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临床下胰腺排斥反应在同时胰腺肾移植后第一年的方案活检中。

Subclinical Pancreas Rejection on Protocol Biopsy Within the First Year of Simultaneous Pancreas Kidney Transplant.

机构信息

Department of Medicine, Mayo Clinic Arizona, Phoenix, Arizona, USA.

Division of Statistics, Mayo Clinic Arizona, Phoenix, Arizona, USA.

出版信息

Clin Transplant. 2024 Oct;38(10):e15467. doi: 10.1111/ctr.15467.

Abstract

This single-center retrospective study investigated subclinical rejection prevalence and significance in simultaneous pancreas and kidney transplant (SPKT) recipients. We analyzed 352 SPKT recipients from July 2003 to April 2022. Our protocol included pancreas allograft surveillance biopsies at 1, 4, and 12months post-transplant. After excluding 153 patients unable to undergo pancreas biopsy, our study cohort comprised 199 recipients. Among the 199 patients with protocol pancreas biopsies, 107 had multiple protocol pancreas biopsies in the first year, totaling 323. Subclinical rejection was identified in 132 episodes (41%). Of these, 72% were Grade 1, 20% were indeterminate, and 8% were Banff Grade 2 or higher. All episodes of subclinical rejection were treated. Rates of pancreas graft loss (10% vs. 7%) and clinical rejection (21% vs. 20%) at 3 years were similar between those with and without subclinical rejection. Subclinical rejection Banff Grade 2 or more was associated with poor pancreas graft survival HR of 5.5 (95% CI: 1.24-24.37, p = 0.025). Of 236 simultaneous protocol kidney and pancreas biopsies, 102 (43%) showed pancreas subclinical rejection, while only 17% had concurrent kidney subclinical rejection. Our findings suggest limited predictive value of pancreatic enzymes and euglycemia in detecting pancreas rejection. Furthermore, poor concordance existed between pancreas and kidney subclinical rejection.

摘要

本单中心回顾性研究调查了胰肾联合移植(SPKT)受者亚临床排斥反应的流行率和意义。我们分析了 2003 年 7 月至 2022 年 4 月的 352 例 SPKT 受者。我们的方案包括移植后 1、4 和 12 个月进行胰腺同种异体移植监测活检。排除 153 例无法进行胰腺活检的患者后,我们的研究队列包括 199 例受者。在这 199 例接受方案胰腺活检的患者中,107 例在第一年进行了多次方案胰腺活检,共 323 例。在 132 个亚临床排斥反应(41%)中发现了亚临床排斥反应。其中,72%为 1 级,20%为不确定,8%为 Banff 2 级或更高。所有亚临床排斥反应均进行了治疗。在 3 年内,有和无亚临床排斥反应的患者胰腺移植物丢失率(10%比 7%)和临床排斥反应率(21%比 20%)相似。Banff 2 级或更高的亚临床排斥反应与胰腺移植物存活率降低相关(HR:5.5,95%CI:1.24-24.37,p=0.025)。在 236 例同时进行的方案肾脏和胰腺活检中,102 例(43%)显示胰腺亚临床排斥反应,而只有 17%的患者同时发生肾脏亚临床排斥反应。我们的研究结果表明,胰腺酶和血糖正常在检测胰腺排斥反应方面的预测价值有限。此外,胰腺和肾脏亚临床排斥反应之间存在不一致性。

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