Department of Pediatrics, Indiana University School of Medicine and Riley Hospital for Children, Indianapolis, IN.
Indiana University School of Medicine, Indianapolis, IN.
Diabetes Care. 2018 Feb;41(2):318-325. doi: 10.2337/dc17-1373. Epub 2017 Nov 28.
Type 2 diabetes is a growing health problem among both adults and adolescents. To better understand the differences in the pathogenesis of diabetes between these groups, we examined differences in β-cell function along the spectrum of glucose tolerance.
We evaluated 89 adults and 50 adolescents with normal glucose tolerance (NGT), dysglycemia, or type 2 diabetes. Oral glucose tolerance test results were used for C-peptide and insulin/glucose minimal modeling. Model-derived and direct measures of insulin secretion and insulin sensitivity were compared across glycemic stages and between age-groups at each stage.
In adolescents with dysglycemia, there was marked insulin resistance (insulin sensitivity index: adolescents, median [interquartile range] 1.8 [1.1-2.4] × 10; adults, 5.0 [2.3-9.9]; = 0.01). The nature of β-cell dysfunction across stages of dysglycemia differed between the groups. We observed higher levels of secretion among adolescents than adults (total insulin secretion: NGT, 143 [103-284] × 10/min adolescent vs. 106 [71-127], = 0.001); adults showed stepwise impairments in static insulin secretion (NGT, 7.5 [4.0-10.3] × 10/min; dysglycemia, 5.0 [2.3-9.9]; type 2 diabetes, 0.7 [0.1-2.45]; = 0.003), whereas adolescents showed diabetes-related impairment in dynamic secretion (NGT, 1,905 [1,630-3,913] × 10; dysglycemia, 2,703 [1,323-3,637]; type 2 diabetes, 1,189 [269-1,410]; = 0.001).
Adults and adolescents differ in the underlying defects leading to dysglycemia, and in the nature of β-cell dysfunction across stages of dysglycemia. These results may suggest different approaches to diabetes prevention in youths versus adults.
2 型糖尿病是成年人和青少年中日益严重的健康问题。为了更好地了解这两个群体中糖尿病发病机制的差异,我们研究了葡萄糖耐量谱中β细胞功能的差异。
我们评估了 89 名成年人和 50 名糖耐量正常(NGT)、糖调节受损或 2 型糖尿病的青少年。根据口服葡萄糖耐量试验结果,使用 C 肽和胰岛素/葡萄糖最小模型进行评估。在每个血糖阶段,比较模型衍生和直接测量的胰岛素分泌和胰岛素敏感性,并在每个阶段的年龄组之间进行比较。
在糖调节受损的青少年中,存在明显的胰岛素抵抗(胰岛素敏感指数:青少年,中位数[四分位数范围]1.8[1.1-2.4]×10;成年人,5.0[2.3-9.9];P=0.01)。糖调节受损各阶段β细胞功能障碍的性质在两组之间不同。我们观察到青少年的分泌水平高于成年人(总胰岛素分泌:NGT,143[103-284]×10/min 青少年 vs. 106[71-127],P=0.001);成年人表现出逐步的静态胰岛素分泌受损(NGT,7.5[4.0-10.3]×10/min;糖调节受损,5.0[2.3-9.9];2 型糖尿病,0.7[0.1-2.45];P=0.003),而青少年则表现出与糖尿病相关的动态分泌受损(NGT,1,905[1,630-3,913]×10;糖调节受损,2,703[1,323-3,637];2 型糖尿病,1,189[269-1,410];P=0.001)。
成年人和青少年在导致糖调节受损的潜在缺陷以及糖调节受损各阶段的β细胞功能障碍的性质上存在差异。这些结果可能表明在青少年和成年人中预防糖尿病的方法不同。