a Department of Nephrology and Department of Medical and Health Sciences , Linköping University , Linköping , Sweden.
b Department of Health Technologies , Technomedicum, Tallinn University of Technology , Tallinn , Estonia.
Scand J Clin Lab Invest. 2019 May;79(3):174-181. doi: 10.1080/00365513.2019.1576218. Epub 2019 Feb 18.
Rapid progression of vascular calcification (VC) in hemodialysis (HD) patients is caused by several factors including inflammation and an imbalance between active inducers and inhibitors of VC. Growing evidence shows that online hemodiafiltration (ol-HDF), a combination of diffusive and convective solute transport, has positive effects on the uremic environment that affects patients on dialysis. However, we recently reported that serum 25-hydroxyvitamin D (25(OH)D) decreased after a switch from HD to ol-HDF. As a consequence of this finding, the present study was undertaken to investigate if inducers and inhibitors of VC (i.e. the inactive matrix Gla protein fractions dp-ucMGP and t-ucMGP, fetuin-A, Gla-rich protein (GRP), osteopontin (OPN), bone-specific alkaline phosphatase (BALP), and osteoprotegerin (OPG)) also are affected by ol-HDF. This non-comparative prospective study comprised 35 prevalent patients who were investigated 6, 12, and 24 months after their switch from HD to ol-HDF. Most patients had increased levels of the calcification inhibitors OPN and OPG; and of the inactive calcification inhibitor dp-ucMGP during the study period irrespective of the dialysis modality. BALP and t-ucMGP were mostly within the reference interval, but fetuin-A was mostly below the reference interval during the study period. OPN was significantly associated with BALP and parathyroid hormone, r = 0.62 and r = 0.65 (p < .001), respectively. In conclusion, in contrast to decreased 25(OH)D levels, no differences were found for any of the measured biomarkers of VC following the switch from HD to ol-HDF. Further studies are needed to elucidate how these biomarkers can contribute to calcification risk assessment.
血管钙化(VC)在血液透析(HD)患者中的快速进展是由多种因素引起的,包括炎症和 VC 的活性诱导剂和抑制剂之间的失衡。越来越多的证据表明,在线血液透析滤过(ol-HDF),即弥散和对流溶质转运的结合,对影响透析患者的尿毒症环境有积极影响。然而,我们最近报告说,从 HD 切换到 ol-HDF 后,血清 25-羟维生素 D(25(OH)D)降低。基于这一发现,本研究旨在探讨 VC 的诱导剂和抑制剂(即无活性基质 Gla 蛋白 dp-ucMGP 和 t-ucMGP、胎球蛋白-A、富含 Gla 蛋白(GRP)、骨桥蛋白(OPN)、骨特异性碱性磷酸酶(BALP)和骨保护素(OPG))是否也受 ol-HDF 影响。这项非比较性前瞻性研究包括 35 名普遍患者,他们在从 HD 切换到 ol-HDF 后 6、12 和 24 个月接受了调查。在研究期间,大多数患者的钙化抑制剂 OPN 和 OPG 水平升高;以及无活性钙化抑制剂 dp-ucMGP 水平升高,无论透析方式如何。BALP 和 t-ucMGP 大多在参考区间内,但在研究期间胎球蛋白-A 大多低于参考区间。OPN 与 BALP 和甲状旁腺激素显著相关,r 分别为 0.62 和 0.65(p<0.001)。总之,与 25(OH)D 水平降低相反,从 HD 切换到 ol-HDF 后,没有发现任何 VC 测量生物标志物存在差异。需要进一步研究阐明这些生物标志物如何有助于钙化风险评估。