Winther Simon, Christensen Jeppe Hagstrup, Flyvbjerg Allan, Schmidt Erik Berg, Jørgensen Kaj Anker, Skou-Jørgensen Hanne, Svensson My
Clin Nephrol. 2013 Sep;80(3):161-7. doi: 10.5414/CN107803.
Patients treated with hemodialysis (HD) have an increased mortality, mainly caused by cardiovascular disease (CVD). Osteoprotegerin (OPG) is a glycoprotein involved in the regulation of the vascular calcification process. Previous studies have demonstrated that OPG is a prognostic marker of mortality. The aim of this study was to investigate if OPG was a prognostic marker of all-cause mortality in high-risk patients with end-stage renal disease and CVD.
We prospectively followed 206 HD patients with CVD. OPG was measured at baseline and the patients were followed for 2 years or until reaching the primary endpoint, i.e., all-cause mortality.
All-cause mortality during follow-up was 44% (90/206). High OPG was associated with increased mortality, using the first tertile as reference, with an unadjusted HR of 1.70 (CI 1.00 - 2.88) for the second tertile and HR of 1.63 (CI 0.96 - 2.78) for the third tertile. In a multivariate Cox-regression analysis age, CRP and OPG in both the second and third tertile were significantly associated with increased mortality In the unadjusted survival analysis, a test for trend of OPG yielded a p-value of 0.08; in the adjusted analyses, the p-value for trend was 0.03.
In a high-risk population of hemodialysis patients with previously documented cardiovascular disease, a high level of OPG was an independent risk marker of all-cause mortality.
接受血液透析(HD)治疗的患者死亡率增加,主要由心血管疾病(CVD)引起。骨保护素(OPG)是一种参与血管钙化过程调节的糖蛋白。先前的研究表明,OPG是死亡率的预后标志物。本研究的目的是调查OPG是否是终末期肾病和CVD高危患者全因死亡率的预后标志物。
我们前瞻性地随访了206例患有CVD的HD患者。在基线时测量OPG,并对患者进行2年随访或直至达到主要终点,即全因死亡率。
随访期间全因死亡率为44%(90/206)。以第一个三分位数为参照,高OPG与死亡率增加相关,第二个三分位数的未调整风险比(HR)为1.70(95%置信区间[CI] 1.00 - 2.88),第三个三分位数的HR为1.63(CI 0.96 - 2.78)。在多变量Cox回归分析中,第二个和第三个三分位数的年龄、C反应蛋白(CRP)和OPG均与死亡率增加显著相关。在未调整的生存分析中,OPG趋势检验的p值为0.08;在调整分析中,趋势的p值为0.03。
在先前有心血管疾病记录的血液透析高危患者群体中,高水平的OPG是全因死亡率的独立风险标志物。