Geusens P, Dequeker J, Gielen J, Schot L P
Arthritis and Metabolic Bone Disease Research Unit, University Hospital, K.U. Leuven, Belgium.
Maturitas. 1991 Jun;13(2):155-62. doi: 10.1016/0378-5122(91)90099-c.
The results of a 2-year placebo-controlled study in 38 female patients with osteoporosis are presented. This study was conducted to evaluate the efficacy of a daily oral dose of 2.5 mg Org OD 14 ((7 alpha, 17 alpha)-17-hydroxy-7-methyl-19-norpregn-5(10)-en-20-yn-3-one) in the treatment of established osteoporosis. Org OD 14 is a steroid which shows combined weak oestrogenic, androgenic and progestational activity. A total of 31 patients completed a 12-month study period (17 placebo, 14 Org OD 14) and 25 of these went on to complete the full 24-months (15 placebo, 10 Org OD 14). A significant increase in bone mineral density as measured by dual photon absorptiometry was recorded in the lumbar spine in the Org OD 14-treated patients at 8, 16 and 24 months. The gain in bone mass after 8 months averaged 4% (P less than 0.01) and after 24 months 8% (P less than 0.001). In the control group, a bone loss rate of 2% per year was recorded in the lumbar spine. No significant changes in bone density in the forearm as assessed by single photon absorptiometry were found in either group. The increase in spinal bone density in the Org OD 14 group was non-linear and followed an S-shaped upward pattern. Org OD 14, while inducing no appreciable endometrial stimulation, was found to be a bone-active compound with anti-resorbing as well as anabolic activity. Org OD 14 warrants consideration not only for the long-term prevention of bone loss but also for curative treatment of post-menopausal osteoporosis.
本文展示了一项针对38名骨质疏松女性患者进行的为期2年的安慰剂对照研究结果。本研究旨在评估每日口服2.5毫克Org OD 14((7α, 17α)-17-羟基-7-甲基-19-去甲孕-5(10)-烯-20-炔-3-酮)对已确诊骨质疏松症的治疗效果。Org OD 14是一种具有微弱雌激素、雄激素和孕激素活性的类固醇。共有31名患者完成了为期12个月的研究期(17名服用安慰剂,14名服用Org OD 14),其中25名继续完成了整个24个月的研究(15名服用安慰剂,10名服用Org OD 14)。通过双能光子吸收法测量,服用Org OD 14的患者在第8、16和24个月时腰椎骨矿物质密度显著增加。8个月后骨量增加平均为4%(P<0.01),24个月后为8%(P<0.001)。在对照组中,腰椎每年的骨质流失率为2%。两组通过单能光子吸收法评估的前臂骨密度均未发现显著变化。Org OD 14组脊柱骨密度的增加呈非线性,呈S形上升模式。Org OD 14虽然未引起明显的子宫内膜刺激,但被发现是一种具有抗吸收和合成代谢活性的骨活性化合物。Org OD 14不仅值得考虑用于长期预防骨质流失,也值得考虑用于绝经后骨质疏松症的治疗。