Zhang Li, Sun Haichen, Liu Shuang, Gao Jinhuan, Xia Jinggang
1Department of Geriatrics, Xuanwu Hospital, Capital Medical University, China National Clinical Research Center for Geriatric Medicine, Beijing, 100053 China.
2Surgical Laboratory, Xuanwu Hospital, Capital Medical University, Beijing, 100053 China.
Diabetol Metab Syndr. 2019 Aug 19;11:67. doi: 10.1186/s13098-019-0464-4. eCollection 2019.
The present study identified whether glycemic variability (GV) was associated with vascular calcification and explored the underlying mechanisms.
Eighty-four consecutive type 2 diabetic patients with unstable angina (UA) were included from January 2018 to June 2018 to calculate calcification scores using computerized tomographic angiography (CTA), and the patients were divided into 2 groups: high calcification score group (HCS group) and low calcification score group (LCS group). Intergroup differences in GV were determined via comparisons of the standard deviation (SD) of blood glucose. Calcification staining, content measurement, apoptosis evaluation and Western blot analysis of endoplasmic reticulum (ER) stress-related apoptosis, Wnt1, galectin-3 and bone morphogenetic protein-2 (BMP-2) were compared in cell cultures from rat vascular smooth muscle cells in the different degrees of GV.
The SD increased significantly with the increases in calcification scores from human studies (HCS group 2.37 ± 0.82 vs. LCS group 1.87 ± 0.78, = 0.007). Multivariate logistic regression analysis suggested that increased SD and serum creatinine were independent predictors of calcification. The high GV group had a higher apoptotic rate, higher calcification content and higher expressions of glucose-regulated protein, caspase-3, Wnt1, galectin-3 and BMP-2 markers compared to the low GV group in the in vitro studies (< 0.001).
We report the novel finding that GV is associated with vascular calcification, and ER stress-related apoptosis, Wnt1, galectin-3 and BMP-2 may be involved in this regulation.
本研究确定血糖变异性(GV)是否与血管钙化相关,并探讨其潜在机制。
纳入2018年1月至2018年6月连续收治的84例2型糖尿病合并不稳定型心绞痛(UA)患者,采用计算机断层血管造影(CTA)计算钙化评分,并将患者分为两组:高钙化评分组(HCS组)和低钙化评分组(LCS组)。通过比较血糖标准差(SD)确定两组间GV的差异。对不同程度GV的大鼠血管平滑肌细胞进行细胞培养,比较钙化染色、含量测定、凋亡评估以及内质网(ER)应激相关凋亡、Wnt1、半乳糖凝集素-3和骨形态发生蛋白-2(BMP-2)的蛋白质印迹分析结果。
人体研究显示,随着钙化评分增加,SD显著升高(HCS组2.37±0.82 vs. LCS组1.87±0.78,P = 0.007)。多因素逻辑回归分析表明,SD升高和血清肌酐是钙化的独立预测因素。体外研究显示,高GV组的凋亡率、钙化含量以及葡萄糖调节蛋白、半胱天冬酶-3、Wnt1、半乳糖凝集素-3和BMP-2标志物的表达均高于低GV组(P < 0.001)。
我们报告了一个新发现,即GV与血管钙化相关,并且ER应激相关凋亡、Wnt1、半乳糖凝集素-3和BMP-2可能参与了这一调控过程。