| Literature DB >> 30198148 |
Jia Shen1,2, Yang Zhou3, Yawen Chen3, Xiaofeng Li3,4, Wenhua Lei1,2, Jun Ge3,4, Wenhan Peng1,2, Jianyong Wu1,2, Guangjun Liu1,2, Gongda Yang3,4, Haifeng Shi3, Jianghua Chen1,2, Tingya Jiang4, Rending Wang1,2,5.
Abstract
Donor-derived cell-free DNA (ddcfDNA) is reported to be a promising noninvasive biomarker for acute rejection in organ transplant. However, studies on monitoring ddcfDNA dynamics during the early periods after organ transplantation are scarce. Our study assessed the dynamic variation in ddcfDNA in early period with various types and status of kidney transplantation. Target region capture sequencing used identifies ddcfDNA level in 21 kidney transplant recipients. Median ddcfDNA level was 20.69% at the initial time post-transplant, and decreased to 5.22% on the first day and stayed at the stable level after the second day. The ddcfDNA level in DCD (deceased donors) group (44.99%) was significantly higher than that in LDRT (living donor) group (10.24%) at initial time, P < 0.01. DdcfDNA level in DGF (delayed graft function) recipients was lower (23.96%) than that in non-DGF (47.74%) at the initial time, P = 0.89 (19.34% in DGF and 4.46% in non-DGF on the first day, P = 0.17). DdcfDNA level at initial time significantly correlated with serum creatinine (r2 = 0.219, P = 0.032) and warm ischemia time (r2 = 0.204, P = 0.040). Plasma ddcfDNA level decreased rapidly follow an L-shaped curve post-transplant, and level in DGF declined slower than non-DGF. The rebound of ddcfDNA level may indicate the occurrence of acute rejection.Entities:
Keywords: acute rejection; delayed graft function; donor-derived cell-free DNA; kidney transplant; target region capture sequencing
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Year: 2018 PMID: 30198148 DOI: 10.1111/tri.13341
Source DB: PubMed Journal: Transpl Int ISSN: 0934-0874 Impact factor: 3.782