Vitamin D Supplementation, Serum 25(OH)D Concentrations and Cardiovascular Disease Risk Factors: A Systematic Review
Naghmeh Mirhosseini1, Jacqueline Rainsbury2, Samantha M Kimball1,3
1Pure North S'Energy Foundation, Calgary, AB, Canada.
Insights
Vitamin D supplementation significantly improves cardiovascular disease risk factors, including blood pressure, cholesterol, and inflammation markers. This meta-analysis of RCTs suggests a protective role for vitamin D in cardiovascular health.
Area of Science:
- Endocrinology
- Cardiovascular Medicine
- Nutritional Science
Background:
- Observational studies link low 25-hydroxyvitamin D (25(OH)D) to cardiovascular disease (CVD) risk factors.
- Clinical trial results on vitamin D supplementation and CVD risk factors are inconsistent.
- This study addresses the need for a comprehensive analysis of existing randomized controlled trials (RCTs).
Purpose of the Study:
- To systematically review and meta-analyze RCTs evaluating vitamin D supplementation's effect on CVD risk factors.
- To assess the impact of increased serum 25(OH)D concentrations on cardiovascular health markers.
- To synthesize evidence on vitamin D's efficacy in managing blood pressure, lipid profiles, and inflammatory markers.
Main Methods:
- Systematic search of MEDLINE, CINAHL, EMBASE, and Google Scholar for RCTs (1992-2017).
- Meta-analysis using a random-effects model and inverse variance method to calculate standardized mean differences (SMD).
- Sensitivity analyses and publication bias assessments were performed.
Main Results:
- Vitamin D supplementation significantly reduced systolic and diastolic blood pressure.
- Significant reductions observed in parathyroid hormone (PTH), hs-CRP, total cholesterol, LDL, and triglycerides.
- A significant increase in HDL was noted; however, no significant effects on PWV or AI were found.
Conclusions:
- Vitamin D supplementation demonstrates a beneficial effect on key cardiovascular risk factors.
- Findings suggest vitamin D may protect against CVD by improving blood pressure, lipid profiles, PTH levels, and inflammation.
- Further research may clarify optimal vitamin D dosing for cardiovascular benefits.
Abstract:
Background: Cardiovascular disease (CVD) risk factors are associated with low serum 25 hydroxyvitamin D (25(OH)D) concentrations in observational studies; however, clinical trial findings are inconsistent. Objective: We assessed the effect of vitamin D supplementation and increased serum 25(OH)D concentrations on CVD risk factors in a systemic review and meta-analysis of randomized controlled trials (RCTs). Design: MEDLINE, CINAHL, EMBASE, and Google Scholar were searched for RCTs that evaluated vitamin D supplementation and cardiovascular outcomes [blood pressure, parathyroid hormone (PTH), serum high-sensitivity C-reactive protein (hs-CRP), total cholesterol, high and low density lipoprotein (HDL and LDL, respectively), triglycerides, peak wave velocity (PWV) and Augmentation Index (AI)] from 1992 through 2017. Meta-analysis was based on a random-effects model and inverse variance method to calculate standardized mean difference (SMD) as effect sizes, followed by a leave-one-out method for sensitivity analysis. Risk of publication bias was assessed using Cochrane checklist and Begg funnel plots. The systematic review is registered as CRD42015025346. Results: We identified 2341 studies from which 81 met inclusion criteria. The meta-analysis indicated a significant reduction in systolic blood pressure (SMD = -0.102 ± 0.04 mmHg, 95% confidence interval (CI), -0.20 to -0.03), diastolic blood pressure (SMD = -0.07 ± 0.03 mmHg, 95% CI, -0.14 to -0.006), serum PTH (SMD = -0.66 ± 0.08 ng/L, 95% CI, -0.82 to -0.49), hs-CRP (SMD = -0.20 ± 0.07 mg/L, 95% CI, -0.34 to -0.06), total cholesterol (SMD = -0.15 ± 0.06 mmol/L, 95% CI, -0.25 to -0.04), LDL (SMD = -0.10 ± 0.05 mmol/L, 95% CI, -0.20 to -0.003), triglycerides (SMD = -0.12 ± 0.06 mmol/L, 95% CI, -0.23 to -0.003) and a significant increase in HDL (SMD = 0.09 ± 0.04 mmol/L, 95% CI, 0.00 to 0.17) with vitamin D supplementation. These findings remained significant in sensitivity analyses for blood pressure, lipid profile, serum PTH, and serum hs-CRP. There was no significant effect of vitamin D supplementation on PWV (SMD = -0.20 ± 0.13 m/s, 95% CI, -0.46 to 0.06, p = 0.14) and AI (SMD = -0.09 ± 0.14%, 95% CI, -0.37 to 0.19, p = 0.52) for vitamin D supplemented groups. Conclusion: These findings suggest that vitamin D supplementation may act to protect against CVD through improving risk factors, including high blood pressure, elevated PTH, dyslipidemia, and inflammation.
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