Department of Medicine, Division of Hospital Medicine, Emory University School of Medicine, Atlanta, GA, USA.
Emory Global Diabetes Research Center, Hubert Department of Global Health, Emory University, Atlanta, GA, USA.
Diabetes Res Clin Pract. 2020 Mar;161:108075. doi: 10.1016/j.diabres.2020.108075. Epub 2020 Feb 11.
To examine the clinical utility of 30-min plasma glucose (30-min-PG) measurement during an oral glucose tolerance (OGTT) in predicting type 2 diabetes (T2DM).
Data from a 3-year, randomized, controlled, primary prevention trial among 548 Asian Indians with prediabetes were analyzed. Participants underwent OGTT with PG measurements at fasting, 30-min, and 2-h at baseline and annually until the end of the study. Multivariable Cox regression models were constructed to calculate the risk of developing diabetes based on 30-min-PG levels. Improvement in prediction performance gained by adding an elevated level of 30-min-PG over prediabetic categories was calculated using the area-under-curve (AUC), net-reclassification (NRI), and integrated discrimination improvement (IDI) statistics.
At the end of follow-up, 30.4% of individuals had been diagnosed with T2DM by ADA criteria. Based on the maximally selected log-rank statistics, the optimal 30-min-PG cut point for predicting incident T2DM was >182 mg/dl. Multivariable-adjusted Cox regression models showed an independent association between elevated 30-min-PG (>182 mg/dl) and incident diabetes (hazard ratio (95% CI): 1.85 [1.32, 2.59]; D = 0.353, c-statistic = 0.676). The addition of an elevated 30-min-PG (>182 mg/dl) model significantly improved the prediction of diabetes (Δdeviance: -15.4; ΔAUC: 0.11; NRI: 0.51; IDI: 0.08) compared with IFG model alone) in individuals with prediabetes.
In prediabetic individuals, baseline 30-min-PG independently predicted T2DM and significantly improved reclassification and discrimination. Therefore, 30-min-PG should be considered as part of the routine testing in addition to FPG and 2-h-PG for better risk stratification.
探讨口服葡萄糖耐量试验(OGTT)30 分钟时的血浆葡萄糖(30-min-PG)测量在预测 2 型糖尿病(T2DM)中的临床应用价值。
分析了一项为期 3 年、随机、对照、一级预防试验的数据,该试验纳入了 548 名患有前驱糖尿病的亚洲印第安人。参与者在基线时和每年进行 OGTT,检测空腹、30 分钟和 2 小时的 PG 水平,直至研究结束。采用多变量 Cox 回归模型,根据 30-min-PG 水平计算发生糖尿病的风险。通过计算曲线下面积(AUC)、净重新分类(NRI)和综合判别改善(IDI)统计量,评估在预测糖尿病方面,增加 30 分钟高血糖水平相对于前驱糖尿病分类的预测性能改善情况。
随访结束时,根据 ADA 标准,30.4%的人被诊断为 T2DM。基于最大选择对数秩统计量,预测新发 T2DM 的最佳 30 分钟 PG 切点为>182mg/dl。多变量调整后的 Cox 回归模型显示,升高的 30 分钟 PG(>182mg/dl)与新发糖尿病之间存在独立关联(风险比(95%CI):1.85[1.32,2.59];D=0.353,c 统计量=0.676)。与仅 IFG 模型相比,添加升高的 30 分钟 PG(>182mg/dl)模型显著改善了糖尿病的预测(偏差变化:-15.4;AUC 变化:0.11;NRI:0.51;IDI:0.08)。
在前驱糖尿病患者中,基线 30 分钟 PG 独立预测 T2DM,并显著改善了重新分类和判别能力。因此,除了 FPG 和 2 小时 PG 之外,30 分钟 PG 应被视为常规检测的一部分,以更好地进行风险分层。