Cited by 260Bone health and osteoporosis researchPharmaceutical Practices and Patient OutcomesBone Metabolism and Diseases

β-Adrenergic Blockers Reduce the Risk of Fracture Partly by Increasing Bone Mineral Density: Geelong Osteoporosis Study

Pasco, Julie A, Henry, Margaret J, Sanders, Kerrie M, Kotowicz, Mark A, Seeman, Ego, Nicholson, Geoffrey C·2004·Journal of Bone and Mineral Research

Abstract

Unlabelled This population-based study documented beta-blocker use in 59/569 cases with incident fracture and 112/775 controls. OR for fracture associated with beta-blocker use was 0.68 (95%CI, 0.49-0.96). Beta-blockers were associated with higher BMD at the total hip (2.5%) and UD forearm (3.6%) after adjusting for age, anthropometry, and thiazide use. Beta-blocker use is associated with reduced fracture risk and higher BMD. Introduction Animal data suggests that bone formation is under beta-adrenergic control and that beta-blockers stimulate bone formation and/or inhibit bone resorption. Materials and methods We evaluated the association between beta-blocker use, bone mineral density (BMD), and fracture risk in a population-based study in Geelong, a southeastern Australian city with a single teaching hospital and two radiological centers providing complete fracture ascertainment for the region. Beta-blocker use was documented for 569 women with radiologically confirmed incident fractures and 775 controls without incident fracture. Medication use and lifestyle factors were documented by questionnaire. Results Odds ratio for fracture associated with beta-blocker use was 0.68 (95% CI, 0.49-0.96) for any fracture. Adjusting for age, weight, medications, and lifestyle factors had little effect on the odds ratio. Beta-blocker use was associated with a higher BMD at the total hip (2.5%, p = 0.03) and ultradistal forearm (3.6%, p = 0.04) after adjustment for age, anthropometry, and…

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Crossref · 10.1359/jbmr.0301214

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  • A type I collagen α1 first-intron polymorphism and high homocysteine can affect fracture risk independently of BMD.

    “A polymorphism of the first intron of the gene coding for the type I collagen α1 chain and increased levels of homocysteine can influence fracture risk independent of BMD”

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Authors
Pasco, J. A., Henry, M. J., Sanders, K. M., Kotowicz, M. A., Seeman, E., & Nicholson, G. C.
Affiliations
  • Barwon Health (AU)
  • The University of Melbourne (AU)
Corresponding author
Pasco, Julie A
Venue
Journal of Bone and Mineral Research
Published
2004-01-01
Volume
19
Issue
1
Pages
19-24
ISSN
  • 0884-0431 (ISSN-L)
  • 1523-4681
OpenAlex
W2046396082
Cited by
260
References
3
Citations by year
2026: 7 · 2025: 5 · 2024: 7 · 2023: 10 · 2022: 4 · 2021: 9 · 2020: 8 · 2019: 6 · 2018: 8 · 2017: 9 · 2016: 2 · 2015: 11 · 2014: 15 · 2013: 13 · 2012: 12
FWCI
21.93
Type
journal article
Language
en
Open access
closed
Locations
  • Journal of Bone and Mineral Research (publishedVersion)
  • PubMed (publishedVersion)
Funders
Geelong Region Medical Research Foundation
Topics
  • Health Sciences › Medicine › Orthopedics and Sports Medicine › Bone health and osteoporosis research
  • Health Sciences › Medicine › Geriatrics and Gerontology › Pharmaceutical Practices and Patient Outcomes
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bone Metabolism and Diseases
Keywords
beta-blockers, fracture risk, bone mineral density, osteoporosis, hip bone density, forearm bone mineral density, thiazide diuretics, women, Geelong Osteoporosis Study
MeSH terms
Adrenergic beta-Antagonists, Aged, Anthropometry, Bones of Upper Extremity, Australia, Bone and Bones, Cardiovascular Diseases, Female, Femur, Femur Neck, Humans, Lumbar Vertebrae, Middle Aged, Surveys and Questionnaires, Regression Analysis, Bone Density, Odds Ratio, Case-Control Studies, Fractures, Bone

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