At Least One Cyclic Teriparatide Administration Can Be Helpful to Delay Initial Onset of a New Osteoporotic Vertebral Compression Fracture
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Purpose: Teriparatide markedly increases bone formation and strength, while reducingthe incidence of new-onset osteoporotic vertebral compression fractures (OVCFs). In some countries, expenses for teriparatide use are covered by medical insurance for up to 6 months; however, the national medical insurance of the authors’country does not cover these expenses. This retrospective cohort study comparedthe therapeutic effects of teriparatide on the initial onset of a new OVCF aftertreatment of osteoporosis and/or related OVCFs with regard to therapeutic durations of longer than 3 months (LT3M) or shorter than 3 months (ST3M). Materialsand Methods: From May 2007 to February 2012, 404 patients who were prescribed and administered teriparatide and who could be followed-up for longer than 12 months were enrolled. They were divided into two groups depending on teriparatide duration: LT3M (n=132) and ST3M (n=272). Results: The group with the teriparatide duration of LT3M showed significantly less development of an initialOVCF within 1 year (p=0.004, chi-square). Duration of teriparatide use, body mass index, pre-teriparatide lowest spinal bone mineral density, and severity of osteoporosissignificantly affected multiple regression analysis results (p<0.05). Survivalanalysis of first new-onset OVCFs demonstrated a significantly better survivalrate for the LT3M group (log rank, p=0.005). Also, the ST3M group showed a higher odds ratio of 54.00 for development of an initial OVCF during follow-up than the LT3M group (Mantel-Haenzel common odds ratio, p=0.006). Conclusion: At least one cyclic teriparatide administration is recommended to provide a protectiveeffect against the initial onset of a new OVCF for up to one year after therapy.
Abstract
Purpose: Teriparatide markedly increases bone formation and strength, while reducingthe incidence of new-onset osteoporotic vertebral compression fractures (OVCFs). In some countries, expenses for teriparatide use are covered by medical insurance for up to 6 months; however, the national medical insurance of the authors’country does not cover these expenses. This retrospective cohort study comparedthe therapeutic effects of teriparatide on the initial onset of a new OVCF aftertreatment of osteoporosis and/or related OVCFs with regard to therapeutic durations of longer than 3 months (LT3M) or shorter than 3 months (ST3M). Materialsand Methods: From May 2007 to February 2012, 404 patients who were prescribed and administered teriparatide and who could be followed-up for longer than 12 months were enrolled. They were divided into two groups depending on teriparatide duration: LT3M (n=132) and ST3M (n=272). Results: The group with the teriparatide duration of LT3M showed significantly less development of an initialOVCF within 1 year (p=0.004, chi-square). Duration of teriparatide use, body mass index, pre-teriparatide lowest spinal bone mineral density, and severity of osteoporosissignificantly affected multiple regression analysis results (p<0.05). Survivalanalysis of first new-onset OVCFs demonstrated a significantly better survivalrate for the LT3M group (log rank, p=0.005). Also, the ST3M group showed a higher odds ratio of 54.00 for development of an initial OVCF during follow-up than the LT3M group (Mantel-Haenzel common odds ratio, p=0.006). Conclusion: At least one cyclic teriparatide administration is recommended to provide a protectiveeffect against the initial onset of a new OVCF for up to one year after therapy.
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