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Oral L-arginine supplementation in acute myocardial infarction therapy: a meta-analysis of randomized controlled
Tao Sun1, Wen-Bai Zhou, Xin-Ping Luo
1Department of Cardiology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai 200040, P.R. China.
Insights
Oral L-arginine supplementation does not improve clinical outcomes for patients experiencing acute myocardial infarction (AMI). This meta-analysis found no significant difference in event rates or mortality between L-arginine and placebo groups.
Area of Science:
- Cardiovascular Research
- Clinical Nutrition
- Medical Interventions
Background:
- Oral L-arginine improves endothelial function in stable coronary artery disease (CAD).
- The efficacy of L-arginine in acute myocardial infarction (AMI), a form of unstable CAD, remains uncertain.
Purpose of the Study:
- To evaluate the impact of oral L-arginine supplementation on clinical outcomes in patients with AMI.
- To synthesize evidence from completed randomized controlled trials.
Main Methods:
- Systematic literature search of PubMed, Cochrane Library, Embase, and reference lists.
- Meta-analysis of randomized, placebo-controlled trials involving L-arginine supplementation in AMI patients.
- Independent assessment of trials by two reviewers, with consensus for discrepancies.
Main Results:
- Two trials with 927 participants were included in the meta-analysis.
- No significant difference in event rates was observed between L-arginine and placebo groups.
- A non-significant 7% reduction in mortality was noted in the L-arginine group (RR: 0.93, 95% CI: 0.74-1.17).
Conclusions:
- Oral L-arginine supplementation demonstrates no significant effect on clinical outcomes for patients with acute myocardial infarction.
- Current evidence does not support the use of L-arginine for improving outcomes in AMI patients.
Objective:
The objective was to analyze completed trials assessing the effect of oral L-arginine supplementation on clinical outcomes of patients with acute myocardial infarction (AMI).
Background:
Prior trials suggest that oral L-arginine administration improves endothelial function in patients with stable coronary artery disease (CAD). However, it is still unclear whether oral supplementation of L-arginine has any effect on clinical outcomes in patients with unstable CAD, such as AMI.
Methods:
We systematically searched PubMed, Cochrane Library, Embase, reviews, and reference lists of relevant articles. The search strategy paired the term "arginine" with the following: "coronary heart disease," "myocardial infarction," "cardiovascular disease," "ischemia," and "trial." We conducted a meta-analysis of randomized, placebo-controlled L-arginine supplementation trials that evaluated clinical outcomes in AMI patients. Two reviewers independently assessed the trials. Differences were resolved by consensus.
Results:
Only 2 trials (927 participants) were included. None of the 2 studies showed a significant difference in event rate between the L-arginine and placebo groups. In an overall pooled estimate, there was a 7% reduction in mortality in the L-arginine treatment group (105/459, 22.9%) compared with the control group (111/455, 24.4%), which did not reach statistical significance (risk ratio [RR]: 0.93, 95% confidence interval [CI]: 0.74-1.17; P = 0.54).
Conclusion:
Oral L-arginine supplementation has no effect on the clinical outcomes of patients with AMI.
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