Folic Acid Supplementation and the Risk of Cardiovascular Diseases: A Meta‐Analysis of Randomized Controlled Trials

Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Aug 2016
Citations:217
Influential Citations:11
Systematic Reviews / Meta-Analyses
81
S2 IconPDF Icon

Enhanced Details

Methods
Design: meta-analysis of randomized controlled trials (RCTs). Participants: 82,334 adults across 30 RCTs; mean age 50 years; 53% male; populations included individuals with preexisting cardiovascular disease, renal disease, or neither; trials conducted across North America, Europe, Asia, and Australia; follow-up durations varied; average folic acid supplementation duration across trials was 3.2 years.
Intervention
Folic acid supplementation, daily oral; dose ranged from 0.5 mg/day to 15 mg/day, with one ESRD trial using 40 mg/day; duration about 3.2 years on average (7 trials <2 years, 18 trials 2-4 years, 5 trials ≥5 years); regimens included folic acid alone or folic acid with vitamin B6 and/or B12.
Results
Folic acid supplementation reduced stroke risk by 10% (RR 0.90; 95% CI 0.84-0.96; P=0.002) and reduced overall cardiovascular disease risk by 4% (RR 0.96; 95% CI 0.92-0.99; P=0.02). No significant effect on coronary heart disease risk (RR 1.04; 95% CI 0.99-1.09; P=0.16). Benefits were greater among participants with lower baseline plasma folate and among those without preexisting CVD, and with larger reductions in homocysteine. The form of supplementation (folic acid alone vs with B vitamins) did not significantly modify CHD risk. Conclusion: folic acid provides a modest reduction in stroke and overall CVD risk, particularly in folate-deficient individuals or those without prior CVD; no clear CHD benefit.
Limitations
Limitations include heterogeneity across trials in fortification status, dosing regimens, and co-supplementation; variability in participant characteristics and outcome definitions; potential residual publication bias not fully excluded; not all trials reported homocysteine changes or MTHFR genotype data; some trials involved renal disease populations, which may limit generalizability.

Abstract

Background Results from observational and genetic epidemiological studies suggest that lower serum homocysteine levels are associated with lower incidence of cardiovascular disease (CVD). Numerous randomized controlled trials have investigated the ef...