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Predictors of teriparatide treatment failure in patients with low bone mass
INTRODUCTION: While teriparatide is the only skeletal anabolic agent approved in the United States, treatment failure is a major concern which complicates its clinical utility. We sought to identify factors that predict response failure in patients with low bone mass. METHOD: We performed a retrospe...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4926837/ https://www.ncbi.nlm.nih.gov/pubmed/28326338 http://dx.doi.org/10.1016/j.bonr.2015.11.001 |
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author | Elraiyah, Tarig Ahmed, Adil H. Wang, Zhen Farr, Joshua N. Murad, Mohammad H. Drake, Matthew T. |
author_facet | Elraiyah, Tarig Ahmed, Adil H. Wang, Zhen Farr, Joshua N. Murad, Mohammad H. Drake, Matthew T. |
author_sort | Elraiyah, Tarig |
collection | PubMed |
description | INTRODUCTION: While teriparatide is the only skeletal anabolic agent approved in the United States, treatment failure is a major concern which complicates its clinical utility. We sought to identify factors that predict response failure in patients with low bone mass. METHOD: We performed a retrospective study of adults with osteopenia or osteoporosis (T-scores < − 1.0 and − 2.5 SD below normal, respectively, at the total hip or lumbar spine) treated with teriparatide at the Mayo Clinic (Rochester, Minnesota) between November 2002–December 2012. Trained study investigators blinded to patient outcomes collected electronic medical record data. Potential response failure predictors were identified using univariate analysis. Multivariable logistic regression modeling was used to identify independent predictors of treatment failure based on either osteoporotic fragility fracture or BMD response. RESULTS: During the 10-year period, 494 patients received teriparatide treatment and met eligibility criteria. Thirty-five patients had osteoporotic fractures, while 172 did not achieve a ≥ 3% BMD increase. Among predictors as defined by BMD change, both prior bisphosphonate treatment [odds ratio (95% confidence interval), 1.50 (1.01–2.24)] and vitamin D therapy [1.50 (1.01–2.22)] were significantly (P < 0.05) associated with teriparatide treatment failure. By contrast, no predictors were associated with treatment failure when fracture was the endpoint. CONCLUSION: These data suggest that prior bisphosphonate or vitamin D exposure may predict response failure to teriparatide therapy. Although these findings may, in part, reflect increased severity or longer duration of disease, this knowledge should help guide clinicians and patients when therapy choices are made. |
format | Online Article Text |
id | pubmed-4926837 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-49268372017-03-21 Predictors of teriparatide treatment failure in patients with low bone mass Elraiyah, Tarig Ahmed, Adil H. Wang, Zhen Farr, Joshua N. Murad, Mohammad H. Drake, Matthew T. Bone Rep Article INTRODUCTION: While teriparatide is the only skeletal anabolic agent approved in the United States, treatment failure is a major concern which complicates its clinical utility. We sought to identify factors that predict response failure in patients with low bone mass. METHOD: We performed a retrospective study of adults with osteopenia or osteoporosis (T-scores < − 1.0 and − 2.5 SD below normal, respectively, at the total hip or lumbar spine) treated with teriparatide at the Mayo Clinic (Rochester, Minnesota) between November 2002–December 2012. Trained study investigators blinded to patient outcomes collected electronic medical record data. Potential response failure predictors were identified using univariate analysis. Multivariable logistic regression modeling was used to identify independent predictors of treatment failure based on either osteoporotic fragility fracture or BMD response. RESULTS: During the 10-year period, 494 patients received teriparatide treatment and met eligibility criteria. Thirty-five patients had osteoporotic fractures, while 172 did not achieve a ≥ 3% BMD increase. Among predictors as defined by BMD change, both prior bisphosphonate treatment [odds ratio (95% confidence interval), 1.50 (1.01–2.24)] and vitamin D therapy [1.50 (1.01–2.22)] were significantly (P < 0.05) associated with teriparatide treatment failure. By contrast, no predictors were associated with treatment failure when fracture was the endpoint. CONCLUSION: These data suggest that prior bisphosphonate or vitamin D exposure may predict response failure to teriparatide therapy. Although these findings may, in part, reflect increased severity or longer duration of disease, this knowledge should help guide clinicians and patients when therapy choices are made. Elsevier 2015-11-17 /pmc/articles/PMC4926837/ /pubmed/28326338 http://dx.doi.org/10.1016/j.bonr.2015.11.001 Text en © 2015 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Elraiyah, Tarig Ahmed, Adil H. Wang, Zhen Farr, Joshua N. Murad, Mohammad H. Drake, Matthew T. Predictors of teriparatide treatment failure in patients with low bone mass |
title | Predictors of teriparatide treatment failure in patients with low bone mass |
title_full | Predictors of teriparatide treatment failure in patients with low bone mass |
title_fullStr | Predictors of teriparatide treatment failure in patients with low bone mass |
title_full_unstemmed | Predictors of teriparatide treatment failure in patients with low bone mass |
title_short | Predictors of teriparatide treatment failure in patients with low bone mass |
title_sort | predictors of teriparatide treatment failure in patients with low bone mass |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4926837/ https://www.ncbi.nlm.nih.gov/pubmed/28326338 http://dx.doi.org/10.1016/j.bonr.2015.11.001 |
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