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Vertebral fracture risk after once-weekly teriparatide injections: follow-up study of Teriparatide Once-Weekly Efficacy Research (TOWER) trial
- Source :
- Current medical research and opinion. 29(3)
- Publication Year :
- 2012
-
Abstract
- To evaluate fracture risk and bone mineral density (BMD) in patients with primary osteoporosis, 1 year after completing 72 weeks of weekly teriparatide injections.After 72 weeks of teriparatide injections or placebo (original trial), treatment was unblinded and subjects were subsequently treated with bisphosphonates or other therapeutic regimens at the discretion of their physicians and followed for 1 year. Spine radiographs and BMD measurements at the lumbar spine, femoral neck, and total hip by dual energy X-ray absorptiometry were performed.Incident vertebral fracture rate.A total of 465 patients were enrolled and 447 (96.1%) completed the study. In the 1 year follow-up period, new morphometric vertebral fractures occurred in 7/203 (3.4%) in the post-teriparatide group and 33/241 (13.7%) in the post-placebo group (relative risk [RR]: 0.23, 95% confidence interval [CI]: 0.10 to 0.52, P 0.05). The cumulative incidences from the start of the original trial were 4.9% and 22.8%, respectively (RR: 0.18, 95% CI: 0.09 to 0.36, P 0.05). There were no significant differences in incidences of vertebral fractures between subsequent therapeutic regimens in the post-teriparatide group. In subjects treated with bisphosphonates, mean BMD values further significantly increased by 9.6%, 2.9%, and 4.1% at the lumbar spine, femoral neck, and total hip, respectively (P 0.05).The reduced risk of vertebral fracture was sustained for 1 year after completion of 72 weeks of weekly teriparatide injections. The effects did not differ between subsequent therapeutic regimens. BMD gains continued with sequential bisphosphonate treatment, but not with the other sequential therapeutic regimens. Bisphosphonates seem to be a useful choice as a subsequent treatment to weekly teriparatide.This study was an observational follow-up study and the regimens of subsequent medication after discontinuation of the original TOWER trial were not randomly allocated.
- Subjects :
- Male
Risk
medicine.medical_specialty
Placebo
law.invention
Placebos
Fractures, Bone
Randomized controlled trial
law
Bone Density
Teriparatide
medicine
Humans
Risk factor
Vitamin D
Femoral neck
Aged
Aged, 80 and over
Hip
Bone Density Conservation Agents
Diphosphonates
business.industry
General Medicine
Confidence interval
Spine
Surgery
Clinical trial
medicine.anatomical_structure
Spinal Injuries
Relative risk
Dietary Supplements
Osteoporosis
Spinal Fractures
Calcium
Female
business
medicine.drug
Follow-Up Studies
Subjects
Details
- ISSN :
- 14734877
- Volume :
- 29
- Issue :
- 3
- Database :
- OpenAIRE
- Journal :
- Current medical research and opinion
- Accession number :
- edsair.doi.dedup.....436f1c12e92fab3b4a6c8f7ba3354d74