Raloxifene versus continuous combined estrogen/progestin therapy: densitometric and biochemical effects in healthy postmenopausal Taiwanese women

Osteoporos Int. 2001 Dec;12(12):1020-5. doi: 10.1007/s001980170011.

Abstract

We treated 116 healthy postmenopausal women (age 47-66 years, mean 57 years) in Taiwan with either raloxifene (RLX) 60 mg (n = 92) or 0.625 mg conjugated equine estrogen plus 5 mg medroxyprogesterone acetate (CCEP, n = 24) daily for 12 months in a randomized, double-masked, active-controlled fashion. The results showed that both regimens increased bone mineral density (BMD) at hip sites (means: RLX 2.5-4.9%, CCEP 4.6-7.9%, all p<0.005 compared with baseline), and the difference between the two regimens was not significant. The spinal BMD increased significantly in both groups (1.4% with RLX and 6.0% with CCEP, both p<0.01), and more with CCEP (p<0.003). Osteocalcin levels and urinary type I collagen C-telopeptide/creatinine ratios decreased significantly in both regimens, but the decreases were significantly larger with CCEP. Compared with baseline, both RLX and CCEP decreased the total cholesterol (median 4.9% and 8.6% respectively, p<0.001) and LDL-cholesterol (median 11% and 19% respectively, p<0.001), and increased HDL-cholesterol (median 8.6% and 10.7% respectively, p<0.01). Both regimens increased triglyceride levels (median 3.2% and 18.9% respectively, both p<0.05), although to a lesser extent with RLX than with CCEP (p<0.05). Only 3 subjects (3.3%) reported vaginal bleeding in the RLX group, as compared with 31% (7/22) with CCEP (p<0.05). We conclude that in healthy, postmenopausal Taiwanese women, RLX 60 mg given daily has favorable results in BMD, bone turnover and serum lipids, although the dosage we used showed a potency less than that of conventional CCEP.

Publication types

  • Clinical Trial
  • Comparative Study
  • Multicenter Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Bone Density / drug effects*
  • Double-Blind Method
  • Drug Combinations
  • Endometrium / anatomy & histology
  • Endometrium / drug effects
  • Estrogen Replacement Therapy*
  • Estrogens, Conjugated (USP) / pharmacology
  • Female
  • Hip Joint / physiology
  • Humans
  • Lipids / blood
  • Lumbar Vertebrae / physiology
  • Medroxyprogesterone Acetate / pharmacology
  • Middle Aged
  • Postmenopause / physiology*
  • Progesterone Congeners / pharmacology
  • Raloxifene Hydrochloride / pharmacology*
  • Selective Estrogen Receptor Modulators / pharmacology
  • Uterus / anatomy & histology
  • Uterus / drug effects

Substances

  • Drug Combinations
  • Estrogens, Conjugated (USP)
  • Lipids
  • Progesterone Congeners
  • Selective Estrogen Receptor Modulators
  • Raloxifene Hydrochloride
  • Medroxyprogesterone Acetate