Nephrology and Dialysis Unit, Department of Medicine, G. d'Annunzio University, Chieti-Pescara, SS. Annunziata Hospital, Via dei Vestini, 66013 Chieti, Italy.
Nephrology Department, Campus Can Ruti, Germans Trias i Pujol Research Institute (IGTP), REMAR-IGTP Group, Germans Trias i Pujol University Hospital, Carretera de Can Ruti, Camí de les Escoles s/n, 08916 Barcelona, Spain.
Int J Mol Sci. 2020 Jul 31;21(15):5489. doi: 10.3390/ijms21155489.
Peritoneal dialysis (PD) is an established home care, cost-effective renal replacement therapy (RRT), which offers several advantages over the most used dialysis modality, hemodialysis. Despite its potential benefits, however, PD is an under-prescribed method of treating uremic patients. Infectious complications (primarily peritonitis) and bio-incompatibility of PD solutions are the main contributors to PD drop-out, due to their potential for altering the functional and anatomical integrity of the peritoneal membrane. To improve the clinical outcome of PD, there is a need for biomarkers to identify patients at risk of PD-related complications and to guide personalized interventions. Several recent studies have shown that proteomic investigation may be a powerful tool in the prediction, early diagnosis, prognostic assessment, and therapeutic monitoring of patients on PD. Indeed, analysis of the proteome present in PD effluent has uncovered several proteins involved in inflammation and pro-fibrotic insult, in encapsulating peritoneal sclerosis, or even in detecting early changes before any measurable modifications occur in the traditional clinical parameters used to evaluate PD efficacy. We here review the proteomic studies conducted thus far, addressing the potential use of such omics methodology in identifying potential new biomarkers of the peritoneal membrane welfare in relation to dialytic prescription and adequacy.
腹膜透析 (PD) 是一种已确立的家庭护理、具有成本效益的肾脏替代疗法 (RRT),与最常用的透析方式相比,PD 具有多项优势。然而,尽管 PD 具有潜在的益处,但它是一种处方不足的尿毒症患者治疗方法。感染并发症(主要是腹膜炎)和 PD 溶液的生物不相容性是 PD 退出的主要原因,因为它们有可能改变腹膜的功能和解剖完整性。为了改善 PD 的临床结果,需要生物标志物来识别有 PD 相关并发症风险的患者,并指导个性化干预。最近的几项研究表明,蛋白质组学研究可能是预测、早期诊断、预后评估和 PD 患者治疗监测的有力工具。事实上,对 PD 流出液中存在的蛋白质组的分析揭示了几种参与炎症和促纤维化损伤的蛋白质,在包裹性腹膜硬化症中,甚至在使用传统的临床参数评估 PD 疗效之前,在任何可测量的变化发生之前,就可以检测到早期变化。我们在这里回顾了迄今为止进行的蛋白质组学研究,探讨了这种组学方法在确定与透析方案和充分性相关的腹膜福利的潜在新生物标志物方面的潜在用途。