A randomized double-blind trial to compare the efficacy of teriparatide [recombinant human parathyroid hormone (1-34)] with alendronate in postmenopausal women with osteoporosis
Autor: | Anthony B. Hodsman, Paul D. Miller, Ricardo Correa-Rotter, Jean-Jacques Body, Anne Peretz, Wim H. Scheele, Robin K. Dore, David C. Cumming, Gregory A Gaich, Pandurang M. Kulkarni, Alexandra Papaioannou |
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Rok vydání: | 2002 |
Předmět: |
musculoskeletal diseases
Adult medicine.medical_specialty Bone disease Endocrinology Diabetes and Metabolism Clinical Biochemistry Osteoporosis Biochemistry Bone resorption Bone and Bones Collagen Type I Bone remodeling Fractures Bone Endocrinology Calcitriol Double-Blind Method Bone Density Internal medicine Teriparatide medicine Humans Bone Resorption Osteoporosis Postmenopausal Aged Bone mineral Aged 80 and over Alendronate business.industry Alendronic acid Biochemistry (medical) Middle Aged medicine.disease Alkaline Phosphatase Body Height Alendronate Sodium Female Bone Remodeling Collagen business Peptides Biomarkers medicine.drug |
Zdroj: | The Journal of clinical endocrinology and metabolism. 87(10) |
ISSN: | 0021-972X |
Popis: | Teriparatide (rDNA origin) injection [recombinant human PTH (1–34)] stimulates bone formation, increases bone mineral density (BMD), and restores bone architecture and integrity. In contrast, bisphosphonates reduce bone resorption and increase BMD. We compared the effects of teriparatide and alendronate sodium on BMD, nonvertebral fracture incidence, and bone turnover in 146 postmenopausal women with osteoporosis. Women were randomized to either once-daily sc injections of teriparatide 40 μg plus oral placebo (n = 73) or oral alendronate 10 mg plus placebo injection (n = 73). Median duration of treatment was 14 months. At 3 months, teriparatide increased lumbar spine BMD significantly more than did alendronate (P < 0.001). Lumbar spine-BMD increased by 12.2% in the teriparatide group and 5.6% in the alendronate group (P < 0.001 teriparatide vs. alendronate). Teriparatide increased femoral neck BMD and total body bone mineral significantly more than did alendronate, but BMD at the one third distal radius decreased, compared with alendronate (P ≤ 0.05). Nonvertebral fracture incidence was significantly lower in the teriparatide group than in the alendronate group (P < 0.05). Both treatments were well tolerated despite transient mild asymptomatic hypercalcemia with teriparatide treatment. In conclusion, teriparatide, a bone formation agent, increased BMD at most sites and decreased nonvertebral fractures more than alendronate. |
Databáze: | OpenAIRE |
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