Table 1
The possible treatments of vascular calcification in CKD.
| General principle | | (1) Treat hypertension, hyperlipidemia, and hyperglycemia as usual | | (2) Body weight control | | (3) Control serum and urine phosphate | | (4) Avoid hypercalcemia | | (5) Avoid magnesium, Iron, and L-lysine deficiency | | (6) Nutritional vitamin-D (NVD) supplement (avoid high dose of VDRAs) | | (7) Possible fractionated heparin for dialysis | | (8) AST-120 | |
| Manipulating the complex biology of vascular calcification | | (1) Pyrophosphate | | (2) Na thiosulfate | | (3) Vit-K (especially in warfarin user) | | (4) Avoid zinc deficiency | | (5) Avoid excess of vit-E, vit-A, vit-C, and fluoride | | (6) Antioxidants (?) | |
| Patients with high turnover bone disorder (e.g., hyperparathyroid bone disorder; iPTH > 300 pg/mL + high level BAP) | | (1) VDRA (paricalcitol/calcitriol) + NVD (cholecalciferol/ergocalciferol) or calcimimetics + NVD | | (2) Non-metal-containing phosphate binders—sevelamer (for phosphorus) | | (3) Bisphosphonate + VDRA/NVD (for high PTH + hypercalcemia + low bone mass) | | (4) Denosumab + VDRA/NVD (for high PTH + hypercalcemia + low bone mass) | |
| Patients with low turnover bone disorder (e.g., adynamic bone disorder; bone alkaline phosphatase < 20 ng/mL, and iPTH < 100 pg/mL) | | (1) NVD + low dose VDRA | | (2) Teriparatide | | (3) Non-metal-containing phosphate binders—sevelamer (for oxidative stress and inflammation) | |
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