TY - JOUR
T1 - Effects of paricalcitol on calcium and phosphate metabolism and markers of bone health in patients with diabetic nephropathy
T2 - Results of the VITAL study
AU - Coyne, Daniel W.
AU - Andress, Dennis L.
AU - Amdahl, Michael J.
AU - Ritz, Eberhard
AU - De Zeeuw, Dick
N1 - Funding Information:
AbbVie provided funding for the VITAL study and was involved in the study design, research analysis, interpretation of data, and reviewing and approval of the publication. The principal investigators of the VITAL study and authors for the primary Lancet publication prepared the manuscript and designed the figures without compensation. Medical writing and editorial support, funded by AbbVie, were provided under the direction of the authors by Larry Nelson and Chris Lawrence, MedThink SciCom.
PY - 2013/9
Y1 - 2013/9
N2 - Background. Chronic kidney disease (CKD) is associated with elevations in serum phosphate, calcium-phosphorus product and bone-specific alkaline phosphatase (BAP), with attendant risks of cardiovascular and bone disorders. Active vitamin D can suppress parathyroid hormone (PTH), but may raise serum calcium and phosphate concentrations. Paricalcitol, a selective vitamin D activator, suppressed PTH in CKD patients (stages 3 and 4) with secondary hyperparathyroidism (SHPT) with minimal changes in calcium and phosphate metabolism. Methods. The VITAL study enrolled patients with CKD stages 2-4. We examined the effect and relationship of paricalcitol to calcium and phosphate metabolism and bone markers in a post hoc analysis of VITAL. The study comprised patients with diabetic nephropathy enrolled in a double-blind, placebo-controlled, randomized trial of paricalcitol (1 or 2 μg/day). Urinary and serum calcium and phosphate, serum BAP, and intact PTH (iPTH) concentrations were measured throughout the study. Results. Baseline demographics and calcium, phosphate, PTH (49% with iPTH <70 pg/mL), and BAP concentrations were similar between groups. A transient, modest yet significant increase in phosphate was observed for paricalcitol 2 μg/day (+0.29 mg/dL; P < 0.001). Dose-dependent increases in serum and urinary calcium were observed; however, there were few cases of hypercalcemia: one in the 1-μg/day group (1.1%) and three in the 2-μg/day group (3.2%). Significant reductions in BAP were observed that persisted for 60 days after paricalcitol discontinuation (P < 0.001 for combined paricalcitol groups versus placebo). Paricalcitol dose-dependent reductions in iPTH were observed. Paricalcitol in CKD patients (±SHPT) was associated with modest increases in calcium and phosphate. Conclusion. Paricalcitol reduces BAP levels, which may be beneficial for reducing vascular calcification. Trial registration. Trial is registered with ClinicalTrials.gov, number NCT00421733.
AB - Background. Chronic kidney disease (CKD) is associated with elevations in serum phosphate, calcium-phosphorus product and bone-specific alkaline phosphatase (BAP), with attendant risks of cardiovascular and bone disorders. Active vitamin D can suppress parathyroid hormone (PTH), but may raise serum calcium and phosphate concentrations. Paricalcitol, a selective vitamin D activator, suppressed PTH in CKD patients (stages 3 and 4) with secondary hyperparathyroidism (SHPT) with minimal changes in calcium and phosphate metabolism. Methods. The VITAL study enrolled patients with CKD stages 2-4. We examined the effect and relationship of paricalcitol to calcium and phosphate metabolism and bone markers in a post hoc analysis of VITAL. The study comprised patients with diabetic nephropathy enrolled in a double-blind, placebo-controlled, randomized trial of paricalcitol (1 or 2 μg/day). Urinary and serum calcium and phosphate, serum BAP, and intact PTH (iPTH) concentrations were measured throughout the study. Results. Baseline demographics and calcium, phosphate, PTH (49% with iPTH <70 pg/mL), and BAP concentrations were similar between groups. A transient, modest yet significant increase in phosphate was observed for paricalcitol 2 μg/day (+0.29 mg/dL; P < 0.001). Dose-dependent increases in serum and urinary calcium were observed; however, there were few cases of hypercalcemia: one in the 1-μg/day group (1.1%) and three in the 2-μg/day group (3.2%). Significant reductions in BAP were observed that persisted for 60 days after paricalcitol discontinuation (P < 0.001 for combined paricalcitol groups versus placebo). Paricalcitol dose-dependent reductions in iPTH were observed. Paricalcitol in CKD patients (±SHPT) was associated with modest increases in calcium and phosphate. Conclusion. Paricalcitol reduces BAP levels, which may be beneficial for reducing vascular calcification. Trial registration. Trial is registered with ClinicalTrials.gov, number NCT00421733.
KW - Bone-specific alkaline phosphatase
KW - Calcitriol
KW - Hypercalcemia
KW - Hyperphosphatemia
KW - Paricalcitol
KW - Vitamin D receptor activation
UR - https://www.scopus.com/pages/publications/84884514624
U2 - 10.1093/ndt/gft227
DO - 10.1093/ndt/gft227
M3 - Article
C2 - 23787544
AN - SCOPUS:84884514624
SN - 0931-0509
VL - 28
SP - 2260
EP - 2268
JO - Nephrology Dialysis Transplantation
JF - Nephrology Dialysis Transplantation
IS - 9
ER -