Bone loss during gonadotropin releasing hormone agonist treatment and use of nasal calcitonin

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Nasal calcitonin at 100 or 200 IU daily did not prevent bone loss in women treated with a GnRH agonist for endometriosis.

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This prospective, double-masked randomized study evaluated whether nasal salmon calcitonin (sCT), at 100 IU or 200 IU daily, could prevent bone loss during GnRH agonist therapy in 40 patients with endometriosis treated for 6 months with triptorelin plus daily calcium. Bone mineral density was assessed by dual-energy X-ray absorptiometry along with biochemical markers of bone metabolism. After 6 months, estradiol and bone turnover markers were at postmenopausal levels and there were no differences between placebo and either sCT dose, with no difference in bone loss at any measured site. This paper is centrally about endometriosis — it tests nasal salmon calcitonin as a preventive adjunct to GnRH agonist–associated bone loss in women with endometriosis.

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Abstract

Gonadotropin releasing hormone (GnRH) agonists have shown to be effective in the treatment of several sex-hormone-dependent conditions. However, their use could be limited by the bone loss they induce. To evaluate the use of nasal salmon calcitonin (sCT) in preventing this bone loss, 40 patients with endometriosis were treated for 6 months with triptoreline (3.75 mg monthly) and calcium (1 g daily), and randomized in three groups-placebo, sCT 100 IU daily and sCT 200 IU daily-in a prospective double-masked study. Dual-energy X-ray absorptiometry and biochemical parameters were used to evaluate the benefit of the treatment. At baseline, there were no statistically significant differences between the groups. After 6 months, estradiol and biochemical markers of bone metabolism were at postmenopausal levels, with no difference between the groups. There was no difference in bone loss in the three groups, at all sites. Mean lumbar bone loss was 4.01 +/- 2.59% (mean +/- SD) in this population. In this study dosages of 100 IU and 200 IU daily of nasal sCT were insufficient to prevent bone loss during GnRH agonist treatment.
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Abstract

Gonadotropin releasing hormone (GnRH) agonists have shown to be effective in the treatment of several sex-hormone-dependent conditions. However, their use could be limited by the bone loss they induce. To evaluate the use of nasal salmon calcitonin (sCT) in preventing this bone loss, 40 patients with endometriosis were treated for 6 months with triptoreline (3.75 mg monthly) and calcium (1 g daily), and randomized in three groups — placebo, sCT 100 IU daily and sCT 200 IU daily — in a prospective double-masked study. Dual-energy X-ray absorptiometry and biochemical parameters were used to evaluate the benefit of the treatment. At baseline, there were no statistically significant differences between the groups. After 6 months, estradiol and biochemical markers of bone metabolism were at postmenopausal levels, with no difference between the groups. There was no difference in bone loss in the three groups, at all sites. Mean lumbar bone loss was 4.01±2.59% (mean±SD) in this population. In this study dosages of 100 IU and 200 IU daily of nasal sCT were insufficient to prevent bone loss during GnRH agonist treatment. Similar content being viewed by others

References

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Author information Authors and Affiliations Rights and permissions About this article Cite this article Roux, C., Pelissier, C., Listrat, V. et al. Bone loss during gonadotropin releasing hormone agonist treatment and use of nasal calcitonin. Osteoporosis Int 5, 185–190 (1995). https://doi.org/10.1007/BF02106098 Received: Accepted: Issue date: DOI: https://doi.org/10.1007/BF02106098

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Condition tags

endometriosis

MeSH descriptors

Bone Diseases, Metabolic Bone Diseases, Metabolic Calcitonin Gonadotropin-Releasing Hormone Triptorelin Pamoate Absorptiometry, Photon Administration, Intranasal Adult Animals Bone Density Bone Density Bone Diseases, Metabolic Calcitonin Calcitonin Calcitonin Double-Blind Method Endometriosis Endometriosis Female Gonadotropin-Releasing Hormone

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