Donor-derived cell-free DNA as a diagnostic marker for kidney-allograft rejection: a systematic review and meta-analysis-testni naslov

Yanbo Xing, Qiang Guo, Cong Wang, Haoying Shi, Jiarui Zheng, Yijun Jia, Chengyong Li, Chuan Hao
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Abstract

Testni abstrakt - Donor-derived cell-free DNA (dd-cfDNA) is a promising biomarker for the detection of graft rejection. We evaluated the accuracy and clinical value of applying it to kidney transplant rejection. Relevant literature on dd-cfDNA diagnosis of kidney transplant rejection was searched in PubMed, Embase, Cochrane Library, and Web of Science databases from the time of construction to 2023. Data and study characteristics were extracted independently by two researchers, and disagreements were resolved by negotiation. We merged diagnostic accuracy data distinguishing major rejection (MRE) and antibody-mediated rejection (AMR) separately. Potential heterogeneity was analyzed by subgroup analysis or meta-regression. Funnel plots were used to clarify the presence or absence of publication bias. A total of 17 publications provided data on the accuracy of dd-cfDNA in diagnosing patients with MRE. The pooled sensitivity, specificity, and the area under the receiver operating characteristic curve with 95% confidence intervals (CI) were 0.60 (95% CI, 0.51-0.69), 0.85 (95% CI, 0.81-0.89), and 0.83 (95% CI, 0.79-0.86), respectively. Additionally, 12 studies focused on the diagnostic efficacy of dd-cfDNA for ABMR, showing pooled sensitivity, specificity, and the area under the receiver operating characteristic curve with 95% CI of 0.81 (95% CI, 0.72–0.88), 0.80 (95% CI, 0.73–0.86), and 0.87 (95% CI, 0.84-0.90), respectively. The type of study, age group, and sample size were responsible for the heterogeneity. In summary, Due to significant heterogeneity, the accuracy of Dd-cfDNA in diagnosing patients with MRE is not very reliable. However, Dd-cfDNA can serve as a biomarker for diagnosing ABMR.
作为肾移植排斥反应诊断标志物的供体源性无细胞 DNA:系统综述和荟萃分析--Testni naslov
Testni abstrakt - 捐献者来源的无细胞DNA(dd-cfDNA)是一种很有前景的检测移植物排斥反应的生物标志物。我们评估了将其应用于肾移植排斥反应的准确性和临床价值。我们在PubMed、Embase、Cochrane Library和Web of Science数据库中检索了自建库至2023年有关dd-cfDNA诊断肾移植排斥反应的相关文献。数据和研究特征由两名研究人员独立提取,分歧通过协商解决。我们合并了诊断准确性数据,分别区分了主要排斥反应(MRE)和抗体介导的排斥反应(AMR)。通过亚组分析或元回归分析潜在的异质性。漏斗图用于明确是否存在发表偏倚。共有 17 篇文献提供了 dd-cfDNA 诊断 MRE 患者准确性的数据。汇总的敏感性、特异性和接收者操作特征曲线下面积(95% 置信区间,CI)分别为 0.60(95% CI,0.51-0.69)、0.85(95% CI,0.81-0.89)和 0.83(95% CI,0.79-0.86)。此外,12 项研究关注了 dd-cfDNA 对 ABMR 的诊断疗效,结果显示,集合敏感性、特异性和接收者操作特征曲线下面积的 95% CI 分别为 0.81(95% CI,0.72-0.88)、0.80(95% CI,0.73-0.86)和 0.87(95% CI,0.84-0.90)。研究类型、年龄组和样本量是造成异质性的原因。总之,由于存在明显的异质性,Dd-cfDNA 诊断 MRE 患者的准确性并不十分可靠。但是,Dd-cfDNA 可以作为诊断 ABMR 的生物标志物。
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