Deep Medicine, Nuffield Department of Women's and Reproductive Health, University of Oxford, Hayes House 1F, George St., Oxford, OX1 2BQ, UK.
NIHR Oxford Biomedical Centre, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
Osteoporos Int. 2022 Feb;33(2):315-326. doi: 10.1007/s00198-021-06190-0. Epub 2021 Oct 13.
Blood pressure and bone metabolism appear to share commonalities in their physiologic regulation. Specific antihypertensive drug classes may also influence bone mineral density. However, current evidence from existing observational studies and randomised trials is insufficient to establish causal associations for blood pressure and use of blood pressure-lowering drugs with bone health outcomes, particularly with the risks of osteoporosis and fractures. The availability and access to relevant large-scale biomedical data sources as well as developments in study designs and analytical approaches provide opportunities to examine the nature of the association between blood pressure and bone health more reliably and in greater detail than has ever been possible. It is unlikely that a single source of data or study design can provide a definitive answer. However, with appropriate considerations of the strengths and limitations of the different data sources and analytical techniques, we should be able to advance our understanding of the role of raised blood pressure and its drug treatment on the risks of low bone mineral density and fractures. As elevated blood pressure is highly prevalent and blood pressure-lowering drugs are widely prescribed, even small effects of these exposures on bone health outcomes could be important at a population level.
血压和骨代谢在生理调节方面似乎有共同之处。特定的降压药物类别也可能影响骨密度。然而,现有观察性研究和随机试验的证据不足以确定血压和使用降压药物与骨骼健康结果之间的因果关系,特别是与骨质疏松症和骨折的风险之间的关系。相关大型生物医学数据源的可用性和可及性以及研究设计和分析方法的发展为更可靠、更详细地研究血压与骨骼健康之间的关系提供了机会,这是以前从未有过的。单一数据源或研究设计不太可能提供明确的答案。然而,通过适当考虑不同数据源和分析技术的优势和局限性,我们应该能够加深对高血压及其药物治疗对低骨密度和骨折风险的影响的理解。由于高血压的患病率很高,降压药物广泛应用,即使这些暴露对骨骼健康结果的影响很小,但从人群水平来看,也可能很重要。