Islet-after-kidney transplantation versus kidney alone in kidney transplant recipients with type 1 diabetes (KAIAK): a population-based target trial emulation in France.

IF 44 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM
The Lancet Diabetes & Endocrinology Pub Date : 2024-10-01 Epub Date: 2024-09-06 DOI:10.1016/S2213-8587(24)00241-9
Mehdi Maanaoui, Rémi Lenain, Yohann Foucher, Fanny Buron, Gilles Blancho, Corinne Antoine, Sophie Caillard, Laurence Kessler, Moglie Le Quintrec, Orianne Villard, Dany Anglicheau, Matthias Büchler, Albane Brodin-Sartorius, Luc Frimat, Paolo Malvezzi, Sandrine Lablanche, Lionel Badet, Laure Esposito, Mikael Chetboun, Aghiles Hamroun, Julie Kerr-Conte, Thierry Berney, Marie-Christine Vantyghem, Marc Hazzan, François Pattou
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引用次数: 0

Abstract

Background: Islet transplantation has been associated with better metabolic control and quality of life than insulin treatment alone, but direct evidence of its effect on hard clinical endpoints is scarce. We aimed to assess the effect of islet transplantation on patient-graft survival in kidney transplant recipients with type 1 diabetes.

Methods: In this retrospective cohort study, we enrolled all patients with type 1 diabetes who received a kidney graft in France during the study period, identified from the CRISTAL nationwide registry. Non-inclusion criteria included recipients from transplant centres that never proposed islet transplantation during the study period, recipients with a functional pancreas throughout the follow-up duration, recipients with more than two kidney transplants, HLA-sensitised recipients, recipients with less than 1 year of follow-up after kidney transplantation, misclassified recipients with type 2 diabetes, recipients aged over 65 years, recipients of kidney grafts from Donation after Circulatory Death donors, recipient with HIV or hepatitis, recipients with cancer, and recipients of combined liver-kidney transplants. Patients who also received islet-after-kidney (IAK) transplantation were compared with controls who received kidney transplantation alone according to a 1:2 matching method based on time-dependent propensity scores, ensuring patients comparability at the time of islet transplantation. The primary outcome was patient-graft survival, a composite outcome defined by death, re-transplantation, or return to dialysis.

Findings: Between Jan 1, 2000, and Dec 31, 2017, 2391 patients with type 1 diabetes were identified as having received a kidney transplant, 47 patients of whom also received an islet transplantation. 2002 patients were not eligible for islet transplantation and 62 were excluded due to missing data. 327 eligible recipients from 15 centres were included in the study dataset for the target trial emulation. 40 patients who received IAK transplantation were successfully matched to 80 patients who received kidney transplantation alone. 13 (33%) of 40 patients in the IAK transplantation group returned to dialysis or died, compared with 36 (45%) of 80 patients in the kidney transplantation alone group. We found a significant benefit of islet transplantation compared with kidney transplantation alone on patient-graft survival, with a hazard ratio (HR) of 0·44 (95% CI 0·23-0·88; p=0·022), mainly explained by a protective effect on the risk of death (HR 0·41, 0·13-0·91; p=0·042). There was no meaningful association between IAK and death-censored graft survival (0·73, 0·30-1·89; p=0·36).

Interpretation: In kidney transplant recipients with type 1 diabetes, IAK transplantation was associated with a significantly better patient-graft survival compared with kidney transplantation alone, mainly due to a protective effect on the risk of death. These results potentially serve as compelling grounds for advocating wider access to islet transplantation in patients with type 1 diabetes undergoing kidney transplant, as reimbursement of islet transplantation is provided in few countries worldwide.

Funding: Programme Hospitalier de la Recherche Clinique, Fondation pour la Recherche Medicale, and Fonds de Dotation Line Renaud-Loulou Gasté.

1型糖尿病肾移植受者肾移植后换肾与单纯换肾的比较(KAIAK):在法国进行的基于人群的目标试验。
背景:与单纯胰岛素治疗相比,胰岛素移植可改善代谢控制和生活质量,但很少有直接证据表明胰岛素移植对硬性临床终点有影响。我们的目的是评估胰岛移植对 1 型糖尿病肾移植受者患者-移植物存活率的影响:在这项回顾性队列研究中,我们登记了研究期间在法国接受肾移植的所有 1 型糖尿病患者,这些患者均来自 CRISTAL 全国登记处。非纳入标准包括:在研究期间来自移植中心但从未建议过胰岛移植的受者、在整个随访期间胰腺功能正常的受者、接受过两次以上肾移植的受者、对 HLA 敏感的受者、肾移植后随访时间少于 1 年的受者、被误认为患有 2 型糖尿病的受者、65 岁以上的受者、接受循环死亡后捐献者肾移植的受者、患有艾滋病或肝炎的受者、癌症受者以及接受肝肾联合移植的受者。同时接受肾移植后胰岛(IAK)移植的患者与仅接受肾移植的对照组进行了比较,比较采用的是基于时间倾向评分的1:2匹配法,以确保患者在接受胰岛移植时的可比性。主要结果是患者-移植物存活率,这是一种综合结果,由死亡、再次移植或恢复透析定义:2000年1月1日至2017年12月31日期间,2391名1型糖尿病患者被确认接受了肾移植,其中47名患者同时接受了胰岛移植。2002名患者不符合胰岛移植条件,62名患者因数据缺失而被排除。来自 15 个中心的 327 名符合条件的受者被纳入目标试验模拟的研究数据集。40 名接受 IAK 移植的患者与 80 名单独接受肾移植的患者配型成功。IAK移植组的40名患者中有13人(33%)重返透析或死亡,而单纯肾移植组的80名患者中有36人(45%)重返透析或死亡。我们发现,与单纯肾移植相比,胰岛移植对患者-移植物存活率有明显益处,危险比(HR)为0-44(95% CI 0-23-0-88;P=0-022),主要原因是对死亡风险有保护作用(HR 0-41,0-13-0-91;P=0-042)。IAK与死亡校正后的移植物存活率(0-73,0-30-1-89;P=0-36)之间没有明显关联:在患有1型糖尿病的肾移植受者中,与单纯肾移植相比,IAK移植能显著提高患者与移植物的存活率,这主要是由于IAK对死亡风险具有保护作用。由于世界上只有少数几个国家提供胰岛移植报销服务,这些结果可能成为倡导更多接受肾移植的1型糖尿病患者接受胰岛移植的有力依据:医院临床研究计划》、《医学研究基金会》和《雷诺-卢卢-加斯特捐赠基金》。
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来源期刊
The Lancet Diabetes & Endocrinology
The Lancet Diabetes & Endocrinology ENDOCRINOLOGY & METABOLISM-
CiteScore
61.50
自引率
1.60%
发文量
371
期刊介绍: The Lancet Diabetes & Endocrinology, an independent journal with a global perspective and strong clinical focus, features original clinical research, expert reviews, news, and opinion pieces in each monthly issue. Covering topics like diabetes, obesity, nutrition, and more, the journal provides insights into clinical advances and practice-changing research worldwide. It welcomes original research advocating change or shedding light on clinical practice, as well as informative reviews on related topics, especially those with global health importance and relevance to low-income and middle-income countries. The journal publishes various content types, including Articles, Reviews, Comments, Correspondence, Health Policy, and Personal Views, along with Series and Commissions aiming to drive positive change in clinical practice and health policy in diabetes and endocrinology.
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