Yozgatli K, Lefrandt J D, Noordzij M J, Oomen P H N, Brouwer T, Jager J, Castro Cabezas M, Smit A J
Department of Internal Medicine, University of Groningen, University Medical Centre Groningen.
Department of Internal Medicine, Medical Centre Leeuwarden.
Diabet Med. 2018 Apr 23. doi: 10.1111/dme.13651.
The United Kingdom Prospective Diabetes Study (UKPDS) study showed that glycaemic control (HbA ) can predict vascular complications in Type 2 diabetes mellitus. The Diabetes Control and Complications Trial (DCCT) study showed that accumulation of advanced glycation end products (AGEs) from skin biopsies predicts vascular complications in Type 1 diabetes. Previously, we showed that tissue AGEs can be measured non-invasively using skin autofluorescence (SAF). The aim of this study was to compare the predictive value of HbA and SAF for new macrovascular events and microvascular complications in people with Type 2 diabetes.
A prospective cohort study of 563 participants, median age 64 years [interquartile range (IQR) 57-72], diabetes duration of 13 years, from five Dutch hospitals was performed.
After a median follow-up of 5.1 (IQR 4.3-5.9) years, 79 (15%) participants had died and 49 (9%) were lost to follow-up. Some 133 (26%) developed a microvascular complication and 189 (37%) a macrovascular event. Tertiles of HbA were significantly associated with development of microvascular complications (log rank P = 0.022), but not with macrovascular events. Tertiles of SAF were significantly associated with macrovascular events (log rank P = 0.003). Cox regression analysis showed SAF was associated with macrovascular events: crude hazard ratio (HR) 1.53 (P < 0.001) per unit increase, HR 1.28 (P = 0.03) after correction for UKPDS score. HbA was predictive for microvascular complications: crude HR 1.20 (P = 0.004), HR 1.20 (P = 0.004) after correction for UKPDS score.
This study shows that tissue accumulation of AGEs, assessed by SAF, is associated with development of macrovascular events in people with Type 2 diabetes, whereas HbA is associated with the development of microvascular complications.
英国前瞻性糖尿病研究(UKPDS)表明,血糖控制(糖化血红蛋白)可预测2型糖尿病患者的血管并发症。糖尿病控制与并发症试验(DCCT)显示,通过皮肤活检测得的晚期糖基化终末产物(AGEs)的积累可预测1型糖尿病患者的血管并发症。此前,我们曾表明可利用皮肤自发荧光(SAF)对组织AGEs进行无创测量。本研究旨在比较糖化血红蛋白和SAF对2型糖尿病患者新发大血管事件和微血管并发症的预测价值。
对来自五家荷兰医院的563名参与者进行了一项前瞻性队列研究,这些参与者的年龄中位数为64岁[四分位间距(IQR)为57 - 72岁],糖尿病病程为13年。
在中位随访5.1(IQR 4.3 - 5.9)年后,79名(15%)参与者死亡,49名(9%)失访。约133名(26%)发生了微血管并发症,189名(37%)发生了大血管事件。糖化血红蛋白三分位数与微血管并发症的发生显著相关(对数秩检验P = 0.022),但与大血管事件无关。SAF三分位数与大血管事件显著相关(对数秩检验P = 0.003)。Cox回归分析显示,SAF与大血管事件相关:每单位增加的粗风险比(HR)为1.53(P < 0.001),校正UKPDS评分后HR为1.28(P = 0.03)。糖化血红蛋白可预测微血管并发症:粗HR为1.20(P = 0.004),校正UKPDS评分后HR为1.20(P = 0.004)。
本研究表明,通过SAF评估的AGEs组织积累与2型糖尿病患者大血管事件的发生相关,而糖化血红蛋白与微血管并发症的发生相关。