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Does sufficient evidence exist to support a causal association between vitamin D status and cardiovascular disease
Patricia G Weyland1, William B Grant2, Jill Howie-Esquivel3
1Department of Physiological Nursing, School of Nursing, University of California, San Francisco (UCSF), #2 Koret Way Box 0610, San Francisco, CA 94143, USA. patricia.weyland@ucsf.edu.
Insights
Low vitamin D levels (25-hydroxyvitamin D) are causally linked to increased cardiovascular disease (CVD) risk factors. Evidence supports vitamin D deficiency as a significant risk factor for heart disease.
Area of Science:
- Endocrinology
- Cardiology
- Nutritional Science
Background:
- Serum 25-hydroxyvitamin D (25(OH)D) levels are inversely associated with cardiovascular disease (CVD) risk factors.
- These risk factors include dyslipidemia, hypertension, and diabetes mellitus.
Purpose of the Study:
- To review evidence for a causal association between low 25(OH)D levels and increased CVD risk.
- To evaluate existing studies using Hill's criteria for causality.
Main Methods:
- Systematic review of journal articles.
- Evaluation of studies based on Hill's criteria (strength, consistency, temporality, biological gradient, plausibility, experimental evidence, analogy).
Main Results:
- Numerous studies demonstrate a statistically significant inverse association between 25(OH)D levels and CVD risk factors.
- A consistent, dose-response relationship was observed across diverse populations.
- Plausible biological mechanisms link low 25(OH)D to CVD, mediated by factors like dyslipidemia and hypertension.
Conclusions:
- All relevant Hill criteria for causality are met.
- Low serum 25(OH)D levels are indicated as a causal risk factor for cardiovascular disease.
Unlabelled:
Serum 25-hydroxyvitamin D (25(OH)D) levels have been found to be inversely associated with both prevalent and incident cardiovascular disease (CVD) risk factors; dyslipidemia, hypertension and diabetes mellitus. This review looks for evidence of a causal association between low 25(OH)D levels and increased CVD risk. We evaluated journal articles in light of Hill's criteria for causality in a biological system. The results of our assessment are as follows. Strength of association: many randomized controlled trials (RCTs), prospective and cross-sectional studies found statistically significant inverse associations between 25(OH)D levels and CVD risk factors. Consistency of observed association: most studies found statistically significant inverse associations between 25(OH)D levels and CVD risk factors in various populations, locations and circumstances. Temporality of association: many RCTs and prospective studies found statistically significant inverse associations between 25(OH)D levels and CVD risk factors. Biological gradient (dose-response curve): most studies assessing 25(OH)D levels and CVD risk found an inverse association exhibiting a linear biological gradient. Plausibility of biology: several plausible cellular-level causative mechanisms and biological pathways may lead from a low 25(OH)D level to increased risk for CVD with mediators, such as dyslipidemia, hypertension and diabetes mellitus. Experimental evidence: some well-designed RCTs found increased CVD risk factors with decreasing 25(OH)D levels. Analogy: the association between serum 25(OH)D levels and CVD risk is analogous to that between 25(OH)D levels and the risk of overall cancer, periodontal disease, multiple sclerosis and breast cancer.
Conclusion:
all relevant Hill criteria for a causal association in a biological system are satisfied to indicate a low 25(OH)D level as a CVD risk factor.
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