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Effect of atorvastatin on bone mineral density in patients with acute coronary syndrome
J L Pérez-Castrillón1, L Abad, G Vega
1Department of Medicine, Rio Hortega University Hospital, Valladolid, Spain. castrv@terra.es
Insights
Atorvastatin improves bone mineral density in patients with acute ischemic heart disease, particularly in males with sufficient vitamin D levels. This cholesterol-lowering drug also boosts vitamin D levels, reducing insufficiency.
Area of Science:
- Cardiology
- Endocrinology
- Metabolic Bone Disease
Background:
- Acute ischemic heart disease (AIHD) patients often have comorbidities affecting bone health.
- Statins, like atorvastatin, are primarily used for cholesterol management but may have pleiotropic effects.
Purpose of the Study:
- To investigate the impact of atorvastatin on bone mineral density (BMD) in patients with AIHD.
- To assess atorvastatin's effect on vitamin D levels and bone metabolism markers.
Main Methods:
- Eighty-three patients with acute coronary syndrome received low-dose (20 mg) or high-dose (40-80 mg) atorvastatin.
- Bone mineral density (spine and hip) and serum levels of cholesterol, triglycerides, calcium, phosphorus, and 25-hydroxyvitamin D were measured at baseline and after one year.
Main Results:
- Atorvastatin significantly increased vitamin D levels by 33% (p = 0.007), reducing vitamin D insufficiency.
- Spine bone mineral density increased by 1.31% (p = 0.02), with significance noted in males and patients with baseline vitamin D > 30 nmol/l.
Conclusions:
- Atorvastatin demonstrates a beneficial effect on bone metabolism in AIHD patients, primarily by increasing BMD.
- The positive effect on bone mineral density is more pronounced in males and contingent upon adequate baseline vitamin D levels (> 30 nmol/l).
Objective:
The aim of this paper is to evaluate the effect of atorvastatin on bone mineral density in patients with acute ischemic heart disease.
Material And Methods:
Eighty-three patients (52 male and 31 female) with acute coronary syndrome were studied. They received treatment with atorvastatin using low doses (20 mg) and high doses (40 mg-80 mg). Initial and final cholesterol, triglyceride, calcium, phosphorus, 25-hydroxyvitamin D were obtained from every patient. Spine and hip bone mineral density were performed at the beginning and one year later.
Results:
Atorvastatin treatment increases vitamin D (33%, p = 0.007) and decreases the individuals with vitamin D insufficiency. Bone mineral density increased in the spine (1.31%, p = 0.02), but it was significant only in male and patients presenting vitamin D levels higher than 30 nmol/l.
Conclusion:
Atorvastatin has a beneficial effect on bone metabolism in patients with acute ischemic heart disease (mainly males) by incrementing bone mineral density in which vitamin D levels are required to be higher than 30 nmol/l for the drug to be effective.
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