Key result
Calcium supplements are linked to ~30% higher risk of myocardial infarction in randomized trials.
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Calcium supplements reduce bone turnover and slow the rate of bone loss. However, few studies have demonstrated reduced fracture incidence with calcium supplements, and meta-analyses show only a 10% decrease in fractures, which is of borderline statistical and clinical significance. Trials in normal older women and in patients with renal impairment suggest that calcium supplements increase the risk of cardiovascular disease. To further assess their safety, we recently conducted a meta-analysis of trials of calcium supplements, and found a 27%-31% increase in risk of myocardial infarction, and a 12%-20% increase in risk of stroke. These findings are robust because they are based on pre-specified analyses of randomized, placebo-controlled trials and are consistent across the trials. Co-administration of vitamin D with calcium does not lessen these adverse effects. The increased cardiovascular risk with calcium supplements is consistent with epidemiological data relating higher circulating calcium concentrations to cardiovascular disease in normal populations. There are several possible pathophysiological mechanisms for these effects, including effects on vascular calcification, vascular cells, blood coagulation and calcium-sensing receptors. Thus, the non-skeletal risks of calcium supplements appear to outweigh any skeletal benefits, and are they appear to be unnecessary for the efficacy of other osteoporosis treatments.
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Ian R. Reid (2013) conducted a review in Osteoporosis / Bone loss and cardiovascular disease risk. Calcium supplements vs. Placebo was evaluated on Myocardial infarction and stroke (27%-31% increase in risk of MI; 12%-20% increase in risk of stroke). Calcium supplements are associated with a 27%-31% increased risk of myocardial infarction and a 12%-20% increased risk of stroke in randomized placebo-controlled trials.
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