Dechant K L, Goa K L
Adis International Limited, Auckland, New Zealand.
Drugs Aging. 1994 Oct;5(4):300-17. doi: 10.2165/00002512-199405040-00006.
A synthetic form of calcitriol (1,25-dihydroxycholecalciferol; 1,25-dihydroxyvitamin D3), the most physiologically active metabolite of vitamin D, has shown efficacy in the treatment of postmenopausal osteoporosis and promise in corticosteroid-induced osteoporosis. Although results of small studies investigating calcitriol in the treatment of postmenopausal osteoporosis have been conflicting, a clinical trial in 622 women with postmenopausal osteoporosis demonstrated that patients with mild to moderate disease who received calcitriol (0.25 microgram twice daily) had a significant 3-fold lower rate of new vertebral fractures after 3 years of treatment, compared with patients receiving elemental calcium 1000 mg/day. In patients commencing long term treatment with prednisone or prednisolone, calcitriol 0.5 to 1.0 micrograms/day plus calcium 1000 mg/day, administered with or without intranasal calcitonin 400 IU/day, prevented steroid-induced bone loss. Overall, calcitriol is well tolerated. As shown in clinical studies, at recommended dosages hypercalcaemia is infrequent and mild, generally responding to reductions in calcium intake and/or calcitriol dosage. The narrow 'therapeutic window' of calcitriol requires that its use be adequately supervised, with periodic monitoring of serum calcium and creatinine levels. However, significant renal toxicity has not been seen in patients with osteoporosis treated with calcitriol in high dosages for several years in comparative and noncomparative trials. In conclusion, as with other drugs currently used in the management of patients with osteoporosis, questions remain to be answered regarding the efficacy of calcitriol relative to other agents, and its tolerability in such patients during the very long term. Nonetheless, at this stage, calcitriol should be considered a useful treatment option in patients with mild to moderate postmenopausal osteoporosis.
骨化三醇(1,25 - 二羟胆钙化醇;1,25 - 二羟基维生素D3)是维生素D最具生理活性的代谢产物,其合成形式已显示出对绝经后骨质疏松症的治疗效果,并有望用于治疗糖皮质激素诱导的骨质疏松症。尽管关于骨化三醇治疗绝经后骨质疏松症的小型研究结果相互矛盾,但一项针对622名绝经后骨质疏松症女性的临床试验表明,与每日服用1000毫克元素钙的患者相比,接受骨化三醇(每日两次,每次0.25微克)治疗的轻至中度疾病患者在治疗3年后新椎体骨折发生率显著降低了3倍。在开始长期使用泼尼松或泼尼松龙治疗的患者中,每日服用0.5至1.0微克骨化三醇加1000毫克钙,无论是否联合每日400国际单位的鼻内降钙素,均可预防类固醇诱导的骨质流失。总体而言,骨化三醇耐受性良好。临床研究表明,在推荐剂量下,高钙血症很少见且症状较轻,一般通过减少钙摄入量和/或骨化三醇剂量即可缓解。骨化三醇狭窄的“治疗窗”要求其使用受到充分监督,定期监测血清钙和肌酐水平。然而,在比较性和非比较性试验中,使用高剂量骨化三醇治疗数年的骨质疏松症患者未出现明显的肾毒性。总之,与目前用于治疗骨质疏松症患者的其他药物一样,关于骨化三醇相对于其他药物的疗效及其在这类患者中长期的耐受性,仍有待解答。尽管如此,现阶段,骨化三醇应被视为轻至中度绝经后骨质疏松症患者的一种有效治疗选择。