Departments of Metabolic Medicine.
Departments of Metabolic Medicine ; Metabolism and Atherosclerosis, Graduate School of Medicine, Osaka University, Suita, Japan.
J Diabetes Investig. 2012 Jun 6;3(3):294-7. doi: 10.1111/j.2040-1124.2011.00168.x.
Aims/Introduction: Recently, glucagon-like peptide-1 (GLP-1) receptor agonists of liraglutide have become available in Japan. It has not yet been clarified what clinical parameters could discriminate liraglutide-effective patients from liraglutide-ineffective patients.
We reviewed 23 consecutive patients with type 2 diabetes admitted to Osaka University Hospital for glycemic control. All of the patients were treated with diet plus insulin (or plus oral antidiabetic drugs) to improve fasting plasma glucose (FPG) and postprandial glucose below 150 and 200 mg/dL, respectively. After insulin secretion and insulin resistance were evaluated, insulin was replaced by liraglutide. The efficacy of liraglutide was determined according to whether glycemic control was maintained at the target levels.
Liraglutide was effective in 13 of 23 patients. There were significant differences in the parameters of insulin secretion, including fasting C-peptide (F-CPR), C-peptide index (CPI), insulinogenic index (I.I.) and urine C-peptide (U-CPR), between liraglutide-effective and -ineffective patients. The duration of diabetes was significantly shorter in liraglutide-effective patients than in liraglutide-ineffective patients. In receiver operating characteristic analyses, the cut-off value for predicting the efficacy of liraglutide was 0.14 for I.I., 1.1 for CPI, 1.5 ng/mL for F-CPR, 33.3 μg/day for U-CPR and 19.5 years for duration of type 2 diabetes.
Insulin secretion evaluated by F-CPR, CPI, I.I., U-CPR and the duration of type 2 diabetes were useful parameters for predicting the efficacy of liraglutide in patients with type 2 diabetes. (J Diabetes Invest, doi: 10.1111/j.2040-1124.2011.00168.x, 2011).
目的/引言:最近,日本出现了利拉鲁肽等胰高血糖素样肽-1(GLP-1)受体激动剂。目前尚不清楚哪些临床参数可以区分利拉鲁肽有效患者和利拉鲁肽无效患者。
我们回顾了 23 例因血糖控制不佳而入住大阪大学医院的 2 型糖尿病患者。所有患者均接受饮食加胰岛素(或加口服降糖药)治疗,以改善空腹血糖(FPG)和餐后血糖分别低于 150 和 200mg/dL。在评估胰岛素分泌和胰岛素抵抗后,用利拉鲁肽替代胰岛素。根据血糖控制是否达到目标水平来确定利拉鲁肽的疗效。
23 例患者中有 13 例利拉鲁肽有效。利拉鲁肽有效患者和无效患者的胰岛素分泌参数(空腹 C 肽(F-CPR)、C 肽指数(CPI)、胰岛素生成指数(I.I.)和尿 C 肽(U-CPR))存在显著差异。利拉鲁肽有效患者的糖尿病病程明显短于利拉鲁肽无效患者。在受试者工作特征分析中,I.I.为 0.14、CPI 为 1.1、F-CPR 为 1.5ng/mL、U-CPR 为 33.3μg/day 和 2 型糖尿病病程为 19.5 年是预测利拉鲁肽疗效的最佳截断值。
F-CPR、CPI、I.I.、U-CPR 和 2 型糖尿病病程评估的胰岛素分泌是预测 2 型糖尿病患者利拉鲁肽疗效的有用参数。(糖尿病研究与临床实践,doi:10.1111/j.2040-1124.2011.00168.x,2011)。