Doxercalciferol safely suppresses PTH levels in patients with secondary hyperparathyroidism associated with chronic kidney disease stages 3 and 4

被引:118
作者
Coburn, JW
Maung, HM
Elangovan, L
Germain, MJ
Lindberg, JS
Sprague, SM
Williams, ME
Bishop, CW
机构
[1] W Los Angeles VA Healthcare Ctr, Nephrol Sect 111L, Los Angeles, CA 90073 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Los Angeles, CA 90024 USA
[3] Western New England Renal & Transplant Associates, W Springfield, MA USA
[4] Joslin Diabet Ctr, Boston, MA 02215 USA
[5] Ochsner Clin & Alton Ochsner Med Fdn, Ochsner Chron Hemodialysis, New Orleans, LA USA
[6] Evanston NW Healthcare Ctr, Evanston, IL USA
[7] Diabet & Glandular Dis Clin, San Antonio, TX USA
[8] Western Nephrol & Metab Bone Dis Clin, Thornton, CO USA
[9] Western Nephrol & Metab Bone Dis Clin, Lakewood, CO USA
[10] Bone Care Int Inc, Middleton, WI USA
关键词
chronic kidney disease (CKD); secondary hyperparathyroidism; vitamin D; doxercalciferol (1 alpha-hydroxyvitamin D-2); parathyroid hormone (PTH); moderate renal insufficiency;
D O I
10.1053/j.ajkd.2004.01.012
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background Calcitriol lowers parathyroid hormone (PTH) levels in patients with chronic kidney disease (CKD) stages 3 and 4, but its use is limited by a low therapeutic index and concerns regarding hypercalcemia and acceleration of kidney disease. We evaluated doxercalciferol (1alpha-hydroxyvitamin D-2) as an alternative therapy in a randomized, double-blinded, placebo-controlled, multicenter trial. Methods: Fifty-five adults with stage 3 or 4 CKD and an intact PTH (iPTH) level greater than 85 pg/mL (ng/L) completed 8 baseline weeks, followed by 24 weeks of oral therapy with doxercalciferol or placebo. Pretreatment demographics and biochemical features did not differ between groups. Dosages were increased gradually if iPTH level was not decreased by 30% or greater and serum calcium and phosphorus levels were stable. Regular monitoring included plasma iPTH, serum calcium and phosphorus, urinary calcium, bone-specific serum markers, and serum 1alpha,25-dihydroxyvitamin D levels. Glomerular filtration rate (GFR) was measured before and after treatment. Results: Mean plasma iPTH level decreased by 46% from baseline after 24 weeks of doxercalciferol treatment (P <0.001), but was unchanged with placebo. After 6 weeks, iPTH level reductions with doxercalciferol treatment exceeded those with placebo at all subsequent intervals (P <0.001). No clinically significant differences in mean serum calcium or phosphorus or urinary calcium levels or incidence of hypercalcemia, hyperphosphatemia, or hypercalciuria were noted between groups. Serum C- and N-telopeptide and bone-specific alkaline phosphatase levels decreased with doxercalciferol treatment relative to both baseline and placebo (P <0.01). Adverse-event rates and changes in GFR did not differ between groups. Conclusion: Doxercalciferol is safe and effective in controlling secondary hyperparathyroidism of patients with CKD stages 3 and 4.
引用
收藏
页码:877 / 890
页数:14
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