Nakano Toshiaki, Kitamura Hiromasa, Tsuneyoshi Shoji, Tsuchimoto Akihiro, Torisu Kumiko, Tsujikawa Hiroaki, Kawanishi Hideki, Tsuruya Kazuhiko, Kitazono Takanari
Department of Medicine and Clinical Science, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.
Department of Internal Medicine, Fukuoka Dental College, Fukuoka, Japan.
Clin Exp Nephrol. 2025 Feb;29(2):212-220. doi: 10.1007/s10157-024-02565-9. Epub 2024 Oct 4.
Encapsulated peritoneal sclerosis (EPS) is a serious complication in patients undergoing peritoneal dialysis (PD). Neutral-pH dialysate is associated with less peritoneal damage and a lower incidence of EPS than conventional PD solution. However, monitoring for peritoneal damage and predicting EPS remain important during PD therapy.
We measured the mesothelial cell area, dialysate-to-plasma ratio of creatinine after 4 h, and concentrations of the potential biological markers effluent fibrin degradation products (eFDPs), cancer antigen-125, and interleukin-6 in the effluent dialysate from patients who had been undergoing PD therapy for > 5 years in our hospital. These biomarkers were obtained from the drainage fluid of the final measurement of peritoneal equilibration testing before withdrawal from PD therapy. The concentrations of these potential biomarkers were measured in 39 patients who withdrew from PD therapy and were enrolled in the study.
Three participants developed EPS after withdrawing PD. The dialysate-to-plasma ratio of creatinine, area of mesothelial cells, and interleukin-6 appearance rate in participants who developed EPS tended to be higher than those in patients who did not, but there were no significant differences. Significantly more eFDPs were in participants who developed EPS than in those who did not (138.5 ± 15.1 vs. 32.9 ± 7.4 µg/mL, P = 0.002). There was no difference in the cancer antigen-125 appearance rate between the groups. A cut-off value of eFDPs ≥ 119.1 µg/mL was optimal for predicting EPS (P = 0.006, specificity = 0.972, sensitivity = 1.000).
This study shows that eFDPs may be a useful biological marker for predicting EPS in patients undergoing PD using neutral-pH dialysate.
包裹性腹膜硬化(EPS)是腹膜透析(PD)患者的一种严重并发症。与传统腹膜透析液相比,中性pH值透析液对腹膜的损伤较小,EPS发生率较低。然而,在腹膜透析治疗期间,监测腹膜损伤和预测EPS仍然很重要。
我们测量了我院接受腹膜透析治疗超过5年的患者腹透液中肌酐的4小时透析液与血浆比值、间皮细胞面积以及潜在生物标志物流出液纤维蛋白降解产物(eFDPs)、癌抗原125和白细胞介素-6的浓度。这些生物标志物取自停止腹膜透析治疗前最后一次腹膜平衡试验的引流液。在39名停止腹膜透析治疗并纳入本研究的患者中测量了这些潜在生物标志物的浓度。
3名参与者在停止腹膜透析后发生了EPS。发生EPS的参与者的肌酐透析液与血浆比值、间皮细胞面积和白细胞介素-6出现率往往高于未发生EPS的患者,但差异无统计学意义。发生EPS的参与者的eFDPs明显多于未发生EPS的参与者(138.5±15.1 vs. 32.9±7.4 μg/mL,P = 0.002)。两组之间癌抗原125出现率没有差异。eFDPs≥119.1 μg/mL的临界值最适合预测EPS(P = 0.006,特异性 = 0.972,敏感性 = 1.000)。
本研究表明,eFDPs可能是预测使用中性pH值透析液进行腹膜透析患者发生EPS的有用生物标志物。