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用于肾移植排斥反应监测的分散式供体来源游离DNA检测方法的评估

Evaluation of a Decentralized Donor-Derived Cell-Free DNA Assay for Kidney Allograft Rejection Monitoring.

作者信息

Loupy Alexandre, Certain Anaïs, Tangprasertchai Narin S, Racapé Maud, Ursule-Dufait Cindy, Benbadi Kawthar, Raynaud Marc, Vaskova Evgeniya, Marchis Corina, Casas Sílvia, Hague Tim, Bestard Oriol, Kervella Delphine, Lefaucheur Carmen, Viard Thierry, Aubert Olivier

机构信息

Université Paris Cité, Institut national de la santé et de la recherche médicale (INSERM) U970, Paris Institute for Transplantation and Organ Regeneration PITOR, Paris, France.

Department of Kidney Transplantation, Necker Hospital, Assistance Publique - Hôpitaux de Paris, Paris, France.

出版信息

Transpl Int. 2024 Dec 17;37:13919. doi: 10.3389/ti.2024.13919. eCollection 2024.

Abstract

Donor-derived cell-free DNA (dd-cfDNA) is an emerging non-invasive biomarker for allograft injury detection. This study aimed to evaluate a new, decentralized dd-cfDNA testing kit against a centralized dd-cfDNA testing service broadly utilized in the United States. Kidney transplant recipients with decentralized and centralized dd-cfDNA measurements and concomitant kidney allograft biopsies were included in the study. 580 kidney allograft recipients from 3 referral centers were included for 603 total evaluations. Correlation between assays was evaluated using r-squared ( ) and Spearman's rank correlation test, and associations with rejection using logistic regression analyses and discrimination using area under the curve. Mean dd-cfDNA levels from decentralized and centralized tests were 0.51% ± 0.81% and 0.43% ± 0.78%, respectively. The assays were highly correlated, with = 0.95 and Spearman's rank correlation 0.88 ( < 0.0001). Both tests showed significant association with allograft rejection ( < 0.0001) and good and similar discriminations to predict rejection (AUC: 0.758 for the decentralized and AUC: 0.760 for the centralized dd-cfDNA; = 0.8466). Consistency between the assays was also confirmed across clinical scenarios including post-transplant timepoint, allograft stability, and allograft rejection subcategories. This decentralized dd-cfDNA assessment demonstrates high accuracy and value to non-invasively monitor kidney recipients.

摘要

供体来源的游离DNA(dd-cfDNA)是一种用于检测同种异体移植损伤的新兴非侵入性生物标志物。本研究旨在评估一种新型的去中心化dd-cfDNA检测试剂盒,并与美国广泛使用的中心化dd-cfDNA检测服务进行对比。本研究纳入了接受去中心化和中心化dd-cfDNA检测并同时进行肾移植活检的肾移植受者。来自3个转诊中心的580名肾移植受者共接受了603次评估。使用决定系数( )和Spearman等级相关检验评估检测方法之间的相关性,并使用逻辑回归分析评估与排斥反应的关联,以及使用曲线下面积评估鉴别能力。去中心化检测和中心化检测的平均dd-cfDNA水平分别为0.51%±0.81%和0.43%±0.78%。两种检测方法高度相关,决定系数 = 0.95,Spearman等级相关性为0.88( < 0.0001)。两种检测均显示与同种异体移植排斥反应显著相关( < 0.0001),并且在预测排斥反应方面具有良好且相似的鉴别能力(曲线下面积:去中心化检测为0.758,中心化dd-cfDNA检测为0.760; = 0.8466)。在包括移植后时间点、同种异体移植稳定性和同种异体移植排斥反应亚类等临床场景中,两种检测方法之间的一致性也得到了证实。这种去中心化的dd-cfDNA评估显示出在非侵入性监测肾移植受者方面具有高准确性和价值。

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