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用于糖尿病治疗的β细胞替代治疗结局的定义:来自 IPITA/EPITA 意见领袖研讨会的 Igls 标准共识报告。

Defining outcomes for β-cell replacement therapy in the treatment of diabetes: a consensus report on the Igls criteria from the IPITA/EPITA opinion leaders workshop.

机构信息

Department of Medicine, Division of Endocrinology, Diabetes & Metabolism, Institute for Diabetes, Obesity & Metabolism, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Department of Surgery, Division of Transplantation, University of California at San Francisco, San Francisco, CA, USA.

出版信息

Transpl Int. 2018 Apr;31(4):343-352. doi: 10.1111/tri.13138.

Abstract

β-cell replacement therapy, available currently as pancreas or islet transplantation, has developed without a clear definition of graft functional and clinical outcomes. The International Pancreas & Islet Transplant Association (IPITA) and European Pancreas & Islet Transplantation Association (EPITA) held a workshop to develop consensus for an IPITA/EPITA Statement on the definition of function and failure of current and future forms of β-cell replacement therapy. There was consensus that β-cell replacement therapy could be considered as a treatment for β-cell failure, regardless of etiology and without requiring undetectable C-peptide, accompanied by glycemic instability with either problematic hypoglycemia or hyperglycemia. Glycemic control should be assessed at a minimum by glycated hemoglobin (HbA ) and the occurrence of severe hypoglycemia. Optimal β-cell graft function is defined by near-normal glycemic control [HbA  ≤ 6.5% (48 mmol/mol)] without severe hypoglycemia or requirement for insulin or other antihyperglycemic therapy, and with an increase over pretransplant measurement of C-peptide. Good β-cell graft function requires HbA  < 7.0% (53 mmol/mol) without severe hypoglycemia and with a significant (>50%) reduction in insulin requirements and restoration of clinically significant C-peptide production. Marginal β-cell graft function is defined by failure to achieve HbA  < 7.0% (53 mmol/mol), the occurrence of any severe hypoglycemia, or less than 50% reduction in insulin requirements when there is restoration of clinically significant C-peptide production documented by improvement in hypoglycemia awareness/severity, or glycemic variability/lability. A failed β-cell graft is defined by the absence of any evidence for clinically significant C-peptide production. Optimal and good functional outcomes are considered successful clinical outcomes.

摘要

β 细胞替代治疗,目前可通过胰腺或胰岛移植实现,其疗效评估缺乏明确的移植物功能和临床结局定义。国际胰腺和胰岛移植协会(IPITA)和欧洲胰腺和胰岛移植协会(EPITA)召开了一次研讨会,旨在为当前和未来形式的β 细胞替代治疗的 IPITA/EPITA 声明制定关于功能和失败的共识定义。与会者一致认为,β 细胞替代治疗可以被视为β 细胞衰竭的一种治疗方法,无论病因如何,都不需要检测不到的 C 肽,并且伴有血糖不稳定,表现为严重低血糖或高血糖。血糖控制应至少通过糖化血红蛋白(HbA )和严重低血糖的发生情况进行评估。最佳β 细胞移植物功能定义为接近正常的血糖控制[HbA ≤ 6.5%(48mmol/mol)],无严重低血糖或需要胰岛素或其他抗高血糖治疗,并且 C 肽较移植前增加。良好的β 细胞移植物功能需要 HbA < 7.0%(53mmol/mol),无严重低血糖,胰岛素需求显著减少(>50%),并恢复有临床意义的 C 肽产生。边缘β 细胞移植物功能定义为无法实现 HbA < 7.0%(53mmol/mol),出现任何严重低血糖,或在有临床意义的 C 肽产生恢复时胰岛素需求减少不足 50%,同时有低血糖意识/严重程度或血糖变异性/不稳定性的改善。不存在任何有临床意义的 C 肽产生证据则被定义为β 细胞移植物失败。最佳和良好的功能结局被认为是成功的临床结局。

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