Fiedler Roman, Deuber Heinz J, Langer Thomas, Osten Bernd, Mohan Subburaman, Jehle Peter M
Department of Nephrology, Martin Luther University Halle-Wittenberg, Halle, Germany.
Nephron Clin Pract. 2004;96(1):c3-9. doi: 10.1159/000075565.
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.
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 phosphatase (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.
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.
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.
由于骨代谢的相关变化,在血液透析(HD)患者中使用低钙透析液(RDC)的安全性存在争议。在本研究中,我们调查了HD患者接受18个月的RDC治疗是否会导致钙磷乘积(CaxP)、骨代谢以及胰岛素样生长因子(IGF)系统成分发生显著变化。
在这项前瞻性研究中,13名因血清钙水平高而出现骨转换降低或低正常、CaxP高的生化迹象的HD患者,将透析液钙从3.5 mEq/l降至2.5 mEq/l,治疗18个月。通过特异性免疫测定法,测量血清中完整甲状旁腺激素(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D3(25-vit D3)、1,25-二羟基维生素D3(1,25-vit D3)、游离IGF-I、IGF-II以及IGF结合蛋白(IGFBP)-1至-6的水平。
CaxP从5.62(基线)显著降至3.95 mmol²/l²(18个月时),而PTH从基线时的81±57 pg/ml增加至12个月时的236±188(p<0.01),此后保持在该范围内。在RDC治疗期间,骨吸收参数(PYR)以及骨形成参数(B-ALP)显著增加,12个月时达到峰值。尽管口服阿法骨化醇剂量增加,但在RDC治疗期间,25-vit D3和1,25-vit D3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水平降低和IGFBP-1/-4水平升高相关。
RDC治疗有效降低了CaxP,并刺激了骨形成和骨吸收。骨标志物和IGF系统成分的不同变化反映了对骨代谢的复杂影响。