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Calcium Supplements and Risk of CVD: A Meta-Analysis of Randomized Trials
Xiqian Huo1,2, Robert Clarke2, Jim Halsey2
1National Clinical Research Center of Cardiovascular Diseases, State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Calcium supplements, alone or with vitamin D, do not appear to increase risks for cardiovascular disease (CVD) or all-cause mortality. Further research is needed for specific populations and fracture prevention.
Area of Science:
- Cardiovascular Health
- Nutritional Epidemiology
- Gerontology
Background:
- Vitamin D and calcium supplementation efficacy for fracture prevention is debated.
- Potential cardiovascular disease (CVD) risks associated with calcium supplements warrant investigation.
Purpose of the Study:
- To conduct a meta-analysis of placebo-controlled trials on calcium supplements (alone or with vitamin D) and their impact on cardiovascular events and mortality.
- To assess the safety of calcium and vitamin D supplementation regarding coronary heart disease (CHD), stroke, and all-cause mortality.
Main Methods:
- A meta-analysis of 11 randomized controlled trials was performed.
- Included 7 comparisons of calcium alone and 6 of calcium plus vitamin D versus placebo.
- Analyzed aggregated study-level data for myocardial infarction (MI), CHD death, any CHD, stroke, and all-cause mortality.
Main Results:
- Calcium alone was not significantly associated with increased risk of MI, CHD death, any CHD, or stroke.
- Calcium plus vitamin D also showed no significant association with excess risk for these cardiovascular outcomes.
- Neither calcium alone nor combined with vitamin D demonstrated significant associations with all-cause mortality.
Conclusions:
- Calcium supplements, individually or combined with vitamin D, do not pose a significant hazard for CHD, stroke, or all-cause mortality.
- The study excluded excess risks above 0.3%-0.5% per year for CHD or stroke.
- Further trials are recommended for individuals with low 25(OH)D levels to evaluate fracture prevention and other outcomes.
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