Wang Jian-Min, Zhou Jia-Jun, Zheng Qian, Gan Hua, Wang Hang
Department of Nephrology, The First Affiliated Hospital of Chongqing Medical University, ChongQing, China.
Ther Apher Dial. 2014 Feb;18(1):44-50. doi: 10.1111/1744-9987.12040.
Atherosclerosis and accompanying cardiovascular disease are the first causes of mortality in patients undergoing maintenance hemodialysis. Anti-atherosclerotic effects of hemodiafiltration (HDF) have been reported. Our study aimed to investigate the effect of serum derived from a healthy group (n = 23), before and after hemodialysis (HD) therapy (n = 23), and before and after HDF therapy (n = 17) on the expression of microRNA-33a and its target genes adenosine triphosphate-binding cassette transporter A1,G1 (ABCA1, ABCG1) in THP-1 macrophages. Meanwhile, blood lipids and high-sensitivity C-reactive protein (hs-CRP) were measured in these groups. Our data showed that the expression of miRNA-33a was lower (P < 0.05) and ABCA1 and ABCG1 were higher (P < 0.05) in the healthy group than pre-HD and pre-HDF. miR-33a was significantly decreased (P < 0.05) but ABCA1, ABCG1 was significantly increased (P < 0.05) in post-HDF compared with pre-HDF, while these parameters in pre- and post- HD groups did not show any significant change (P > 0.05). High density lipoprotein cholesterol (HDL-C) was higher and hs-CRP was lower in the healthy group than pre-HD and pre-HDF groups. Moreover, a significant increase of HDL-C (P < 0.05) and decrease (P < 0.05) of hs-CRP was shown in post-HDF compared with pre-HDF, but HD appeared to have no significant change in these subjects. HDF therapy can downregulate miR-33a expression, and then result in ABCA1, ABCG1 upregulation and an increase in circulating HDL-C, leading to a possible anti-atherosclerosis effect to some extent.
动脉粥样硬化及伴随的心血管疾病是维持性血液透析患者死亡的首要原因。已有报道称血液透析滤过(HDF)具有抗动脉粥样硬化作用。我们的研究旨在探讨健康组(n = 23)、血液透析(HD)治疗前后(n = 23)以及HDF治疗前后(n = 17)的血清对THP - 1巨噬细胞中微小RNA - 33a及其靶基因三磷酸腺苷结合盒转运体A1、G1(ABCA1、ABCG1)表达的影响。同时,对这些组的血脂和高敏C反应蛋白(hs - CRP)进行了检测。我们的数据显示,健康组中miRNA - 33a的表达低于HD治疗前和HDF治疗前(P < 0.05),而ABCA1和ABCG1的表达高于HD治疗前和HDF治疗前(P < 0.05)。与HDF治疗前相比,HDF治疗后miR - 33a显著降低(P < 0.05),但ABCA1、ABCG1显著升高(P < 0.05),而HD治疗前后这些参数未显示任何显著变化(P > 0.05)。健康组的高密度脂蛋白胆固醇(HDL - C)高于HD治疗前和HDF治疗前组,hs - CRP低于HD治疗前和HDF治疗前组。此外,与HDF治疗前相比,HDF治疗后HDL - C显著升高(P < 0.05),hs - CRP显著降低(P < 0.05),但HD在这些受试者中似乎没有显著变化。HDF治疗可下调miR - 33a的表达,进而导致ABCA1、ABCG1上调以及循环HDL - C增加,在一定程度上可能产生抗动脉粥样硬化作用。