Tavintharan S, Pek Li Ting Sharon, Liu Jian Jun, Ng Xiao Wei, Yeoh Lee Ying, Su Chi Lim, Chee Fang Sum
Diabetes Centre, Khoo Teck Puat Hospital, Singapore Division of Endocrinology, Khoo Teck Puat Hospital, Singapore
Clinical Research Unit, Khoo Teck Puat Hospital, Singapore.
Diab Vasc Dis Res. 2014 Sep;11(5):359-62. doi: 10.1177/1479164114539712. Epub 2014 Jul 7.
Osteoprotegerin (OPG) is a glycoprotein from tumour necrosis factor receptor superfamily, responsible for osteoclastogenesis inhibition and associated with arterial calcification and stiffness. We describe the association between metabolic syndrome (MS) and OPG in type 2 diabetes mellitus patients.
We consecutively enrolled 1220 patients from our institution's Diabetes Centre from August 2011. Anthropometric data such as fasting blood/urine were obtained, and OPG was measured by enzyme-linked immunosorbent assay (ELISA).
Mean (standard deviation (SD)) of age and diabetes duration was 57.4 (10.9) years and 11.2 (8.9) years, respectively. Prevalence of MS was 64.3% (95% confidence interval (CI): 61.3%-67.2%) and associated with significantly higher OPG (5.44 vs 4.47 pmol/L) and microvascular complications. The presence of microvascular complications was associated with higher OPG: nephropathy (5.54 (2.20) vs 4.65 (1.70) pmol/L, p < 0.0001), neuropathy (6.33 (2.64) vs 5.06 (1.91) pmol/L, p < 0.0001) and retinopathy (6.08 (2.47) vs 5.00 (1.95) pmol/L, p < 0.0001). After adjusting for age, gender, ethnicity, glucose and microvascular complications, OPG remained an independent predictor of MS: (odds ratio (OR) = 1.102 (95% CI: 1.015-1.196), p = 0.021).
Higher OPG levels were associated with risk of MS and microvascular complications. Studies are needed to test whether OPG could be a useful biomarker identifying patients at risk of vascular complications and whether further exploration of this pathway may lead novel therapeutic options.
骨保护素(OPG)是一种来自肿瘤坏死因子受体超家族的糖蛋白,负责抑制破骨细胞生成,并与动脉钙化和僵硬有关。我们描述了2型糖尿病患者中代谢综合征(MS)与OPG之间的关联。
我们从2011年8月起连续纳入了我院糖尿病中心的1220例患者。获取了诸如空腹血/尿等人体测量数据,并通过酶联免疫吸附测定(ELISA)法测量OPG。
年龄和糖尿病病程的均值(标准差(SD))分别为57.4(10.9)岁和11.2(8.9)年。MS的患病率为64.3%(95%置信区间(CI):61.3%-67.2%),且与显著更高的OPG水平(5.44对4.47 pmol/L)和微血管并发症相关。微血管并发症的存在与更高的OPG水平相关:肾病(5.54(2.20)对4.65(1.70)pmol/L,p<0.0001)、神经病变(6.33(2.64)对5.06(1.91)pmol/L,p<0.0001)和视网膜病变(6.08(2.47)对5.00(1.95)pmol/L,p<0.0001)。在调整年龄、性别、种族、血糖和微血管并发症后,OPG仍然是MS的独立预测因子:(比值比(OR)=1.102(95%CI:1.015-1.196),p=0.021)。
更高的OPG水平与MS和微血管并发症的风险相关。需要开展研究来检验OPG是否可能是一种识别有血管并发症风险患者的有用生物标志物,以及进一步探索该途径是否可能带来新的治疗选择。