Clinical Research Unit, Khoo Teck Puat Hospital, Singapore.
Clinical Research Unit, Khoo Teck Puat Hospital, Singapore; Diabetes Centre, Admiralty Medical Centre, Khoo Teck Puat Hospital, Singapore.
Diabetes Res Clin Pract. 2020 Mar;161:107992. doi: 10.1016/j.diabres.2019.107992. Epub 2020 Feb 4.
Poor glycaemic control elevates the risk for vascular complications. Biomarkers for predicting susceptibility to glycaemic worsening are lacking. This 3-year prospective analysis assessed the utility of several circulating diabetes-related biomarkers for predicting loss of glycaemic control, and their contribution to albuminuria progression in type 2 diabetes mellitus (T2DM).
T2DM subjects with adequately-controlled diabetes (HbA1c < 8%) at initial recruitment were analysed (N = 859). Baseline plasma levels of osteoprotegerin (OPG), C-reactive protein (CRP), adiponectin, intercellular-cell adhesion molecule-1, and vascular-cell adhesion molecule-1 were quantified using immunoassay. Definitions for development of uncontrolled diabetes and albuminuria progression were HbA1c ≥ 8.0% and increase in albuminuria category at follow-up, respectively.
At follow-up, 185 subjects developed uncontrolled diabetes. Higher baseline CRP and OPG levels were observed in the high-risk individuals, and predicted increased risk for developing uncontrolled diabetes. OPG, but not CRP, was associated with albuminuria progression after multivariable adjustment. The relationship was attenuated following adjustment for development of uncontrolled diabetes, which emerged as a significant associate. Mediation analysis revealed that loss of glycaemic control explained 64.5% of the relationship between OPG and albuminuria progression.
OPG outperformed other diabetes-related biomarkers to be a potentially useful biomarker for predicting loss of glycaemic control and its associated albuminuria deterioration.
血糖控制不佳会增加血管并发症的风险。目前缺乏预测血糖恶化易感性的生物标志物。本 3 年前瞻性分析评估了几种循环糖尿病相关生物标志物预测血糖控制丧失的效用,以及它们对 2 型糖尿病(T2DM)白蛋白尿进展的贡献。
在初始招募时,对血糖控制良好(HbA1c<8%)的 T2DM 患者进行了分析(N=859)。使用免疫测定法定量检测基线血浆骨保护素(OPG)、C 反应蛋白(CRP)、脂联素、细胞间黏附分子-1 和血管细胞黏附分子-1 的水平。未控制糖尿病和白蛋白尿进展的定义分别为 HbA1c≥8.0%和随访时白蛋白尿类别增加。
随访时,185 例患者出现未控制的糖尿病。高危患者的基线 CRP 和 OPG 水平较高,预测发生未控制糖尿病的风险增加。OPG 与多变量调整后的白蛋白尿进展相关,但 CRP 无此相关性。在调整未控制糖尿病的发展后,这种关系减弱,该因素成为一个显著的关联。中介分析表明,血糖控制丧失解释了 OPG 与白蛋白尿进展之间 64.5%的关系。
OPG 优于其他糖尿病相关生物标志物,是预测血糖控制丧失及其相关白蛋白尿恶化的潜在有用生物标志物。