Purdie D W, Hay A W, Everett M
Department of Obstetrics and Gynaecology, University of Leeds, U.K.
Maturitas. 1992 Mar;14(3):189-99. doi: 10.1016/0378-5122(92)90114-j.
Forty-five healthy postmenopausal women participated in a study designed to examine the effects on bone and mineral metabolism of SHD 386L, a new hormone replacement therapy (HRT) regime. This oral preparation delivers 2 mg estradiol valerate daily and 75 micrograms of levonorgestrel from days 17-28 inclusive of a 28-day cycle. The study was double-blind, randomized and placebo controlled. Patients who received SHD 386L exhibited significant falls in plasma calcium, ionised calcium, phosphate and total alkaline phosphatase. No alteration, however, was observed in plasma osteocalcin. No significant changes in mineral metabolism were observed in a parallel group receiving levonorgestrel alone. The results indicate that SHD 386L is likely to be protective to the skeleton through inhibition of bone resorption and that such actions are attributable to the estrogen component. The preparation was well tolerated, compliance was satisfactory and serious adverse affects were not seen. The above biochemical evidence for skeletal protection will require to be supplemented by prospective biophysical evidence of the effect of SHD 386L on bone mineral density.
45名健康的绝经后女性参与了一项研究,该研究旨在检验一种新型激素替代疗法(HRT)方案SHD 386L对骨骼和矿物质代谢的影响。这种口服制剂在28天的周期中,从第17天至第28天每天提供2毫克戊酸雌二醇和75微克左炔诺孕酮。该研究为双盲、随机且安慰剂对照试验。接受SHD 386L治疗的患者血浆钙、离子钙、磷酸盐和总碱性磷酸酶显著下降。然而,血浆骨钙素未观察到变化。在单独接受左炔诺孕酮的平行组中,矿物质代谢未观察到显著变化。结果表明,SHD 386L可能通过抑制骨吸收对骨骼起到保护作用,且这种作用归因于雌激素成分。该制剂耐受性良好,依从性令人满意,未观察到严重不良反应。上述骨骼保护的生化证据还需要通过SHD 386L对骨矿物质密度影响的前瞻性生物物理证据加以补充。