Department of Nephrology, Institute of Nephrology, West China Hospital of Sichuan University, Chengdu, China.
Department of Nephrology, The Second People's Hospital of Yibin, Yibin, China.
Kidney Blood Press Res. 2024;49(1):718-726. doi: 10.1159/000540657. Epub 2024 Jul 31.
Biomarkers are urgently required to identify peritoneal dialysis (PD) patients at risk of cardiovascular (CV) events. This study aimed to investigate the predictive value of soluble suppression of tumorigenicity-2 (sST2) for CV events in patients undergoing incident PD.
In this prospective cohort study, incident PD patients were enrolled. Blood samples to measure sST2 levels were obtained before PD catheter implantation. The patients underwent a standard peritoneal equilibration test (PET) after initiation of PD for 4-6 weeks. The sST2 levels in both serum and dialysate were determined using enzyme-linked immunosorbent assay. CV events were recorded during the follow-up period.
A total of 137 patients were enrolled. During the follow-up period of 17.3 months, 49 (35.76%) patients experienced CV events. When patients were dichotomized based on the median values and the calculated cutoff values of sST2, the higher sST2 group had 2.980- and 3.048-fold increased risks of CV events, respectively, when compared with the lower sST2 group. Moreover, the prognostic value of sST2 remained significant as a continuous variable (per 1 standard deviation increase, hazard ratio [HR] = 1.037, 95% confidence interval [CI] 1.010-1.066, p = 0.008). N-terminal pro-brain natriuretic peptide (NT-proBNP) levels were found to indicate a higher risk only when dichotomized based on the calculated cutoff values. Furthermore, serum sST2 and NT-proBNP levels simultaneously above the calculated cutoff values were associated with a higher risk of CV events (HR = 3.398, 95% CI 1.813-6.367, p < 0.001).
Baseline serum sST2 level is an independent predictor of the risk of CV events in patients receiving incident PD, and in combination with NT-proBNP level, it can provide a more accurate predictive value.
目前急需生物标志物来识别发生心血管(CV)事件风险的腹膜透析(PD)患者。本研究旨在探讨可溶性肿瘤抑制物 2(sST2)对开始 PD 治疗 4-6 周后进行标准腹膜平衡试验(PET)的新发生 PD 患者发生 CV 事件的预测价值。
这是一项前瞻性队列研究,纳入了新发生 PD 的患者。在 PD 导管植入前采集血样以测量 sST2 水平。在开始 PD 后 4-6 周进行标准腹膜平衡试验。采用酶联免疫吸附试验测定血清和透析液中的 sST2 水平。在随访期间记录 CV 事件。
共纳入 137 例患者。在 17.3 个月的随访期间,49 例(35.76%)患者发生 CV 事件。根据 sST2 的中位数和计算的截断值将患者分为两组,较高 sST2 组发生 CV 事件的风险分别是较低 sST2 组的 2.980 倍和 3.048 倍。此外,sST2 作为连续变量的预后价值仍然显著(每增加 1 个标准差,风险比[HR] = 1.037,95%置信区间[CI] 1.010-1.066,p = 0.008)。仅当根据计算的截断值将 N 末端脑利钠肽前体(NT-proBNP)水平分为两组时,才发现其提示更高的风险。此外,同时高于计算的截断值的血清 sST2 和 NT-proBNP 水平与 CV 事件的风险增加相关(HR = 3.398,95%CI 1.813-6.367,p < 0.001)。
基线血清 sST2 水平是接受新发生 PD 治疗的患者发生 CV 事件风险的独立预测因子,与 NT-proBNP 水平相结合,可以提供更准确的预测价值。