Berezina Tetiana A, Berezin Alexander E
VitaCenter, Department of Internal Medicine and Nephrology, Zaporozhye, 69000, Ukraine.
Paracelsus Medical University, Department of Internal Medicine II, Division of Cardiology, Salzburg, 5020, Austria.
Epigenomics. 2023 Sep;15(17):879-890. doi: 10.2217/epi-2023-0255. Epub 2023 Oct 4.
Circulating cell-free DNA (cf-DNA) is released from dead and/or apoptotic leukocytes and due to neutrophil extracellular traps contributing to an inflammatory response. Previous clinical studies have reported that the peak concentrations and dynamic changes of cf-DNA may be used as a noninvasive biomarker of worsening kidney function as well as a guide to the management of kidney allograft rejection. We hypothesized that the pattern and dynamic changes of cf-DNA might be a plausible predictive biomarker for patients at risk of chronic kidney disease (CKD), including individuals with type 2 diabetes mellitus, heart failure, cardiovascular disease and established CKD. Along with it, pre- and posthemodialysis levels of serum cf-DNA appear to be a independent predictor for all-cause mortality in patients with end-stage kidney disease.
循环游离DNA(cf-DNA)由死亡和/或凋亡的白细胞释放,并且由于中性粒细胞胞外诱捕网而促成炎症反应。先前的临床研究报道,cf-DNA的峰值浓度和动态变化可用作肾功能恶化的非侵入性生物标志物以及肾移植排斥反应管理的指导。我们假设,cf-DNA的模式和动态变化可能是慢性肾脏病(CKD)风险患者(包括2型糖尿病、心力衰竭、心血管疾病患者以及已确诊的CKD患者)的一种合理的预测生物标志物。与此同时,血液透析前后血清cf-DNA水平似乎是终末期肾病患者全因死亡率的独立预测指标。