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基于尿液的GSTP1甲基化自动检测在疑似前列腺癌患者诊断中的临床意义。

Clinical significance of urine-based automated detection of GSTP1 methylation for the diagnosis of suspected prostate cancer patients.

作者信息

Ji Ruidong, Zhang Liang, Xing Yaping, Zhu Yifei, Mao Kaifeng, Wang Mingchi, Xuan Kenan, Yang Yu, Lo Richard, Luo Bingfeng, Lu Zhenquan

机构信息

Division of Urology, Department of Surgery, The University of Hong Kong-Shenzhen Hospital, Shenzhen, China.

Maternal and Child Health Research Institute, Translational Medicine Center, Guangdong Women and Children Hospital, Guangzhou, China.

出版信息

Transl Androl Urol. 2025 May 30;14(5):1204-1213. doi: 10.21037/tau-2024-689. Epub 2025 May 27.

Abstract

BACKGROUND

Glutathione S-transferase Pi-1 (GSTP1) methylation is detectable in prostate cancer (PCa) tissues, blood, and urine post-prostate massage, with elevated levels in urine samples. But its role in urine samples for PCa diagnosis is still unclear. This study aimed to investigate the clinical significance of urine-based automated detection of GSTP1 methylation technology in the diagnosis of clinical suspected PCa patients.

METHODS

A retrospective study was performed on 120 patients who underwent prostate biopsy at The University of Hong Kong-Shenzhen Hospital from September 2022 to June 2024. All patients underwent digital rectal examination (DRE) prior to biopsy, with post-DRE urine samples used for GSTP1 methylation testing. Using biopsy pathology as the gold standard, we compared the sensitivity, specificity, and accuracy of urinary GSTP1 methylation with prostate-specific antigen (PSA) for diagnosing PCa. Additionally, we developed a diagnostic prediction model integrating urinary GSTP1 methylation and PSA to assess the combined method's value in enhancing diagnostic efficacy.

RESULTS

The sensitivity and specificity of urinary GSTP1 methylation for PCa diagnosis were 81.4% and 83.6%, respectively, with positive predictive value (PPV) of 82.8% and accuracy of 82.5%. In contrast, PSA had sensitivity and specificity of 67.8% and 54.1%, respectively, with PPV of 58.8% and accuracy of 60.8%. Urinary GSTP1 methylation showed no significant difference in sensitivity compared to PSA (P=0.16) but significantly higher specificity (P=0.001). In the PSA gray zone (4.0-10.0 ng/mL), GSTP1 methylation had sensitivity and specificity of 87.5% and 86.2%, respectively, achieving accuracy of 86.7%, demonstrating good diagnostic efficacy. The area under the curve (AUC) for the combined urinary GSTP1 methylation and PSA method was 0.89 [95% confidence interval (CI): 0.84-0.95], P<0.001, significantly superior to PSA alone, notably improving diagnostic efficacy.

CONCLUSIONS

Automated detection of urinary GSTP1 methylation significantly enhanced PCa diagnostic value, outperforming PSA in sensitivity, specificity, and accuracy. Combining urinary GSTP1 methylation with PSA notably improved accuracy, especially in the PSA gray zone (4.0-10.0 ng/mL), demonstrating excellent efficacy. This non-invasive, easily performed method showed high diagnostic efficacy, indicating strong clinical potential.

摘要

背景

在前列腺癌(PCa)组织、血液以及前列腺按摩后的尿液中均可检测到谷胱甘肽S-转移酶Pi-1(GSTP1)甲基化,尿液样本中的水平有所升高。但其在尿液样本用于PCa诊断中的作用仍不明确。本研究旨在探讨基于尿液的GSTP1甲基化自动检测技术在临床疑似PCa患者诊断中的临床意义。

方法

对2022年9月至2024年6月在香港大学深圳医院接受前列腺活检的120例患者进行回顾性研究。所有患者在活检前均接受了直肠指检(DRE),DRE后的尿液样本用于GSTP1甲基化检测。以活检病理作为金标准,我们比较了尿液GSTP1甲基化与前列腺特异性抗原(PSA)在诊断PCa时的敏感性、特异性和准确性。此外,我们开发了一个整合尿液GSTP1甲基化和PSA的诊断预测模型来评估联合方法在提高诊断效能方面的价值。

结果

尿液GSTP1甲基化诊断PCa的敏感性和特异性分别为81.4%和83.6%,阳性预测值(PPV)为82.8%,准确性为82.5%。相比之下,PSA的敏感性和特异性分别为67.8%和54.1%,PPV为58.8%,准确性为60.8%。尿液GSTP1甲基化与PSA相比,敏感性无显著差异(P=0.16),但特异性显著更高(P=0.001)。在PSA灰色区域(4.0 - 10.0 ng/mL),GSTP1甲基化的敏感性和特异性分别为87.5%和86.2%,准确性达到86.7%,显示出良好的诊断效能。尿液GSTP1甲基化与PSA联合方法的曲线下面积(AUC)为0.89 [95%置信区间(CI):0.84 - 0.95],P<0.001,显著优于单独使用PSA,明显提高了诊断效能。

结论

尿液GSTP1甲基化的自动检测显著提高了PCa的诊断价值,在敏感性、特异性和准确性方面均优于PSA。将尿液GSTP1甲基化与PSA相结合显著提高了准确性,尤其是在PSA灰色区域(4.0 - 10.0 ng/mL),显示出优异的效能。这种非侵入性、易于操作的方法显示出高诊断效能,具有很强的临床潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81d4/12170280/c0509ed64381/tau-14-05-1204-f1.jpg

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