Novel urine-based DNA methylation biomarkers for urothelial bladder carcinoma detection in patients with hematuria

IF 1.3 Q3 UROLOGY & NEPHROLOGY Arab Journal of Urology Pub Date : 2023-05-14 DOI:10.1080/2090598x.2023.2208492
Hassan F. Abol-Elnazer, Amira Awadalla, Asmaa E. Ahmed, Hassan Abol-Enein, Munir Ali Al Ganzouri, Amr A. Elsawy
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Abstract

Background Urothelial bladder carcinoma (UBC) is usually detected during work-up for hematuria. Cystoscopy and/or contrast-enhanced imaging are the gold standard tools for UBC diagnosis, despite limited by being invasive, expensive and low yield in small flat tumors.Objectives To assess the diagnostic performance of urine-based DNA methylation of six genes (GATA4, P16, P14, APC, CDH1 and CD99) for UBC detection in patients with hematuria.Patients and methods Voided urine was collected from consecutive patients presented with hematuria for urine cytology and DNA methylation assay of the assigned genes using methylation-specific Polymerase Chain Reaction (PCR). Further assessment by office cystoscopy and imaging with subsequent inpatient cystoscopic biopsy for positive findings was done. The diagnostic characteristics of DNA methylation and urine cytology were assessed based on its capability to predict UBC.Results We included 246 patients in the study with identified macroscopic hematuria in 204 (82.9%) patients. Positive cytology was found in 78 (31.7%) patients. DNA methylation of GATA4, P16, P14, APC, CDH1 and CD99 genes was identified in 127 (51.6%), 52 (21.1%), 117 (47.6%), 106 (43.1%), 90 (36.6%) and 71 (28.9%) patients, respectively. The sensitivity of the assigned genes for UBC detection ranges from 35% (95%CI: 31–39) to 83% (95%CI: 79–87). Optimal specificity (SP) (100%) was noted for P16, APC and CDH1 genes. While for the other genes (GATA4, P14 and CD99), the SP was 95% (95%CI: 92–98), 96% (95%CI: 92–99) and 97% (95%CI: 93–99), respectively. On multivariate logistic regression analysis, all genes exclusively demonstrated independent prediction of UBC. On receiver operator characteristic (ROC) analysis, all tested genes methylation showed superior area under the curve (AUC) when compared to urine cytology.Conclusions We have developed a novel urine-based DNA methylation assay for detection of UBC in patients with hematuria with superior diagnostic performance and independent predictive capacity over urine cytology.
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血尿患者尿路上皮性膀胱癌检测的新型尿液DNA甲基化生物标志物
背景尿路上皮性膀胱癌(UBC)通常在血尿检查中被发现。膀胱镜检查和/或对比增强成像是UBC诊断的金标准工具,尽管在小的扁平肿瘤中存在侵入性、昂贵和低收益的限制。目的评价尿中6个基因(GATA4、P16、P14、APC、CDH1和CD99) DNA甲基化对血尿患者UBC检测的诊断价值。患者和方法收集连续出现血尿的患者的空尿,进行尿细胞学检查,并采用甲基化特异性聚合酶链反应(methyl- specific Polymerase Chain Reaction, PCR)对指定基因进行DNA甲基化检测。通过办公室膀胱镜检查和成像以及随后的住院膀胱镜活检来进一步评估阳性结果。DNA甲基化和尿细胞学的诊断特点是基于其预测UBC的能力进行评估。结果我们纳入了246例患者,其中204例(82.9%)患者肉眼可见血尿。细胞学阳性78例(31.7%)。GATA4、P16、P14、APC、CDH1和CD99基因甲基化分别在127例(51.6%)、52例(21.1%)、117例(47.6%)、106例(43.1%)、90例(36.6%)和71例(28.9%)患者中检测到。指定基因检测UBC的灵敏度范围为35% (95%CI: 31-39)至83% (95%CI: 79-87)。P16、APC和CDH1基因的最佳特异性(SP)为100%。其他基因GATA4、P14和CD99的SP分别为95% (95% ci: 92 ~ 98)、96% (95% ci: 92 ~ 99)和97% (95% ci: 93 ~ 99)。多因素logistic回归分析显示,所有基因均能独立预测UBC。在受试者操作特征(ROC)分析中,与尿细胞学相比,所有测试基因甲基化显示出优越的曲线下面积(AUC)。我们开发了一种新的基于尿液的DNA甲基化检测方法,用于血尿患者的UBC检测,具有优于尿细胞学的诊断性能和独立预测能力。
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来源期刊
Arab Journal of Urology
Arab Journal of Urology UROLOGY & NEPHROLOGY-
CiteScore
2.80
自引率
0.00%
发文量
40
期刊介绍: The Arab Journal of Urology is a peer-reviewed journal that strives to provide a high standard of research and clinical material to the widest possible urological community worldwide. The journal encompasses all aspects of urology including: urological oncology, urological reconstructive surgery, urodynamics, female urology, pediatric urology, endourology, transplantation, erectile dysfunction, and urinary infections and inflammations. The journal provides reviews, original articles, editorials, surgical techniques, cases reports and correspondence. Urologists, oncologists, pathologists, radiologists and scientists are invited to submit their contributions to make the Arab Journal of Urology a viable international forum for the practical, timely and state-of-the-art clinical urology and basic urological research.
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