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Fracture risk reduction during treatment with teriparatide is independent of pretreatment bone turnover.
Bone. 2006 Aug; 39(2):237-43.BONE

Abstract

INTRODUCTION

Teriparatide is a bone formation agent that increases bone turnover and mass, resulting in an increase in bone strength and a decrease in fracture risk.

METHODS

The primary purpose of this analysis was to evaluate the association between pretreatment bone turnover marker (BTM) concentrations and the absolute and relative fracture risks after adjusting for baseline femoral neck BMD, number of prevalent vertebral fractures, and age. Because femoral neck BMD is commonly attained in the assessment of patients at risk for osteoporosis, we examined the ability of a multivariate assessment including pretreatment BTM concentration and femoral neck BMD to predict future fracture risk after adjusting for the number of prevalent vertebral fractures. We examined data from the Fracture Prevention Trial, a study designed to determine the effect of teriparatide 20 mcg/day and teriparatide 40 mcg/day on vertebral and nonvertebral fracture risk in postmenopausal women with osteoporosis. BTM were analyzed in two subsets of women within the Fracture Prevention Trial, and included serum bone-specific alkaline phosphatase (BSAP), serum carboxy-terminal extension peptide of procollagen type I (PICP), serum amino-terminal extension peptide of procollagen type I (PINP), urinary free deoxypyridinoline (DPD), and urinary N-terminal telopeptide (NTX).

RESULTS

Teriparatide significantly reduced the risk of fracture [four BTM subset (n = 520), placebo = 14.3%, teriparatide = 5.8%, P < 0.05; PINP subset (n = 771), placebo = 17.7%, teriparatide = 5.5%, P < 0.05]. Subjects with the highest pretreatment BTM concentrations had the greatest fracture risk. Teriparatide-mediated absolute risk reduction was greatest for women with high pretreatment bone turnover; however, the relative fracture risk reduction was independent of pretreatment bone turnover. After adjusting for pretreatment BTM and number of prevalent vertebral fractures, baseline femoral neck BMD was not a significant predictor of fracture risk.

CONCLUSION

Teriparatide-mediated relative fracture risk reduction was independent of pretreatment bone turnover, demonstrating that this therapy offers clinical benefit to patients across a range of disease severity.

Authors+Show Affiliations

INSERM Research Unit 403, Claude Bernard University of Lyon, Lyon, France. delmas@lyon.inserm.frNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Clinical Trial
Journal Article
Randomized Controlled Trial
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

16563890

Citation

Delmas, P D., et al. "Fracture Risk Reduction During Treatment With Teriparatide Is Independent of Pretreatment Bone Turnover." Bone, vol. 39, no. 2, 2006, pp. 237-43.
Delmas PD, Licata AA, Reginster JY, et al. Fracture risk reduction during treatment with teriparatide is independent of pretreatment bone turnover. Bone. 2006;39(2):237-43.
Delmas, P. D., Licata, A. A., Reginster, J. Y., Crans, G. G., Chen, P., Misurski, D. A., Wagman, R. B., & Mitlak, B. H. (2006). Fracture risk reduction during treatment with teriparatide is independent of pretreatment bone turnover. Bone, 39(2), 237-43.
Delmas PD, et al. Fracture Risk Reduction During Treatment With Teriparatide Is Independent of Pretreatment Bone Turnover. Bone. 2006;39(2):237-43. PubMed PMID: 16563890.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Fracture risk reduction during treatment with teriparatide is independent of pretreatment bone turnover. AU - Delmas,P D, AU - Licata,A A, AU - Reginster,J Y, AU - Crans,G G, AU - Chen,P, AU - Misurski,D A, AU - Wagman,R B, AU - Mitlak,B H, Y1 - 2006/03/24/ PY - 2005/08/24/received PY - 2005/11/02/revised PY - 2006/02/01/accepted PY - 2006/3/28/pubmed PY - 2006/8/26/medline PY - 2006/3/28/entrez SP - 237 EP - 43 JF - Bone JO - Bone VL - 39 IS - 2 N2 - INTRODUCTION: Teriparatide is a bone formation agent that increases bone turnover and mass, resulting in an increase in bone strength and a decrease in fracture risk. METHODS: The primary purpose of this analysis was to evaluate the association between pretreatment bone turnover marker (BTM) concentrations and the absolute and relative fracture risks after adjusting for baseline femoral neck BMD, number of prevalent vertebral fractures, and age. Because femoral neck BMD is commonly attained in the assessment of patients at risk for osteoporosis, we examined the ability of a multivariate assessment including pretreatment BTM concentration and femoral neck BMD to predict future fracture risk after adjusting for the number of prevalent vertebral fractures. We examined data from the Fracture Prevention Trial, a study designed to determine the effect of teriparatide 20 mcg/day and teriparatide 40 mcg/day on vertebral and nonvertebral fracture risk in postmenopausal women with osteoporosis. BTM were analyzed in two subsets of women within the Fracture Prevention Trial, and included serum bone-specific alkaline phosphatase (BSAP), serum carboxy-terminal extension peptide of procollagen type I (PICP), serum amino-terminal extension peptide of procollagen type I (PINP), urinary free deoxypyridinoline (DPD), and urinary N-terminal telopeptide (NTX). RESULTS: Teriparatide significantly reduced the risk of fracture [four BTM subset (n = 520), placebo = 14.3%, teriparatide = 5.8%, P < 0.05; PINP subset (n = 771), placebo = 17.7%, teriparatide = 5.5%, P < 0.05]. Subjects with the highest pretreatment BTM concentrations had the greatest fracture risk. Teriparatide-mediated absolute risk reduction was greatest for women with high pretreatment bone turnover; however, the relative fracture risk reduction was independent of pretreatment bone turnover. After adjusting for pretreatment BTM and number of prevalent vertebral fractures, baseline femoral neck BMD was not a significant predictor of fracture risk. CONCLUSION: Teriparatide-mediated relative fracture risk reduction was independent of pretreatment bone turnover, demonstrating that this therapy offers clinical benefit to patients across a range of disease severity. SN - 8756-3282 UR - https://www.unboundmedicine.com/medline/citation/16563890/Fracture_risk_reduction_during_treatment_with_teriparatide_is_independent_of_pretreatment_bone_turnover_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S8756-3282(06)00260-2 DB - PRIME DP - Unbound Medicine ER -