Evaluating the clinical performance of SDC2/NDRG4 methylation for colorectal cancer detection.

IF 3 4区 医学 Q2 GENETICS & HEREDITY Epigenomics Pub Date : 2024-01-01 Epub Date: 2024-01-16 DOI:10.2217/epi-2023-0290
Ke Zhang, Qing He, Qin Cao, Jun Chuan, Ang Qin, Lin Tang, Xinyue Zhang, Changhe Xiao, Biyin Zhu, Meiling Hu, Lei Chang, Zhong Xin Bu, Lanqi Fu, Ting Yang, Yu Wang, Weidong Liu
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Abstract

Purpose: The performance and clinical accuracy of combined SDC2/NDRG4 methylation were evaluated in diagnosing colorectal cancer (CRC) and advanced adenoma. Methods: A total of 2333 participants were enrolled to assess the sensitivity and specificity of biomarkers in diagnosing CRC in a multicenter clinical trial through feces DNA methylation tests. Results: SDC2/NDRG4 methylation showed excellent performance for CRC detection in biomarker research and the real world. Its sensitivity for detecting CRC, early CRC and advanced adenoma were 92.06%, 91.45% and 62.61%, respectively. Its specificity was 94.29%, with a total coincidence rate of 88.28%. When interference samples were included, the specificity was still good (82.61%). Therefore, the SDC2/NDRG4 methylation test showed excellent performance in detecting CRC and advanced adenoma under clinical application.

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评估 SDC2/NDRG4 甲基化在结直肠癌检测中的临床表现。
目的:评估 SDC2/NDRG4 联合甲基化在诊断结直肠癌(CRC)和晚期腺瘤方面的性能和临床准确性。方法:在一项多中心临床试验中,通过粪便 DNA 甲基化测试评估生物标志物诊断 CRC 的灵敏度和特异性。结果SDC2/NDRG4 甲基化在生物标记物研究和现实世界中检测 CRC 方面表现出色。其检测 CRC、早期 CRC 和晚期腺瘤的灵敏度分别为 92.06%、91.45% 和 62.61%。其特异性为 94.29%,总吻合率为 88.28%。当包括干扰样本时,特异性仍然良好(82.61%)。因此,在临床应用中,SDC2/NDRG4 甲基化检测在检测 CRC 和晚期腺瘤方面表现出色。
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来源期刊
Epigenomics
Epigenomics GENETICS & HEREDITY-
CiteScore
5.80
自引率
2.60%
发文量
95
审稿时长
>12 weeks
期刊介绍: Epigenomics provides the forum to address the rapidly progressing research developments in this ever-expanding field; to report on the major challenges ahead and critical advances that are propelling the science forward. The journal delivers this information in concise, at-a-glance article formats – invaluable to a time constrained community. Substantial developments in our current knowledge and understanding of genomics and epigenetics are constantly being made, yet this field is still in its infancy. Epigenomics provides a critical overview of the latest and most significant advances as they unfold and explores their potential application in the clinical setting.
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