Netelenbos J C, Asscheman H, Lips P, Van der Vijgh W J, Jongen M J, Van Ginkel F, Hackeng W H
J Clin Endocrinol Metab. 1986 Jul;63(1):246-8. doi: 10.1210/jcem-63-1-246.
Nineteen patients with primary hyperparathyroidism were treated with 25 micrograms 24,25-dihydroxyvitamin D3 or placebo daily for 3 months according to double-blind cross-over protocol. Serum immunoreactive PTH, total and ionized calcium, urinary calcium excretion, tubular reabsorption of phosphate/glomerular filtrate, and urinary hydroxyproline excretion did not change significantly. Serum 24,25-dihydroxyvitamin D3 levels increased significantly from 1.4 +/- 2.2 (SD) nmol/liter to 38 +/- 11 nmol/liter during the treatment period. Serum 25-hydroxyvitamin D3 and 1,25-dihydroxyvitamin D3 levels did not change. We conclude that pharmacological doses of 24,25-dihydroxyvitamin D3 have no suppressive effect on parathyroid function in primary hyperparathyroidism.
根据双盲交叉试验方案,19例原发性甲状旁腺功能亢进患者每日接受25微克24,25 - 二羟维生素D3或安慰剂治疗,为期3个月。血清免疫反应性甲状旁腺激素、总钙和离子钙、尿钙排泄、肾小管对磷酸盐的重吸收/肾小球滤过率以及尿羟脯氨酸排泄均无显著变化。治疗期间,血清24,25 - 二羟维生素D3水平从1.4±2.2(标准差)纳摩尔/升显著升至38±11纳摩尔/升。血清25 - 羟维生素D3和1,25 - 二羟维生素D3水平未发生变化。我们得出结论,药理剂量的24,25 - 二羟维生素D3对原发性甲状旁腺功能亢进患者的甲状旁腺功能无抑制作用。