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Long-term continuous combined hormone replacement therapy in the prevention of postmenopausal bone loss: a comparison of high- and low-dose estrogen-progestin regimens.

AbstractWe studied the effect of four continuous combined estradiol valerate (E2V) and medroxyprogesterone acetate (MPA) dose combinations in six treatment groups (n = 70 per group) receiving regimens containing 1 mg or 2 mg E2V combined to 2.5 mg or 5 mg MPA, on bone mineral density (BMD) and endometrium in 419 healthy postmenopausal women over 4 treatment years. In two groups the 1 mg dose of E2V was increased to 2 mg after the first 6 months, while the MPA doses remained constant (2.5 mg or 5 mg). The remaining four groups received 1 E2V + 2.5 mg MPA, 1 mg E2V + 5 mg MPA, 2 mg E2V + 2.5 mg MPA, or 2 mg E2V + 5 mg MPA throughout the study. BMD at the spine and hip was measured by dual-energy X-ray absorptiometry and endometrial biopsy samples were taken at 6, 12, 24, 36 and 48 month follow-ups. Combinations containing the low dose of 1 mg of E2V (with 2.5 mg or 5 mg MPA) resulted in a mean BMD increase of 6.2% at the spine and 2.9% at the femoral neck after 4 years of treatment. With 2 mg E2V the corresponding increases were 7.4% and 2.9%, respectively. The largest increases in BMD were seen in women for whom the E2V dose was doubled after the initial 6 months of treatment: 8.9% at the spine and 4.2% in the femoral neck. Both MPA doses (2.5 mg and 5 mg) effectively prevented estrogen-induced stimulation of the endometrium. No endometrial hyperplasia was observed in any of the treatment groups. Lower-dose combinations of continuous combined estrogen-progestin regimens are effective in increasing and maintaining BMD and provide a good endometrial safety profile for the long-term prevention of osteoporosis in postmenopausal women.
AuthorsJ Heikkinen, R Vaheri, P Kainulainen, U Timonen (Affiliation: The Deaconess Institute of Oulu, Isokatu, Finland.)
JournalOsteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA (Osteoporos Int) Vol. 11 Issue 11 Pg. 929-37 ( 2000) ISSN: 0937-941X England
PMID11193245 (Publication Type: Clinical Trial, Comparative Study, Journal Article, Randomized Controlled Trial)
Chemical References
  • Drug Combinations
  • Estradiol Congeners
  • Progesterone Congeners
  • Estradiol
  • Medroxyprogesterone 17-Acetate
Topics
  • Aged
  • Analysis of Variance
  • Bone Density (drug effects)
  • Double-Blind Method
  • Drug Combinations
  • Endometrium (drug effects)
  • Estradiol (administration & dosage)
  • Estradiol Congeners (administration & dosage)
  • Estrogen Replacement Therapy (methods)
  • Female
  • Humans
  • Medroxyprogesterone 17-Acetate (administration & dosage)
  • Middle Aged
  • Osteoporosis, Postmenopausal (prevention & control)
  • Progesterone Congeners (administration & dosage)
  • Single-Blind Method
  • Treatment Outcome