Department of Surgery, Division of Transplantation, SUNY Upstate Medical University, Syracuse, New York.
Department of Pathology and Laboratory Medicine, SUNY Upstate Medical University, Syracuse, New York.
Transplant Proc. 2024 Jul-Aug;56(6):1259-1263. doi: 10.1016/j.transproceed.2024.02.023. Epub 2024 Jul 16.
Transcriptomic kidney profile testing and donor-derived cell-free DNA (dd-cfDNA) testing are new methods shown to provide early markers of graft inflammation during the post-transplant period. This study focused on utilizing clinical data to evaluate the application of these tests in detecting transplant rejection by comparing tests results to biopsy reports.
We conducted a retrospective analysis of a prospectively collected database of all adult kidney transplant patients at SUNY Upstate Medical Hospital from 1 January 2014 to 1 December 2022. Inclusion criteria were patients with concurrent transcriptomic kidney profile test and kidney biopsy results.
Biopsies identified 33 kidney transplant rejections. For diagnosis of kidney rejection, transcriptomic kidney profile testing had a 52.83% positive predictive value and 92.77% negative predicative value, while dd-cfDNA testing had a 54.83% positive predictive value and 86.45% negative predictive value. Transcriptomic kidney profile testing showed an 82.35% sensitivity and 75.49% specificity, while dd-cfDNA testing showed a 56.66% sensitivity and 85.56% specificity. Positive transcriptomic kidney profile and dd-cfDNA tests detected 51.51% of rejections. Combined negative tests were observed in 70.21% of biopsies without rejection.
Despite certain discrepancies and limitations, we believe transcriptomic profile testing and dd-cfDNA testing are useful for detecting early-stage rejections and can guide patient care. Additionally, dd-cfDNA testing avoids invasive screening biopsies. Following negative test results, the probability patients are not having rejection is 86.45%. The transcriptomic profile test's high sensitivity and specificity allow possible detection of transplant rejections that may have otherwise not been identified by biopsy.
转录组肾脏特征检测和供体游离细胞 DNA(dd-cfDNA)检测是新的方法,它们在移植后期间提供了炎症的早期标志物。本研究通过将测试结果与活检报告进行比较,利用临床数据评估这些测试在检测移植排斥反应中的应用。
我们对 2014 年 1 月 1 日至 2022 年 12 月 1 日期间在纽约州立大学上州医科大学医院接受同种异体肾移植的所有成年患者的前瞻性收集数据库进行了回顾性分析。纳入标准为同时进行转录组肾脏特征检测和肾活检的患者。
活检确定了 33 例肾移植排斥反应。对于肾移植排斥的诊断,转录组肾脏特征检测的阳性预测值为 52.83%,阴性预测值为 92.77%,而 dd-cfDNA 检测的阳性预测值为 54.83%,阴性预测值为 86.45%。转录组肾脏特征检测的敏感性为 82.35%,特异性为 75.49%,而 dd-cfDNA 检测的敏感性为 56.66%,特异性为 85.56%。阳性的转录组肾脏特征和 dd-cfDNA 检测检测到 51.51%的排斥反应。无排斥反应的活检中,70.21%观察到联合阴性检测。
尽管存在一些差异和局限性,但我们认为转录组特征检测和 dd-cfDNA 检测有助于早期检测排斥反应,并可指导患者的护理。此外,dd-cfDNA 检测避免了有创性的筛查活检。在阴性检测结果后,患者未发生排斥反应的概率为 86.45%。转录组特征检测的高敏感性和特异性允许检测到可能被活检遗漏的移植排斥反应。