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与低通量膜相比,高通量透析器治疗的透析患者中β2微球蛋白与血细胞的结合增加,这导致β2微球蛋白浓度降低。一项交叉研究的结果。

Increased binding of beta-2-microglobulin to blood cells in dialysis patients treated with high-flux dialyzers compared with low-flux membranes contributed to reduced beta-2-microglobulin concentrations. Results of a cross-over study.

作者信息

Traut Mario, Haufe Christoph C, Eismann Ulrike, Deppisch Reinhold M, Stein Gunter, Wolf Gunter

机构信息

Department of Internal Medicine III, University of Jena, Jena, Germany.

出版信息

Blood Purif. 2007;25(5-6):432-40. doi: 10.1159/000110069. Epub 2007 Oct 23.

DOI:10.1159/000110069
PMID:17957097
Abstract

BACKGROUND

Patients on long-term dialysis eventually develop amyloid deposits with beta2-microglobulin as a predominant component. Although several studies have suggested that high-flux membranes reduce beta2-microglobulin in plasma compared with low-flux dialyzers, the mechanisms underlying this observation are still discussed.

METHODS

We revisited this important subject and measured beta2-microglobulin in the plasma of healthy individuals (n = 8), and patients undergoing hemodialysis (n = 20) who for assigned periods of time were either treated with a low-flux membrane (cuprophan) or high-flux (polyamide) dialyzer with an ELISA. The number of blood cells was determined by FACS. Beta2-microglobulin was also measured on the surface of granulocytes, lymphocytes, and monocytes before, directly after, and 4 h after hemodialysis. Expression of beta2-microglobulin, c-fos, tumor necrosis factor-alpha (TNF-alpha), and interleukin-1 mRNA was determined in whole blood samples with quantitative RT-PCR using an internal standard in parallel. In the second part of the study, patients were assigned in a two-group cross-over design either to low- or high-flux dialyzers (n = 9 in each group), and dialyzer membranes were changed every 4 weeks for two consecutive periods. Serum beta2-microglobulin concentrations were measured at the end of each period.

RESULTS

Healthy controls had a low plasma beta2-microglobulin level of 1.2 +/- 0.3 mg/l. Before hemodialysis, patients on low-flux dialyzers had a plasma beta2-microglobulin level of 42.0 +/- 14.0 mg/l, patients treated with high-flux dialyzers 21.5 +/- 10.8 mg/l (p < 0.05 vs. low-flux dialyzers). In contrast, there was no significant difference in plasma concentrations of active transforming growth factor-beta1 with the two different membrane types. The difference in serum beta2-microglobulin between low- and high-flux membranes was more prominent directly after hemodialysis as well as 4 h after hemodialysis compared with the values directly before the start of treatment. At all studied time-points, leukocytes and platelets were significantly higher in patients on low-flux membranes. Healthy control persons exhibited a significantly higher amount of beta2-microglobulin bound to granulocytes, lymphocytes, and monocytes compared with dialysis patients. Interestingly, beta2-microglobulin bound to granulocytes, lymphocytes, and monocytes was significantly increased in patients treated with high-flux membranes compared with low-flux filters. Quantitative RT-PCR revealed no significant difference in beta2-microglobulin expression in whole blood before hemodialysis, directly after hemodialysis, and 4 h after hemodialysis. However, TNF-alpha and c-fos transcripts were significantly higher in whole blood obtained from patients treated with low-flux membranes compared to high-flux dialyzers. The two-group cross-over study over three periods of 4 weeks revealed that switching from low-flux to high-flux dialyzers significantly reduced serum beta2-microglobulin levels.

CONCLUSION

Patients treated with a polyamide high-flux membrane had lower beta2-microglobulin concentrations compared with those patients on low-flux dialyzers. This difference might not be mediated by an increase in beta2-microglobulin mRNA, but may be caused by less beta2-microglobulin released from the blood cells in patients treated with high-flux dialyzers, in addition to a better beta2-microglobulin clearance.

摘要

背景

长期透析患者最终会形成以β2-微球蛋白为主要成分的淀粉样沉积物。尽管多项研究表明,与低通量透析器相比,高通量膜可降低血浆中的β2-微球蛋白,但这一现象背后的机制仍在探讨中。

方法

我们重新审视了这个重要课题,使用酶联免疫吸附测定法(ELISA)测量了健康个体(n = 8)以及接受血液透析的患者(n = 20)血浆中的β2-微球蛋白。这些接受血液透析的患者在指定时间段内分别使用低通量膜(铜仿膜)或高通量(聚酰胺)透析器进行治疗。通过荧光激活细胞分选术(FACS)测定血细胞数量。在血液透析前、透析刚结束后以及透析后4小时,还对粒细胞、淋巴细胞和单核细胞表面的β2-微球蛋白进行了测量。使用内标通过定量逆转录聚合酶链反应(RT-PCR)在全血样本中平行测定β2-微球蛋白、c-fos、肿瘤坏死因子-α(TNF-α)和白细胞介素-1 mRNA的表达。在研究的第二部分,患者被分配到两组交叉设计中,分别使用低通量或高通量透析器(每组n = 9),透析器膜每4周更换一次,连续进行两个周期。在每个周期结束时测量血清β2-微球蛋白浓度。

结果

健康对照组血浆β2-微球蛋白水平较低,为1.2±0.3 mg/l。血液透析前,使用低通量透析器的患者血浆β2-微球蛋白水平为42.0±14.0 mg/l,使用高通量透析器治疗的患者为21.5±10.8 mg/l(与低通量透析器相比,p < 0.05)。相比之下,两种不同膜类型的活性转化生长因子-β1血浆浓度没有显著差异。与治疗开始前的值相比,低通量和高通量膜之间血清β2-微球蛋白的差异在血液透析刚结束后以及透析后4小时更为明显。在所有研究的时间点,使用低通量膜的患者白细胞和血小板显著更高。与透析患者相比,健康对照者与粒细胞、淋巴细胞和单核细胞结合的β2-微球蛋白量显著更高。有趣的是,与低通量滤器相比,使用高通量膜治疗的患者与粒细胞、淋巴细胞和单核细胞结合的β2-微球蛋白显著增加。定量RT-PCR显示血液透析前、透析刚结束后以及透析后4小时全血中β2-微球蛋白表达没有显著差异。然而,与高通量透析器相比,从使用低通量膜治疗的患者获得的全血中TNF-α和c-fos转录本显著更高。为期4周的三个周期的两组交叉研究表明,从低通量透析器转换为高通量透析器可显著降低血清β2-微球蛋白水平。

结论

与使用低通量透析器的患者相比,使用聚酰胺高通量膜治疗的患者β2-微球蛋白浓度更低。这种差异可能不是由β2-微球蛋白mRNA增加介导的,而是除了更好的β2-微球蛋白清除率外,可能是由于使用高通量透析器治疗的患者血细胞释放的β2-微球蛋白减少所致。

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