Department of Internal Medicine, Faculty of Medicine, "Grigore T Popa" University of Medicine and Pharmacy, University Street nr 16, 700115 Iasi, Romania.
Prof. Dr. George I.M. Georgescu Institute of Cardiovascular Diseases, 700503 Iasi, Romania.
Biomolecules. 2023 Feb 18;13(2):389. doi: 10.3390/biom13020389.
Patients with chronic kidney disease have an increased risk of all-cause death. The value of collagen biomarkers such as procollagen type I carboxy-terminal propeptide (PICP) and procollagen type III N-terminal peptide (P3NP), in end-stage renal disease (ESRD), has not yet been defined (in the literature and in clinics). The purpose of this study was to determine the potential value of these new biomarkers in the prediction of mortality in this population. Plasma PICP and P3NP levels were determined in 140 patients with ESRD, not yet on dialysis, who were followed up for 36 ± 5.3 months. During follow-up, 58 deaths were recorded (41.4%), with the majority of them being cardiovascular deaths (43, 74.13%). Using the ROC curve, the cut-off value for the prediction of mortality for PICP was 297.31 µg/L, while for P3NP, the cut-off value was 126.67 µg/L. In univariate analysis, a value of PICP above the cut-off point was associated with a fivefold increased risk of mortality (hazard ratio (HR) 5.071, 95% confidence interval 1.935-13.29, = 0.001) and a value of P3NP above the cut-off point was associated with a twofold increased risk of mortality (HR 2.089, 95% CI 1.044-4.178, = 0.002). In a multivariable Cox proportional hazards model, PICP values remained independent predictors of mortality (HR 1.22, 95% CI 1.1-1.31, < 0.0001). Our data suggest that the collagen biomarker PICP is an independent predictor of mortality in ESRD patients who are not yet on dialysis.
患有慢性肾脏疾病的患者全因死亡风险增加。在终末期肾病(ESRD)中,Ⅰ型前胶原羧基端前肽(PICP)和Ⅲ型前胶原 N 端肽(P3NP)等胶原生物标志物的价值尚未确定(在文献和临床实践中)。本研究旨在确定这些新的生物标志物在预测该人群死亡率方面的潜在价值。在未接受透析的 140 名 ESRD 患者中测定了血浆 PICP 和 P3NP 水平,这些患者随访了 36 ± 5.3 个月。在随访期间,记录了 58 例死亡(41.4%),其中大多数为心血管死亡(43 例,占 74.13%)。使用 ROC 曲线,PICP 预测死亡率的截断值为 297.31 µg/L,而 P3NP 的截断值为 126.67 µg/L。在单因素分析中,PICP 值高于截断值与死亡率增加五倍相关(风险比(HR)5.071,95%置信区间 1.935-13.29, = 0.001),而 P3NP 值高于截断值与死亡率增加两倍相关(HR 2.089,95%CI 1.044-4.178, = 0.002)。在多变量 Cox 比例风险模型中,PICP 值仍然是死亡率的独立预测因素(HR 1.22,95%CI 1.1-1.31, < 0.0001)。我们的数据表明,在尚未接受透析的 ESRD 患者中,胶原生物标志物 PICP 是死亡率的独立预测因素。