Division of Nephrology, Department of Medicine, Helsinki University Central Hospital, Folkhälsan Institute of Genetics, Folkhälsan Research Center, and the Diabetes and Obesity Research Program, Research Program's Unit, University of Helsinki, Helsinki, Finland.
Second Clinical Department, "Carol Davila" University of Medicine and Pharmacy, Bucharest, Romania.
Diabetes Care. 2014 Sep;37(9):2593-600. doi: 10.2337/dc14-0065. Epub 2014 Jun 26.
Osteopontin (OPN) is a multifunctional protein suggested to be a player in the arterial disease of patients with type 2 diabetes. However, its role for complications in patients with type 1 diabetes (T1D) is unknown. We therefore investigated the associations between OPN and diabetic vascular complications and all-cause mortality in patients with T1D.
Serum OPN was measured in 2,145 adults with T1D without end-stage renal disease (ESRD; dialysis or transplantation) as part of the Finnish Diabetic Nephropathy (FinnDiane) Study. Data on renal status, cardiovascular disease (CVD), and all-cause mortality during follow-up were verified from medical files, hospital discharge registries, and the Finnish National Death Registry, respectively. The median follow-up time was 10.5 (interquartile range 8.9-11.8) years.
Serum OPN was higher at baseline in patients who developed incident microalbuminuria (16.0 ± 0.9 vs. 14.1 ± 0.2 µg/L; P = 0.04), progressed to ESRD (28.3 ± 1.7 vs. 15.4 ± 0.2 µg/L; P < 0.001), suffered an incident CVD event (20.2 ± 1.2 vs. 15.5 ± 0.2 µg/L; P < 0.001), or died (23.3 ± 1.4 vs. 15.8 ± 0.2 µg/L; P < 0.001) during follow-up. In multivariate Cox regression analysis, OPN was independently associated with the development of incident microalbuminuria, an incident CVD event, and death, after adjustments for associated risk factors. Even after calculating reclassification indexes, OPN was predictive of CVD and all-cause mortality beyond the Framingham risk score covariates and hs-CRP.
Serum OPN is a strong predictor of incipient diabetic nephropathy, a first-ever CVD event, and all-cause mortality in patients with T1D. Serum OPN may be of clinical significance for the risk prediction of CVD events in patients with T1D.
骨桥蛋白(OPN)是一种多功能蛋白,被认为是 2 型糖尿病患者动脉疾病的参与者。然而,其在 1 型糖尿病(T1D)患者并发症中的作用尚不清楚。因此,我们研究了 OPN 与 T1D 患者的糖尿病血管并发症和全因死亡率之间的关系。
作为芬兰糖尿病肾病(FinnDiane)研究的一部分,在 2145 名无终末期肾病(透析或移植)的 T1D 成年人中测量了血清 OPN。肾功能、心血管疾病(CVD)和全因死亡率的数据分别从病历、医院出院登记处和芬兰国家死亡登记处核实。中位随访时间为 10.5 年(四分位距 8.9-11.8 年)。
在发生微量白蛋白尿(16.0 ± 0.9 与 14.1 ± 0.2 µg/L;P = 0.04)、进展为终末期肾病(28.3 ± 1.7 与 15.4 ± 0.2 µg/L;P < 0.001)、发生首次 CVD 事件(20.2 ± 1.2 与 15.5 ± 0.2 µg/L;P < 0.001)或随访期间死亡(23.3 ± 1.4 与 15.8 ± 0.2 µg/L;P < 0.001)的患者中,基线时血清 OPN 更高。在调整相关危险因素后,多变量 Cox 回归分析显示,OPN 与微量白蛋白尿、首次 CVD 事件和死亡的发生独立相关。即使在计算重新分类指数后,OPN 仍然可以预测 CVD 和全因死亡率,超出了 Framingham 风险评分协变量和 hs-CRP。
血清 OPN 是 T1D 患者早期糖尿病肾病、首次 CVD 事件和全因死亡率的强有力预测因子。血清 OPN 可能对 T1D 患者 CVD 事件的风险预测具有临床意义。