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Published on: October 12, 2014
Pyridoxine improves endothelial function in cardiac transplant recipients
S E Miner1, D E Cole, J Evrovski
1Department of Medicine, University of Toronto, Toronto, Ontario, Canada.
Insights
Pyridoxine supplementation significantly improved endothelial function in cardiac transplant recipients, unlike folate. This suggests pyridoxine may help prevent transplant coronary artery disease by enhancing vascular health.
Area of Science:
- Cardiology
- Transplantation Medicine
- Vascular Biology
Background:
- Endothelial dysfunction is prevalent in cardiac transplant recipients and a predictor of transplant coronary artery disease.
- Hyperhomocysteinemia, common in transplant recipients, is linked to endothelial dysfunction and transplant coronary artery disease.
- Therapies reducing homocysteine may improve endothelial function and mitigate transplant coronary artery disease risk.
Purpose of the Study:
- To investigate the impact of folate or pyridoxine supplementation on endothelial function in cardiac transplant recipients.
Main Methods:
- A double-blind, randomized, placebo-controlled trial involving 31 cardiac transplant recipients.
- Participants were assigned to receive pyridoxine (100 mg/day), folate (5 mg/day), or placebo for 10 weeks.
- Endothelial function was assessed using brachial artery flow-mediated dilatation; homocysteine levels were also measured.
Main Results:
- Pyridoxine supplementation led to a significant improvement in endothelial function.
- No significant changes in homocysteine concentrations were observed in any group.
- Folate supplementation or placebo did not result in significant changes in endothelial function.
Conclusions:
- Pyridoxine supplementation, but not folate, significantly enhances endothelial function in cardiac transplant recipients.
- These findings suggest a potential therapeutic role for pyridoxine in managing endothelial dysfunction post-cardiac transplantation.
Background:
Endothelial dysfunction is common in cardiac transplant recipients and predicts the development of transplant coronary artery disease. Hyperhomocysteinemia is associated with endothelial dysfunction in the general population, is common in transplant recipients, and has been associated with transplant coronary artery disease. Thus therapy that decreases homocysteine concentrations might also improve endothelial function and decrease the risk of transplant coronary artery disease. Folate and pyridoxine are important cofactors in distinct aspects of homocysteine metabolism. The purpose of this study was to determine whether folate or pyridoxine supplementation improves endothelial function in cardiac transplant recipients.
Methods And Results:
This was a double-blind, randomized, placebo-controlled trial. We assigned 31 transplant recipients to either pyridoxine (n = 11:100 mg/day), folate (n = 12:5 mg/day), or placebo (n = 8) for 10 weeks. Fasting and post-methionine-load (methionine 100 mg/kg orally) homocysteine concentrations were determined. Brachial artery flow-mediated dilatation was used as a measure of endothelial function. At follow-up, we noted no significant changes in homocysteine concentrations in any of the groups. However, pyridoxine supplementation was associated with a significant improvement in endothelial function (2.8 +/- 6.7 to 6.9 +/- 6.3, p = 0.05). No significant changes were seen in patients treated with folate or placebo.
Conclusions:
Pyridoxine, but not folate supplementation, significantly improves endothelial function in cardiac transplant recipients.
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