Prevention of early postmenopausal bone loss with cyclical etidronate therapy (a double-blind, placebo-controlled study and 1-year follow-up)

J Clin Endocrinol Metab. 1997 Sep;82(9):2784-91. doi: 10.1210/jcem.82.9.4073.


The objective of the study was to evaluate the effects of cyclical therapy with etidronate and calcium on spinal and femoral bone loss in the early post menopausal period. Fifty-four women, 53 +/- 2.8 yr old (mean +/- SD) and 2.3 +/- 1.3 yr post menopause received oral doses of either 400 mg/day etidronate for 2 weeks followed by 500 mg/day elemental calcium for 11 weeks, or placebo for 14 days followed by calcium for 11 weeks, repeated over a total of 24 months. A statistically significant increase in spinal bone mineral density (BMD) was observed after 6 months in the etidronate group. At 2 yr, the mean treatment differences in spinal and femoral neck BMD were +2.93% (P < 0.02) and 2.02% (P < 0.03), respectively. Serum osteocalcin and urinary crossLaps/creatinine excretion were decreased significantly by etidronate. Etidronate was well tolerated with a safety profile similar to that of placebo. Thirty-seven women participated in a 1-yr open-label follow-up study. Twelve months after treatment withdrawal, spinal BMD in the former etidronate group decreased by 1.43% and serum osteocalcin and urinary crossLaps returned to pretreatment values. In conclusion, cyclical etidronate is an effective therapy for the prevention of both trabecular and cortical bone loss in the early menopause and has a good safety profile.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial

MeSH terms

  • Biomarkers / blood
  • Biomarkers / urine
  • Bone Density / drug effects
  • Bone and Bones / drug effects
  • Bone and Bones / metabolism
  • Bone and Bones / pathology
  • Double-Blind Method
  • Drug Administration Schedule
  • Etidronic Acid / administration & dosage*
  • Etidronic Acid / adverse effects
  • Etidronic Acid / therapeutic use
  • Female
  • Follow-Up Studies
  • Humans
  • Middle Aged
  • Organ Size / drug effects
  • Osteoporosis, Postmenopausal / prevention & control*


  • Biomarkers
  • Etidronic Acid