Dimitropoulou Nefeli M, Eussen Simone J P M, Schalkwijk Casper G, de Galan Bastiaan E
Department of Internal Medicine, Maastricht University Medical Centre+, Maastricht, the Netherlands.
Cardiovascular Research Institute Maastricht (CARIM), Maastricht University, Maastricht, the Netherlands.
Diabetologia. 2025 Jun 20. doi: 10.1007/s00125-025-06469-5.
AIMS/HYPOTHESIS: Glucose variability in people with type 2 diabetes has been associated with increased risk of CVD, and AGEs might be an underlying mechanism. Therefore, this study investigates associations of glucose variability with AGEs in the skin in people with and without impaired fasting glucose, impaired glucose tolerance or diabetes.
We used data from the Maastricht Study, a population-based cohort study. Glucose variability and AGEs in skin were measured by continuous glucose monitoring (CGM) and skin autofluorescence (SAF), respectively. Multiple linear regression was used to test the association of CGM-metrics CV and SD with SAF and adjusted for age, sex, CVD risk factors, nutritional factors and educational level. Interaction analysis was used to test the effect of glucose metabolism status on the association of CV and SD with SAF.
We included 795 participants (mean ± SD age 59 ± 8.7 years; 49% were female). Glucose metabolism status was stratified into normal glucose metabolism (n = 459), prediabetes (n = 174) and type 2 diabetes (n = 162). Individuals with type 2 diabetes had higher values of SAF (mean ± SD 2.3 ± 0.6 arbitrary units [AU]) than those with prediabetes (2.1 ± 0.4 AU, p = 0.014) and normal glucose metabolism (2.0 ± 0.4 AU, p = 0.007). In the cohort, both SD (0.152 AU [IQR 0.088-0.217]) and CV (0.014 AU [IQR 0.005-0.017]) were significantly associated with SAF in fully adjusted analyses. Glucose metabolism status did not modify the associations of SD and CV with SAF.
CONCLUSIONS/INTERPRETATION: A higher glucose variability is associated with higher levels of SAF, suggesting that glucose variability plays a role in the formation of AGEs.
目的/假设:2型糖尿病患者的血糖变异性与心血管疾病(CVD)风险增加相关,晚期糖基化终末产物(AGEs)可能是潜在机制。因此,本研究调查了空腹血糖受损、糖耐量受损或糖尿病患者与非此类患者的血糖变异性与皮肤中AGEs的关联。
我们使用了马斯特里赫特研究的数据,这是一项基于人群的队列研究。分别通过连续血糖监测(CGM)和皮肤自发荧光(SAF)测量血糖变异性和皮肤中的AGEs。采用多元线性回归检验CGM指标CV和SD与SAF的关联,并对年龄、性别、CVD危险因素、营养因素和教育水平进行校正。交互分析用于检验糖代谢状态对CV和SD与SAF关联的影响。
我们纳入了795名参与者(平均年龄±标准差59±8.7岁;49%为女性)。糖代谢状态分为正常糖代谢(n = 459)、糖尿病前期(n = 174)和2型糖尿病(n = 162)。2型糖尿病患者的SAF值(平均±标准差2.3±0.6任意单位[AU])高于糖尿病前期患者(2.1±0.4 AU,p = 0.014)和正常糖代谢患者(2.0±0.4 AU,p = 0.007)。在该队列中,在完全校正分析中,SD(0.152 AU[四分位间距0.088 - 0.217])和CV(0.014 AU[四分位间距0.005 - 0.017])均与SAF显著相关。糖代谢状态并未改变SD和CV与SAF的关联。
结论/解读:较高的血糖变异性与较高水平的SAF相关,表明血糖变异性在AGEs形成中起作用。