Nephrology, Dialysis and Transplantation Unit, Department of Emergency and Organ Transplantation, University of Bari "A. Moro", Piazza G. Cesare 11, 70122, Bari, Italy.
Nephrology, Dialysis and Transplantation Unit, Department of Medical and Surgical Sciences, University of Foggia, Foggia, Italy.
J Nephrol. 2021 Dec;34(6):1989-1997. doi: 10.1007/s40620-020-00958-z. Epub 2021 Mar 24.
Hemodialysis patients present a dramatic increase in cardiovascular morbidity/mortality. Circulating immune cells, activated by both uremic milieu and dialysis, play a key role in the pathogenesis of dialysis-related vascular disease. The aim of our study was to identify, through a high-throughput approach, differences in gene expression profiles in the peripheral blood mononuclear cells (PBMCs) of patients treated with on-line hemodiafiltration and bicarbonate hemodialysis.
The transcriptomic profile was investigated in PBMCs isolated from eight patients on on-line hemodiafiltration and eight patients on bicarbonate hemodialysis by microarray analysis. The results were evaluated by statistical and functional pathway analysis and validated by real time PCR (qPCR) in an independent cohort of patients (on-line hemodiafiltration N = 20, bicarbonate hemodialysis n = 20).
Eight hundred and forty-seven genes were differentially expressed in patients treated with on-line hemodiafiltration and bicarbonate hemodialysis. Thirty-seven functional gene networks were identified and atherosclerosis signaling was the top canonical pathway regulated by on-line hemodiafiltration. Among the genes of this pathway, on-line hemodiafiltration was associated with a reduced expression of Platelet-derived growth factor A chain (PDGF A), Clusterin, Monoamine Oxidase A, Interleukin-6 (IL-6) and Vascular Endothelial Growth Factor C (VEGF-)C and with an increase of Apolipoprotein E. qPCR confirmed the microarray results. Platelet derived growth factor AA (PDGF-AA), IL-6 and VEGF-C serum levels were significantly lower in the on-line hemodiafiltration group. Finally, 10 patients previously on bicarbonate hemodialysis were switched to on-line hemodiafiltration and PBMCs were harvested after 6 months. The qPCR results from this perspective group confirmed the modulation of atherosclerotic genes observed in the cross-sectional analysis.
Our data suggest that type of dialysis (on-line hemodiafiltration versus bicarbonate hemodialysis) may modulate the expression of several genes involved in the pathogenesis of atherosclerotic disease.
血液透析患者心血管发病率和死亡率显著增加。循环免疫细胞被尿毒症环境和透析激活,在透析相关血管疾病的发病机制中发挥关键作用。我们的研究目的是通过高通量方法鉴定在线血液透析滤过和碳酸氢盐血液透析治疗患者外周血单个核细胞(PBMCs)中的基因表达谱差异。
通过微阵列分析研究了 8 名在线血液透析滤过患者和 8 名碳酸氢盐血液透析患者的 PBMCs 转录组谱。通过统计和功能途径分析评估结果,并在独立患者队列中通过实时 PCR(qPCR)验证(在线血液透析滤过 N=20,碳酸氢盐血液透析 n=20)。
在线血液透析滤过和碳酸氢盐血液透析治疗的患者中,有 847 个基因表达差异。确定了 37 个功能基因网络,动脉粥样硬化信号是受在线血液透析滤过调节的主要经典途径。在该途径的基因中,在线血液透析滤过与血小板衍生生长因子 A 链(PDGF A)、载脂蛋白 E、簇蛋白、单胺氧化酶 A、白细胞介素-6(IL-6)和血管内皮生长因子 C(VEGF-C)的表达降低有关,与载脂蛋白 E 的表达升高有关。qPCR 证实了微阵列结果。在线血液透析滤过组血小板衍生生长因子 AA(PDGF-AA)、IL-6 和 VEGF-C 血清水平明显降低。最后,10 名先前接受碳酸氢盐血液透析的患者改为在线血液透析滤过,6 个月后采集 PBMCs。从这个角度来看,前瞻性组的 qPCR 结果证实了在横断面分析中观察到的动脉粥样硬化基因的调节。
我们的数据表明,透析类型(在线血液透析滤过与碳酸氢盐血液透析)可能调节参与动脉粥样硬化疾病发病机制的几个基因的表达。