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如何在长效胰岛素研究中提高正常血糖葡萄糖钳夹试验的质量。

How to improve the quality of euglycemic glucose clamp tests in long-acting insulin studies.

作者信息

Yang Yi, Kuang Fu, Zhu XueYing, Li Li, Huang Yao, Liu Yang, Yu Xian

机构信息

Department of Phase I Clinical Trial Center, The Second Affiliated Hospital of ChongQing Medical University, ChongQing, China.

出版信息

Trials. 2025 Feb 1;26(1):37. doi: 10.1186/s13063-025-08749-2.

Abstract

BACKGROUND

The euglycemic clamp test stands as the best method for assessing the pharmacokinetic and pharmacodynamic properties of long-acting insulin. However, despite its widespread use, there remains a notable absence of an established gold standard for evaluating the test's quality. Existing recommendations from regulatory agencies lack specific threshold values, particularly concerning long-acting insulin. This study aimed to determine the evaluation criteria for assessing the quality of the long-acting insulin euglycemic glucose clamp test and to improve the overall quality of this testing method.

METHODS

Fifty-three healthy volunteers were administered a single dose of insulin degludec (0.4 IU/kg) and underwent a 24-h euglycemic clamp test. Blood samples were collected to evaluate the pharmacokinetics and pharmacodynamics of insulin degludec. Volunteers were separated into group A (coefficient of variation in blood glucose [CVBG] ≤ 3.5%) and group B (CVBG > 3.5%). The quality difference of the clamp test between the groups was assessed using various quality control indices. Volunteers were also categorized into group C (C-peptide reduction rate < 50%) and group D (C-peptide reduction rate ≥ 50%). The clamp test quality, pharmacokinetics, and pharmacodynamics of groups C and D were compared.

RESULTS

According to CVBG, group A had a mean CVBG of 2.95%, group B had a mean CVBG of 4.15%, and group A had a significantly lower CVBG than group B (p < 0.001). CVBG was positively correlated with other quality control indicators, such as the percentage of glucose excursion from the target range (GEFTR), duration of GEFTR, and area under the curve (AUC) of GEFTR. According to the reduction of C-peptide levels: group D had significantly higher C-peptide reduction than group C (p < 0.001). Groups C and D had CVBG < 3.5%. The quality of groups C and groups D was evaluated by the quality control indicators of the clamp test. Only the AUC of GEFTR was statistically different between Groups C and D (p = 0.043, < 0.05), and there was no statistical difference in other indicators between the two groups.

CONCLUSIONS

CVBG could be used as a standard for evaluating the quality of long-acting insulin euglycemic glucose clamp test, and the test quality was superior with a CVBG ≤ 3.5%. A C-peptide reduction ratio ≥ 50% indicated sufficient endogenous insulin inhibition; however, when the glucose fluctuation is small (CVBG is maintained at a low level) during the clamp test, even if the clamp test quality is slightly different, it is not sufficient to interfere with endogenous insulin secretion.

摘要

背景

正常血糖钳夹试验是评估长效胰岛素药代动力学和药效学特性的最佳方法。然而,尽管其广泛应用,但仍明显缺乏评估该试验质量的既定金标准。监管机构现有的建议缺乏具体阈值,尤其是关于长效胰岛素的阈值。本研究旨在确定评估长效胰岛素正常血糖葡萄糖钳夹试验质量的评估标准,并提高该检测方法的整体质量。

方法

53名健康志愿者单次注射德谷胰岛素(0.4 IU/kg),并进行24小时正常血糖钳夹试验。采集血样以评估德谷胰岛素的药代动力学和药效学。志愿者被分为A组(血糖变异系数[CVBG]≤3.5%)和B组(CVBG>3.5%)。使用各种质量控制指标评估两组之间钳夹试验的质量差异。志愿者还被分为C组(C肽降低率<50%)和D组(C肽降低率≥50%)。比较C组和D组的钳夹试验质量、药代动力学和药效学。

结果

根据CVBG,A组的平均CVBG为2.95%,B组的平均CVBG为4.15%,A组的CVBG显著低于B组(p<0.001)。CVBG与其他质量控制指标呈正相关,如血糖偏离目标范围的百分比(GEFTR)、GEFTR的持续时间以及GEFTR的曲线下面积(AUC)。根据C肽水平的降低:D组的C肽降低显著高于C组(p<0.001)。C组和D组的CVBG<3.5%。通过钳夹试验的质量控制指标评估C组和D组的质量。C组和D组之间仅GEFTR的AUC存在统计学差异(p=0.043,<0.05),两组之间的其他指标无统计学差异。

结论

CVBG可作为评估长效胰岛素正常血糖葡萄糖钳夹试验质量的标准,CVBG≤3.5%时试验质量更佳。C肽降低率≥50%表明内源性胰岛素抑制充分;然而,当钳夹试验期间血糖波动较小(CVBG维持在低水平)时,即使钳夹试验质量略有差异,也不足以干扰内源性胰岛素分泌。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9481/11786465/2e8e5ffca917/13063_2025_8749_Fig1_HTML.jpg

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