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量化胰岛移植后维持胰岛移植功能所需的胰岛素治疗剂量。

Quantifying Insulin Therapy Requirements to Preserve Islet Graft Function Following Islet Transplantation.

作者信息

Orr Chris, Stratton Jeannette, Rao Irram, Al-Sayed Mohamad, Smith Craig, El-Shahawy Mohamed, Dafoe Donald, Mullen Yoko, Al-Abdullah Ismail, Kandeel Fouad

机构信息

Southern California Islet Cell Resources Center, Department of Diabetes, Endocrinology, and Metabolism, Beckman Research Institute of the City of Hope, Duarte, CA, USA.

出版信息

Cell Transplant. 2016;25(1):83-95. doi: 10.3727/096368915X687958. Epub 2015 Apr 7.

Abstract

A mathematical nonlinear regression model of several parameters (baseline insulin intake, posttransplant 2-h postprandial blood glucose, and stimulated C-peptide) from type 1 diabetics with HbA1c <6.5% who do not require insulin therapy and have no hypoglycemic instances was developed for accurately predicting supplemental insulin requirements in the posttransplant period. An insulin deficit threshold of 0.018 U/kg/day was defined as the average first-year calculated insulin deficit (CID), above which HbA1c rose to >6.5% during year 2 of the posttransplant period. When insulin-untreated subjects were divided into two groups based on whether the average CID was smaller (group I) or greater (group II) than the insulin deficit threshold, HbA1c was found to be similar in the two groups in year 1, but increased significantly in group II to above 6.5% (with mean glucose of 121.9 mg/dl) but remained below 6.5% in group I subjects (with mean glucose of 108.7 mg/dl) in year 2 of the follow-up period. The greater insulin deficit in group II was also associated with a higher susceptibility to hyperglycemia during periods of low serum Rapamune and Prograf levels (combined levels below 11.2 and 4.7 ng/ml, respectively). Although the differences between predicted insulin requirement (PIR) and actual empirical insulin intake in the insulin-treated subjects were generally small, they were nonetheless sufficient to identify over- and underinsulinization at each follow-up visit for all subjects (n = 14 subjects, 135 observations). The newly developed model can effectively identify underinsulinized islet transplant recipients at risk for graft dysfunction due to inadequate supplemental insulin intake or those potentially susceptible to graft function loss due to inadequate immunosuppression. While less common following islet cell therapy, the model can also identify overinsulinized subjects who may be at risk for hypoglycemia.

摘要

针对糖化血红蛋白(HbA1c)<6.5%、无需胰岛素治疗且无低血糖情况的1型糖尿病患者,建立了一个包含多个参数(基础胰岛素摄入量、移植后餐后2小时血糖和刺激后的C肽)的数学非线性回归模型,以准确预测移植后阶段的补充胰岛素需求。将0.018 U/kg/天的胰岛素缺乏阈值定义为移植后第一年的平均计算胰岛素缺乏量(CID),高于此阈值时,在移植后第二年HbA1c升至>6.5%。当未接受胰岛素治疗的受试者根据平均CID小于(I组)或大于(II组)胰岛素缺乏阈值分为两组时,发现两组在第一年的HbA1c相似,但在随访期的第二年,II组显著升高至6.5%以上(平均血糖为121.9 mg/dl),而I组受试者仍低于6.5%(平均血糖为108.7 mg/dl)。II组更大的胰岛素缺乏还与血清西罗莫司和他克莫司水平较低(分别低于11.2和4.7 ng/ml)时对高血糖的易感性增加有关。尽管胰岛素治疗受试者的预测胰岛素需求量(PIR)与实际经验性胰岛素摄入量之间的差异通常较小,但仍足以在每次随访时识别所有受试者(n = 14名受试者,135次观察)的胰岛素过量和不足情况。新开发的模型可以有效识别因补充胰岛素不足而有移植功能障碍风险的胰岛素不足的胰岛移植受者,或因免疫抑制不足而可能易发生移植功能丧失的受者。虽然在胰岛细胞治疗后不太常见,但该模型也可以识别可能有低血糖风险的胰岛素过量的受试者。

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