# Combined B-vitamin supplementation on homocysteine and vascular outcomes in coronary heart disease: a meta-analysis

**Authors:** Liping Guo, Xiangfen Shi, Gaobiao Wang, Wenchao Han, Rui Ding, Shihao Wang, Dongdong Yuan

PMC · DOI: 10.1080/07853890.2026.2622208 · Annals of Medicine · 2026-01-30

## TL;DR

Combined B-vitamin supplements lower homocysteine and reduce vascular restenosis in heart disease patients, but do not significantly affect major cardiovascular events or mortality.

## Contribution

A meta-analysis showing combined B-vitamins reduce homocysteine and vascular restenosis in coronary heart disease.

## Key findings

- Combined B-vitamin supplementation significantly reduces serum homocysteine levels in CHD patients.
- The intervention group had lower vascular restenosis compared to controls.
- No significant effect on major cardiovascular events or mortality was observed.

## Abstract

Hyperhomocysteinemia (Hcy) independently predicts coronary heart disease (CHD) and adverse cardiovascular events. Although folic acid plays a key role in Hcy metabolism, the effect of combined B-vitamin supplementation (folic acid, VB6, and VB12) on clinical outcomes in CHD remains uncertain.

A systematic search of PubMed, Embase, and the Cochrane Library was conducted from inception through April 2025 using MeSH terms including “folic acid,” “vitamin B6,” “vitamin B12,” “coronary heart disease,” and “homocysteine.” A random-effects model was used for meta-analysis.

Thirteen studies involving 14,539 participants were included in the meta-analysis (7,338 patients treated with folic acid combined with vitamin B complex and 7,301 controls). Combined B-vitamin supplementation significantly reduced serum Hcy levels [mean difference: −2.36; 95% confidence interval (CI): (−3.09 to −1.62); p < 0.01] compared with any single-nutrient regimen. The incidence of vascular restenosis was lower in the intervention group than in the control group (risk ratio: 0.65; 95% CI: 0.44–0.95; p < 0.05). However, no significant differences were observed in the incidence of major cardiovascular events (p = 0.78) or cardiovascular-related mortality (risk ratio: 0.96; 95% CI: 0.85–1.07; p = 0.44).

Combined B-vitamin supplementation effectively lowers serum Hcy levels and the incidence of vascular restenosis in patients with CHD. However, its impact on cardiovascular events and mortality remains inconclusive.

Meta-analysis of 13 RCTs (n = 14,539): combined B vitamins lower serum Hcy

Combined B-vitamin supplementation lowers vascular restenosis in CHD patients

Exerts no significant impact on major CV events or mortality

Hcy-lowering appears CHD-specific; broader CV benefits remain unproven

## Linked entities

- **Chemicals:** folic acid (PubChem CID 135398658), vitamin B6 (PubChem CID 1054), vitamin B12 (PubChem CID 73415824)
- **Diseases:** coronary heart disease (MONDO:0005010)

## Full-text entities

- **Genes:** CTH (cystathionine gamma-lyase) [NCBI Gene 1491] {aka CGL, CSE}, MTR (5-methyltetrahydrofolate-homocysteine methyltransferase) [NCBI Gene 4548] {aka HMAG, MS, cblG}, CBS (cystathionine beta-synthase) [NCBI Gene 875] {aka HIP4}
- **Diseases:** venous thromboembolism (MESH:D054556), Hcy (MESH:D020138), DVT (MESH:D020246), lumen stenosis (MESH:D003251), cerebral infarction (MESH:D002544), vitamin B12 deficiency (MESH:D014806), Stroke (MESH:D020521), inflammation (MESH:D007249), endothelial injury (MESH:D057772), acute myocardial infarction (MESH:D009203), coronary artery stenosis (MESH:D023921), endothelial dysfunction (MESH:D014652), vascular restenosis (MESH:D006083), platelet aggregation (MESH:D001791), cardiovascular (MESH:D002318), Death (MESH:D003643), CHD (MESH:D003327), restenosis (MESH:D023903), atherosclerosis (MESH:D050197)
- **Chemicals:** B (MESH:D001895), PLP (MESH:D011732), vitamin B6 (MESH:D025101), Cysteine (MESH:D003545), B6 (-), methionine (MESH:D008715), glutathione (MESH:D005978), Vitamin B12 (MESH:D014805), FA (MESH:D005492), reactive oxygen species (MESH:D017382), Hcy (MESH:D006710), B12 (MESH:C034730), serine (MESH:D012694), 5-methyltetrahydrofolate (MESH:C005984), cystathionine (MESH:D003540)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** C677T

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## References

45 references — full list in the complete paper: https://tomesphere.com/paper/PMC12862861/full.md

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Source: https://tomesphere.com/paper/PMC12862861