Comparative effect of oral or intravenous calcitriol on secondary hyperparathyroidism in chronic hemodialysis patients
- PMID: 7816008
Comparative effect of oral or intravenous calcitriol on secondary hyperparathyroidism in chronic hemodialysis patients
Abstract
The suppressive effects of intravenous (IVC) and oral (ORC) 1,25(OH)2D3 (calcitriol) therapies on parathyroid hormone (PTH) secretion were compared in 10 hemodialysis (HD) patients with secondary hyperparathyroidism (SHPT). These patients were randomized to receive either IVC or ORC therapy for 12 weeks, both followed by a 12-week washout period. After the washout, the patients who received IVC then switched to ORC therapy for another 12 weeks, and the patients who received ORC switched to IVC therapy. The mean dose of IVC was 2.45 +/- 0.30 micrograms/dialysis session (approximately equal to 1.05 micrograms/day) and that of ORC was 0.69 +/- 0.07 micrograms/day. A significant reduction in serum levels of intact PTH was observed after 8 weeks and that of C-PTH after 10 weeks of ORC therapy, but both fell after 6 weeks of IVC treatment. There was a concomitant reduction in serum alkaline phosphatase (AP), but it became significant 4 weeks later than in intact PTH. The maximal reductions of serum levels of intact PTH, C-PTH and AP were 74.28, 64.91, 41.97%, respectively, after IVC, and 31.57, 24.39, 22.50%, respectively, after ORC therapy. Serum calcium rose faster during ORC treatment. There were no significant changes in serum levels of phosphorus, magnesium, and albumin throughout the treatment period. We conclude that both IVC or ORC treatments result in a significant decrement in blood levels of PTH in chronic HD patients with SHPT. However, this PTH-suppressive effect is more pronounced with IVC therapy, and cannot be totally explained by either the higher dose or elevated serum calcium.
Similar articles
-
1alpha(OH)D3 One-alpha-hydroxy-cholecalciferol--an active vitamin D analog. Clinical studies on prophylaxis and treatment of secondary hyperparathyroidism in uremic patients on chronic dialysis.Dan Med Bull. 2008 Nov;55(4):186-210. Dan Med Bull. 2008. PMID: 19232159 Review.
-
Effect of the mode of calcitriol administration on PTH-ionized calcium relationship in uraemic patients with secondary hyperparathyroidism.Nephrol Dial Transplant. 1995;10(5):665-70. Nephrol Dial Transplant. 1995. PMID: 7566580 Clinical Trial.
-
Effects of 22-oxacalcitriol and calcitriol on PTH secretion and bone mineral metabolism in a crossover trial in hemodialysis patients with secondary hyperparathyroidism.Ther Apher Dial. 2007 Jun;11(3):202-9. doi: 10.1111/j.1744-9987.2007.00422.x. Ther Apher Dial. 2007. PMID: 17498002 Clinical Trial.
-
A crossover comparison of intermittent oral and intravenous administration of calcitriol on the parathyroid hormone concentration in hemodialysis patients.Miner Electrolyte Metab. 1997;23(1):13-8. Miner Electrolyte Metab. 1997. PMID: 9058364
-
Guidelines for dosing of intravenous calcitriol in dialysis patients with hyperparathyroidism.Nephrol Dial Transplant. 1996;11 Suppl 3:96-101. doi: 10.1093/ndt/11.supp3.96. Nephrol Dial Transplant. 1996. PMID: 8840322 Review.
Cited by
-
Comparison of oral and intravenous alfacalcidol in chronic hemodialysis patients.BMC Nephrol. 2014 Feb 4;15:27. doi: 10.1186/1471-2369-15-27. BMC Nephrol. 2014. PMID: 24495277 Free PMC article.
-
Intravenous calcitriol therapy in an early stage prevents parathyroid gland growth.Nephrol Dial Transplant. 2008 Nov;23(11):3662-9. doi: 10.1093/ndt/gfn264. Epub 2008 May 30. Nephrol Dial Transplant. 2008. PMID: 18515308 Free PMC article. Clinical Trial.
-
Calcitriol administration in end-stage renal disease: intravenous or oral?Pediatr Nephrol. 1996 Jun;10(3):331-6. doi: 10.1007/BF00866773. Pediatr Nephrol. 1996. PMID: 8792399 Review.
-
The Use of Vitamin D Metabolites and Analogues in the Treatment of Chronic Kidney Disease.Endocrinol Metab Clin North Am. 2017 Dec;46(4):983-1007. doi: 10.1016/j.ecl.2017.07.008. Epub 2017 Sep 29. Endocrinol Metab Clin North Am. 2017. PMID: 29080646 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Medical