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Calcification of Vascular Smooth Muscle Cells and Imaging of Aortic Calcification and Inflammation
Published on: May 31, 2016
Cardiovascular drugs and bone
1Department of Endocrinology and Metabolism C, Aarhus Sygehus, Aarhus, University Hospital, Aarhus, Denmark. rejnmark@post6.tele.dk
Insights
Many cardiovascular drugs appear safe for bone health, but some, like loop diuretics, may increase fracture risk. Further research is needed for definitive conclusions on certain medications.
Area of Science:
- Cardiology
- Geriatrics
- Bone Metabolism
Background:
- Cardiovascular diseases and osteoporosis are prevalent in the elderly.
- Understanding the bone effects of cardiovascular drugs is crucial for patient safety.
Purpose of the Study:
- To evaluate the impact of common cardiovascular medications on bone health.
- To identify potential risks or benefits associated with these treatments.
Main Methods:
- Review of existing studies, including randomized controlled trials (RCTs) and epidemiological research.
- Analysis of drug classes such as thiazide diuretics, statins, ACE-inhibitors, and others.
Main Results:
- Thiazide diuretics, statins, digoxin, ACE-inhibitors, and organic nitrates generally show no adverse bone effects and may improve bone strength.
- Loop diuretics are associated with increased parathyroid hormone and decreased bone mineral density in RCTs, and increased fracture risk in epidemiological studies.
- Amiodarone is linked to increased fracture risk in epidemiological studies.
- Conflicting results exist for oral anticoagulants, beta-blockers, and calcium channel blockers.
Conclusions:
- Most cardiovascular drugs appear safe for bone, but definitive fracture prevention recommendations cannot be made due to limited RCT data.
- Loop diuretics and amiodarone warrant caution due to potential negative bone effects and fracture risk.
- Further research is needed for definitive conclusions on anticoagulants, beta-blockers, and calcium channel blockers.
Abstract:
Cardiovascular diseases are common and occur mainly in the elderly in whom osteoporotic fractures also are very common. Because of this, it is of importance to establish whether drugs used in the treatment of cardiovascular diseases affect bone, in order to minimise any possible adverse effects. In the majority of studies, treatment with thiazide diuretics, statins, digoxin, angiotensin-converting enzyme (ACE)-inhibitors, and organic nitrates have not been associated with harmful effects on bone. On the contrary, treatment with these drugs may improve bone strength but because there is a lack of randomised controlled trials (RCTs) with fracture as a primary outcome measure, these drugs should not be prescribed for fracture prevention. In RCTs, treatment with loop diuretics have been shown to increase plasma levels of parathyroid hormone and decrease bone mineral density. In epidemiological studies, treatment with loop diuretics as well as treatment with amiodarone has been associated with an increased risk of fracture. In view of the conflicting results from published studies, no conclusions can be drawn on potential bone effects of treatment with oral anticoagulants, beta-blockers, and calcium channel blockers.
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