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Association of Beta Blocker Use With Bone Mineral Density in the Framingham Osteoporosis Study: A Cross‐Sectional Study
Some, but not all, prior observational studies have shown that beta blocker (BB) use is associated with lower fracture risk and higher bone mineral density (BMD). Rodent studies show the mechanism to involve the reduction in the effects of beta‐adrenergic signaling on bone remodeling. Because previo...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7507481/ https://www.ncbi.nlm.nih.gov/pubmed/32995691 http://dx.doi.org/10.1002/jbm4.10388 |
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author | Lary, Christine W Hinton, Alexandra C Nevola, Kathleen T Shireman, Theresa I Motyl, Katherine J Houseknecht, Karen L Lucas, F. Lee Hallen, Sarah Zullo, Andrew R Berry, Sarah D Kiel, Douglas P |
author_facet | Lary, Christine W Hinton, Alexandra C Nevola, Kathleen T Shireman, Theresa I Motyl, Katherine J Houseknecht, Karen L Lucas, F. Lee Hallen, Sarah Zullo, Andrew R Berry, Sarah D Kiel, Douglas P |
author_sort | Lary, Christine W |
collection | PubMed |
description | Some, but not all, prior observational studies have shown that beta blocker (BB) use is associated with lower fracture risk and higher bone mineral density (BMD). Rodent studies show the mechanism to involve the reduction in the effects of beta‐adrenergic signaling on bone remodeling. Because previous studies did not have detailed information on dose, duration, and beta‐1 selectivity, we examined these in a cross‐sectional analysis of the association between BB use and hip and spine BMD using DXA with the Offspring Cohort of the Framingham Heart Study. The sample size was n = 1520, and 397 individuals used BBs. We used propensity score modeling to balance a comprehensive set of covariates using inverse probability of treatment weighting (IPTW) to minimize bias due to treatment indication. We found significant differences in BMD between BB users and non‐users for three of four BMD measurements (femoral neck: 3.1%, 95% CI, 1.1% to 5.0%; total femur: 2.9%, 95% CI, 0.9% to 4.9%; femoral trochanter: 2.4%, 95% CI, −0.1% to 5.0%; and lumbar spine: 2.7%, 95% CI, 0.2% to 5.0%). Results were found to be similar between sexes although the magnitude of association was larger for women. Similar differences were estimated for beta‐1 selective and nonselective BBs compared with no BB use. We modeled dose in categories (no BB use, low‐dose, high‐dose) and as a continuous variable and found an increasing dose response that levels off at higher doses. Finally, associations were similar for short‐term versus long‐term (≤4 years versus >4 years) use. In summary, this large comprehensive study shows that BB use is associated with higher BMD in a dose‐related manner regardless of beta‐1 specificity and duration of use, which supports the conduct of a randomized clinical trial of BBs for achieving improvements in BMD for individuals at risk of bone loss with aging. © 2020 The Authors. JBMR Plus published by Wiley Periodicals LLC. on behalf of American Society for Bone and Mineral Research. |
format | Online Article Text |
id | pubmed-7507481 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75074812020-09-28 Association of Beta Blocker Use With Bone Mineral Density in the Framingham Osteoporosis Study: A Cross‐Sectional Study Lary, Christine W Hinton, Alexandra C Nevola, Kathleen T Shireman, Theresa I Motyl, Katherine J Houseknecht, Karen L Lucas, F. Lee Hallen, Sarah Zullo, Andrew R Berry, Sarah D Kiel, Douglas P JBMR Plus Original Articles Some, but not all, prior observational studies have shown that beta blocker (BB) use is associated with lower fracture risk and higher bone mineral density (BMD). Rodent studies show the mechanism to involve the reduction in the effects of beta‐adrenergic signaling on bone remodeling. Because previous studies did not have detailed information on dose, duration, and beta‐1 selectivity, we examined these in a cross‐sectional analysis of the association between BB use and hip and spine BMD using DXA with the Offspring Cohort of the Framingham Heart Study. The sample size was n = 1520, and 397 individuals used BBs. We used propensity score modeling to balance a comprehensive set of covariates using inverse probability of treatment weighting (IPTW) to minimize bias due to treatment indication. We found significant differences in BMD between BB users and non‐users for three of four BMD measurements (femoral neck: 3.1%, 95% CI, 1.1% to 5.0%; total femur: 2.9%, 95% CI, 0.9% to 4.9%; femoral trochanter: 2.4%, 95% CI, −0.1% to 5.0%; and lumbar spine: 2.7%, 95% CI, 0.2% to 5.0%). Results were found to be similar between sexes although the magnitude of association was larger for women. Similar differences were estimated for beta‐1 selective and nonselective BBs compared with no BB use. We modeled dose in categories (no BB use, low‐dose, high‐dose) and as a continuous variable and found an increasing dose response that levels off at higher doses. Finally, associations were similar for short‐term versus long‐term (≤4 years versus >4 years) use. In summary, this large comprehensive study shows that BB use is associated with higher BMD in a dose‐related manner regardless of beta‐1 specificity and duration of use, which supports the conduct of a randomized clinical trial of BBs for achieving improvements in BMD for individuals at risk of bone loss with aging. © 2020 The Authors. JBMR Plus published by Wiley Periodicals LLC. on behalf of American Society for Bone and Mineral Research. John Wiley & Sons, Inc. 2020-07-30 /pmc/articles/PMC7507481/ /pubmed/32995691 http://dx.doi.org/10.1002/jbm4.10388 Text en © 2020 The Authors. JBMR Plus published by Wiley Periodicals LLC. on behalf of American Society for Bone and Mineral Research. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Lary, Christine W Hinton, Alexandra C Nevola, Kathleen T Shireman, Theresa I Motyl, Katherine J Houseknecht, Karen L Lucas, F. Lee Hallen, Sarah Zullo, Andrew R Berry, Sarah D Kiel, Douglas P Association of Beta Blocker Use With Bone Mineral Density in the Framingham Osteoporosis Study: A Cross‐Sectional Study |
title | Association of Beta Blocker Use With Bone Mineral Density in the Framingham Osteoporosis Study: A Cross‐Sectional Study |
title_full | Association of Beta Blocker Use With Bone Mineral Density in the Framingham Osteoporosis Study: A Cross‐Sectional Study |
title_fullStr | Association of Beta Blocker Use With Bone Mineral Density in the Framingham Osteoporosis Study: A Cross‐Sectional Study |
title_full_unstemmed | Association of Beta Blocker Use With Bone Mineral Density in the Framingham Osteoporosis Study: A Cross‐Sectional Study |
title_short | Association of Beta Blocker Use With Bone Mineral Density in the Framingham Osteoporosis Study: A Cross‐Sectional Study |
title_sort | association of beta blocker use with bone mineral density in the framingham osteoporosis study: a cross‐sectional study |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7507481/ https://www.ncbi.nlm.nih.gov/pubmed/32995691 http://dx.doi.org/10.1002/jbm4.10388 |
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