Kramer Caroline K, Ye Chang, Hanley Anthony J G, Connelly Philip W, Sermer Mathew, Zinman Bernard, Retnakaran Ravi
Leadership Sinai Centre for Diabetes, Mount Sinai Hospital, 60 Murray Street, Suite L5-025, Mailbox-21, Toronto, Ontario, Canada, M5T 3L9.
Diabetologia. 2015 Jun;58(6):1354-62. doi: 10.1007/s00125-015-3551-6. Epub 2015 Mar 12.
AIMS/HYPOTHESIS: On cross-sectional assessment, a delayed timing of the peak blood glucose level at ≥60 min post-challenge on an OGTT is associated with beta cell dysfunction. In this context, we hypothesised that longitudinal changes in the timing of this peak might predict changes in glucose metabolism. We thus sought to evaluate the longitudinal associations of changes in the timing of the peak glucose level with changes over time in insulin sensitivity, beta cell function and glucose tolerance.
A total of 532 women underwent an OGTT at both 3 months and 12 months postpartum. The participants were stratified into four groups according to the change in timing of their glucose peak between the two visits: women with no change in timing of the glucose peak at 30 min (n = 217), those whose glucose peak shifted to an earlier time point (n = 120), those whose peak shifted to a later time point (n = 87) and women with an unchanged glucose peak at ≥60 min (n = 108). Beta cell function was measured using the Insulin Secretion-Sensitivity Index-2 (ISSI-2).
Compared with an unchanged glucose peak at 30 min, both the shift of the glucose peak to a later time point and a peak that was unchanged at ≥60 min were independently associated with declining ISSI-2 scores (β = -127.5, p < 0.001 and β = -98.8, p = 0.006, respectively) and increased 2 h post-challenge glucose levels (β = 1.28, p < 0.001 and β = 0.91, p < 0.001, respectively) between the two visits. Furthermore, both these patterns of change in peak were independently associated with worsening glucose tolerance (from normal to prediabetes [defined as impaired fasting glucose or impaired glucose tolerance]/diabetes or from prediabetes to diabetes) (OR 8.1, 95% CI 3.0, 22.1 and OR 3.7, 95% CI 1.2, 11.7, respectively).
CONCLUSIONS/INTERPRETATION: A delayed timing of the post-challenge peak glucose level is associated with declining beta cell function and worsening glucose tolerance over time.
目的/假设:在横断面评估中,口服葡萄糖耐量试验(OGTT)中挑战后≥60分钟时血糖峰值出现延迟与β细胞功能障碍有关。在此背景下,我们假设该峰值时间的纵向变化可能预测葡萄糖代谢的变化。因此,我们试图评估血糖峰值时间变化与胰岛素敏感性、β细胞功能和葡萄糖耐量随时间变化之间的纵向关联。
共有532名女性在产后3个月和12个月时进行了OGTT。根据两次就诊时血糖峰值时间的变化,将参与者分为四组:30分钟时血糖峰值时间无变化的女性(n = 217)、血糖峰值提前的女性(n = 120)、血糖峰值延迟的女性(n = 87)以及≥60分钟时血糖峰值无变化的女性(n = 108)。使用胰岛素分泌-敏感性指数-2(ISSI-2)测量β细胞功能。
与30分钟时血糖峰值无变化相比,血糖峰值延迟以及≥60分钟时血糖峰值无变化均与两次就诊之间ISSI-2评分下降(分别为β = -127.5,p < 0.001和β = -98.8,p = 0.006)以及挑战后2小时血糖水平升高(分别为β = 1.28,p < 0.001和β = 0.91,p < 0.001)独立相关。此外,这两种峰值变化模式均与葡萄糖耐量恶化(从正常到糖尿病前期[定义为空腹血糖受损或葡萄糖耐量受损]/糖尿病或从糖尿病前期到糖尿病)独立相关(分别为OR 8.1,95%CI 3.0,22.1和OR 3.7,95%CI 1.2,11.7)。
结论/解读:挑战后血糖峰值时间延迟与β细胞功能下降和随时间推移葡萄糖耐量恶化有关。