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Effects of Reduced Dialysate Calcium on Calcium-Phosphorus Product and Bone Metabolism in Hemodialysis Patients

机译:透析液钙减少对血液透析患者钙磷产物和骨代谢的影响

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Background: The safety of using reduced calcium dialysate (RDC) in hemodialysis (HD) patients is controversial due to related changes in bone metabolism. In the present study we investigated whether an 18-month treatment period with RDC may induce significant changes in calcium-phosphorus product (CaxP), bone metabolism, and components of the insulin-like growth factor (IGF) system in HD patients. Study Design: In this prospective study, 13 HD patients with biochemical signs of diminished or low-normal bone turnover and high CaxP due to high serum calcium level were treated by lowering dialysate calcium from 3.5 to 2.5 mEq/l for 18 months. By specific immunometric assays, serum levels of intact parathyroid hormone (PTH), bone alkaline phos-phatase (B-ALP), pyridinoline (PYR), desoxypyridinoline (D-PYR), 25-OH-vitamin D_3 (25-vit D_3), 1,25-(OH)_2-vitamin D_3 (1,25-vit D_3), free IGF-I, IGF-II, and IGF-binding protein (IGFBP)-1 to -6 were measured. Results: CaxP decreased significantly from 5.62 (baseline) to 3.95 mmol~2/l~2 (at 18 months), whereas PTH increased from 81 +- 57 pg/ml at baseline to 236 +- 188 at 12 months (p<0.01), remaining in this range thereafter. Parameters of bone resorption (PYR) as well as formation (B-ALP) significantly increased during RDC, with peak levels after 12 months. Despite increasing doses of oral alfacalcidol, levels of 25-vit D_3 and 1,25-vit D_3 subsequently declined during RDC. In parallel with the changes in bone markers, free IGF-I levels decreased (baseline: 1.9 +- 0.9 ng/ml, after 18 months: 1.1 +- 0.7; p < 0.01). The decline of free IGF-I correlated with decreasing levels of IGFBP-3 and increasing levels of IGFBP-1/-4. Conclusion: The treatment with RDC effectively lowered CaxP and stimulated bone formation and resorption. The different changes in bone markers and IGF system components mirror the complex effects on bone metabolism.
机译:背景:由于骨代谢的相关变化,在血液透析(HD)患者中使用还原性钙透析液(RDC)的安全性存在争议。在本研究中,我们调查了在HD患者中使用RDC治疗18个月是否会引起钙磷产物(CaxP),骨代谢以及胰岛素样生长因子(IGF)系统组成的显着变化。研究设计:在此前瞻性研究中,通过将透析液钙从3.5 mEq / l降低至18个月来治疗13例HD患者,这些患者的生化迹象是骨代谢减少或正常低下,并且由于血清钙水平高而导致CaxP升高。通过特定的免疫测定法,检测完整甲状旁腺激素(PTH),骨碱性磷酸酶(B-ALP),吡啶啉(PYR),脱氧吡啶啉(D-PYR),25-羟基维生素D_3(25-vit D_3)分别测定了1,25-(OH)_2-维生素D_3(1,25-vit D_3),游离IGF-I,IGF-II和IGF结合蛋白(IGFBP)-1至-6。结果:CaxP从5.62(基线)显着降低至3.95 mmol〜2 / l〜2(在18个月时),而PTH从基线时的81 +-57 pg / ml升高到12个月时的236 +-188(p <0.01) ),此后保持在此范围内。 RDC期间骨吸收(PYR)和形成(B-ALP)的参数显着增加,在12个月后达到峰值。尽管口服阿法骨化醇的剂量增加,但是在RDC期间25-vit D_3和1,25-vit D_3的水平随后下降。与骨标志物的变化同时,游离IGF-I水平降低(基线:1.9±0.9 ng / ml,18个月后:1.1±0.7; p <0.01)。游离IGF-I的下降与IGFBP-3水平的降低和IGFBP-1 / -4水平的提高相关。结论:RDC治疗可有效降低CaxP并刺激骨形成和吸收。骨标志物和IGF系统组成的不同变化反映了对骨代谢的复杂影响。

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