagnostic Performance of DNA Hypermethylation Markers in Peripheral Blood for the Detection of Colorectal Cancer: A Meta-Analysis and Systematic Review
title_short Diagnostic Performance of DNA Hypermethylation Markers in Peripheral Blood for the Detection of Colorectal Cancer: A Meta-Analysis and Systematic Review
title_sort diagnostic performance of dna hypermethylation markers in peripheral blood for the detection of colorectal cancer: a meta-analysis and systematic review
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4861294/
https://www.ncbi.nlm.nih.gov/pubmed/27158984
http://dx.doi.org/10.1371/journal.pone.0155095
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