Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
Division of Endocrinology, Department of Internal Medicine, Leiden University Medical Center, Leiden, The Netherlands.
Metabolomics. 2021 Jun 9;17(6):57. doi: 10.1007/s11306-021-01806-2.
Insulin is the key regulator of glucose metabolism, but it is difficult to dissect direct insulin from glucose-induced effects. We aimed to investigate the effects of hyperinsulemia on metabolomic measures under euglycemic conditions in nondiabetic participants.
We assessed concentrations of 151 metabolomic measures throughout a two-step hyperinsulinemic euglycemic clamp procedure. We included 24 participants (50% women, mean age = 62 [s.d. = 4.2] years) and metabolomic measures were assessed under baseline, low-dose (10 mU/m/min) and high-dose (40 mU/m/min) insulin conditions. The effects of low- and high-dose insulin infusion on metabolomic measures were analyzed using linear mixed-effect models for repeated measures.
After low-dose insulin infusion, 90 metabolomic measures changed in concentration (p < 1.34e), among which glycerol (beta [Confidence Interval] = - 1.41 [- 1.54, - 1.27] s.d., p = 1.28e) and three-hydroxybutyrate (- 1.22 [- 1.36, - 1.07] s.d., p = 1.44e) showed largest effect sizes. After high-dose insulin infusion, 121 metabolomic measures changed in concentration, among which branched-chain amino acids showed the largest additional decrease compared with low-dose insulin infusion (e.g., Leucine, - 1.78 [- 1.88, - 1.69] s.d., P = 2.7e). More specifically, after low- and high-dose insulin infusion, the distribution of the lipoproteins shifted towards more LDL-sized particles with decreased mean diameters.
Metabolomic measures are differentially insulin sensitive and may thus be differentially affected by the development of insulin resistance. Moreover, our data suggests insulin directly affects metabolomic measures previously associated with increased cardiovascular disease risk.
胰岛素是葡萄糖代谢的关键调节剂,但很难将其与葡萄糖引起的作用区分开来。我们旨在研究在非糖尿病参与者的正常血糖条件下,高胰岛素血症对代谢组学测量的影响。
我们在两步高胰岛素正常血糖钳夹过程中评估了 151 种代谢组学测量的浓度。我们纳入了 24 名参与者(女性占 50%,平均年龄 62[标准差 4.2]岁),并在基础状态、低剂量(10mU/m/min)和高剂量(40mU/m/min)胰岛素条件下评估代谢组学测量值。使用重复测量线性混合效应模型分析低剂量和高剂量胰岛素输注对代谢组学测量值的影响。
低剂量胰岛素输注后,90 种代谢组学测量值的浓度发生变化(p<1.34e),其中甘油(beta[置信区间] = -1.41[-1.54,-1.27]标准差,p=1.28e)和β-羟基丁酸(-1.22[-1.36,-1.07]标准差,p=1.44e)的效应量最大。高剂量胰岛素输注后,121 种代谢组学测量值的浓度发生变化,其中支链氨基酸与低剂量胰岛素输注相比表现出最大的额外降低(例如亮氨酸,-1.78[-1.88,-1.69]标准差,P=2.7e)。更具体地说,在低剂量和高剂量胰岛素输注后,脂蛋白的分布向更小的 LDL 大小颗粒转移,平均直径减小。
代谢组学测量值对胰岛素具有不同的敏感性,因此可能会受到胰岛素抵抗发展的不同影响。此外,我们的数据表明胰岛素直接影响代谢组学测量值,这些测量值与心血管疾病风险增加有关。