Effects of Transdermal Estradiol Delivered by a Matrix Patch on Bone Density in Hysterectomized, Postmenopausal Women: A 2-year Placebo-Controlled Trial

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Abstract
This 2-year, double-masked, randomized, placebo-controlled trial was designed to evaluate the safety and efficacy in preventing bone loss in postmenopausal women of two doses of transdermal 17β-estradiol (estradiol) delivered by a matrix patch, compared with placebo. One hundred and sixty healthy, hysterectomized postmenopausal volunteers aged 40–60 years with serum estradiol levels n= 53), oestradiol, 50 mg/day (E-50, n= 54), placebo (P-100, placebo to E-100, n= 27 or P-50, placebo to E-50, n= 26). Treatment was continued for up to 2 years. After 24 months, BMD of the lumbar spine in the E-100 group differed by 7.7% [5.8–9.5%] (mean [95% confidence interval]) from the placebo group and showed a mean (s.e.m.) increase in BMD from baseline of 5.9% (0.69%). For the E-50 group the difference compared with placebo was 6.2% [4.4–8.0%] and the absolute increase was 4.5% (0.62%); in the placebo group, the absolute change was –2.3% (0.48%). In the total wrist, the changes were: E-100: difference compared with placebo 2.5% [1.5–3.6%], absolute increase 0.6% (0.3%); E-50: difference compared with placebo 2.9% [1.8–3.9%], absolute increase 0.7% (0.25%); and absolute change on placebo: –2.5% (0.35%). In the total hip, the changes were: E-100: difference compared with placebo 3.7% [2.2–5.2%], absolute increase 2.8% (0.5%); E-50: difference compared with placebo: 3.2% [1.8–4.7%], absolute change 2.4% (0.36%); and absolute change on placebo –1.4% (0.66%). Three markers of bone turnover – serum bone-specific alkaline phosphatase, serum osteocalcin and urinary CTX – fell significantly during the trial. Breast pain was reported by 8% of women on placebo, by 6% of women on E-50 and by 17% of women on E-100. Estradiol delivered by the E-50 matrix patch effectively reversed bone loss in hysterectomized postmenopausal women with few side-effects. The marginal additional gain in BMD with the higher dose may be offset by a more important side effect profile.

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