Kidney Disease Center, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310003, China.
Key Laboratory of Kidney Disease Prevention and Control Technology, Hangzhou 310003, China.
Biomolecules. 2024 Mar 14;14(3):348. doi: 10.3390/biom14030348.
Mitochondria are essential organelles that possess their own DNA. Mitochondrial dysfunction has been revealed in many kidney diseases, including BK polyomavirus-associated nephropathy (BKPyVAN). In this study, we introduce an innovative approach for non-invasive monitoring of mitochondrial impairment through urinary donor-derived cell-free mitochondrial DNA (ddcfmtDNA), addressing the crucial challenge of BKPyVAN diagnosis. Urinary samples were collected at the time of biopsy from a total of 60 kidney transplant recipients, comprising 12 with stable function, 22 with T cell-mediated rejection, and 21 with biopsy-proven BKPyVAN. Our findings reveal that the ddcfmtDNA-to-ddcfDNA ratio exhibits superior capability in distinguishing BKPyVAN from other conditions, with a cutoff value of 4.96% (area under curve = 0.933; sensitivity: 71.4%; and specificity: 97.1%). Notably, an elevation of ddcfmtDNA levels is associated with mitochondrial damage, as visualized through electron microscopy. These results underscore the promise of non-invasive monitoring for detecting subtle mitochondrial damage and its potential utility in BKPyVAN diagnosis. Further investigations are required to advance this field of research.
线粒体是具有自身 DNA 的必需细胞器。线粒体功能障碍已在许多肾脏疾病中被揭示,包括 BK 多瘤病毒相关性肾病(BKPyVAN)。在这项研究中,我们介绍了一种通过尿源性供体细胞游离线粒体 DNA(ddcfmtDNA)进行非侵入性监测线粒体损伤的创新方法,解决了 BKPyVAN 诊断的关键难题。共采集了 60 名接受肾移植的患者的活检时尿液样本,其中 12 名患者肾功能稳定,22 名患者存在 T 细胞介导的排斥反应,21 名患者经活检证实为 BKPyVAN。我们的研究结果表明,ddcfmtDNA 与 ddcfDNA 的比值在区分 BKPyVAN 与其他情况方面具有更好的能力,其截断值为 4.96%(曲线下面积=0.933;灵敏度:71.4%;特异性:97.1%)。值得注意的是,ddcfmtDNA 水平的升高与电子显微镜下观察到的线粒体损伤有关。这些结果强调了非侵入性监测在检测微妙的线粒体损伤及其在 BKPyVAN 诊断中的潜在应用的潜力。需要进一步的研究来推进这一研究领域。