Jenkins E A, Walker-Bone K E, Wood A, McCrae F C, Cooper C, Cawley M I
Milton Keynes District Hospital, Eaglestone, UK.
Scand J Rheumatol. 1999;28(3):152-6. doi: 10.1080/03009749950154211.
A prospective, randomised, double-blind, placebo controlled primary prevention trial was undertaken in 28 patients commencing low to moderate doses of corticosteroids for the first time. Patients were randomised to intermittent cyclical etidronate (400 mg daily for 2 weeks) and calcium (500 mg daily for 11 weeks) or intermittent cyclical placebo with calcium. After 52 weeks of treatment, lumbar spine BMD increased by 1.8% in the etidronate group, while it decreased by 3.7% in the placebo group. The differences in bone loss rate were statistically significant (p<0.01) at both 6 and 12 months. Similar trends were observed at the proximal femur, but differences were not statistically significant. These results suggest that intermittent cyclical etidronate therapy is effective in the primary prevention of corticosteroid-induced bone loss at the lumbar spine.
一项前瞻性、随机、双盲、安慰剂对照的一级预防试验纳入了28例首次开始使用低至中等剂量皮质类固醇的患者。患者被随机分为间歇周期性依替膦酸(每日400毫克,共2周)加钙(每日500毫克,共11周)组或间歇周期性安慰剂加钙组。治疗52周后,依替膦酸组腰椎骨密度增加了1.8%,而安慰剂组降低了3.7%。在6个月和12个月时,骨丢失率的差异均具有统计学意义(p<0.01)。在股骨近端也观察到了类似趋势,但差异无统计学意义。这些结果表明,间歇周期性依替膦酸疗法在皮质类固醇诱导的腰椎骨丢失的一级预防中是有效的。