K. Kurokawa et al., EFFECT OF 22-OXACALCITRIOL ON HYPERPARATHYROIDISM OF DIALYSIS PATIENTS - RESULTS OF A PRELIMINARY-STUDY, Nephrology, dialysis, transplantation, 11, 1996, pp. 121-124
Intermittent high dose administration of calcitriol or alfacalcidol is
effective in suppressing secondary hyperparathyroidism in chronic dia
lysis patients, however calcaemic action of these vitamin D derivative
s is a major obstacle. 22-Oxacalcitriol (OCT) has been reported to hav
e less calcaemic action than calcitriol, while preserving a comparable
suppressive effect on parathyroid hormone (PTH) secretion. This preli
minary study was conducted to examine the effects of OCT on secondary
hyperparathyroidism in chronic dialysis patients. OCT was administrate
d intravenously immediately after every haemodialysis session three ti
mes a week for 12 weeks to three haemodialysis patients with secondary
hyperparathyroidism. An initial dose of OCT of 5.5 mu g/haemodialysis
session was increased stepwise by 5.5 mu g/haemodialysis up to 22 mu
g/haemodialysis according to the suppression of PTH and calcaemic acti
on. OCT was discontinued for at least a week when serum calcium adjust
ed to albumin concentration measured just before haemodialysis exceede
d 11.5 mg/dl. Marked reduction in plasma PTH, alkaline phosphatase and
tartrate-resistant acid phosphatase was observed in all three patient
s. Although the dose of OCT was increased to 22 mu g/haemodialysis in
one patient, the final dose of OCT remained 5.5 mu g/haemodialysis in
the other two patients because of hypercalcaemia. It is concluded that
OCT is highly effective in suppressing PTH in dialysis patients with
secondary hyperparathyroidism. Hypercalcaemia may be a major factor wh
ich limits the use of OCT, though it may occur with higher doses of OC
T than those of calcitriol usually given to suppress PTH hypersecretio
n.