Literature DB >> 11344179

Effect of combined risedronate and hormone replacement therapies on bone mineral density in postmenopausal women.

S T Harris1, E F Eriksen, M Davidson, M P Ettinger, A H Moffett, D J Baylink, C E Crusan, A A Chines.   

Abstract

Both hormone replacement therapy (HRT) and bisphosphonates are efficacious in the prevention and treatment of postmenopausal osteoporosis. Combined therapy with bisphosphonate and HRT is likely to be used in clinical practice, and limited data are available regarding its efficacy and safety. This was a 1-yr, double blind, placebo-controlled study in which 524 postmenopausal women received daily treatment with conjugated equine estrogens (0.625 mg) alone or in combination with risedronate (5 mg). Women who had not undergone hysterectomy received medroxyprogesterone acetate (up to 5 mg, daily or cyclically) at the discretion of the investigator. The primary efficacy end point was the percent change from baseline in mean lumbar spine bone mineral density (BMD) at 1 yr. Changes in BMD at the proximal femur and forearm, bone turnover markers, and histology and histomorphometry were also assessed. At 12 months, significant (P < 0.05) increases from baseline in lumbar spine BMD were observed in both treatment groups (HRT-only, 4.6%; combined risedronate-HRT, 5.2%); the difference between the two groups was not statistically significant. Both therapies led to significant increases in BMD at 12 months at the femoral neck (1.8% and 2.7%, respectively), femoral trochanter (3.2% and 3.7%), distal radius (1.7% and 1.6%), and midshaft radius (0.4% and 0.7%). The differences between groups were statistically significant (P < 0.05) at the femoral neck and midshaft radius. Both combined risedronate-HRT and HRT-only produced significant decreases in the biochemical markers of bone turnover, with somewhat greater decreases in the combined treatment group. Bone biopsy data showed normal bone structure and normal mineralization with either treatment. Expected decreases in bone turnover were observed and were greater in the combined treatment group (68-79% reduction relative to baseline values, P < 0.005). Overall, combined treatment had a safety profile similar to that of HRT-only, including bone and gastrointestinal safety profiles. In conclusion, the combined treatment with risedronate and HRT had a favorable effect on BMD similar to that of HRT alone at the lumbar spine and slightly, but significantly, greater than that of HRT alone at the femoral neck and midshaft radius. The combined treatment was well tolerated, and there were no adverse effects on the skeleton.

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Year:  2001        PMID: 11344179     DOI: 10.1210/jcem.86.5.7505

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  34 in total

Review 1.  Management of post-menopausal osteoporosis: something new on the horizon?

Authors:  M L Brandi
Journal:  J Endocrinol Invest       Date:  2003-02       Impact factor: 4.256

Review 2.  An update on bisphosphonates.

Authors:  Stanley B Cohen
Journal:  Curr Rheumatol Rep       Date:  2004-02       Impact factor: 4.592

Review 3.  The use of combination therapy in the treatment of postmenopausal osteoporosis.

Authors:  Juliet Compston
Journal:  Endocrine       Date:  2011-10-29       Impact factor: 3.633

Review 4.  Combination therapy for osteoporosis: considerations and controversy.

Authors:  Neil Binkley; Diane Krueger
Journal:  Curr Rheumatol Rep       Date:  2005-03       Impact factor: 4.592

Review 5.  Combination therapy for osteoporosis: considerations and controversy.

Authors:  Neil Binkley; Diane Krueger
Journal:  Curr Osteoporos Rep       Date:  2005-12       Impact factor: 5.096

6.  In vivo magnetic resonance detects rapid remodeling changes in the topology of the trabecular bone network after menopause and the protective effect of estradiol.

Authors:  Felix W Wehrli; Glenn A Ladinsky; Catherine Jones; Maria Benito; Jeremy Magland; Branimir Vasilic; Andra M Popescu; Babette Zemel; Andrew J Cucchiara; Alexander C Wright; Hee K Song; Punam K Saha; Helen Peachey; Peter J Snyder
Journal:  J Bone Miner Res       Date:  2008-05       Impact factor: 6.741

7.  H-tetracycline as a proxy for Ca for measuring dietary perturbations of bone resorption.

Authors:  Connie Weaver; Jennifer Cheong; George Jackson; David Elmore; George McCabe; Berdine Martin
Journal:  Nucl Instrum Methods Phys Res B       Date:  2007       Impact factor: 1.377

Review 8.  Atypical femoral fractures: a review of the literature.

Authors:  Pingal A Desai; Parth A Vyas; Joseph M Lane
Journal:  Curr Osteoporos Rep       Date:  2013-09       Impact factor: 5.096

Review 9.  Long-term tolerability of the bisphosphonates in postmenopausal osteoporosis: a comparative review.

Authors:  Raheem B Kherani; Alexandra Papaioannou; Jonathan D Adachi
Journal:  Drug Saf       Date:  2002       Impact factor: 5.606

10.  Daily and intermittent oral ibandronate normalize bone turnover and provide significant reduction in vertebral fracture risk: results from the BONE study.

Authors:  P D Delmas; R R Recker; C H Chesnut; A Skag; J A Stakkestad; R Emkey; J Gilbride; R C Schimmer; C Christiansen
Journal:  Osteoporos Int       Date:  2004-04-08       Impact factor: 4.507

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