Department of Laboratory Medicine, Pomeranian Medical University of Szczecin, Powstancow Wielkopolskich 72, 70-111, Szczecin, Poland.
Department of Nephrology, Transplantology and Internal Medicine, Pomeranian Medical University of Szczecin, Powstancow Wielkopolskich 72, 70-111, Szczecin, Poland.
Int Urol Nephrol. 2019 Oct;51(10):1831-1840. doi: 10.1007/s11255-019-02190-6. Epub 2019 Jun 13.
Chronic kidney disease (CKD) is a systemic disease affecting many organs. Progression of renal failure aggravates ongoing inflammation and increases oxidative stress. In the final stage of CKD, it is necessary to use renal replacement therapy. A side effect of dialysis therapy is the synthesis of proinflammatory factors and increased oxidative stress, which activates platelets and immune cells.
To determine the regenerative potential of platelets in patients with CKD based on the analysis of the relationships between substances with potential regenerative action, as well as analysis of the influence of the type of renal replacement therapy used on regeneration of platelets.
The study group consisted of 117 patients. Based on the type of therapy used, patients were divided into four groups: hemodialysis, peritoneal dialysis, kidney transplant patients, and conservative treatment (30, 30, 27, and 30 patients). The control group consisted of 30 healthy volunteers. The concentrations of IGF-1, TGF-β, and PDGF-B in the blood serum were measured by ELISA methods.
It was shown that renal replacement therapy significantly influences the concentration of platelet growth factors (IGF-1: p = 0.025 and PDGF-B: p = 0.012). There was a relationship between the type of renal replacement therapy and the duration of dialysis, and the concentration of IGF-1, PDGF-B (p < 0.00001, p < 0.001).
The type of renal replacement therapy has a different effect on the concentration of platelet-derived growth factors IGF-1 and PDGF-B. PD patients had the highest concentrations of all growth factors, and this may be due to the presence of inflammation induced by dialysis-related advanced end-products of glycosylation (AGE).
慢性肾脏病(CKD)是一种影响多个器官的全身性疾病。肾衰竭的进展加剧了持续的炎症和增加的氧化应激。在 CKD 的终末期,需要使用肾脏替代疗法。透析治疗的一个副作用是促炎因子的合成和氧化应激的增加,这会激活血小板和免疫细胞。
根据具有潜在再生作用的物质之间的关系分析,以及分析所使用的肾脏替代治疗类型对血小板再生的影响,来确定 CKD 患者血小板的再生潜力。
研究组包括 117 名患者。根据所使用的治疗类型,患者被分为四组:血液透析、腹膜透析、肾移植患者和保守治疗(30、30、27 和 30 名患者)。对照组包括 30 名健康志愿者。通过 ELISA 方法测量血清中 IGF-1、TGF-β 和 PDGF-B 的浓度。
研究表明,肾脏替代治疗显著影响血小板生长因子的浓度(IGF-1:p=0.025 和 PDGF-B:p=0.012)。肾脏替代治疗的类型与透析的持续时间以及 IGF-1、PDGF-B 的浓度之间存在关系(p<0.00001,p<0.001)。
肾脏替代治疗的类型对血小板衍生生长因子 IGF-1 和 PDGF-B 的浓度有不同的影响。PD 患者所有生长因子的浓度最高,这可能是由于透析相关的晚期糖基化终产物(AGE)引起的炎症所致。