Hodsman A B, Wong E G, Sherrard D J, Brickman A S, Lee D B, Singer F R, Norman A W, Coburn J W
Am J Med. 1983 Mar;74(3):407-14. doi: 10.1016/0002-9343(83)90959-2.
Fifteen patients with dialysis osteomalacia were treated with 24,25-dihydroxyvitamin D3 in dosages up to 10 micrograms per day for two to 24 months. All had previously had no improvement during treatment with calcitriol but had been remarkably susceptible to hypercalcemia. When 24,25-dihydroxyvitamin D3 was given with either calcitriol or dihydrotachysterol, serum calcium levels were significantly lower than during treatment with calcitriol or dihydrotachysterol alone. Eight of nine patients who received combined therapy with 24,25-dihydroxyvitamin D3 and calcitriol for longer than two months had clinical improvement; six patients underwent repeated bone biopsy and showed evidence of improved bone mineralization. Patients who received 24,25-dihydroxyvitamin D3 alone did not improve clinically. Since 24,25-dihydroxyvitamin D3 appears to improve calcium homeostasis and bone mineralization in some patients with severe dialysis osteomalacia when administered with 1-hydroxylated vitamin D metabolites, further controlled studies are warranted.
15名患有透析性骨软化症的患者接受了剂量高达每日10微克的24,25 - 二羟基维生素D3治疗,为期2至24个月。所有患者此前在使用骨化三醇治疗期间均无改善,但对高钙血症极为敏感。当24,25 - 二羟基维生素D3与骨化三醇或双氢速甾醇合用时,血清钙水平显著低于单独使用骨化三醇或双氢速甾醇治疗期间。9名接受24,25 - 二羟基维生素D3与骨化三醇联合治疗超过两个月的患者中有8名临床症状得到改善;6名患者接受了重复骨活检,显示有骨矿化改善的证据。单独接受24,25 - 二羟基维生素D3治疗的患者临床症状未改善。由于24,25 - 二羟基维生素D3与1 - 羟化维生素D代谢产物合用时,似乎能改善一些重度透析性骨软化症患者的钙稳态和骨矿化,因此有必要进行进一步的对照研究。