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1
Progressive decline of function in renal allografts with normal 1-year biopsies: Gene expression studies fail to identify a classifier.在 1 年活检正常的同种异体肾移植物中功能逐渐下降:基因表达研究未能确定分类器。
Clin Transplant. 2021 Dec;35(12):e14456. doi: 10.1111/ctr.14456. Epub 2021 Nov 9.
2
Utility of Serial Protocol Biopsies Performed After 1 Year in Predicting Long-Term Kidney Allograft Function According to Histologic Phenotype.根据组织学表型,1年后进行的系列协议活检在预测长期肾移植功能方面的效用。
Exp Clin Transplant. 2018 Aug;16(4):391-400. doi: 10.6002/ect.2016.0323. Epub 2017 Dec 5.
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Biopsy transcriptome expression profiling to identify kidney transplants at risk of chronic injury: a multicentre, prospective study.通过活检转录组表达谱分析识别有慢性损伤风险的肾移植:一项多中心前瞻性研究。
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Am J Transplant. 2019 Oct;19(10):2846-2854. doi: 10.1111/ajt.15380. Epub 2019 May 6.
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Interstitial fibrosis is the critical determinant of impaired renal function in transplant glomerulopathy.间质纤维化是移植性肾小球病中肾功能受损的关键决定因素。
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Capillary C4d and Kidney Allograft Outcome in Relation to Morphologic Lesions Suggestive of Antibody-Mediated Rejection.与提示抗体介导排斥反应的形态学病变相关的毛细血管C4d与肾移植结果
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本文引用的文献

1
Prediction system for risk of allograft loss in patients receiving kidney transplants: international derivation and validation study.移植肾受者移植肾丢失风险预测系统:国际推导和验证研究。
BMJ. 2019 Sep 17;366:l4923. doi: 10.1136/bmj.l4923.
2
Modeling graft loss in patients with donor-specific antibody at baseline using the Birmingham-Mayo (BirMay) predictor: Implications for clinical trials.使用伯明翰-梅奥(BirMay)预测器对基线时具有供体特异性抗体的患者进行移植物丢失建模:对临床试验的影响。
Am J Transplant. 2019 Aug;19(8):2274-2283. doi: 10.1111/ajt.15312. Epub 2019 Mar 13.
3
A method to reduce variability in scoring antibody-mediated rejection in renal allografts: implications for clinical trials - a retrospective study.一种减少肾移植中抗体介导排斥反应评分变异性的方法:对临床试验的影响-一项回顾性研究。
Transpl Int. 2019 Feb;32(2):173-183. doi: 10.1111/tri.13340. Epub 2018 Oct 2.
4
A 2018 Reference Guide to the Banff Classification of Renal Allograft Pathology.2018 年肾移植病理的班夫分类参考指南。
Transplantation. 2018 Nov;102(11):1795-1814. doi: 10.1097/TP.0000000000002366.
5
Development and clinical validity of a novel blood-based molecular biomarker for subclinical acute rejection following kidney transplant.新型血液分子生物标志物在肾移植后亚临床急性排斥反应中的研发及临床验证。
Am J Transplant. 2019 Jan;19(1):98-109. doi: 10.1111/ajt.15011. Epub 2018 Aug 31.
6
The Banff 2017 Kidney Meeting Report: Revised diagnostic criteria for chronic active T cell-mediated rejection, antibody-mediated rejection, and prospects for integrative endpoints for next-generation clinical trials.Banff 2017 年会肾脏报告:慢性活动性 T 细胞介导排斥反应、抗体介导排斥反应的修订诊断标准,以及下一代临床试验综合终点的前景。
Am J Transplant. 2018 Feb;18(2):293-307. doi: 10.1111/ajt.14625. Epub 2018 Jan 21.
7
Real Time Central Assessment of Kidney Transplant Indication Biopsies by Microarrays: The INTERCOMEX Study.实时通过微阵列对肾移植适应证活检进行中央评估:INTERCOMEX 研究。
Am J Transplant. 2017 Nov;17(11):2851-2862. doi: 10.1111/ajt.14329. Epub 2017 May 30.
8
Unique molecular changes in kidney allografts after simultaneous liver-kidney compared with solitary kidney transplantation.肾移植和肝移植同期与单独肾移植后肾脏移植物的独特分子变化。
Kidney Int. 2017 May;91(5):1193-1202. doi: 10.1016/j.kint.2016.12.016. Epub 2017 Feb 21.
9
Biopsy transcriptome expression profiling to identify kidney transplants at risk of chronic injury: a multicentre, prospective study.通过活检转录组表达谱分析识别有慢性损伤风险的肾移植:一项多中心前瞻性研究。
Lancet. 2016 Sep 3;388(10048):983-93. doi: 10.1016/S0140-6736(16)30826-1. Epub 2016 Jul 22.
10
The Substantial Loss of Nephrons in Healthy Human Kidneys with Aging.健康人肾脏中肾单位随衰老而大量丧失。
J Am Soc Nephrol. 2017 Jan;28(1):313-320. doi: 10.1681/ASN.2016020154. Epub 2016 Jul 8.

在 1 年活检正常的同种异体肾移植物中功能逐渐下降:基因表达研究未能确定分类器。

Progressive decline of function in renal allografts with normal 1-year biopsies: Gene expression studies fail to identify a classifier.

机构信息

Mayo Clinic Rochester, Rochester, Minnesota, USA.

Henry Ford Hospital, Detroit, Michigan, USA.

出版信息

Clin Transplant. 2021 Dec;35(12):e14456. doi: 10.1111/ctr.14456. Epub 2021 Nov 9.

DOI:10.1111/ctr.14456
PMID:34717009
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8702476/
Abstract

Histologic findings on 1-year biopsies such as inflammation with fibrosis and transplant glomerulopathy predict renal allograft loss by 5 years. However, almost half of the patients with graft loss have a 1-year biopsy that is either normal or has only interstitial fibrosis. The goal of this study was to determine if there was a gene expression profile in these relatively normal 1-year biopsies that predicted subsequent decline in renal function. Using transcriptome microarrays we measured intragraft mRNA levels in a retrospective Discovery cohort (170 patients with a normal/minimal fibrosis 1-year biopsy, 54 with progressive decline in function/graft loss and 116 with stable function) and developed a nested 10-fold cross-validated gene classifier that predicted progressive decline in renal function (positive predictive value = 38 ± 34%%; negative predictive value = 73 ± 30%, c-statistic = .59). In a prospective, multicenter Validation cohort (270 patients with Normal/Interstitial Fibrosis [IF]), the classifier had a 20% positive predictive value, 85% negative predictive value and .58 c-statistic. Importantly, the majority of patients with graft loss in the prospective study had 1-year biopsies scored as Normal or IF. We conclude predicting graft loss in many renal allograft recipients (i.e., those with a relatively normal 1-year biopsy and eGFR > 40) remains difficult.

摘要

1 年活检的组织学发现,如纤维化炎症和移植肾小球病,可预测 5 年内的肾移植丢失。然而,近一半的移植丢失患者的 1 年活检结果正常或仅有间质纤维化。本研究的目的是确定这些相对正常的 1 年活检中是否存在可预测肾功能随后下降的基因表达谱。我们使用转录组微阵列在回顾性发现队列(170 例 1 年活检正常/轻度纤维化患者,54 例肾功能下降/移植丢失,116 例肾功能稳定)中测量了移植内 mRNA 水平,并开发了一种嵌套的 10 倍交叉验证基因分类器,该分类器可预测肾功能的进行性下降(阳性预测值=38±34%;阴性预测值=73±30%,c 统计量=0.59)。在前瞻性、多中心验证队列(270 例正常/间质纤维化[IF]患者)中,该分类器的阳性预测值为 20%,阴性预测值为 85%,c 统计量为 0.58。重要的是,前瞻性研究中大多数移植丢失患者的 1 年活检评分正常或 IF。我们得出结论,预测许多肾移植受者(即 1 年活检相对正常且 eGFR>40 的受者)的移植丢失仍然困难。