Weill Cornell Medicine in Qatar, Qatar Foundation, Education City, Doha, Qatar.
Faculty of Science and Engineering, Manchester Metropolitan University, Manchester, UK.
J Diabetes Investig. 2021 Nov;12(11):2002-2009. doi: 10.1111/jdi.13582. Epub 2021 Jun 19.
AIMS/INTRODUCTION: This study aimed to investigate whether insulin resistance (IR) in individuals with type 2 diabetes undergoing intensive glycemic control determines the extent of improvement in neuropathy.
This was an exploratory substudy of an open-label, randomized controlled trial of individuals with poorly controlled type 2 diabetes treated with exenatide and pioglitazone or insulin to achieve a glycated hemoglobin <7.0% (<53 mmol/mol). Baseline IR was defined using homeostasis model assessment of IR, and change in neuropathy was assessed using corneal confocal microscopy.
A total of 38 individuals with type 2 diabetes aged 50.2 ± 8.5 years with (n = 25, 66%) and without (n = 13, 34%) IR were studied. There was a significant decrease in glycated hemoglobin (P < 0.0001), diastolic blood pressure (P < 0.0001), total cholesterol (P < 0.01) and low-density lipoprotein (P = 0.05), and an increase in bodyweight (P < 0.0001) with treatment. Individuals with homeostasis model assessment of IR <1.9 showed a significant increase in corneal nerve fiber density (P ≤ 0.01), length (P ≤ 0.01) and branch density (P ≤ 0.01), whereas individuals with homeostasis model assessment of IR ≥1.9 showed no change. IR was negatively associated with change in corneal nerve fiber density after adjusting for change in bodyweight (P < 0.05).
Nerve regeneration might be limited in individuals with type 2 diabetes and IR undergoing treatment with pioglitazone plus exenatide or insulin to improve glycemic control.
目的/引言:本研究旨在探讨 2 型糖尿病患者强化血糖控制下的胰岛素抵抗(IR)是否决定神经病变改善的程度。
这是一项针对接受艾塞那肽和吡格列酮或胰岛素治疗以实现糖化血红蛋白<7.0%(<53mmol/mol)的控制不佳的 2 型糖尿病患者的开放性、随机对照试验的探索性亚研究。使用稳态模型评估胰岛素抵抗来定义基线 IR,使用角膜共聚焦显微镜评估神经病变的变化。
共纳入 38 名年龄为 50.2±8.5 岁的 2 型糖尿病患者,其中 25 名(66%)存在 IR,13 名(34%)无 IR。治疗后糖化血红蛋白(P<0.0001)、舒张压(P<0.0001)、总胆固醇(P<0.01)和低密度脂蛋白(P=0.05)显著降低,体重增加(P<0.0001)。稳态模型评估胰岛素抵抗<1.9 的患者角膜神经纤维密度(P≤0.01)、长度(P≤0.01)和分支密度(P≤0.01)显著增加,而稳态模型评估胰岛素抵抗≥1.9 的患者则无变化。在调整体重变化后,IR 与角膜神经纤维密度的变化呈负相关(P<0.05)。
在接受吡格列酮加艾塞那肽或胰岛素治疗以改善血糖控制的 2 型糖尿病和 IR 患者中,神经再生可能受到限制。