Parathyroid Hormone(1–84) Treatment of Postmenopausal Women with Low Bone Mass Receiving Hormone Replacement Therapy
Autor: | Ignac Fogelman, J. Fox, Claus Christiansen, J. N. Fordham, William D. Fraser, S. A. Morris, Tim D. Spector |
---|---|
Rok vydání: | 2008 |
Předmět: |
musculoskeletal diseases
medicine.medical_specialty Endocrinology Diabetes and Metabolism medicine.medical_treatment Osteoporosis Parathyroid hormone Placebo Bone remodeling Endocrinology Bone Density Internal medicine medicine Humans Orthopedics and Sports Medicine Hypercalciuria Osteoporosis Postmenopausal Femoral neck Bone mineral Lumbar Vertebrae Femur Neck business.industry Estrogen Replacement Therapy Estrogens Hormone replacement therapy (menopause) Middle Aged medicine.disease Radiography medicine.anatomical_structure Parathyroid Hormone Spinal Fractures Drug Therapy Combination Female Bone Remodeling Progestins business |
Zdroj: | Calcified Tissue International. 83:85-92 |
ISSN: | 1432-0827 0171-967X |
Popis: | Treatment of postmenopausal osteoporosis (PMO) is based primarily on antiresorptive agents, including hormone replacement therapy (HT). To evaluate whether anabolic therapy together with HT provides additional benefits in the treatment of PMO, we evaluated the effects of parathyroid hormone (PTH) 1-84 in postmenopausal women with low bone mineral density (BMD) who were receiving chronic (> or =6 months) HT. Subjects were randomized to receive 100 microg PTH(1-84) or placebo injections daily for 24 months (n = 90/group). The primary efficacy outcome was change from baseline in lumbar spine BMD. Secondary end points included changes in hip and distal radius BMD, bone turnover markers, and fracture incidence. The study was terminated early following recommendations regarding HT for PMO. At 18 months, the mean increase in lumbar spine BMD was 7.9% for PTH(1-84) subjects vs. 1.5% for those receiving HT alone; between-group differences were significant at 6 months and persisted throughout the study. Lumbar spine BMD increased in 94% of women receiving PTH(1-84) compared to 59% for HT alone. Femoral neck BMD and bone turnover markers were significantly higher in PTH(1-84)-treated subjects, but the changes in total hip and distal radius BMD were not significant. PTH(1-84) treatment was generally well-tolerated, with hypercalciuria, hypercalcemia, nausea, vomiting, and dizziness reported more frequently in the HT + PTH(1-84) group. In conclusion, addition of PTH(1-84) to stable HT produced marked increases in lumbar spine BMD and may represent an additional approach to the treatment of PMO women receiving HT. |
Databáze: | OpenAIRE |
Externí odkaz: |