Department of Primate Medicine, Davis, California;, Email:
Department of Primate Medicine, Davis, California.
Comp Med. 2021 Jun 1;71(3):247-255. doi: 10.30802/AALAS-CM-20-000075. Epub 2021 May 25.
Treating and monitoring type 2 diabetes mellitus (T2DM) in NHP can be challenging. Multiple insulin and hypoglycemic therapies and management tools exist, but few studies demonstrate their benefits in a NHP clinical setting. The insulins glargine and degludec are long-acting insulins; their duration of action in humans exceeds 24 and 42 h, respectively. In the first of this study's 2 components, we evaluated whether insulin degludec could be dosed daily at equivalent units to glargine to achieve comparable blood glucose (BG) reduction in diabetic rhesus macaques () with continuous glucose monitoring (CGM) devices. The second component assessed the accuracy of CGM devices in rhesus macaques by comparing time-stamped CGM interstitial glucose values, glucometer BG readings, and BG levels measured by using an automated clinical chemistry analyzer from samples that were collected at the beginning and end of each CGM device placement. The CGM devices collected a total of 21,637 glucose data points from 6 diabetic rhesus macaques that received glargine followed by degludec every 24 h for 1 wk each. Ultimately, glucose values averaged 29 mg/dL higher with degludec than with glargine. Glucose values were comparable between the CGM device, glucometer, and chemistry analyzer, thus validating that CGM devices as reliable for measuring BG levels in rhesus macaques. Although glargine was superior to degludec when given at the same dose (units/day), both are safe and effective treatment options. Glucose values from CGM, glucometers, and chemistry analyzers provided results that were analogous to BG values in rhesus macaques. Our report further highlights critical clinical aspects of using glargine as compared with degludec in NHP and the benefits of using CGM devices in macaques.
治疗和监测 2 型糖尿病(T2DM)在非人类灵长类动物(NHP)中具有挑战性。存在多种胰岛素和降血糖治疗和管理工具,但很少有研究证明它们在 NHP 临床环境中的益处。甘精胰岛素和地特胰岛素是长效胰岛素;它们在人类中的作用持续时间分别超过 24 和 42 小时。在这项研究的第一部分的 2 个组成部分中,我们评估了地特胰岛素是否可以以与甘精胰岛素相当的单位剂量每天给药,以在使用连续血糖监测(CGM)设备的糖尿病恒河猴中实现可比的血糖(BG)降低。第二部分通过比较标记时间的 CGM 间质葡萄糖值、血糖仪 BG 读数和通过在每个 CGM 设备放置开始和结束时收集的样本使用自动化临床化学分析仪测量的 BG 水平,评估了 CGM 设备在恒河猴中的准确性。CGM 设备总共从接受甘精胰岛素随后每 24 小时接受地特胰岛素治疗 1 周的 6 只糖尿病恒河猴中收集了 21637 个葡萄糖数据点。最终,地特胰岛素的葡萄糖值平均比甘精胰岛素高 29mg/dL。CGM 设备、血糖仪和化学分析仪之间的葡萄糖值具有可比性,从而验证了 CGM 设备可用于测量恒河猴的 BG 水平。虽然在相同剂量(单位/天)下甘精胰岛素优于地特胰岛素,但两者都是安全有效的治疗选择。CGM、血糖仪和化学分析仪的葡萄糖值提供的结果与恒河猴的 BG 值相似。我们的报告进一步强调了在 NHP 中使用甘精胰岛素与地特胰岛素相比的关键临床方面,以及在恒河猴中使用 CGM 设备的益处。